用于治疗或预防人乳头瘤病毒感染的多型HPV肽的组合物和方法与流程

文档序号:11245025阅读:1924来源:国知局
用于治疗或预防人乳头瘤病毒感染的多型HPV肽的组合物和方法与流程
本申请是中国专利申请cn200880120046.x的分案申请,原申请是国际申请号pct/us2008/082290于2010年6月10日进入中国国家阶段的申请。本申请要求2007年11月2日提交的美国临时专利申请序列号61/001,630和61/001,629的优先权,其通过引用全部并入本文中。本发明得到美国国立卫生研究院(nih)资助的基金号为p50ca098252的政府支持。政府享有本发明中的某些权益。本发明的实施方案一般地涉及生物学和医学。在本发明的某些实施方案中涉及使用多型(multitype)hpv多肽的组合物和方法。
背景技术
:生殖器热带人乳头瘤病毒(hpv)感染被认为是美国最常见的性传播感染(疾病预防控制中心(cdc)向国会的报告,preventionofgenitalhumanpapillomavirus,2004年1月)。肛门生殖器hpv的主要表现包括:生殖器疣(尖锐湿疣)以及外阴、宫颈、肛门或阴茎的上皮内赘生物。小部分持续高风险hpv感染,如果未得到治疗的话,将发展为癌症(例如,宫颈癌,偶尔是头颈癌,以及某些类型的非黑素瘤皮肤癌)。据报道,全球范围内99.7%的宫颈癌中存在hpv的dna,这提示hpv感染是这种癌症的必要原因,并且可利用预防性hpv疫苗接种来预防该疾病(walboomers等,1999)。除了生殖器疣以外,hpv感染可导致寻常疣、跖疣或平疣(planarwart)。疣可以不同的形式存在,这取决于相关的hpv类型和所涉及的上皮。寻常疣(verrucavulgaris)通常发生在手上,呈肉色至褐色、外生型的角化过度丘疹(hyperkeratoticpapule)。跖疣(verrucaplantaris)出现在脚底,可能会非常疼。通过去除表层显露出形成血栓的毛细血管,可将它们与胼胝进行区分。扁平疣或平疣(verrucaplana)在儿童中最常见,可发生于面部、颈部、胸部以及前臂和腿的屈肌表面。在多于100种hpv亚型中约35种是特异性针对肛门生殖器上皮的并具有不同的恶性病变潜能(munoz等,2003)。在15种致癌生殖器hpv类型中,hpv16是最常见的,其次是hpv18和hpv45(分别占宫颈癌病例的~50%、~20%和~10%)。尽管通过实施宫颈细胞学筛查方案来减少宫颈癌发生率和死亡率的公众卫生努力已取得成功,然而未接受定期筛查的女性占侵袭性癌患者的大多数(hoffman和cavanagh,1995),并且宫颈癌仍是全球范围内第二常见的妇女癌症死亡原因以及撒哈拉以南非洲、中美洲、南-中亚和美拉尼西亚(大洋洲的分区,从西太平洋西侧延伸至阿拉弗拉海(arafurasea),澳大利亚以北和东北;该称谓最初用于指示区别于波利尼西亚和密克罗尼西亚的种族和地理集群)妇女中最普遍的癌症(parkin,2001)。每年诊断出约471,000个侵袭性宫颈癌病例(parkin,2001)。hpv基因组被60nm的无包膜二十面体衣壳所包绕(baker等,1991),所述衣壳包含两种遗传上不相关的主要衣壳蛋白l1和次要衣壳蛋白l2。重组l1自组装成病毒样颗粒(vlp),其在形态上和免疫学上与天然病毒粒子类似(kirnbauer等,1992)。基于l1vlp的疫苗对用于产生该免疫原之乳头瘤病毒类型对应的感染具有高度保护性(同源疫苗),但是对除了最密切相关之hpv类型以外的所有hpv类型都无效(roden等,2000)。经许可的hpv疫苗已通过设计多价疫苗制剂规避了这一障碍;cervarixtm包含源自hpv16和hpv18的l1vlp,而gardasiltm还含有用于预防良性生殖器疣的hpv6和hpv11l1vlp。遗憾的是,目前这些l1vlp疫苗的费用以及需要冷藏的事实使得将其用于最需要它们的资源缺乏的偏远地区变得不实际。此外,由于这些疫苗对致癌hpv类型的相当一部分是无效的,因此昂贵的细胞学筛查方案仍是必要的。为了在全球范围内实现全面有效的hpv预防,疫苗应该是安全有效的,其在环境温度下是稳定的从而有利于运送至偏远地区,制造成本低廉,无需针即可施用,优选采用单剂量制剂的形式。由众多的hpv类型带来的疾病负担表明广泛保护的疫苗是必需的。因此,需要另外的交叉中和性hpv疫苗。技术实现要素:本发明的实施方案涉及多型肽组合物。本发明的另一些实施方案涉及这些多型肽组合物作为免疫原或疫苗的用途。本发明的多型肽组合物包含代表病原生物之多种同种型或类型或者生物之不同免疫原性肽的两种或更多种肽(免疫原性肽,即诱导对象中免疫应答的肽)。所述生物可以是多种类型或变体的靶标生物、同属生物或同科生物。在另一些方面,所述肽可来自不同的病原性生物(例如hpv和hsv)。在某些方面,不同的病原性生物在传播方式(例如性传播疾病(sexuallytransmitteddisease,std))或者被感染的器官或器官系统(例如生殖系统、皮肤等)方面是相关的。一方面,所述多型肽组合物可以包含源自多种生物变体或类型的多种肽,使其具有广泛的交叉中和性免疫应答。hpv类型的交叉中和是此类交叉中和性多型肽组合物的一个实例。在另一些方面,多型肽组合物可包含源自不同病原体的肽,例如性传播病毒、细菌或真菌,其包括但不限于乳头瘤病毒(pv)、hpv、巨细胞病毒(cmv)、疱疹病毒、乙型肝炎病毒、人免疫缺陷病毒(hiv/aids)、卡波西氏肉瘤相关疱疹病毒(kshv/hhv8)、软下疳(软下疳嗜血杆菌(haemophilusducreyi))、多诺万病(donovanosis)(腹股沟肉芽肿(granulomainguinale)或肉芽肿鞘杆菌(calymmatobacteriumgranulomatis))、淋病(淋病奈瑟菌(neisseriagonorrhoeae))、淋巴肉芽肿(lymphogranulomavenereum,lgv)(沙眼衣原体(chlamydiatrachomatis))、非淋球菌性尿道炎(non-gonococcalurethritis,ngu)(解尿素支原体(ureaplasmaurealyticum)或人型支原体(mycoplasmahominis))、金黄色葡萄球菌、梅毒(梅毒螺旋体(treponemapallidum))等。hpv是可通过使用本文所述的多型肽组合物进行靶向的生物的一个实例。hpv感染导致了世界范围内人类癌症的5%。细胞学(pap)筛查可鉴定并随之切除宫颈癌癌前病变。如经许可疫苗gardasiltm(merck)和cervarixtm(gsk)所描述地,预防hpv感染将消除hpv相关癌症及其癌前病变。然而,所述经许可疫苗源自l1衣壳蛋白,并且仅靶向一部分致癌hpv类型(因此仍然需要pap筛查方案)。本发明人描述了基于施用多型hpvl2肽组合物而广泛地预防良性和致癌性hpv感染及其后遗症的组合物和方法。所述多型hpvl2肽组合物将包含源自两种或更多种hpv类型的多种多肽区段。所述区段或肽可以来自同源多肽的相应区域(即,来自另一类型或变体之生物的、与第一多肽功能等价的多肽),或者可来自同源多肽的不同区段,或者可以来自不同类型的不同多肽。所述多肽区段(或肽)可以通过缀合或制备成融合蛋白、脂质体、纳米颗粒、聚合物或肽树状分子(dendrimer)(分支多肽)来构建成多型肽组合物。在某些实施方案中,分离的多肽组合物包含来自至少2、3、4、5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、21、22、23、24、25、26、27、28、29、30、40、50、60、70、80、90、100、200或更多种不同分离物或类型之感染性生物之对应或同源多肽的至少2、3、4、5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、21、22、23、24、25、26、27、28、29、30、40、50、60、70、80、90、100、200或更多种免疫原性肽,其中含有第一多肽之第一肽的氨基酸序列的第一免疫原性肽可与来自第二多肽的第二对应或同源免疫原性肽有效偶联。“有效偶联”是指肽直接或间接地与第二肽连结。例如,与第二多肽连结的官能团可通过其部分(例如肽键)与第一肽或表面直接连结。或者,官能团可经由中间组分与肽或表面连结,所述中间组分使官能团与肽或表面连结。这种中间组分常称为“接头”。接头是双功能性分子,其可具有与第一肽化学连结的一个部分以及与官能团化学连结的第二部分。本发明涵盖任意数目的中间组分,并且这是本领域技术人员已知的。在一个实施方案中,本发明人描述了用于预防多种pv类型感染的多型pv肽组合物。在某些方面,多型pv肽组合物是包含来自不同pv类型之两种或更多种pv蛋白区段或免疫原性肽的非天然多肽,其被构建成线性(串联体(concatamer))或分支多肽结构,多型pvl2多肽。所述pvl2肽可包括如下病毒之l2蛋白质的所有或部分氨基酸序列:乳多空病毒科;多瘤病毒科;乳头瘤病毒科和/或α属或β、γ、δ、ε、ζ、η、θ、ι、κ、λ、μ、ν、ξ、o、π属的乳头瘤病毒(参见devilliers等,classificationofpapillomaviruses.virology.2004年6月20日;324(1)∶17-27);和/或人乳头瘤病毒:hpv1,hpv2,hpv3,hpv4,hpv5,hpv6,hpv7,hpv8,hpv9,hpv10,hpv11,hpv12,hpv13,hpy14,hpv15,hpv16,hpv17,hpv18,hpv19,hpv20,hpv21,hpv22,hpv23,hpv24,hpv25,hpv26,hpv27,hpv28,hpv29,hpv30,hpv31,hpv32,hpv33,hpv34,hpv35,hpv36,hpv37,hpv38,hpv39,hpv40,hpv41,hpv42,hpv43,hpv44,hpv45,hpv46,hpv47,hpv48,hpv49,hpv50,hpv51,hpv52,hpv53,hpv54,hpv55,hpv56,hpv57,hpv58,hpv59,hpv60,hpv61,hpv62,hpv63,hpv64,hpv65,hpv66,hpv67,hpv68,hpv69,hpv70,hpv71,hpv72,hpv73,hpv74,hpv75,hpv76,hpv77,hpv78,hpv79,hpv80,hpv81,hpv82,hpv83,hpv84,hpv85,hpv86,hpv87,hpv88,hpv89,hpv90,hpv91,hpv92,hpv93,hpv94,hpv95,hpv96,hpv97,hpv98,hpv99,hpv100,hpv101,hpv102,hpv103,hpv104,hpv105,hpv106,hpv107,hpv108,hpv109,hpv110,hpv111;和/或动物乳头瘤病毒:1型牛乳头瘤病毒(bpv1)、2型牛乳头瘤病毒(bpv2)、4型牛乳头瘤病毒(bpv4)、棉尾兔乳头瘤病毒(crpv)、鹿乳头瘤病毒(dpv)、欧洲麇鹿乳头瘤病毒(eepv)、犬口腔乳头瘤病毒(copv)、恒河猴乳头瘤病毒(rhpv)和兔口腔乳头瘤病毒(ropv)。本发明的pv抗原或表位或肽或多肽区段可包含乳头瘤病毒l2多肽(例如seqidno:1-70)的5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、25、30、35、40、45、50、55、60、65、70、75、80、85、90、95、100、125、150、200、250、300、350、400、450、500个连续氨基酸,并包括其间的所有数值和范围。在另一方面,多肽区段可包含l2多肽(例如seqidno:1-70)的至多、至少或大约氨基酸位置1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139,140,141,142,143,144,145,146,147,148,149,150,151,152,153,154,155,156,157,158,159,160,161,162,163,164,165,166,167,168,169,170,171,172,173,174,175,176,177,178,189,180,181,182,183,184,185,186,187,188,189,190,191,192,193,193,194,195,196,197,198,199,200,201,202,203,204,205,206,207,208,209,210,211,212,213,214,215,216,217,218,219,220,221,222,223,224,225,226,227,228,229,230,231,232,233,234,235,236,237,238,239,240,241,242,243,244,245,246,247,248,249,250,251,252,253,254,255,256,257,258,259,260,261,262,263,264,265,266,267,268,269,270,271,272,273,274,275,276,277,278,289,280,281,282,283,284,285,286,287,288,289,290,291,292,293,293,294,295,296,297,298,299,300,301,302,303,304,305,306,307,308,309,310,311,312,313,314,315,316,317,318,319,320,321,322,323,324,325,326,327,328,329,330,331,332,333,334,335,336,337,338,339,340,341,342,343,344,345,346,347,348,349,350,351,352,353,354,355,356,357,358,359,360,361,362,363,364,365,366,367,368,369,370,371,372,373,374,375,376,377,378,389,380,381,382,383,384,385,386,387,388,389,390,391,392,393,393,394,395,396,397,398,399,400,401,402,403,404,405,406,407,408,409,410,411,412,413,414,415,416,417,418,419,420,421,422,423,424,425,426,427,428,429,430,431,432,433,434,435,436,437,438,439,440,441,442,443,444,445,446,447,448,449,450,451,452,453,454,455,456,457,458,459,460,461,462,463,464,465,466,467,468,469,470,471,472,473,474,475,476,477,478,489,480,481,482,483,484,485,486,487,488,489,490或更多至氨基酸位置10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,89,80,81,82,83,84,85,86,87,88,89,90,91,92,93,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139,140,141,142,143,144,145,146,147,148,149,150,151,152,153,154,155,156,157,158,159,160,161,162,163,164,165,166,167,168,169,170,171,172,173,174,175,176,177,178,189,180,181,182,183,184,185,186,187,188,189,190,191,192,193,193,194,195,196,197,198,199,200,201,202,203,204,205,206,207,208,209,210,211,212,213,214,215,216,217,218,219,220,221,222,223,224,225,226,227,228,229,230,231,232,233,234,235,236,237,238,239,240,241,242,243,244,245,246,247,248,249,250,251,252,253,254,255,256,257,258,259,260,261,262,263,264,265,266,267,268,269,270,271,272,273,274,275,276,277,278,289,280,281,282,283,284,285,286,287,288,289,290,291,292,293,293,294,295,296,297,298,299,300,301,302,303,304,305,306,307,308,309,310,311,312,313,314,315,316,317,318,319,320,321,322,323,324,325,326,327,328,329,330,331,332,333,334,335,336,337,338,339,340,341,342,343,344,345,346,347,34g,349,350,351,352,353,354,355,356,357,358,359,360,361,362,363,364,365,366,367,368,369,370,371,372,373,374,375,376,377,378,389,380,381,382,383,384,385,386,387,388,389,390,391,392,393,393,394,395,396,397,398,399,400,401,402,403,404,405,406,407,408,409,410,411,412,413,414,415,416,417,418,419,420,421,422,423,424,425,426,427,428,429,430,431,432,433,434,435,436,437,438,439,440,441,442,443,444,445,446,447,448,449,450,451,452,453,454,455,456,457,458,459,460,461,462,463,464,465,466,467,468,469,470,471,472,473,474,475,476,477,478,489,480,481,482,483,484,485,486,487,488,489,490,491,492,493,494,495,496,497,498,499,500或更多。在又一方面中,l2肽包括这样的多肽区段,所述多肽区段包含本文seqidno:1中公开之l2多肽或seqidno:2-70之对应区域或其共有序列的至多、至少或大约17-36、13-45、11-88或11-200位氨基酸。每个位置可以是大致的氨基酸位置,并且可以在±1、2、3、4、5、6、7、8、9、10或更多个氨基酸位置内变化。氨基酸位置的确定是基于针对hpv16l2蛋白质(seqidno:1)的编号。来自其它hpv类型的l2蛋白的氨基酸位置可以不同,但是本领域技术人员能够将任意l2氨基酸序列与hpv16进行比对,并确定对应于hpv16l2氨基酸位置的肽序列。在某些实施方案中,所述l2肽是hpv16l2蛋白质(seqidno:1)的区段、hpv18l2蛋白质(seqidno:2)的区段、hpv45l2蛋白质(seqidno:3)的区段、hpv6l2蛋白质(seqidno:9)的区段、hpv1l2蛋白质(seqidno:4)的区段、hpv2l2蛋白质(seqidno:5)的区段、hpv63l2蛋白质(seqidno:62)的区段、hpv5l2蛋白质(seqidno:8)的区段、hpv8l2蛋白质(seqidno:11)的区段、hpv11l2蛋白质(seqidno:14)的区段、hpv31l2蛋白质(seqidno:32)的区段、hpv33l2蛋白质(seqidno:34)的区段、hpv35l2蛋白质(seqidno:36)的区段、hpv39l2蛋白质(seqidno:40)的区段、hpv51l2蛋白质(seqidno:50)的区段、hpv52l2蛋白质(seqidno:51)的区段、hpv56l2蛋白质(seqidno:55)的区段、hpv58l2蛋白质(seqidno:57)的区段、hpv59l2蛋白质(seqidno:58)的区段、hpv68l2蛋白质(seqidno:66)的区段、hpv73l2蛋白质(seqidno:69)的区段和/或hpv82l2蛋白质(seqidno:70)的区段。在某些方面中,多型多肽具有如下通式:[表位x(a)-l-表位x+1(b)-l-表位x+n(c)](d),其中a和/或b和/或c和/或d彼此独立地是1、2、3、4、5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、21、22、23、24、25;n独立地是1~98;肽x、肽x+1、肽x+n是选自一种或多种性传播生物的不同免疫原性表位;(l)可代表接头、化学偶联、肽键。该式的肽可源自同种蛋白质或源自同种生物或病原体的不同蛋白质,或者这些肽可源自不同病原生物的同源或异源蛋白质。在一个实施方案中,肽x是hpv多肽;肽x+1是不同的hpv肽或来自另一病原生物的肽;肽x+n是来自任意hpv类型或其它病原生物的一种或多种其它不同肽。所述“-l-”代表接头、化学接头、肽接头、化学偶联或多肽融合情形中的肽键,或者本领域已知的肽-肽连接或肽-基质连接的其它偶联或连接方式。本发明的实施方案包括seqidno:71-92、94-106和/或110-112的两种或更多种肽序列的至多、至少或大约2、3、4、5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、21、22、23、24、25、50、100、150、200、250、500或更多。在另一些方面,本发明的肽包括seqidno:1-70和其它hpvl2多肽的对应序列。在某些方面,l2多肽区段与seqidno:71-92、94-106、110-112和/或seqidno:1-70的对应序列和/或seqidno:1-70的区段和/或其它pvl2多肽或其区段具有至少或大于50%、55%、60%、65%、70%、75%、80%、85%、90%、91%、92%、93%、94%、95%、96%、97%、98%、99%或100%的同一性。可使用一种或多种所述多肽作为预防、治疗或防止乳头瘤病毒感染的疫苗组合物。在某些方面中,所述组合物可以与药物载体联用。在暴露于乳头瘤病毒之前向个体施用所述疫苗组合物以最小化或防止乳头瘤病毒感染,或者在患者已感染之后施用以降低感染的严重程度以及延缓/阻止疾病的发展或者防止乳头瘤病毒从被感染宿主向另一未被乳头瘤病毒感染的个体传播。本文所用的术语“抗原”或“免疫原性肽”是能够与抗体或t细胞受体结合的分子。抗原还能诱导体液免疫应答和/或细胞免疫应答,导致b淋巴细胞和/或t淋巴细胞的产生。引起生物应答的抗原结构方面在本文中称作“抗原决定簇”。b淋巴细胞通过产生抗体对外来抗原决定簇产生应答,而t淋巴细胞是细胞免疫的媒介物。因此,抗原决定簇或表位是被抗体(在mhc情形中,是被t细胞受体)所识别的抗原部分。通常,抗原是源自病原生物(例如hpv)表达之蛋白质的肽。抗原决定簇不必是连续的蛋白质序列或区段,其可包含彼此不紧邻的多种序列。在某些方面中,抗原决定簇是pv多肽区段、pv肽。对于特定的氨基酸序列来说,“表位”是这样一组氨基酸残基,其参与特定免疫球蛋白的识别,或者在t细胞的情形中,其为t细胞受体蛋白和/或主要组织相容性复合物(mhc)受体识别所必需的那些残基。表位的氨基酸残基不必是连续的。在体内或体外的免疫系统设置中,表位是分子的综合特征,例如一级、二级和三级肽结构以及电荷,其共同形成被免疫球蛋白、t细胞受体或hla分子识别的位点。在本公开通篇中,“表位”和“肽”常互换使用。本文所用的“b细胞表位”或“靶表位”是指在针对含某抗原(例如hpvl2区段或其亚区域)之肽的免疫应答中被b细胞受体识别的该肽或蛋白质的特征结构。本文所用的“hpv”和“人乳头瘤病毒”是指能够感染人类的乳头瘤病毒(pv)属的成员。有两个主要的hpv群(生殖器群和皮肤群),其中每个群含有多种病毒“类型”或“毒株”(例如hpv16、hpv18、hpv31、hpv32等)。本发明中特别关注的是与生殖器感染和恶性病变有关的hpv类型。术语“疫苗”是指含有1、2、3、4、5、6、7、8、9、10或更多种本发明多型hpv肽组合物的制剂。所述多型hpv肽组合物通常采用能够向对象施用的形式,并诱导保护性或治疗性免疫应答,所述应答足以诱导免疫力来预防和/或改善感染和/或减少感染的至少一种症状和/或增强另一抗hpv治疗的功效和/或减弱hpv感染和/或减弱hpv的传播性。通常,疫苗含有本发明组合物混悬或溶解于其中的常规盐水或缓冲水溶液介质。在另一些方面,所述疫苗可以是固体(例如粉末或冻干制剂)。本发明的组合物可方便地用于预防、改善或治疗感染。在引入宿主后,所述组合物能够激发免疫应答,包括但不限于抗体和/或细胞因子的产生和/或细胞毒t细胞、抗原递呈细胞、辅助t细胞、树突细胞的活化和/或其它细胞应答。本文所用的“预防性”疫苗或组合物是设计并施用以预防由病原生物(特别是hpv)引起或与之相关的感染、疾病和/或任何相关后遗症的组合物。本文所用的“治疗性”疫苗或组合物是设计并向已感染病原生物(例如至少一种hpv毒株)的患者施用的组合物。治疗性疫苗(例如治疗性hpv疫苗)用于预防和/或治疗这些被感染对象中良性或恶性肿瘤的进展。当用于权利要求和/或说明书中时,术语“抑制”、“减少”或“预防”或这些术语的任何变型包括任何可测量的降低或完全抑制以实现期望的结果。在权利要求和/或说明书中,当单数名词与术语“包括(包含)”联用时可表示“一个(种)”,也可表示“一个(种)或更多”、“至少一个(种)”以及“一个(种)或多于一个(种)”的含义。在本申请通篇中,术语“约”用于表示数值包括用于确定该数值之设备或方法的标准误差。在权利要求中,术语“或”用于表示“和/或”,除非明确指明仅指替代方案中之一或者各替代方案间相互排斥,但是本公开支持这样的定义,即仅指替代方案以及“和/或”。还应考虑的是,使用术语“或”列出的任何内容还可具体排除。如本说明书和权利要求中所用,表述“包含”(以及“包含”的任何形式,例如“含有”和“含”)、“具有”(以及“具有”的任何形式,例如“有”)、“包括”(以及“包括”的任何形式,例如“涵盖”)或“含有”(以及“含有”的任何形式,如“包含”和“含”)是开放式的,不排除其它未引述的元件或方法步骤。应考虑,本文列出的一个或多个成员可以从本发明的保护范围中特定排除或囊括在其中。本发明的另一些实施方案在本申请通篇中进行了论述。就本发明之一个方面所讨论的任何实施方案也适用于本发明的其它方面,反之亦然。实施例部分中的实施方案应当理解为可适用于本发明所有方面的本发明实施方案。通过如下详细描述,本发明的其它目的、特征和优点将显而易见。然而,应当理解,当涉及本发明具体实施方案时,所述详细描述和具体实施例仅通过举例说明的方式给出,这是因为,通过该详细描述,本发明精神和范围内的各种变动和修改对本领域技术人员是显而易见的。附图说明以下附图构成本说明书的一部分,并进一步说明本发明的某些方面。通过参考这些附图中的一幅或多幅并结合本文中对具体实施方案的详细描述,可以更好地理解本发明。图1.用多型l2疫苗接种小鼠诱导出比单体l2疫苗或l1vlp更广泛交叉中和性的抗体。在第0、15、30天用pbs或者gpi-0100(50μg)佐剂中的25μg不同的l2单体构建物和多型构建物或者无佐剂的hpv16l1vlp或hpv45l1vlp皮下接种balb/c小鼠。使用所示基因型的hpv假病毒,利用从最终免疫两周后的小鼠中收集的两倍稀释的抗血清进行体外中和测定。图示实现50%中和的终点效价。图2.单独的多型l2蛋白质是免疫原性的,并且对于广泛中和性抗体应答来说,其不需要特别的佐剂。在第0、15和30天时,仅用明矾(alum)(1.3mg)或者仅用iss1018(10μg/小鼠)或者pbs或者仅用25μg11-200×3(seqidno:113)或者与明矾(1.3mg)或与iss1018(10μg/小鼠)或与gpi-0100(50μg/小鼠或200μg/小鼠)或与gpi-0100(50μg/小鼠)+tween40(1mg/小鼠)或与明矾和iss1018(10μg/小鼠)一起配制的25μg11-200×3(seqidno:113)皮下接种balb/c小鼠。使用所示基因型的hpv假病毒,利用从最终免疫两周后的小鼠中所收集抗血清的两个稀释度进行体外中和测定。图示实现50%中和的终点效价。图3.用与不同佐剂联用的l211-200×3(seqidno:113)接种小鼠4个月后,进行体内hpv16假病毒攻击。用pbs或不同佐剂中的25μgl211-200×3(seqidno:113)或仅用佐剂,以两周为间隔,接种小鼠3次。以下列出从左至右的各组:仅用pbs、仅用明矾(1.3mg)、仅用iss1018(10μg/小鼠)、仅用11-200×3(seqidno:113)、11-200×3(seqidno:113)+iss1018(10μg/小鼠)、11-200×3(seqidno:113)+明矾(1.3mg)、11-200×3(seqidno:113)+gpi-0100(50μg/小鼠)、11-200×3(seqidno:113)+gpi-0100(200μg/小鼠)、11-200×3(seqidno:113)+gpi-0100(50μg/小鼠)+tween40(1mg/小鼠)、11-200×3(seqidno:113)+明矾+1018(10μg/小鼠)。免疫约4个月后,用电动剃刀剃去每只经麻醉balb/c小鼠腹部上一小片毛发,但不伤到上皮。然后,用10μl0.6%羧甲基纤维素中的3×109hpv16假病毒粒子(100ng)(带有萤光素酶报告构建物)攻击小鼠。三天后,麻醉小鼠并注射萤光素,使用xenogenivis200获得10分钟图像。使用livingimage2.20软件分析包含接种位点的大小相等区域,并对较之于用hpv16l1接种的小鼠受攻击前的相对发光单位来作图。图4.与gardasiltm相比,用l211-200×3(seqidno:113)或11-88×5(seqidno:108)接种小鼠诱导出较低但更广泛交叉中和性的抗体。在第0、15和30天时,用1/5人剂量的gardasiltm或用gpi-0100(50μg)佐剂中的25μgl211-200×3(seqidno:113)或11-88×5(seqidno:108)接种小鼠3次。使用所示基因型的hpv假病毒,利用从最终免疫两周后的小鼠中所收集抗血清的两个稀释度进行体外中和测定。图示实现50%中和的终点效价。具体实施方式第一代hpvl1病毒样颗粒疫苗花费高并且保护类型受限,这使得有必要开发其它广泛保护性的第二代组合物和疫苗。次要衣壳蛋白l2通过诱导中和性抗体来保护动物免于乳头瘤病毒的攻击。尽管l2诱导交叉中和多种乳头瘤病毒类型的抗体,然而本发明人观察到,较之于与进化相关性小的类型,l2特异性抗体通常更有效地中和相关类型。为了增强交叉保护,l2融合蛋白被设计成由不同hpv类型的已知交叉中和性表位组成。将用包含17-36、1-88或11-200位残基的hpv16l2多肽接种与用三种多型l2融合蛋白(11-200×3(seqidno:113)类型(hpv6、16、18)、11-88×5(seqidno:108)类型(hpv1、5、6、16、18)、17-36×22类型(5种皮肤类型、2种粘膜低风险类型和15种致癌类型))接种进行比较。用gpi-0100佐剂中的25μg抗原皮下接种小鼠三次。在所有单型(monotype)多肽中,11-200产生最高的hpv16中和效价。然而,和与其它多型和单型融合蛋白相比,11-200×3诱导出针对hpv45和hpv58以及hpv16、hpv18、hpv6的最高中和效价。用表达萤光素酶的hpv16假病毒攻击经免疫小鼠。使用11-200×3(seqidno:113)接种保护小鼠免于hpv16以及hpv16l1vlp的攻击。对仅用25μg11-200×3(seqidno:113)蛋白或者与明矾或与50μg或200μggpi-0100或50μggpi-0100+tween-40一起接种后所诱导的hpv中和抗体进行比较。佐剂的存在显著加强了针对11-200×3的体液应答,但是佐剂之间没有显著差异。本发明人得出结论,使用与佐剂一起配制的、包含由大肠杆菌产生的hpv6l211-200(seqidno:96)、hpv16l211-200(seqidno:100)和hpv18l211-200(seqidno:101)的单一融合蛋白进行接种是保护性的并且诱导广泛交叉中和性的抗体。还考虑到,这种多型hpv组合物可用于其它病原生物(特别是那些与hpv感染方式相同之疾病(如性传播疾病)相关的病原生物)或用作其模型。因此,本申请有关hpv或多型hpvl2肽的教导可以延伸至其它病原生物。i.治疗性和预防性组合物本发明的实施方案包括含有来自两个或更多hpv类型之两种或更多种hpv多肽区段的hpv肽组合物。在某些方面,所述hpv类型包括对于施用该组合物的特定生物或动物或人对象是致病性的所有或某些hpv类型。在某些实施方案中,所述hpv多肽包含至少两种l2表位或肽。在又一方面,所述hpv多肽包括来自至少两个hpv类型的l2表位。hpv多肽区段在本文中有详细描述。本发明的方法包括治疗由乳头瘤病毒感染(例如hpv感染)引起的或与之相关的疾病或病症。可提供免疫原性多型hpv肽组合物和/或与之结合的抗体在感染有hpv或者疑似暴露于hpv或者处于感染或暴露于hpv风险的人中诱导或提供治疗性应答。该方法可应用于经测试为hpv暴露或其它性传播疾病呈阳性的个体、或者基于可能的暴露或将来的暴露被认定具有感染风险的个体。特别地,本发明包括治疗hpv感染的方法。在某些实施方案中,所述治疗在佐剂或载体或其它抗原(hpv抗原或来自其它病原体(具有与hpv暴露风险相关或一起发生的暴露风险)的抗原存在下施用。此外,在一些实例中,治疗包括施用常用于抗病毒感染的其它药剂,例如一种或多种抗病毒剂。在本发明的某些方面,对本发明的肽进行构建,从而使多种肽以彼此接近的形式呈递给免疫系统的组分。每种肽可刺激免疫系统的多种组分(两种或更多种效应细胞)或免疫系统的单一组分(倾向于识别多种类型或变体之肽的效应细胞)。所述肽可以构建成线性串联体、分支串联体(树状分子)、支持物或基底(例如纳米颗粒、脂质体、聚合物等)的突起物(projection)。识别位点或肽的数目以整体呈现,其间距将决定肽的寡聚程度。例如,四价实体(例如链亲和素)会得到四聚体。然而,更高价也是可能的。优选地,肽的数目在2、3、4、5、6、7、8、9、10至10、20、25、50或更多的范围内(包括其间所有范围)。在某些实施方案中,多型肽组合物是天然聚合物或其衍生物,例如蛋白质、分支多肽(树状分子)、多聚蛋白质或编码这些的核酸。多数肽可以附着至多糖例如葡聚糖、淀粉、纤维素、透明质酸、甲壳素或海藻酸或这些多糖的衍生物;合成聚合物例如聚丙二醇、聚乙二醇(peg);磷脂膜,例如囊泡或脂质体;以及无机颗粒例如聚苯乙烯或丙烯酸珠或磁珠。在某些方面,多型多肽是树状分子。这些树状分子可以例如根据weng和peter,white编,“fmocsolidphasepeptidesynthesis,apracticalapproach”oxforduniversitypress(2000)中第11章“chemoselectiveandorthogonalligationtechniques″以及美国专利公开20080207485”中公开的方案来制备,其通过引用并入本文。用于合成分支多肽的一些其它方法对于本领域技术人员来说是公知的。分支多肽在其两个或更多分支中的预定位点处并入肽。肽的每个分支可具有期望的长度。优选地,各分支的长度小于24个氨基酸。肽的分支可受到通过已知方法利用lys残基在合成期间对肽进行分支的影响。以这种方式,肽在第一赖氨酸残基上分成两个分支,又在另一赖氨酸残基上进行分支,从而形成四价实体。通过包括更多或更少的分支步骤可形成其它价(例如八聚体)。通过对合成肽进行部分分支还可以获得奇数价。在某些实施方案中,多肽的一个或多个末端附着至支持物或基底,例如在一个方面形成从支持物延伸出的多肽环。本发明的肽可包含在不同的递送载体或形式(例如病毒样颗粒(vlp)或脂质体)中,或者在生物可降解颗粒的表面上,或者在珠或微粒或纳米颗粒的表面上。a.感染性病原体本文所用的“感染”或“感染性疾病”是指由感染性生物经表面、局部或系统性侵入宿主而引起的疾病。感染性生物包括细菌、病毒、寄生物、真菌和原生动物。细菌包括革兰氏阴性细菌和革兰氏阳性细菌。革兰氏阳性细菌的实例包括但不限于巴氏杆菌属(pasteurella)物种、葡萄球菌属(staphylococcus)物种包括金黄色葡萄球菌(staphylococcusaureus);链球菌属(streptococcus)物种包括a型化脓性链球菌(streptococcuspyogenesgroupa)、草绿色链球菌(streptococcusviridansgroup)、b型无乳链球菌(streptococcusagalactiaegroupb)、牛链球菌(streptococcusbovis)、厌氧链球菌(streptococcusanaerobicspecies)、肺炎链球菌(streptococcuspneumoniae)和粪链球菌(streptococcusfaecalis);杆菌属(bacillus)物种包括炭疽杆菌(bacillusanthracis);棒状杆菌属(corynebacterium)物种包括白喉杆菌(corynebacteriumdiphtheriae)、需氧棒状杆菌属物种和厌氧棒状杆菌属物种;类白喉菌物种;李斯特氏菌属(listeria)物种包括单核细胞增生性李斯特氏菌(listeriamonocytogenes);丹毒丝菌属(erysipelothrix)物种包括红斑丹毒丝菌(erysipelothrixrhusiopathiae);梭菌属(clostridium)物种包括产气荚膜梭菌(clostridiumperfringens)、破伤风梭菌(clostridiumtetani)和艰难梭菌(clostridiumdifficile)。革兰氏阴性细菌包括但不限于奈瑟菌属(neisseria)物种包括淋病奈瑟菌(neisseriagonorrhoeae)和脑膜炎奈瑟菌(neisseriameningitidis);布兰汉氏菌属(branhamella)物种包括粘膜炎布兰汉氏菌(branhamellacatarrhalis);埃希氏菌属(escherichia)物种包括大肠杆菌(escherichiacoli);肠杆菌属(enterobacter)物种;变形菌属(proteus)物种包括奇异变形菌(proteusmirabilis);假单胞菌属(pseudomonas)物种包括铜绿假单胞菌(pseudomonasaeruginosa)、鼻疽假单胞菌(pseudomonasmallei)和假鼻疽假单胞菌(pseudomonaspseudomallei);克雷伯氏菌属(klebsiella)物种包括肺炎克雷伯氏菌(klebsiellapneumoniae);沙门氏菌属(salmonella)物种;志贺氏菌属(shigella)物种;沙雷氏菌属(serratia)物种;不动杆菌属(acinetobacter)物种;嗜血杆菌属(haemophilus)物种包括流感嗜血杆菌(haemophilusinfluenzae)和杜克雷嗜血杆菌(haemophilusducreyi);布鲁氏菌属(brucella)物种;耶尔森氏菌属(yersinia)物种包括鼠疫耶尔森氏菌(yersiniapestis)和小肠结肠炎耶尔森氏菌(yersiniaenterocolitica);弗朗西斯氏菌属(francisella)物种包括土拉弗朗西斯氏菌(francisellatularensis);巴氏杆菌属物种包括多杀巴氏杆菌(pasteurellamultocida);霍乱弧菌(vibriocholerae);黄杆菌属(flavobacterium)物种;脑膜败血黄杆菌(meningosepticum);弯曲菌属(campylobacter)物种包括空肠弯曲菌(campylobacterjejuni);类杆菌属(bacteroides)物种(口腔、咽部)包括脆弱类杆菌(bacteroidesfragilis);梭杆菌属(fusobacterium)物种包括具核梭杆菌(fusobacteriumnucleatum);肉芽肿鞘杆菌;链杆菌属(streptobacillus)物种包括念珠状链杆菌(streptobacillusmoniliformis);军团菌属(legionella)物种包括嗜肺军团菌(legionellapneumophila)。另外的细菌类型包括抗酸杆菌(acid-fastbacillus)、螺旋体和放线菌。抗酸杆菌的实例包括分枝杆菌属(mycobacterium)物种,其包括结核分枝杆菌(mycobacteriumtuberculosis)和麻风分枝杆菌(mycobacteriumleprae)。螺旋体的实例包括密螺旋体属(treponema)物种(包括梅毒螺旋体(treponemapallidum)、细弱螺旋体(treponemapertenue))、疏螺旋体属(borrelia)物种(包括伯氏疏螺旋体(borreliaburgdorferi)(莱姆病,lymedisease)和回归热疏螺旋体(borreliareacurrentis)以及钩端螺旋体属(leptospira)物种。放线菌的实例包括放线菌属(actinomyces)物种(包括伊氏放线菌(actinomycesisraelii))和诺卡氏菌属(nocardia)物种(包括星状诺卡氏菌(nocardiaasteroides))。病毒的实例包括但不限于:逆转录病毒、人免疫缺陷病毒(包括hiv-1、hdtv-iii、lave、htlv-iii/lav、hiv-iii、hiv-lp)、巨细胞病毒(cmv)、小rna病毒、脊髓灰质炎病毒、甲型肝炎病毒、肠道病毒、人柯萨奇病毒(humancoxsackievirus)、鼻病毒、艾柯病毒、杯状病毒(calcivirus)、披膜病毒、马脑炎病毒、风疹病毒、黄病毒(flavirus)、登革热病毒、脑炎病毒、黄热病病毒、冠状病毒、弹状病毒、疱疹性口腔炎病毒、狂犬病病毒、线状病毒、埃博拉病毒、副粘病毒、副流感病毒、腮腺炎病毒、麻疹病毒、呼吸道合胞病毒(rsv)、正粘病毒、流感病毒、布尼亚病毒(bungavirus)、汉坦病毒、白蛉病毒和纳伊罗病毒(nairovirus)、沙粒病毒(arenavirus)、出血热病毒、呼肠孤病毒、环状病毒、轮状病毒、双rna病毒(bimavirus)、肝dna病毒、乙型肝炎病毒、细小病毒、乳多空病毒科(papovaviridae)、乳头瘤病毒、多瘤病毒、腺病毒、疱疹病毒包括1型和2型单纯疱疹病毒、水痘带状疱疹病毒、痘病毒、天花病毒、牛痘病毒、虹彩病毒(iridovirus)、非洲猪瘟病毒、丁型肝炎病毒、非甲型非乙型肝炎病毒、丙型肝炎病毒、诺沃克病毒、星状病毒以及未分类的病毒。真菌的实例包括但不限于:隐球菌属(cryptococcus)物种包括新型隐球菌(crytococcusneoformans);组织胞浆菌属(histoplasma)物种包括荚膜组织胞浆菌(histoplasmacapsulatum);球孢子菌属(coccidiodes)物种包括粗球孢子菌(coccidiodesimmitis);副球孢子菌属(paracoccidioides)物种包括巴西副球孢子菌(paracoccidioidesbrasiliensis);芽生菌属(blastomyces)物种包括皮炎芽生菌(blastomycesdermatitidis);衣原体属(chlamydia)物种包括沙眼衣原体(chlamydiatrachomatis);念珠菌属(candida)物种包括白色念珠菌(candidaalbicans);孢子丝菌属(sporothrix)物种包括申克孢子丝菌(sporothrixschenckii);曲霉属(aspergillus)物种以及毛霉病的真菌。其它感染性生物包括寄生虫。寄生虫包括疟原虫属(plasmodium)物种,例如包括恶性疟原虫(plasmodiumfalciparum)、三日疟原虫(plasmodiummalariae)、卵形疟原虫(plasmodiumovale)和间日疟原虫(plasmodiumvivax)的疟原虫属物种以及刚地弓形虫(toxoplasmagondii)。血源性和/或组织寄生虫包括疟原虫属物种、巴贝虫属(babesia)物种包括田鼠巴贝虫(babesiamicroti)和分歧巴贝虫(babesiadivergens)、利什曼原虫属(leishmania)物种包括热带利什曼原虫(leishmaniatropica)、巴西利什曼原虫(leishmaniabraziliensis)、杜氏利什曼原虫(leishmaniadonovani);锥虫属(trypanosoma)物种包括冈比亚锥虫(trypanosomagambiense)、罗得西亚锥虫(trypanosomarhodesiense)(非洲睡眠病(africnasleepingsickness))和克氏锥虫(trypanosomacruzi)(查加斯病(chagas’disease))。其它医学相关微生物已在文献中有广泛地描述,例如参见thomas,medicalmicrobiology,baillieretindall,greatbritain1983和murray,medicalmicrobiology(isbn0323033032),2005,其全部内容通过引用并入本文。b.hpv疫苗本发明包括预防或改善hpv感染的组合物。因此,本发明涉及用于主动和被动免疫实施方案中的疫苗。可从含有hpvl2蛋白质区段的多型hpv多肽制备计划用作疫苗的免疫原性组合物。在另一些实施方案中,多型hpvl2多肽可与其它hpv蛋白质或其区段(例如e1、e2、e3、e4、e5、e6、e7、e8和/或l1蛋白质)联用。参见例如美国专利7,425,438、7,416,846、7,416,732、7,407,807、7,374,767、7,201,908、7,189,513和7,288,258,其均通过引用全部并入本文。通常,疫苗以与疫苗制剂相容的方式并以治疗有效量和/或产生免疫原性的量来施用。待施用的量取决于待治疗的对象,包括个体免疫系统合成抗体的能力以及期望的保护程度。所需施用的活性成分的精确量取决于从业者的判断。通常,每次接种或施用可施用0.1、1、5、10、20、30、40、50、60、70、80、90至100ng、μg或mg。首次施用和加强注射的合适方案也可以不同,通常是在首次施用后随后进行接种或其它施用。1.hpv多肽和多肽区段在本发明的某些方面,hpv多肽的不同区段被用作多型hpv多肽疫苗的hpv肽组分。在某些方面,hpv多肽是l2多肽。在另一方面,l2多肽是hpv1,hpv2,hpv3,hpv4,hpv5,hpv6,hpv7,hpv8,hpv9,hpv10,hpv11,hpv12,hpv13,hpv14,hpv15,hpv16,hpv17,hpv18,hpv19,hpv20,hpv21,hpv22,hpv23,hpv24,hpv25,hpv26,hpv27,hpv28,hpv29,hpv30,hpv31,hpv32,hpv33,hpv34,hpv35,hpv36,hpv37,hpv38,hpv39,hpv40,hpv41,hpv42,hpv43,hpv44,hpv45,hpv46,hpv47,hpv48,hpv49,hpv50,hpv51,hpv52,hpv53,hpv54,hpv55,hpv56,hpv57,hpv58,hpv59,hpv60,hpv61,hpv62,hpv63,hpv64,hpv65,hpv66,hpv67,hpv68,hpv69,hpv70,hpv71,hpv72,hpv73,hpv74,hpv75,hpv76,hpv77,hpv78,hpv79,hpv80,hpv81,hpv82,hpv83,hpv84,hpv85,hpv86,hpv87,hpv88,hpv89,hpv90,hpv91,hpv92,hpv93,hpv94,hpv95,hpv96,hpv97,hpv98,hpv99,hpv100或更多(参见seqidno:1-70);以及动物乳头瘤病毒:1型牛乳头瘤病毒(bpv1)、2型牛乳头瘤病毒(bpv2)、4型牛乳头瘤病毒(bpv4)、棉尾兔乳头瘤病毒(crpv)、鹿乳头瘤病毒(dpv)、欧洲麋鹿乳头瘤病毒(eepv)、犬口腔乳头瘤病毒(copv)、恒河猴乳头瘤病毒(rhpv)或兔口腔乳头瘤病毒(ropv)l2肽表位。“人乳头瘤病毒汇编在线版(thehumanpapillomavirusescompendiumonline)”汇编并发布了与人乳头瘤病毒(hpv)和相关动物乳头瘤病毒有关的相关分子数据。可通过互联网访问该汇编(hpv-web.lanl.gov/stdgen/viras/hpv/compendium/htdocs/html_files/hpvcompintro4.html),从本申请的优先权日和申请日起,其通过引用并入本文。l2多肽的实例可以在公众可获得的蛋白质数据库如genbank(gb)、swisspro(sp)、embl等中找到。代表性的数据库条目(按hpv类型列出,括号中为登记号)包括但不限于:hpv2(gb/aay86489,gb/abn49461,gb/abn49469,gb/abo14925,gb/np_077121);hpv3(sp/p36744);hpv7(gb/np_041858.1);hpv10(gb/np_041745);hpv16(gb/aao85414,gb/aao15703,gb/aao15711,gb/aaq10726,gb/aav91650);hpv18(gb/aaf14009,gb/abp99710,gb/abp99718,gb/abp99726,gb/abp99742,gb/abp99766,gb/abp99774,gb/abp99782,gb/abp99790,gb/abp99798,gb/abp99806,gb/np_040316);hpv26(gb/np_041786.1);hpv27(dbj/bae16268,sp/p36755);hpv28(sp/p50799);hpv29(sp/p50800);hpv30(sp/p36756);hpv33(sp/p06418);hpv39(gb/aaa47055);hpv40(sp/p36760);hpv43(sp/q705h5);hpv45(gb/aay86493);hpv45(gb/abp99814,gb/abp99854,gb/abp99862,gb/abp99870,gb/abp99878,gb/abp99894,gb/abp99902,sp/p36761);hpv51(sp/p26539);hpv52(sp/p36763);hpv53(gb/abu54103,gb/abu54117,gb/abu54131,gb/abu54152,gb/abu54159,gb/abu54173,gb/np_041847);hpv56(gb/abo76808,gb/abo76815,gb/abo76822,gb/abo76829,sp/p36765);hpv57(dbj/baf80485,sp/p22164);hpv58(sp/p26538);hpv59(emb/caa54855);hpv61(ref/np_043449);hpv62(sp/q676u7);hpv66(gb/abo76836,gb/abo76843,gb/abo76857,gb/abo76864,gb/abo76885,gb/abo76892,gb/abo76899,sp/q80960);hpv68a(gb/aaz39497);hpv69(sp/q9jh45);hpv70(gb/aac54856);hpv71(gb/aaq95182,gb/aaq95189,gb/aaq95203,ref/np_597937);hpv72(emb/caa63878);hpv77(emb/caa75467);hpv81(emb/caf05697);hpv82(gb/aak28455,sp/q9ir53);hpv83(gb/aad38973);hpv84(gb/aak09276);hpv85(gb/aad24187);hpv86(gb/aal06740);hpv87(emb/cac17717);hpv89(gb/aam92156);hpv90(ref/np_671508);hpv91(gb/aam89135);hpv94(dbj/bad89178,emb/caf05714);hpv97(gb/aaz39505,gb/abo27082);hpv102(gb/aaz39525);或hpv106(gb/aaz39518)。自本申请的申请日起,所述登记号代表的各氨基酸序列通过引用并入本文。在某些方面,来自至少2、3、4、5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、21、22或更多hpv类型的至少2、3、4、5、6、7、8、9、10或更多种l2肽偶联在一起形成多型hpv多肽(参见seqidno:94、108、109和113)。可通过表达或合成融合蛋白、或通过肽的相互化学缀合、或将肽与常规基质或聚合物进行化学缀合来进行区段偶联。本发明的肽可包含从hpvl2多肽的第1,5,10,15,20,25,30,35,40,45,50,55,60,65,70,75,80,85,90,95,100,110,120,130,140,150,160,170,180,190,200,210,220,230,240,250,260,270,280,290,300,310,320330,340,350,360,370,380,390,400,410,420,43,440,450,460,470,480或490位氨基酸(包括其间的所有数值)开始的10,15,20,25,30,35,40,45,50,55,60,65,70,75,80,85,90,95,100,110,120,130,140,150,160,170,180,190,200,210,220,230,240,250,260,270,280,290,300,310,320330,340,350,360,370,380,390,400,410,420,43,440,450,460,470,480或490个连续氨基酸(包括其间的所有数值和范围)。在某些实施方案中,hpvl2多肽包括但不限于seqidno:1至seqidno:70。在某些方面,所述多型hpv多肽包含选自如下的2、3、4、5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、21、22、23、24、25或更多肽的2、3、4、5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、21、22、23、24、25、26、27、28、29、30、60、70、80、90、100、200或更多:hpvl217-36-diypsckisntcppdiqnki(seqidno:72),hpvl217-36-dlyrtckqagtcppdiiprv(seqidno:73),hpvl217-36-diypackvanncppdiqnki(seqidno:74),hpvl217-36-hiyqtckqagtcppdvinkv(seqidno:75),hpvl217-36-hiyqtckqagtcppdvinkv(seqidno:76),hpvl217-36-qlyqtckltgtcppdvipkv(seqidno:77),hpvl217-36-qlyqtckatgtcppdvipkv(seqidno:78),hpvl217-36-qlyktckqagtcppdiipkv(seqidno:71),hpvl217-36-dlyktckqsgtcppdvvpkv(seqidno:79),hpvl217-36-qlyqtckaagtcpsdvipki(seqidno:80),hpvl217-36-qlyqtckatgtcppdvipkv(seqidno:81),hpvl217-36-qlyrtckaagtcppdvipkv(seqidno:82),hpvl217-36-dlyrtckqsgtcppdvvdkv(seqidno:83),hpvl217-36-dlyrtckqsgtcppdvinkv(seqidno:84),hpvl217-36-qlystckaagtcppdvvnkv(seqidno:85),hpvl217-36-qlyqtckasgtcppdvipkv(seqidno:86),hpvl217-36-qlyktcklsgtcpedvvnki(seqidno:87),hpvl217-36-qlyqtckasgtcppdvipkv(seqidno:88),hpvl217-36~dlyktckqagtcpsdvinkv(seqidno:89),hpvl217-36-dlyktckqsgtcpsdvinkv(seqidno:90),hpvl217-36-qlyktckqagtcppdvipkv(seqidno:91)和/或qlystckaagtcppdvipkv(seqidno:92)。又一方面,所述多型hpv多肽包含hpvl217-36x22的氨基酸序列-diypsckisntcppdiqnkidlyrtckqagtcppdiiprvdiypackvanncppdiqnkihiyqtckqagtcppdvinkvhiyqtckqagtcppdvinkvqlyqtckltgtcppdvipkvqlyqtckatgtcppdvipkvqlyktckqagtcppdiipkvdlyktckqsgtcppdvvpkvqlyqtckaagtcpsdvipkiqlyqtckatgtcppdvipkvqlyrtckaagtcppdvipkvdlyrtckqsgtcppdvvdkvdlyrtckqsgtcppdvinkvqlystcxaagtcppdvvnkvqlyqtckasgtcppdvipkvqlyktcklsgtcpedvvnkiqlyqtckasgtcppdvipkvdlyktckqagtcpsdvinkvdlyktckqsgtcpsdvinkvqlyktckqagtcppdvipkvqlystckaagtcppdvipkv(seqidno:93)。另一方面,所述多型hpv多肽包含选自如下的1、2、3、4、5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、21、22、23、24、25或更多肽的2、3、4、5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、21、22、23、24、25、26、27、28、29、30、60、70、80、90、100、200或更多:hpvl211-88-krasatqlyktckqagtcppdiipkvegktiadqilqygsmgvffgglgigtgsgtggrtgyiplgtrpptatdtlap(seqidno:94),hpvl211-88-krasvtdlyktckqsgtcppdvvpkvegttladkilqwsslgiflgglgigtgsgtggrtgyiplggrsntvvdvgpt(seqidno:95),hpvl211-88-kraapkdiypsckisntcppdiqnkiehttiadkilqygslgvflgglgigtargsggrigytplgegggvrvatrpt(seqidno:96),hpvl211-88-krdsvthiyqtckqagtcppdvinkveqttvadnilkygsagvffgglgistgrgtggatgyvplgegpgvrvggtpt(seqidno:97),hpvl211-88-krasatqlyqtckltgtcppdvipkvehntiadqilkwgslgvffgglgigtgsgtggrtgyvplgtsakpsitsgpm(seqidno:98)hpvl211-88satqlyqtckltgtcppdvipkvehntiadqilkwgslgvffgglgigtgsgtggrtgyvplqtsakpsitsgpmakra(seqidno:99),hpvl211-88satqlyktckqagtcppdiipkvegktiadqilqygsmgvffgglgigtgsgtggrtgyiplgtrpptatdtlapra(seqidno:100),hpvl211-88svtdlyktckqsgtcppdvvpkvegttladkilqwsslgiflgglgigtgsgtggrtgyiplggrsntvvdvgptrkra(seqidno:101),hpvl211-88satqlyqtckaagtcpsdvipkiehttiadqilrygsmgvffgglgigsgsgtggrtgyvplstrpstvseasipra(seqidno:102),hpvl211-88satdlyrtckqsgtcppdvvdkvegttladkilqwtslgiflgglgigtgtgtggrtgyiplggrpntvvdvsparra(seqidno:103),hpvl211-88svtqlystckaagtcppdvvnkvegttladkilqwsglgiflgglgigtgsgsggrtgyiplggggrpgvvdiapara(seqidno:104),hpvl211-88satqlyktcklsgtcpedvvnkieqktwadkilqwgslftyfgglgigtgtgsggragyvplgsrpstivdvtparkkra(seqidno:105),and/orhpvl211-88satqlyktckqagtcppdvipkvegstiadnilkygsigvffgglgigsgsgsggrtgyvplstgtpskpveip(seqidno:106)。在某些实施方案中,多型hpv多肽包含hpvl211-88×5的氨基酸-krasatqlyktckqagtcppdiipkvegktiadqilqygsmgvffgglgigtgsgtggrtgyiplgtrpptatdtlapkrasvtdlyktckqsgtcppdvvpkvegttladkilqwsslgflgglgigtgsgtggrtgyiplggrsntvvdvgptkraapkdiypsckisntcppdiqnkiehttiadkilqygslgvflgglgigtargsggrigytplgegggvrvatrptkrdsvthiyqtckqagtcppdvinkveqttvadnilkygsagvffgglgistgrgtggatgyvplgegpgvrvggtptkrasatqlyqtckltgtcppdvipkvehntiadqilkwgslgvffgglgigtgsgtggrtgvplgtsakpsitsgpm(seqidno:107).。在又一实施方案中,多型hpv多肽包含hpvl211-88×8的氨基酸-satqlyqtckltgtcppdvipkvehntiadqilkwgslgvffgglgigtgsgtggrtgyvplqtsakpsitsgpmakrasatqlyktckqagtcppdiipkvegktiadqilqygsmgvffgglgigtgsgtggrtgyiplgtrpptatdtlaprasvtdlyktckqsgtcppdvvpkvegttladkilqwsslgiflgglgigtgsgtggrtgyiplggrsntvvdvgptrkrasatqlyqtckaagtcpsdvipkiehttiadqilrygsmgvffgglgigsgsgtggrtgyvplstrpstvseasiprasatdlyrtckqsgtcppdvvdkvegttladkilqwtslgiflgglgigtgtgtggrtgyiplggrpntvvdvsparrasvtqlystckaagtcppdvvnkvegttladkilqwsglgiflgglgigtgsgsggrtgyiplggggrpgvvdiaparasatqlyktcklsgtcpedvvnkieqktwadkilqwgslftyfgglgigtgtgsggragyvplgsrpstivdvtparkkrasatqlyktckqagtcppdvipkvegstiadnilkygsigvffgglgigsgsgsggrtgyvplstgtpskpveip(seqidno:108).在又一实施方案中,多型hpv多肽包含来自hpv6b、hpv16、hpv18、hpv31、hpv39、hpv51、hpv56和hpv73之l2的同源区。hpvl211-88×8的氨基酸是:masatqlyqtckltgtcppdvipkvehntiadqilkwgslgvffgglgigtgsgtggrtgyvplqtsakpsitsgpmakrasatqlyktckqagtcppdiipkvegktiadqilqygsmgvffgglgigtgsgtggrtgyiplgtrpptatdtlaprasvtdlyktckqsgtcppdvvpkvegttladkilqwsslgiflgglgigtgsgtggrtgyiplggrsntvvdvgptrkrasatqlyqtckaagtcpsdvipkiehttiadqilrygsmgvffgglgigsgsgtggrtgyvplstrpstvseasiprasatdlyrtckqsgtcppdvvdkvegttladkilqwtslgiflgglgigtgtgtggrtgyiplggrpntvvdvsparrasvtqlystckaagtcppdvvnkvegttladkilqwsglgiflgglgigtgsgsggrtgyiplggggrpgvvdiaparasatqlyktcklsgtcpedvvnkieqktwadkilqwgslftyfgglgigtgtgsggragyvplgsrpstivdvtparkkrasatqlyktckqagtcppdvipkvegstiadnilkygsigvffgglgigsgsgsggrtgyvplstgtpskpveip(seqidno:109)。在另一实施方案中,多型hpv多肽包含选自如下的1、2、3、4、5、6、7、8、9、10或更多肽的2、3、4、5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、21、22、23、24、25、26、27、28、29、30、60、70、80、90、100、200或更多:hpvl211-200-krasatqlyqtckasgtcppdiiakveqntladkilkwgslgvffgglgigtgsgtggrtgyvpvqtaprpaipfgptarppiivdtvgpsdssivslvedstiinsaasdfvppiregfeistsetttpaildvsvtthnttstsifknpafaepsivqsqpsveasghvltstytstisshsvedipldt(seqidno:110),hpvl211-200-krasatqlyktckqagtcppdiipkvegktiadqilqygsmgvffgglgigtgsgtggrtgyiplgtrpptatdtlapvrppltvdpvgpsdpsivslveetsfidagaptpvpsippdvsgfsittstdttpaildinntvfttvtthnnptftdpsvlqpptpaetgghftlssstisthnyeeipmdt(seqidno:111)和/或hpvl211-200-krasvtdlyktckqsgtcppdvvpkvegttladkilqwsslgiflgglgigtgsgtggrtgyiplggrsntvvdvgptrppvviepvgptdpsivtliedssvvtsgaprptftgtsgfiditsagtttpavlditpsstsvsisttnftnpafsdpsiievpqtgevagnvfvgtptsgthgyeeiplqt(seqidno:112)。在某些实施方案中,多型hpv多肽包含hpvl211-200×3的氨基酸序列krasatqlyqtckasgtcppdiiakveqntladkilkwgslgvffgglgigtgsgtggrtgyvpvqtaprpaipfgptarppiivdtvgpsdssivslvedstiinsaasdfvppiregfeistsetttpaildvsvtthnttstsifknpafaepsivqsqpsveasghvltstytstisshsvedipldtkmsatqlyktckqagtcppdiipkvegiadqilqygsmgvffgglgigtgsgtggrtgyiplgtrpptatdtlapvrppltvdpvgpsdpsivslveetsfidagaptpvpsippdvsgfsittstdttpaildinntvttvtthnnptftdpsvlqpptpaetgghftlssstisthnyeeipmdtkrasvtdlyktckqsgtcppdvvpkvegtladkilqwsslgiflgglgigtgsgtggrtgyiplggrsntyvdvgptrppvviepvgptdpsivtliedssvvtsgaprptftgtsgfditsagtttpavlditpsstsvsisttnftnpafsdpsiievpqtgevagnvfvgtptsgthgyeeiplqt(seqidno:113)。在某些实施方案中,多型多肽“furindkilk×15”包含来自hpv6b、hpv11、hpv16、hpv18、hpv31、hpv33、hpv35、hpv39、hpv45、hpv51、hpv52、hpv56、hpv58、hpv59和hpv73的l2蛋白质序列。furindkilk×15的氨基酸序列是:masatqlyqtckltgtcppdvipkvehntiadqilkasatqlyqtckatgtcppdvipkvehttiadqilkasatqlyktckqagtcppdiipkvegktiadqilqasvtdlyktckqsgtcppdvvpkvegttladkilqasatqlyqtckaagtcpsdvipkiehttiadqilrasatqlyqtckatgtcppdvipkvegstiadqilkasatqlyrtckaagtcppdvipkvegntvadqilkasatdlyrtckqsgtcppdvvdkvegttladkilqasatdlyrtckqsgtcppdvinkvegttladkilqasvtqlystckaagtcppdvvnkvegttladkilqasatqlyqtckasgtcppdvipkvegttiadqllkasatqlyktcklsgtcpedvvnkieqktwadkilqasatqlyqtckasgtcppdvipkvegttiadqilrasatdlyktckqagtcpsdvinkvegttladkilqasatqlyktckqagtcppdvipkvegstiadnilk(seqidno:114)。本发明的肽通常使用本领域技术人员已知的肽合成方法来合成和/或利用本领域技术人员已知的肽化学性质进行偶联。在另一些方面,可使用本领域技术人员已知的重组技术表达和纯化本发明的肽和多肽。2.接头本发明涵盖包含多种肽的寡聚体或融合蛋白。这种寡聚体可采用共价连接或非共价连接多聚体(包括二聚体、三聚体或更高寡聚体)的形式。在本发明的一方面,所述寡聚体保持刺激免疫应答的能力。本发明的一个实施方案涉及包含通过肽之间共价或非共价接头连接之多个肽的寡聚体。此类接头可以是肽接头(间隔序列)或具有促进寡聚化之特性的肽。亮氨酸拉链和某些源自抗体的多肽属于能够促进其所附着的肽寡聚化的肽。合适的肽接头包括美国专利4,751,180和4,935,233中所描述的那些,其通过引用并入本文。在某些实施方案中,本发明的肽通过肽键连接,在肽之间没有可辨识的接头。3.递送载体已知的疫苗制剂采用多种递送载体用于向哺乳动物免疫系统呈递这种抗原,从而引发针对病原体的保护性或治疗性免疫应答。这种“递送载体”包含作为疫苗的热灭活或化学灭活的完整病毒、完整病毒的蛋白质颗粒、病毒载体(例如腺病毒和牛痘等)以及基于dna的载体或质粒。病毒样颗粒病毒样颗粒(vlp)已被研究作为疫苗。一般地,包衣壳的病毒包含经组装而含有病毒核酸蛋白质的外层或“衣壳”。许多病毒具有能够用分别表达的衣壳蛋白进行“自组装”(在表达衣壳的细胞内(“体内组装”)以及在分离和纯化之后的细胞外(“体外组装”))以形成vlp的衣壳。病毒样颗粒模拟病毒颗粒的整体结构,而不需要包含感染性物质。vlp可不含病毒dna或rna基因组,但保留了真病毒的三维结构。vlp能够刺激b细胞介导的应答、cd4增殖性应答和细胞毒t淋巴细胞应答。参见schirmbeck等(1996)intervirology39,111-119;paliard等(2000)aidsres.hum.retroviruses16,273-282;murata等(2000)pnasusa100,6753-6758。还可参见美国专利公开20070041999,其通过引用全部并入本文。已生产了针对感染人类和其它动物的、超过30种不同病毒的vlp,所述病毒包括诺沃克病毒、乙型和丙型肝炎病毒、乳头瘤病毒、细小病毒和甲型流感病毒。还可以操作病毒样颗粒用作载体分子来递送其它病原体的表位。参见,noad等(2003)trendsinmicrobiology11(9),438-444;sadeyen等(2003)virology309:32-40;pct公开wo2005/005614;美国专利公开2004/0033585和2005/0048082;美国专利6,448,070、6,110,466、6,171,591;brinkman等(2004)lett.drugdes.&disc.1:137-147。可修饰衣壳蛋白使其包含抗原性肽,产生重组病毒衣壳蛋白-抗原性肽的融合物。然后可以在宿主细胞中表达这种衣壳蛋白-抗原性肽融合产物,在体内或体外组装以形成重组病毒或病毒样颗粒,并施用给宿主从而引发免疫应答。纳米颗粒一方面,肽可以与非蛋白质材料(例如,纳米颗粒和其它基质)偶联。纳米颗粒通常直径约为1nm~200nm,其可用于提供给对象以递送免疫原性肽。可通过共价或非共价化学相互作用将一个或多个肽与纳米颗粒附着。非共价化学相互作用可包括亲合作用(例如亲合素/生物素、抗原/抗体、受体/配体)、离子相互作用和/或疏水相互作用。用于将肽附着至固体支持物(如纳米颗粒)的方法在例如美国专利公开2004/0258698中有所描述。具有约50nm至约200nm之直径的纳米颗粒可全身性递送。本文所用的术语“纳米颗粒”是指纳米尺寸范围(约1nm~500nm)的、可制备成具有预定绑定分子规则排布之表面的聚合物球或球状体。优选地,利用自组装单体来形成纳米颗粒。此外,术语“纳米颗粒”涵盖了使用聚合和非聚合的脂质体、bicelle和微团以及病毒衣壳结构。尽管纳米颗粒对于本发明的组合物和方法来说是优选的,但是也可如本领域技术人员公知地使用适合本发明中配体的其它框架、支架及另外的“呈递物(presenter)”,例如树状分子。多价纳米颗粒参见美国公开20030223938。可以以脂质体组合物来施用本发明的肽。本发明的脂质体可以是多层囊泡(multilamellarvesicle,mlv)。所述脂质体包含形成脂质体的脂质,其具有亲水性尾部以及极性或化学反应性部分(其又包含酸、醇、醛、胺或酯)。所述脂质体还可表征为烃链或类固醇尾部基团以及极性头部基团。所述形成脂质体的脂质包括磷脂。合适的磷脂的实例包括但不限于磷脂酸、磷脂酰胆碱、磷脂酰乙醇胺、磷脂酰甘油、磷脂酰肌醇和鞘磷脂。可包封于或偶联至本发明脂质体的物质包括蛋白质和肽。在一些实施方案中,所述物质包括多于一种化合物。本发明的肽可包含或缀合至将该肽定位于脂质表面的亲脂性部分。多型肽可定位于脂质体表面。参见美国专利公开20060035853。c.佐剂和其它免疫刺激或增强组分可通过使用其它非特异性免疫应答刺激物(称为“佐剂”)来增强多肽或肽或多型hpv肽组合物的免疫原性。合适的佐剂包括所有可接受的免疫刺激化合物,例如细胞因子、毒素或合成组合物。多种佐剂可用于增强针对本文所述多型hpv多肽或任何其它组合物的抗体应答。佐剂可用于(1)诱捕体内的抗原从而导致缓慢释放;(2)将参与免疫应答的细胞吸引至施用位点;(3)诱导免疫系统细胞的增殖或活化;或(4)改善抗原在整个对象体内的传播。佐剂制剂包括但不限于水包油乳剂、油包水乳剂、矿物盐、多聚核苷酸和天然物质。可用的特异性佐剂包括il-1、il-2、il-4、il-7、il-12和γ-干扰素、gmcsp、bcg、铝盐(例如氢氧化铝或其它铝化合物)、mdp化合物(例如thur-mdp和nor-mdp)、cgp(mtp-pe)、脂质a和单磷酰脂a(mpl)。ribi,其含有从细菌提取的三种组分,2%角鲨烯/吐温80乳剂中的mpl、海藻糖二霉菌酸酯(trehalosedimycolate,tdm)和细胞壁骨架(cellwallskeleton,cws)、cpg1018和/或gpi-0100,包括其各种组合。在某些方面,佐剂是与tweentm或明矾或其组合之一种或多种联用的cpg1018或gpi-0100。还可以使用mhc抗原。其它佐剂或方法在美国专利6,814,971、5,084,269、6,656,462中举例说明,其均通过引用并入本文。获得针对疫苗之佐剂作用的多种方法包括使用试剂(例如氢氧化铝或磷酸铝盐(明矾)),常以磷酸盐缓冲盐溶液中约0.05至约0.1%的溶液来使用,并混有以约0.25%溶液使用的糖的合成聚合物通过约70℃至约101℃下热处理30秒至2分钟来实现疫苗中蛋白质的聚集。为了获得佐剂作用,还可通过用针对白蛋白的经胃蛋白酶处理的(fab)抗体再活化来进行聚集;与细菌细胞(例如小球隐孢子虫(c.parvum))、革兰氏阴性细菌的内毒素或脂多糖组分混合;在生理可接受的油介质(例如二缩甘露醇一油酸(aracela))中乳化;或与20%的全氟化碳溶液(用作封闭替代物)乳化。典型的佐剂是完全弗氏佐剂(含有灭活的结核分枝杆菌)、不完全弗氏佐剂和氢氧化铝。除了佐剂以外,理想的是共施用生物应答调节剂(biologicalresponsemodifier,brm)来增强免疫应答。已显示,brm上调t细胞免疫性或下调抑制细胞的活性。这样的brm包括但不限于西咪替丁(cimetidine,cim;1200mg/天)(smith/kline,pa);或低剂量环磷酰胺(cyp;300mg/m2)(johnson/mead,nj)和细胞因子如γ-干扰素、il-2或il-12或编码参与免疫辅助功能之蛋白质(例如b-7)的基因。t辅助细胞表位-已描述了主要t淋巴细胞的两种类型:cd8+细胞毒性淋巴细胞(ctl)和cd4辅助细胞(th细胞)。cd8+t细胞是通过t细胞受体(tcr)识别由(例如被病毒或细菌感染之细胞上的)i型mhc分子呈递的外来抗原的效应细胞。识别外来抗原后,cd8+细胞经历活化、成熟和增殖过程。这种分化过程产生ctl克隆,其能够破坏呈递外来抗原的靶细胞。另一方面,t辅助细胞参与体液和细胞介导形式的效应细胞免疫应答。就体液(或抗体)免疫应答而言,抗体由b淋巴细胞通过与th细胞相互作用而产生。具体来说,细胞外抗原(例如循环中的微生物)被专门的抗原呈递细胞(apc)捕获、加工并与ii型主要组织相容性复合物(mhc)分子一起呈递至cd4+th细胞上。这些th细胞继而活化b淋巴细胞,导致抗体的产生。与此相反,细胞介导的免疫应答或细胞免疫应答对于定居于细胞内的微生物(例如成功感染靶细胞后的微生物)发挥中和作用。外来抗原(例如微生物抗原)在被感染细胞内合成,并与i型mhc分子一起呈递于该细胞的表面上。这些表位的呈递导致上述的cd8+ctl的刺激,该过程继而也受到cd4+th细胞的刺激。th细胞由至少两个不同的亚群组成,称为th1和th2细胞。th1和th2亚型代表接触抗原后从共同前体分化而来的th细胞极化群。在某些方面,多型hpv多肽还可包含th1或th2型应答的优选诱导物。高水平的th1型细胞因子倾向于诱导针对给定抗原的细胞介导免疫应答,而高水平的th2型细胞因子倾向于诱导针对抗原的体液免疫应答。th1和th2型免疫应答之间的区别不是绝对的。事实上,个体将支持以th1为主或以th2为主的免疫应答。然而,根据mosmann和coffman(mosmann和coffman,1989)在鼠cd4+t细胞克隆中所描述的细胞因子家族来考虑是方便的。通常,th1型应答与由t淋巴细胞产生的inf-γ和il-2细胞因子有关。常直接与诱导th1型免疫应答有关的其它细胞因子(例如il-12)不是由t细胞产生的。相反地,th2型应答与il-4、il-5、il-6和il-10的分泌有关。在某些方面,th表位包括但不限于源自细菌蛋白质和毒素(例如破伤风和白喉毒素)的t细胞表位。例如,来自破伤风毒素的p2和p30表位、乙型肝炎核心抗原、结核、结核分枝杆菌ra12(mtb32a的亚序列(192~323位氨基酸)(skeiky等1999))、麻疹病毒/犬瘟热病毒的p25蛋白质:klipnaslienctkael(seqidno:117);pv(脊髓灰质炎病毒)序列103-115:klfavwkitykdt(seqidno:118);m5:nkliaypaveals(seqidno:119);tt(破伤风毒素)830-844:qyikanskfigitel(seqidno:120);padre:akxvmwtlkaaa(a=d-ala、x=l-环己基-ala)(seqidno:121);e7p20-29:tdlycyeqln(seqidno:122);e7p45-54:aepdrahyni(seqidno:123);e7p60-79:kcdstlrlcvqsthvirtl(seqidno:124);e7p85-94:gtlgivgpic(seqidno:125);rasp5-17:klvvvgargvgks(seqidno:126);neup42-56:hldmlrhlyqggqvv(seqidno:127);neup783-797:srllgicltstvqlv(seqidno:128)和mage-3121-134:llkyrarepvtkae(seqidno:129)。toll样受体激动剂-目前广泛的共识是,保护性免疫的产生不仅取决于对抗原的暴露,还取决于接触抗原的环境。有许多这样的实例,即向炎性环境下的宿主引入新抗原会产生免疫耐受而非长期免疫,但是在炎性剂(佐剂)存在下暴露于抗原则诱导免疫性(mondino等,1996;pulendran等1998;jenkins等1994;以及keamey等,immunity1:327,1994)。由于可存在耐受与免疫的不同,因此对于发现在感染病原体(其刺激参与产生抗原呈递之合适免疫原环境的分子途径)内存在的“佐剂”方面已作出很多努力。目前已知,许多佐剂活性是由于微生物和病毒产物与免疫细胞上表达之toll样受体(tlr)不同成员之间的相互作用所致的(beutler等,2004;kaisho,2002;akira等2003;以及takeda和akira,2004)。tlr是根据其与果蝇中分子(称为toll,其在发育中发挥作用并参与抗微生物免疫)的同源性来命名的(lernaitre等,1996;以及hashimoto等,1988)。早期工作显示,toll和toll通路分子的哺乳动物同源物对于固有免疫系统之细胞响应于微生物攻击和微生物副产物的能力至关重要(medzhitov等,1997;medzhitov等,1998;medzhitov等,2000;medzhitov等,2000;以及janeway等,2002)。自从lps被鉴定为tlr4激动剂(poltorok等,1998)之后,许多其它tlr激动剂已被描述,例如三酰基多型hpv多肽(tlr1)、肽聚糖、脂磷壁酸和pam3cys(tlr2)、dsrna(tlm)、鞭毛蛋白(tlrs)、二酰基多型hpv多肽如malp-2(tlr6)、咪唑喹啉和单链rna(tlr7、8)、细菌dna、未甲基化cpgdna序列,甚至人类基因组dna抗体复合物(tlr9)。takeuchi等,2001;edwards等,2002;hayashi等,2003;nagase等,2003。在某些方面,tlr2配体包括但不限于脂磷壁酸、甘露糖醛酸、肽聚糖、非典型lps、malp-2和malp-404(脂蛋白)、ospa、孔蛋白、lcrv、脂化甘露聚糖(lipomannan)、gpi锚、溶血磷脂酰丝氨酸、脂磷聚糖(lpg)、糖磷脂酰肌醇(gpi)、酵母聚糖、血凝素及其类似物或衍生物。另一方面,tlr2激动剂包括来自结核分枝杆菌、伯氏疏螺旋体、梅毒螺旋体的细菌脂肽;来自包括金黄色葡萄球菌的肽聚糖;奈瑟菌孔蛋白、细菌菌毛、耶尔森氏菌毒力因子、cmv病毒粒子、麻疹血凝素和来自酵母的酵母聚糖。在某些方面,tlr激动剂是脂质部分。脂质部分包括但不限于脂肪酸,例如棕榈酰基、豆蔻酰基、硬脂酰基和癸酰基或者更一般地任何c2~c30饱和、单不饱和或多不饱和脂肪酰基。在某些方面,所述脂质部分是pam2cys[s-[2,3-双(棕榈酰氧基)丙基]半胱氨酸]或pam3cys[n-棕榈酰基-s-[2,3-双(棕榈酰氧基)丙基]半胱氨酸]部分。pam3cys或pam3cys-oh(wiesmuller等,1983)是跨越革兰阴性细菌之内外膜的布罗氏脂蛋白(braun′slipoprotein)n端部分的合成版本(例如,美国专利5,700,910,其通过引用全部并入本文)。在美国专利公开20080145375中描述了其它tlr激动剂,其通过引用全部并入本文。d.脂质组分和部分在某些实施方案中,本发明涉及包含与多型hpv肽非共价结合的一种或多种脂质的组合物。脂质是不溶于水并且可用有机溶剂进行萃取的物质。除了本文中特别指明的以外,本领域技术人员应将“化合物”理解为脂质,并涵盖在本发明的组合物和方法中。脂质可以是天然脂质或合成脂质。然而,脂质通常是生物物质。生物脂质是本领域众所周知的,并且包括例如中性脂肪、磷脂、磷酸甘油脂、类固醇、萜类、溶血磷脂、鞘糖脂、糖脂、硫脂、带有醚的脂质(lipidwithether)、酯连接的脂肪酸以及聚合脂质,及其组合。与脂质有关的多型hpv肽可分散于含有脂质的溶液中、用脂质溶解、用脂质乳化、与脂质混合、与脂质组合、包含于脂质混悬液中或者与脂质结合。本发明的脂质相关组合物不限于任何特定结构。例如,它们还可以仅仅散布于溶液中,可能形成大小或形状不均一的聚集体。在另一实例中,它们可存在于双层结构(如微团)中或具有“塌陷”结构。在另一非限制性实例中,还考虑lipofectamine(gibcobrl)或superfect(qiagen)复合物。在某些实施方案中,组合物可包含约1%、约2%、约3%、约4%、约5%、约6%、约7%、约8%、约9%、约10%、约11%、约12%、约13%、约14%、约15%、约16%、约17%、约18%、约19%、约20%、约21%、约22%、约23%、约24%、约25%、约26%、约27%、约28%、约29%、约30%、约31%、约32%、约33%、约34%、约35%、约36%、约37%、约38%、约39%、约40%、约41%、约42%、约43%、约44%、约45%、约46%、约47%、约48%、约49%、约50%、约51%、约52%、约53%、约54%、约55%、约56%、约57%、约58%、约59%、约60%、约61%、约62%、约63%、约64%、约65%、约66%、约67%、约68%、约69%、约70%、约71%、约72%、约73%、约74%、约75%、约76%、约77%、约78%、约79%、约80%、约81%、约82%、约83%、约84%、约85%、约86%、约87%、约88%、约89%、约90%、约91%、约92%、约93%、约94%、约95%、约96%、约97%、约98%、约99%重量百分比(或其间任何范围或数值)脂质的特定脂质,脂质类型或非脂质组分例如佐剂、糖、核酸或者本文公开的其它材料等是本领域技术人员公知的。因此,考虑到本发明的组合物可包含采用任何组合或比例范围的任何脂质、脂质类型或其它组分。ii.多肽及其片段的产生a.多肽的合成和/或缀合在某些方面,可采用针对特定氨基酸序列而变化的常规方法来合成多肽。这样的技术包括但不限于肽合成领域技术人员公知的方法,如液相合成(参见finn和hoffman,1976)或固相合成(参见barany和merrifield,1979)或merrifield报道的分步固相合成(1963),其内容均通过引用并入本文。肽合成技术的其它参考包括利用lu等(1981)公开的fmoc-聚酰胺模式固相肽合成而合成的肽、采用fmoc/tbu方法合成的肽(atherton和sheppard,1989)。可从多家供应商获得fmoc氨基酸,例如chem-impexinternational(wooddale,ill.,usa)、merckbiosciences(nottingham,uk)以及bachemukltd.(st.helens,uk)。合成之后或合成期间,肽可与间隔序列、氨基酸、聚合物或脂质缀合。在某些方面,赖氨酸或赖氨酸类似物的末端侧链基团(例如内部赖氨酸的ε氨基)由多种保护基团中的一种所保护。封闭基团或保护基团或遮蔽基团用于保护具有参与偶联反应之活化羧基的氨基酸的氨基基团,或者保护具有参与偶联反应之酰化氨基的氨基酸的羧基基团。为了发生偶联,必须除去封闭基团而不破坏肽键,或者除去与肽之另一部分结合的任何保护基团。可通过本领域公知的方法对肽进行脂化。标准的缩合、加成、取代或氧化(例如,内部赖氨酸或赖氨酸类似物的末端氨基基团与所引入的氨基酸或肽或脂氨基酸(lipoaminoacid)的羧基末端之间形成二硫桥或酰胺键)反应使脂质添加至肽。b.表达系统可通过任何合适的技术来实现本发明多肽及片段的表达、分离和纯化。本发明还提供了包含dna的重组克隆和表达载体,以及包含该重组载体的宿主细胞。包含dna的表达载体可用于制备由所述dna编码的本发明多肽或片段。产生多肽的方法包括在促使所述多肽表达的条件下培养宿主细胞(其转化有编码所述多肽的重组表达载体),然后从培养物中回收表达的多肽。本领域技术人员会了解,用于纯化所表达之多肽的方法将根据如下因素而有所变化,例如所应用的宿主细胞类型以及所述多肽是结合于膜亦或是从宿主细胞分泌的可溶形式。本发明的多肽可包含指导运输或辅助纯化的各种前导序列。可使用任何合适的表达系统。载体包含与合适的转录或翻译调节核苷酸序列(例如源自哺乳动物、微生物、病毒或昆虫基因的那些)有效连接之编码本发明多肽或片段的dna。调节序列的实例包括转录启动子、操纵子、或增强子、mrna核糖体结合位点以及控制转录和翻译起始和终止的合适序列。当调节序列在功能上与所述dna序列相关时,使核苷酸序列有效连接。因此,如果启动子核苷酸序列控制dna序列的转录,则启动子核苷酸序列与dna序列有效连接。表达载体中一般含有使其在期望的宿主细胞中具有复制能力的复制起点以及用于鉴定将选择转化子的选择基因。此外,可将编码合适信号肽(天然或异源)的序列并入表达载体中。可以将信号肽(分泌型前导肽)的dna序列与本发明的核酸序列同框融合,从而使dna首先进行转录,继而mrna翻译成包含信号肽的融合蛋白。在目的宿主细胞中具有功能的信号肽促进多肽的细胞外分泌。多肽从细胞分泌后,信号肽从多肽中切除。本领域技术人员还应了解,信号肽被切除的位置可能与计算机程序所预测的不同,并且可根据例如在表达重组多肽中所用宿主细胞之类型这样的因素而有所变化。蛋白质制备物可包括具有不同n端氨基酸之蛋白质分子的混合物,其由于在多于一个位点切割信号肽而产生。用于表达多肽的合适宿主细胞包括原核细胞、酵母细胞或更高等的真核细胞。一般优选使用哺乳动物细胞或昆虫细胞作为宿主细胞。在例如pouwels等(1985)中描述了用于细菌、真菌、酵母和哺乳动物细胞宿主的合适的克隆和表达载体。使用源自本文公开之dna构建物的rna,还可应用无细胞翻译系统来产生多肽。1.原核系统原核生物包括革兰氏阴性生物或革兰氏阳性生物。用于转化的合适原核宿主细胞包括例如大肠杆菌、枯草芽孢杆菌、鼠伤寒沙门氏菌以及假单胞菌属、链霉菌属和葡萄球菌属中的多个其它物种。在原核宿主细胞(例如大肠杆菌)中,多肽可包含n端甲硫氨酸残基从而有利于重组多肽在原核宿主细胞中表达。可将n端met从所表达的重组多肽中切除。用于原核宿主细胞中的表达载体一般包含一个或多个表型选择标记基因。表型选择标记基因是例如编码赋予抗生素抗性或提供自养需求之蛋白质的基因。可用于原核宿主细胞的表达载体的实例包括源自市售质粒(如克隆载体pbr322(atcc37017))的表达载体。pbr322包含氨苄青霉素和四环素的抗性基因,因而为鉴定转化细胞提供了简单的方法。将适当的启动子和dna序列插入pbr322载体中。其它市售载体包括例如pkk223-3(pharmaciafinechemicals,uppsala,sweden)和pgem1(promegabiotec,madison,wis.,usa)。常用于重组原核宿主细胞表达载体的启动子序列包括β-内酰胺酶(青霉素酶)、乳糖启动子系统(chang等,1978;和goeddel等,1979)、色氨酸(trp)启动子系统(goeddel等,1980;和ep-a-36776)和tac启动子(maniatis,1982)。特别有用的原核宿主细胞表达系统采用了噬菌体λpl启动子和ci857ts热不稳定阻遏物序列。可从美国模式培养物保藏中心(americantypeculturecollection)获得的质粒载体(其并入了λpl启动子的衍生物)包括phub2(于大肠杆菌株jmb9中保存,atcc37092)和pplc28(于大肠杆菌rr1中保存,atcc53082)质粒。2.酵母系统作为替代,所述多肽可在酵母宿主细胞(优选来自酵母菌属(例如,酿酒酵母(s.cerevisiae)))中表达。也可使用其它酵母属,例如毕赤属(pichia)或克鲁维酵母属(kluyveromyces)。酵母载体常包含来自2μ酵母质粒的复制起点序列、自主复制序列(autonomouslyreplicatingsequence,ars)、启动子区域、多聚腺苷酸化序列、转录终止序列和选择标记基因。用于酵母载体的合适启动子序列包括用于金属硫蛋白、3-磷酸甘油酯激酶(hitzeman等,1980)或其它糖酵解酶(hess等,1968;和holland等,1978)例如烯醇化酶、3-磷酸甘油醛脱氢酶、己糖激酶、丙酮酸脱羧酶、磷酸果糖激酶、葡萄糖-6-磷酸异构酶、3-磷酸甘油酯变位酶、丙酮酸激酶、磷酸丙糖异构酶、磷酸葡萄糖异构酶和葡萄糖激酶的启动子等。用于酵母表达中的其它合适载体和启动子在欧洲专利申请73,657中进一步描述。另一选择方案是russell等(1982)和beier等(1982)描述的葡萄糖可阻遏adh2启动子。可通过将用于在大肠杆菌中进行选择和复制的来自pbr322之dna序列(ampr基因和复制起点)插入上述酵母载体中来构建在酵母和大肠杆菌中均可复制的穿梭载体。可使用酵母α-因子前导序列来指导多肽的分泌。所述α-因子前导序列常插至启动子序列和结构基因序列之间。参见例如kurjan等,1982和bitter等,1984。有利于重组多肽从酵母宿主分泌的其它前导序列是本领域技术人员众所周知地。可以在前导序列的3’端附近进行修饰,使其含有一个或多个限制性位点。这将有利于前导序列与结构基因的融合。酵母转化方案对本领域技术人员来说是周知的。hinnen等,1978描述了一个这样的方案。hinnen等人的方案在选择性培养基中选择trp+转化子,其中所述选择性培养基由0.67%酵母氮源、0.5%酪氨基酸、2%葡萄糖、10mg/ml腺嘌呤和20mg/ml尿嘧啶组成。用含有adh2启动子序列之载体转化的酵母宿主细胞可以在“营养”培养基中培养以诱导表达。营养培养基的一个实例是由1%酵母提取物、2%蛋白胨和1%葡萄糖并补充有80mg/ml腺嘌呤和80mg/ml尿嘧啶组成的培养基。当葡萄糖从培养基中耗尽时,发生adh2启动子的解阻遏作用(derepression)。3.哺乳动物或昆虫系统还可以使用哺乳动物或昆虫宿主细胞培养系统来表达重组多肽。luckow和summers,bio/technology6:47(1988)中对杆状病毒系统在昆虫细胞中产生异源蛋白进行了综述。还可使用已建立的哺乳动物来源的细胞系。合适的哺乳动物宿主细胞系的实例包括猴肾细胞的cos-7系(atcccrl1651)(gluzman等,1981)、l细胞、c127细胞、3t3细胞(atccccl163)、中国仓鼠卵巢(cho)细胞、hela细胞和bhk(atcccrl10)细胞系以及mcmahan等(1991)描述的源自非洲绿猴肾细胞系cv1的cv1/ebna细胞系(atccccl70)。已描述了用于将dna引入哺乳动物细胞的已建立方法(kaufman,1990)。使用市售试剂(例如lipofectamine脂质试剂(gibco/brl)或lipofectamine-plus脂质试剂)的其它方案可用于转染细胞(felgner等,1987)。此外,可使用如sambrook等(1989)中的常规方法采用电穿孔来转染哺乳动物细胞。可使用本领域已知的方法(例如对细胞毒性药物的抗性)来选择稳定转化子。kaufman等,1990描述了几种选择方案,例如二氢叶酸还原酶(dihydrofolatereductase,dhfr)抗性。用于dhfr选择的合适宿主株可以是cho株dx-b11,其缺乏dhfr(urlaub和chasin,1980)。可以将表达dhfrcdna的质粒引入dx-b11株,只有含有该质粒的细胞可以在合适的选择培养基中生长。可以并入表达载体的选择标记的其它实例包括赋予抗生素(例如g418和潮霉素b)抗性的cdna。基于对这些化合物的抗性可以选择出携带所述载体的细胞。哺乳动物宿主细胞表达载体的转录和翻译控制序列可从病毒基因组中切下。常用的启动子序列和增强子序列源自多瘤病毒、腺病毒2、猿猴病毒40(sv40)和人巨细胞病毒。源自sv40病毒基因组的dna序列(例如sv40起点、早期和晚期启动子、增强子、剪接和多聚腺苷酸化位点)可为在哺乳动物宿主细胞中表达结构基因序列提供其它的遗传元件。病毒早期和晚期启动子特别有用,这是因为二者易于以片段形式从病毒基因组中获得,其还可以含有病毒复制起点(fiers等,1978;kaufman,1990)。来自哺乳动物表达载体的显示增强异源基因表达的其它控制序列包括这样的元件,例如源自cho细胞的表达增强序列元件(expressionaugmentingsequenceelement,ease)(morris等,animalcelltechnology,1997,529-534页和pct申请wo97/25420)以及来自腺病毒2的三联前导序列(tripartiteleader,tpl)和va基因rna(gingeras等,j.biol.chem.257:13475-13491,1982)。病毒来源的内部核糖体进入位点(internalribosomeentrysite,ires)序列允许双顺反子mrna有效翻译(oh和sarnow,1993;ramesh等,1996)。作为双顺反子mrna之一部分的异源cdna(随后是选择标记基因(例如dhfr))的表达已显示出提高宿主的转染能力和异源cdna的表达(kaufman,1990)。采用双顺反子mrna的示例性表达载体是mosser等(1997)描述的ptr-dc/gfp和morris等(1997)描述的p2a5i。mosley等(1989)描述了有用的高表达载体pcavnot。可以如okayama和berg(1983)中公开地构建用于哺乳动物宿主细胞中的其它表达载体。可以基本如cosman等(1986)中所述地来构建在c127鼠乳腺上皮细胞中稳定高水平表达哺乳动物cdna的有用系统。cosman等(1984)描述的有用的高表达载体pmlsvn1/n4已作为atcc39890进行保藏。其它有用的哺乳动物表达载体描述于ep-a-0367566和wo91/18982中,其通过引用并入本文。在另一替代方案中,所述载体可源自逆转录病毒。还可使用另一些有用的表达载体——和pdc311。技术关键在于将低分子量(1kd)、亲水性标记肽与表达载体表达之重组蛋白的n端融合。pdc311是另一种专门用于在cho细胞中表达蛋白质的载体。pdc311的特征在于包含目的基因和二氢叶酸还原酶(dhfr)基因的双顺反子序列(其具有用于dhfr翻译的内部核糖体结合位点)、表达增强序列元件(ease)、人cmv启动子、三联前导序列和多聚腺苷酸化位点。关于可用的信号肽,需要时,可以用异源信号肽或前导序列代替天然信号肽。信号肽或前导序列的选择可取决于诸如产生重组多肽之宿主细胞类型等因素。为了举例说明,在哺乳动物宿主细胞中发挥功能的异源信号肽的实例包括美国专利4,965,195中所述的白介素-7(il-7)的信号序列;cosman等,nature312:768(1984)中所述的白介素-2受体的信号序列;ep367,566中所述的白介素-4受体信号序列;美国专利4,968,607中所述的白介素-1受体信号肽;以及ep460,846中所述的ii型白介素-1受体信号肽。c.分离和纯化本发明还包括分离和纯化所述多肽及其片段的方法。在一个实施方案中,可通过将本发明的多肽或其片段与另一辅助纯化本发明之多肽或片段的多肽融合来实现对所述重组多肽或片段的纯化。这样的融合伴侣(partner)可包括聚his或上述另一些抗原性识别肽以及fc部分。就任何类型的宿主细胞而言,如本领域技术人员所周知地,纯化重组多肽或片段的方法将根据如下因素而有所变化,例如所用宿主细胞的类型以及重组多肽或片段是否分泌到培养基中。一般地,重组多肽或片段可以从宿主细胞中分离(如果不分泌的话)或者可以从培养基或上清液中分离(如果可溶并且分泌的话),随后是一个或多个的浓缩、盐析、离子交换、疏水相互作用、亲和纯化或体积排阻色谱步骤。就实现这些步骤的具体方法而言,首先可使用市售的蛋白质浓缩滤器(例如amicon或milliporepellicon超滤装置)浓缩培养基。浓缩步骤之后,将浓缩物施加至纯化基质(如凝胶过滤介质)。或者,可应用阴离子交换树脂,例如具有二乙基氨基乙基(deae)侧基的基质。所述基质可以是丙烯酰胺、琼脂糖、葡聚糖、纤维素或在蛋白质纯化中常用的其它类型。或者,可采用阳离子交换步骤。合适的阳离子交换剂包括含有磺丙基或羧甲基的多种不溶性基质。此外,可以使用色谱聚焦步骤(chromatofucusingstep)。或者,可以使用疏水相互作用色谱步骤。合适的基质可以是与树脂结合的苯基或辛基部分。此外,可以使用具有选择性结合重组蛋白之基质的亲和色谱。所用此类树脂的实例是凝集素柱、染料柱和金属螯合柱。最后,可以使用一个或多个采用疏水rp-hplc介质(例如硅胶或具有甲基、辛基、辛癸基或其它脂族基团侧基的聚合物树脂)的反相高效液相色谱(rp-hplc)步骤来进一步纯化所述多肽。采用各种组合的上述某些或全部纯化步骤是公知的,并且可用于提供分离且纯化的重组蛋白质。也可使用包含多肽结合蛋白(例如针对本发明多肽产生的单克隆抗体)的亲和柱来亲和纯化所表达的多肽。可使用常规技术从亲和柱移走这些多肽,例如采用高盐洗脱缓冲液然后透析至较低浓度盐缓冲液中备用来实现,或取决于所用的亲和基质通过改变ph或其它组分来实现,或通过使用亲和部分的天然底物(例如本发明的多肽)竞争性移除来实现。在本发明的这一方面中,多肽结合蛋白(例如可以与本发明多肽相互作用的本发明抗多肽抗体或其它蛋白质)可以与固相支持物(例如适用于识别、分离或纯化细胞(其表面上表达本发明的多肽)的柱色谱基质或类似基质)结合。可通过任何手段来实现将本发明的多肽结合蛋白附着至固相接触表面。从固相上释放所选择的细胞是本领域公知的并包括例如使用酶。这样的酶优选是无毒的且对细胞无损害的,优选涉及切割细胞表面的结合区域。期望的纯度取决于蛋白质的目的用途。例如,当所述多肽将在体内施用时,需要相对高的纯度。在这种情形中,纯化所述多肽从而在sds-聚丙烯酰胺凝胶电泳(sds-page)分析后检测不到对应于其它蛋白质的蛋白质条带。本领域技术人员应当了解,由于不同的糖基化、不同的翻译后加工等原因,通过sds-page可观察到对应于所述多肽的多个条带。最优选地,将本发明的多肽纯化至基本均一,即通过sds-page分析显示单一蛋白质条带。可通过银染、考马斯蓝染色或放射自显影(如果蛋白质经放射性标记的话)来观察蛋白质条带。iii.制剂和施用本文所述组合物的施用方式可有所变化。施用疫苗的任何常规方法均是适用的。相信这些包括利用固体生理可接受基质的口服施加或采用生理可接受的分散剂、胃肠外注射、吸入粉末、经皮贴剂、经阴道灌注等。疫苗的剂量取决于施用途径,并根据对象的体积和健康状况而有所变化。制备含有作为活性成分之多肽或肽序列的疫苗是本领域普遍公知的,如美国专利4,608,251;4,601,903;4,599,231;4,599,230;4,596,792和4,578,770中所举例说明地,其均通过引用并入本文。通常,这种疫苗制备成液体溶液或混悬液的可注射形式;也可以制备适用于在注射前溶于或混悬于液体中的固体形式。所述制备物还可以进行乳化。活性免疫成分常与可药用并与活性成分相容的赋形剂混合。合适的赋形剂有例如水、盐水、右旋葡萄糖、甘油、乙醇等,及其组合。此外,如果需要,疫苗可包含一定量的辅助基质例如润湿剂或乳化剂、ph缓冲剂或增强疫苗有效性的佐剂。在一些具体的实施方案中,疫苗与基质的组合进行配制,如美国专利6,793,923和6,733,754中所述,其通过引用并入本文。疫苗可通过吸入来施用。在一些实施方案中,疫苗可作为气雾剂施用。本文所用的术语“气雾剂”或“气雾组合物”是指气体中的固体或液体颗粒悬浮物。该术语一般可用于指经汽化、雾化或者从固体或液体形式转变为可吸入形式(包括悬浮的固体或液体药物颗粒)的组合物。这种气雾剂可经由呼吸系统来递送疫苗。本文所用的“呼吸系统”是指负责摄入氧并排出二氧化碳的机体器官系统。该系统一般包括从鼻至肺泡的所有气道。在哺乳动物中,一般认为包括肺、支气管、细支气管、气管、鼻道和隔膜。就本公开内容而言,将疫苗递送至呼吸系统是指将药物递送至呼吸系统的一个或多个气道(特别是肺)。适用于其它施用模式的其它制剂包括栓剂(肛门或阴道施用)以及在某些情况下的口服制剂。对于栓剂而言,常规的粘合剂和载体可包括例如聚烷撑乙二醇或甘油三酯;可以用含有约0.5%至约10%、优选约1%至约2%之活性成分的混合物形成这种栓剂。口服制剂包括如下这样常用的赋形剂,例如药物级的甘露醇、乳糖、淀粉、硬脂酸镁、糖精钠、纤维素、碳酸镁等。这些组合物采用溶液、混悬剂、片剂、丸剂、胶囊、持续释放制剂或粉末的形式,并含有约10%至约95%、优选约25%至约70%的活性成分。可将所述多肽、肽和脂肽组合物配制成中性或盐形式的疫苗。可药用盐包括酸加成盐(与肽的游离氨基基团形成)以及与无机酸(例如盐酸或磷酸)或有机酸(例如醋酸、草酸、酒石酸、扁桃酸等)形成的盐。与游离羧基基团形成的盐也可衍生自无机碱(例如,钠、钾、铵、钙或铁的氢氧化物)和有机碱(例如异丙胺、三甲胺、2-乙基氨基乙醇、组氨酸、普鲁卡因等)。在许多情形中,理想的是具有多次疫苗施用,通常至多、至少或不超过1、2、3、4、5、6、7、8、9、10、11、12、13、14、15或更多次免疫接种(包括其间的所有范围)。接种通常以每周/每月/每年1、2、3、4、5、6至5、6、7、8、9、10、11至12次为间隔(包括其间的所有数值和范围),更通常是以3至5周为间隔。通常,以1~15年、通常10年为间隔进行定期加强免疫是维持抗体的保护性水平所期望的。免疫过程后可对针对所述抗原的抗体进行测定,如上所述,美国专利3,791,932、4,174,384和3,949,064,其对这些测定类型进行了举例说明。a.联合治疗本发明的组合物和相关方法(特别是hpv表位的施用,包括向患者/对象施用hpvl2蛋白的多肽或肽)也可与常规hpv筛选和/或其它疫苗的施用(包括但不限于抗体或抗体片段、pap涂片、pcr、southern印迹、施用cervarixtm、gardasiltm、针对hpv或其它感染性病原体的疫苗、hpv病变的消融疗法(ablativetherapy)等)联用。一方面,考虑将hpv肽组合物和/治疗与hpv筛选和/或其它治疗联用。或者,所述治疗可在其它治疗之前或之后、以数分钟至数周为间隔来进行。在其它试剂单独施用的实施方案中,一般要确保在每次递送之间的主要时间段内不失效,从而使所述药剂和抗原性组合物仍能针对对象发挥有利的组合作用。在这种情形中,可考虑将各形式在12~24小时内施用,更优选在约6~12小时内施用。然而,在一些情形中,显著延长施用的时间段可以是理想的,其中在各施用之间间隔数天(2、3、4、5、6或7)至数月(1、2、3、4、5、6、7、8、9、10、11、12)或数年(2、3、4、5、6、7、8、9、10、11、12)。可以采用各种组合,例如多型hpv肽治疗是“a”,作为治疗给出的另一种疫苗或抗体或治疗是“b”:a/b/ab/a/bb/b/aa/a/ba/b/bb/a/aa/b/b/bb/a/b/bb/b/b/ab/b/a/ba/a/b/ba/b/a/ba/b/b/ab/b/a/ab/a/b/ab/a/a/ba/a/a/bb/a/a/aa/b/a/aa/a/b/a根据施用这种化合物的一般方法向患者/对象施用本发明的免疫原性组合物,并考虑到多型hpv多肽组合物或本文所述任何其它抗原或抗原组合之组合物的毒性(如果有的话)。可预期的是,必要时可重复所述治疗周期。还考虑到,可将多种标准疗法(如水合作用(hydration))与所述治疗联用。b.预防和/或治疗方法在一些实施方案中,向对象施用药物组合物。本发明的不同方面涉及向对象施用有效量的组合物。在本发明的一些实施方案中,向患者施用多型hpv肽组合物来保护免受或治疗由至少一种或多种hpv病原体的感染。这样的组合物一般溶于或分散于可药用载体或水性介质中。本文所用的术语“可药用”或“药理学可接受”是指这样的化合物、材料、组合物和或剂型,其在安全的医学判断范围内适于与人和动物的组织接触并且无过度的毒性、刺激、过敏反应或其它疑难并发症(相当于合理的益处/风险比)。术语“可药用载体”表示参与携带或运输化学剂的可药用材料、组合物或运载体(vehicle),例如液体或固体填充剂、稀释剂、赋形剂、溶剂或包封材料。可药用载体包括任何以及所有的溶剂、分散介质、包衣、抗细菌剂和抗真菌剂、等渗剂和吸收延迟剂等。这些介质和试剂用于药物活性物质的用途是本领域公知的。除非任一常规介质或试剂与活性成分不相容,否则考虑将其用于免疫原性组合物和治疗性组合物。本发明的活性化合物可配制成用于胃肠外施用,例如配制成用于经静脉内、肌内、皮下或腹膜内途径注射。除了配制成用于气雾剂或胃肠外施用的化合物(例如用于静脉内或肌内注射的那些),其它可药用形式包括例如片剂或用于口服施用的其它固体;延时释放胶囊。作为游离碱或可药用盐的活性化合物的溶液可以在水中制备,并适当混有表面活性剂(例如羟丙基纤维素)。分散制剂也可在甘油、液体聚乙二醇及其混合物以及在油中制备。在普通的储存和使用条件下,这些制备物含有防腐剂以防止微生物的生长。适于注射用的药物形式包括无菌水溶液或分散制剂;制剂包括芝麻油、花生油或水性丙二醇;以及用于临时制备无菌注射溶液或分散制剂的无菌粉末剂。在所有情形中,所述形式必须是无菌的,并且必须是易于注射的流体。其还应当在制备和储存条件下保持稳定,且必须抵抗微生物(如细菌和真菌)的污染作用。所述多型hpv多肽组合物可配制成中性或盐形式。可药用盐包括酸加成盐(与蛋白质的游离氨基基团形成)以及与无机酸(例如盐酸或磷酸)或有机酸(例如醋酸、草酸、酒石酸、扁桃酸等)形成的盐。与游离羧基基团形成的盐也可衍生自无机碱(例如,钠、钾、铵、钙或铁的氢氧化物)和有机碱(例如异丙胺、三甲胺、组氨酸、普鲁卡因等)。载体也可以是含有例如水、乙醇、多元醇(例如甘油、丙二醇和液体聚乙二醇等)及其适当混合物以及植物油的溶剂或分散介质。例如通过使用包衣(如卵磷脂)、通过维持分散时所需的颗粒大小以及通过使用表面活性剂来维持适当的流动性。可通过各种抗细菌剂和抗真菌剂(如苯甲酸酯、氯丁醇、苯酚、山梨酸、硫柳汞等)防止微生物的作用。在许多情形中,优选包括等渗剂(例如糖或氯化钠)。可通过在组合物中使用吸收延迟剂(例如单硬脂酸铝和明胶)来延长注射组合物的吸收。无菌注射溶液通过将所需量的所述活性化合物掺入含上述各成分的适当溶剂中来制备,需要时在随后进行过滤灭菌。一般地,分散制剂通过将各无菌活性成分掺入含有上述基础分散介质和所需其它成分的无菌载体中来制备。在用于制备无菌注射溶液的无菌粉末剂的情形中,优选的制备方法是真空干燥和冷冻干燥技术,其得到活性成分以及来自先前无菌过滤溶液的任何其它期望成分的粉末。通常,通过任意常见途径来施用本发明的组合物。这包括但不限于口服、经鼻或颊内施用。或者,可通过原位、皮内、皮下、肌内、腹膜内、肛门栓剂、阴道内、呼吸道或静脉内施用。在某些实施方案中,可以吸入疫苗组合物(例如美国专利6,651,655,其通过引用具体并入本文)。这样的组合物通常作为包含生理可接受载体、缓冲剂或其它赋形剂的可药用组合物来施用。例如,对于采用水溶液形式的胃肠外施用来说,必要时,所述溶液应当进行适当缓冲,并且液体稀释剂首先用足量盐水或葡萄糖进行等渗处理。这些特定的水溶液尤其适用于静脉内、肌内、皮下和腹膜内施用。在这方面,本领域技术人员根据本公开内容会知晓可用的无菌水性介质。例如,可将一剂量溶于等渗nacl溶液中,并添加到皮下注射液中或注射至期望的输注位点(参见例如,remington′spharmaceuticalsciences,1990)。取决于对象的状况,必然会出现剂量的某些改变。在任何情况下,负责施用的人员确定针对个体对象的合适剂量。基于预期目的来确定治疗性或预防性组合物的有效量。术语“单位剂量”或“剂量”是指适用于对象的物理离散单元,各单元含有预定量的组合物,经计算其能产生与施用(即合适的途径和方案)有关的上述期望应答。根据治疗次数和单位剂量的待施用的量取决于所期望的保护。所述组合物的精确量还取决于从业者的判断,并且对每个个体是独特的。影响剂量的因素包括对象的身体和临床状态、施用途径、治疗的预期目的(缓解症状亦或治愈)以及具体组合物的效力、稳定性和毒性。配制后,溶液以与制剂剂型相容的方式、以治疗或预防有效量进行施用。所述制剂易于采用多种剂型(例如上述注射溶液类型)施用。1.体外、离体或体内施用本文所用的术语“体外施用”是指利用从动物中取出或在动物以外的细胞(包括但不限于培养的细胞)进行的操作。术语“离体施用”是指将已经体外操作的细胞随后施用于活的动物。术语“体内施用”包括所有在动物内进行的操作。在本发明的某些方面中,可以体外、离体或体内施用所述组合物。在一些体外实施方案中,用多型hpv组合物孵育自体b淋巴细胞系或树突细胞。然后,可将活化细胞用于体外分析,或者任选地用于离体施用。2.抗体和被动免疫本发明的另一方面是制备用于预防或治疗hpv感染的免疫球蛋白的方法,其包括如下步骤:用本发明的疫苗免疫受者,从该受者中分离免疫球蛋白或抗体和/或重组产生这种免疫球蛋白或其片段。本发明的另一方面是通过这种方法制备的免疫球蛋白。本发明的又一方面是包含本发明免疫球蛋白和可药用载体的药物组合物,其可以用于制备治疗或预防hpv感染的药物。本发明的另一方面是治疗或预防hpv感染的方法,其包括向患者施用有效量的本发明药物制备物的步骤。产生多克隆抗体的接种物通常通过将抗原性组合物分散到生理可耐受稀释剂(如盐水或适用于人的其它佐剂)中形成水性组合物来制备。向哺乳动物(例如人)施用免疫刺激量的接种物,然后使经接种的对象维持一段足以使该抗原性组合物诱导出保护性抗体的时间。可通过公知技术(例如亲和色谱)将抗体分离至期望的程度(harlow和lane,antibodies:alaboratorymanual1988)。抗体可包括来自多种常用动物(例如山羊、灵长类、驴、猪、马、豚鼠、大鼠)或人的抗血清制备物。给这些动物放血并回收血清。根据本发明产生的免疫球蛋白可以包括完整抗体、抗体片段或亚片段。抗体可以是任何类型的完整免疫球蛋白,例如igg、igm、iga、igd或ige、具有针对本发明两种或更多种抗原的双特异性嵌合抗体或杂合抗体。其也可以是片段,例如f(ab′)2、fab′、fab、fv等,包括杂合片段。免疫球蛋白还可包括通过结合特异性抗原形成复合物从而发挥抗体作用的天然、合成或遗传改造的蛋白质。可以向受者施用本发明的hpv组合物或疫苗,所述受者然后作为免疫球蛋白的来源,所述免疫球蛋白响应于所述hpv组合物的攻击而产生。经此处理的对象提供血浆,超免疫球蛋白通过常规血浆分离方法从该血浆中获得。向另一对象施用所述超免疫球蛋白从而赋予针对hpv感染的抗性或治疗hpv感染。本发明的超免疫球蛋白特别适用于治疗或预防婴儿、免疫力低下之个体中的hpv感染,或者有治疗需求但没有时间响应于接种而产生抗体之个体中的hpv感染。本发明的另一方面是包含一种或多种对本发明免疫组合物之组分具有反应性的单克隆抗体(或其片段;优选人的或人源化的)的药物组合物,其可用于治疗或预防多种hpv类型的感染。制备单克隆抗体的方法是本领域周知的,可包括脾细胞与骨髓瘤细胞的融合(kohler和milstein,1975;harlow和lane,1988)。或者,可通过筛选合适的噬菌体展示文库获得单克隆fv片段(vaughan等,1998)。单克隆抗体可以是人的、利用已知方法人源化的或部分人源化的。iv.药盒本发明的另一方面是用于根据本发明进行接种或治疗的药盒。在一个实施方案中,所述药盒包含小瓶/管和可选的施用说明包装插页,所述小瓶/管包含用于根据本发明方法施用的多型hpv多肽组合物或疫苗。药盒中可包含本文所述的任何组合物。在一个非限制性实例中,用于制备多型hpv多肽、配制多型hpv多肽和/或施用多型hpv多肽的试剂可包括在药盒内。所述药盒还可包含用于在体外和体内评价脂肽活性的试剂。因此,所述药盒包括在合适容器装置中的多型hpv多肽组合物。在某些方面,所述药盒可包括用于施用的试剂和/或装置,例如吸入器或喷雾器。其还可包括一种或多种用于制备所施用组合物的缓冲剂、化合物或装置。药盒的各组分可采用水性介质或冻干形式进行包装。药盒的容器装置一般包括至少一个小瓶、试管、烧瓶、瓶、注射器或其它容器装置,组分可置于所述容器装置中(优选经过适当分装)。当药盒中有多于一种组分时,所述药盒一般还包含第二、第三或另外附加的容器(另外的组分可单独置于其中)。然而,组分的各种组合也可包含在小瓶/管中。通常,本发明的药盒还包括用于将各容器紧密排放便于出售的装置。这样的容器可包括容纳期望小瓶的注塑或吹塑塑料容器。当药盒的组分以一种和/或多种液体溶液提供时,所述液体溶液是水性溶液,特别优选是无菌水性溶液。然而,药盒的组分可作为干粉提供。当试剂和/或组分作为干粉提供时,可通过添加合适的溶剂使所述粉末重溶。可设想到,所述溶剂也可以提供在另一容器装置中。在其它方面,药盒或装置可包含针对本发明多肽的多克隆或单克隆抗体。这样的药盒或装置可用于检测或鉴定或纯化各种样本和/或患者中的病毒。药盒还包括使用该药盒组分以及使用不包括在药盒内的任何其它试剂的说明。说明可包括可实施的变动。应当理解,这些试剂是本发明药盒的实施方案。然而,这样的药盒不限于上述具体条目,其可包括用于制备和/或施用多型hpv多肽疫苗的任何试剂。v.实施例以下给出的实施例目的在于举例说明本发明的各实施方案,而不意在以任何方式限制本发明。本领域技术人员很容易理解,本发明经适当调整以实现所提及的多种目的并获得结果和优点以及本文固有的这些目的、结果和优点。本实施例连同本文所述的方法代表了优选的实施方案,是示范性的,不意在限制本发明的范围。本领域技术人员会意识到涵盖在本发明宗旨(如权利要求的范围所限定的)内的变化及其它用途,。a.结果基于方便的限制性位点而非免疫原性的考虑,选择早期研究中使用的包含残基11-200和1-88的l2疫苗(campo和jarrett,1994;roden等1994)。因此,它们可以不包含所有相关的中和性表位或者具有最佳的免疫原性和稳定性。但是,这些研究表明中和性l2特异性抗体的存在对于保护性免疫是足够的(embers等,2002;gambhira等,2007)。实际上,用l211-200接种在bpv4、crpv和ropv攻击模型中诱导出交叉中和性抗体和保护(gambhira等,2007;campo和jarrett,1994)。用l21-88肽接种也是保护性的,但也有些提议认为,其交叉中和性和交叉保护可能不如用l211-200接种的动物有效(gambhira等,2007)。与此观点一致,用来自94-112和107-122的l2肽进行接种对同源攻击都具有保护性(embers等,2002)。因此,为了评价l2疫苗中包含这些区域的益处,我们制备了在88、107或200位处终止的n端l2多肽用于疫苗研究(表1)。表1:用不同大小的单体或多聚体l2多肽接种之兔的抗体应答。使用cfa/ifa作为佐剂,用300μg的hpv16l2多肽(a)或多聚l2构建体(b)对兔接种4次。在最后一次免疫后的一个月收集超免疫血清,并用全长hpv16l2(16l2elisa)或hpv16l2/l2假病毒粒子(hpv16elisa)包被的微滴定板通过酶联免疫吸附测定(elisa)测试l2特异性抗体。还测试所述血清针对所示hpv假病毒粒子类型的体外中和(invitroneutralization,ivn)效价。在免疫前血清中未检测到中和效价。#蛋白质表现出在大肠杆菌中显著降解。“rb”兔个体。“无”对应于在所测试的最低稀释度(1∶50)下小于50%中和。“-”未测试。l2对于感染是必需的(roden等,2001),并且可具有多种不同的功能(richards等,2006;bossis等,2005;kamper等,2006)。在感染期间,l2必须经弗林蛋白酶切割从而除去1-13位残基(richards等,2006),这使得保守的中和性表位(17-36位残基之间)更易于接近单克隆抗体rg-1(day等,2008)。此外,针对l21-88或11-200多肽的抗血清交叉中和皮肤以及黏膜乳头瘤病毒类型(pastrana等,2005)。因此,我们制备了从1、11、13或89位残基起始的n端l2多肽用于疫苗研究(表1)。用单体和多型l2多肽接种之兔中的应答:为了对交叉中和性表位进行描绘,在大肠杆菌中表达了带有6-his标签的7种hpv16l2多肽(表1),进行亲和纯化以用于免疫接种研究。尽管所有多肽均易于纯化,但是hpv16l213-88和89-200在储藏期间不稳定。用300μg的每种多肽对兔进行5次免疫,最初采用cfa,在加强免疫采用ifa。首先通过在hpv16l2全长elisa和hpv16l1/l2假病毒粒子elisa中测试超免疫血清来验证每次免疫成功与否。针对各hpv16l2多肽均得到高效价的血清抗体,但是针对两种不稳定抗原(l213-88和89-200)之抗血清的抗hpv16假病毒粒子效价较低。然后,测定了由l2多肽诱导的每只兔抗血清的hpv16中和效价以及hpv6、hpv18、hpv31、hpv45和hpv58的交叉中和性效价。与早前的研究(gambhira等,2007)一致,hpv16l211-200和1-88肽诱导出强的hpv16中和抗体效价。在针对hpv16l213-200、1-107、13-107的抗血清中也观察到相似的强hpv16中和抗体效价。用hpv16l289-200接种产生显著较弱的中和应答,尽管其在两只兔之一中诱导出具有高l2elisa效价的抗体。由各种hpv16l2肽诱导的l2特异性抗血清不仅中和hpv16,还中和广泛的异源乳头瘤病毒类型,包括已进行测试的致癌类型hpv18、hpv31、hpv45和hpv58(表2)。然而,针对hpv16的中和抗体效价显著高于针对其它类型的中和抗体效价,尽管在效价与hpv16遗传距离之间没有明显的关系。表2:多型l2构建物的总结*残基命名基于hpv16氨基酸的编号,同源肽的实际残基编号可能会有所不同,但可以通过与hpv16肽进行序列比对来确定。由于替代的hpv16l2肽基本上不提高针对异源病毒的中和效价,我们检测了由源自不同的医学上显著hpv基因型的数种同源l2肽组成的串联(concatenated)融合蛋白。基于本次和先前的结果,选择对应于hpv16l217-36、11-88和11-200的l2多肽用于融合构建物。由于细菌产生较大尺寸重组蛋白常常不很高效,因此我们测试了包含3拷贝11-200(称为11-200×3)、5拷贝11-88(称为11-88×5)和22拷贝17-36(称为17-36×22)的多型构建物,如表2所示,其中每个拷贝均源自医学上相关的各种hpv基因型(devilliers等,2004)。蛋白质在大肠杆菌中表达,在变性条件下进行亲和纯化,并如针对hpv16l2多肽所述地用于免疫兔。与单型l2肽(表1a)相比,用各多型l2融合蛋白(11-200×3、11-88×5和17-36×22)(采用cfa/ifa佐剂)对兔进行接种诱导出更强的交叉中和效价(表1b),而不减弱hpv16中和效价。特别地,11-88×5诱导出针对所有测试hpv类型(包括三种未用于产生融合蛋白的hpv类型(hpv31、45和58))显著高的中和抗体效价。用gardasiltm接种之兔的应答:用l1vlp接种可诱导出交叉中和相关性非常近之乳头瘤病毒类型(例如hpv18和hpv45)的抗体(smith等2007;lin等,1992;richards等,2006)。因此,我们试图比较由用两种不同浓度的gardasiltm(在明矾中配制)接种与用cfa/ifa中配置的多型l2蛋白接种的交叉中和抗体的水平(表3)。用gardasiltm接种产生针对包含在疫苗中的致癌性hpv类型(hpv16和hpv18)的高效价中和抗体。尽管用l2融合蛋白产生更高的hpv16和hpv18效价,但是这发生在更高剂量抗原以及使用更强效的佐剂时。用gardasiltm接种之兔的血清均含有显著水平的hpv45中和抗体,偶尔有hpv31中和抗体,但是未检测到hpv58中和抗体效价。因此,在gardasiltm接种后,针对不包含在疫苗中之hpv类型的中和抗体效价非常低或偶有出现或检测不到。表3:用gardasiltm接种之兔的抗体应答。用300μg多聚l2构建物11-88×5(使用cfa/ifa作为佐剂)或者用30μg或12μg的gardasiltm对兔进行3次接种。最后一次免疫后1个月收集超免疫血清,并测试针对所示hpv假病毒粒子类型的体外中和(ivn)效价。在免疫前血清中未检测到中和效价。“rb”兔个体。“无”对应于在所测试的最低稀释度(1∶50)下小于50%中和。“-”未测试用单体和多型l2多肽接种之小鼠的应答:可以用hpv假病毒粒子攻击小鼠,通过递送报告基因(如萤光素酶)来定量感染(gambhira等,2007;roberts等,2007)。以两周为间隔,用包含17-36,1-88或11-200位残基的hpv16l2多肽、或三种串联多型l2融合蛋白(11-200×3、11-88×5或17-36×22)之一种接种小鼠3次,其中使用基于皂苷的gpi-0100佐剂(marciani等,2000)。两周后收获其血清,测定针对hpv16、hpv18、hpv45、hpv58(四种常见致癌hpv类型)和hpv6(良性生殖器疣中最常见的类型)的体外中和效价。如在兔中所观察到地,用hpv16l21-88或hpv16l211-200接种诱导出显著效价的针对同源病毒类型hpv16的中和抗体。然而,用含有hpv16l217-36残基的合成肽接种则未诱导出中和抗体或l2特异性抗体(未显示),这可能因为其缺乏该小鼠种系的t辅助表位(alphs等,2008)。在无佐剂的情况下用hpv16l1vlp接种,阳性对照诱导出比hpv16l2构建物更高的效价。相反地,用hpv45l1vlp接种未能诱导出hpv16中和抗体,这与针对l1vlp疫苗的类型限制性应答是一致的(图1)。l211-88×5构建物得到比hpv16l21-88肽增加的hpv16中和抗体效价,但是这在11-200×3对比hpv16l211-200中未观察到。17-36×22更加低效(图1),可能由弱的t辅助细胞导致(alphs等,2008)。出人意料的是,在用hpv16l2多肽接种的小鼠中观察到的交叉中和抗体应答不如接受同样接种的兔中产生的抗体应答强。然而,当比较多型l2与hpv16l211-200和1-88构建物时,用11-200×3和11-88×5进行免疫在诱导针对hpv6、hpv18、hpv45和hpv58的中和抗体方面更加有效(图1)。很明显,所述11-200×3和11-88×5多肽不包含来自hpv45或hpv58的序列,然而却观察到了显著的交叉中和作用。添加佐剂的l2多型多肽:潜在地比明矾更有效的或与明矾互补的数种佐剂已在临床疫苗试验中显现出前景,例如免疫刺激序列(immunostimulatorysequence,iss)1018(一种激活toll样受体9的寡核苷酸)(halperin等,2005;halperin等,2003)和基于皂苷的佐剂gpi-0100(marciani等,2003;slovin等,2005)。为了确定特定佐剂在与多型l2疫苗一起配制时是否对诱导hpv中和抗体更加有效,我们一一比较了针对与多种佐剂及其组合一起配制的25μg11-200×3的免疫应答。第三次免疫两周后从小鼠获得血清,测定hpv16、hpv18、hpv45和hpv58的体外中和效价(图2)。在该时间点,各佐剂组之间的体外中和效价非常相似,并且无一显著优于11-200×3在明矾中的制剂。除了峰值效价以外,佐剂还可以延长抗体应答的时间。为了评估佐剂间的差异随着体液反应之减弱会愈加明显的可能性,在接种4个月后用hpv16假病毒粒子攻击小鼠。在施用携带有萤光素酶报告基因的hpv16假病毒粒子3天后,用萤光素酶的底物(萤光素)注射被攻击的小鼠来检测皮肤感染的生物发光信号。单因素方差分析(带有bonferroni比较的anova)显示单独用11-200×3保护免受hpv16感染与pbs对照免疫具有显著差异(p<0.05;图4)。用任意测试佐剂中的11-200×3接种与pbs对照免疫具有更加显著的差异(p<0.001;图4)。特别地,11-200×3外加明矾+iss1018的制剂比单独的11-200×3更有效(p<0.01)。所测试的gpi-0100制剂外加11-200×3比单独的11-200×3(p<0.001)或11-200×3联合明矾(p<0.01)更有效。与仅用11-200×3相比,仅用明矾外加11-200×3或仅用iss1018外加11-200×3在保护方面未观察到统计学显著性差异。单独用hpv16l1vlp(而非hpv45vlp)接种也得到与用11-200×3外加明矾+iss1018或gpi-0100(p<0.001;未显示)接种相似的保护水平。因此,我们试图比较由用gardasiltm接种之小鼠诱导与用佐剂gpi-0100中的11-200×3或11-88×5接种之小鼠诱导的体外中和抗体效价。与用多型l2构建物接种相比,针对hpv16和hpv18产生的体外中和效价在用gardasiltm接种之小鼠的血清中显著更高(其中l1vlp包含在gardasiltm中)。然而,在用gardasiltm接种之小鼠的血清中没有检测到hpv45或hpv58中和抗体(图4)。相反地,在用11-200×3或11-88×5接种的小鼠血清中检测到强的中和抗体效价,尽管这两种构建物都不含源自hpv45或hpv58的l2序列。几种佐剂在临床试验中已被测试并证明有效且安全,包括明矾、gpi-0100、明矾和免疫刺激序列1018(激活toll样受体9的cpg寡核苷酸)。为了确定多聚l2疫苗是否需要特定的佐剂以及佐剂对多聚l2疫苗产生的中和抗体应答加强的程度,对数种佐剂一一进行了比较。因此,用2514在不同佐剂中的l211-200×3或只用佐剂接种小鼠。各组分别为:(1)只有明矾(1.3mg氢氧化铝/小鼠,sigmaa-8222),(2)单独的cpg1018(10μg/小鼠),(3)pbs,(4)单独的11-200×3,(5)11-200×3+明矾(50%悬浮液),(6)11-200×3+cpg1018(10μg/小鼠,dynavax,berkley,ca),(7)11-200×3+gpi-0100(50μg/小鼠,hawaiibiotech,maui,hi),(8)11-200×3+gpi-0100(200μg/小鼠),(9)11-200×3+gpi-0100(50μg/小鼠)+tween40(1mg/鼠,sigmap-1504),(10)11-200×3+明矾+cpg1018(10μg/小鼠)。最后一次免疫两周后获得血清,并测试hpv6、hpv16和hpv18的体外中和。当与单独的蛋白质相比时,各佐剂组之间的体外中和效价非常相似,这表明多聚l2蛋白本身是免疫原性的以及在接种后紧接着不需要特定的佐剂用于获得广泛的中和抗体应答。表4.佐剂组的anova分析bonferroni多重比校检验ppbsvsalum(1.3mg)p<0.05pbsvs1018单独(10μg/小鼠)p>0.05pbsvs11-200x3单独p<0.05pbsvs11-200x3+cpg1018(10μg)p<0.001pbsvs11-200x3+alum(1.3mg)p<0.001pbsvs11-200x3+alum+1018p<0.001pbsvs11-200x3+gpi(50μg)+tweenp<0.001pbsvs11-200x3+gpi-0100(200μg)p<0.001pbsvs11-200x3+gpi-0100(50μg)p<0.001alum(1.3mg)vs1018单独(10μg/小鼠)p>0.05alum(1.3mg)vs11-200x3单独p>0.05alum(1.3mg)vs11-200x3+cpg1018(10μg)p>0.05alum(1.3mg)vs11-200x3+alum(1.3mg)p>0.05alum(1.3mg)vs11-200x3+alum+1018p<0.001alum(1.3mg)vs11-200x3+gpi(50μg)+tweenp<0.001alum(1.3mg)vs11-200x3+gpi-0100(200μg)p<0.001alum(1.3mg)vs11-200x3+gpi-0100(50μg)p<0.0011018单独(10μg/小鼠)vs11-200x3单独p>0.051018单独(10μg/小鼠)vs11-200x3+cpg1018(10μg)p>0.051018单独(10μg/小鼠)vs11-200x3+alum(1.3mg)p>0.051018单独(10μg/小鼠)vs11-200x3+alum+1018p<0.0011018单独(10μg/小鼠)vs11-200x3+gpi(50μg)+tweenp<0.0011018单独(10μg/小鼠)vs11-200x3+gpi-0100(200μg)p<0.0011018单独(10μg/小鼠)vs11-200x3+gpi-0100(50μg)p<0.00111-200x3单独vs11-200x3+cpg1018(10μg)p>0.0511-200x3单独vs11-200x3+alum(1.3mg)p>0.0511-200x3单独vs11-200x3+alum+1018p<0.0111-200x3单独vs11-200x3+gpi(50μg)+tweenp<0.00111-200x3单独vs11-200x3+gpi-0100(200μg)p<0.00111-200x3单独vs11-200x3+gpi-0100(50μg)p<0.00111-200x3+cpg1018(10μg)vs11-200x3+alum(1.3mg)p>0.0511-200x3+cpg1018(10μg)vs11-200x3+alum+1018p>0.0511-200x3+cpg1018(10μg)vs11-200x3+gpi(50μg)+tweenp<0.0111-200x3+cpg1018(10μg)vs11-200x3+gpi-0100(200μg)p<0.0511-200x3+cpg1018(10μg)vs11-200x3+gpi-0100(50μg)p<0.0111-200x3+alum(1.3mg)vs11-200x3+alum+1018p>0.0511-200x3+alum(1.3mg)vs11-200x3+gpi(50μg)+tweenp<0.00111-200x3+alum(1.3mg)vs11-200x3+gpi-0100(200μg)p<0.0511-200x3+alum(1.3mg)vs11-200x3+gpi-0100(50μg)p<0.0111-200x3+alum+1018vs11-200x3+gpi(50μg)+tweenp>0.0511-200x3+alum+1018vs11-200x3+gpi-0100(200μg)p>0.0511-200x3+alum+1018vs11-200x3+gpi-0100(50μg)p>0.0511-200x3+gpi(50μg)+tweenvs11-200x3+gpi-0100(200μg)p>0.0511-200x3+gpi(50μg)+tweenvs11-200x3+gpi-0100(50μg)p>0.0511-200x3+gpi-0100(200μg)vs11-200x3+gpi-0100(50μg)p>0.05b.方法抗原制备:如前所述,通过pcr产生hpv16l2多肽表达构建物(pastrana等,2005)。通过最低自由能计算将多型l2构建物进行密码子优化以在大肠杆菌中表达,并通过blueheroninc.合成5′bamhi和3′xhol位点以便于克隆。将l2基因亚克隆至pet28a载体(novagen)中,所得六组氨酸(6his)标记的重组多肽表达于大肠杆菌bl21(rosettacells,novagen)中(pastrana等,2005)。通过在8m尿素中结合镍-氨基三乙酸(ni-nta)柱(qiagen)亲和纯化所述重组l2多肽(使用变性条件的qiaexpressionist标准纯化方法),然后在盒(pierce)中对dulbecco′s磷酸缓冲盐溶液(pbs)进行透析。通过sds-page来监测纯度,使用牛血清白蛋白标准通过二喹啉甲酸测试(pierce)来测定蛋白质浓度。酶联免疫吸附测定(elisa):在4℃,用大肠杆菌中制备的100ng/孔的6his-hpv16l2或293tt细胞中产生并在pbs中稀释的hpv16l1/l2假病毒粒子过夜包被immobilon板(nunc)。然后,用1%牛血清白蛋白(bsa)-pbs在室温下对孔封闭1小时,并用2倍稀释的抗血清在室温下孵育1小时。用pbs-0.01%(体积/体积)tween20清洗后,加入1%bsa-pbs中以1∶5000稀释的经过氧化物酶标记之山羊抗兔igg(kplinc,gaithersburg,md)维持1小时。然后,再次清洗板,用2,2′-次偶氮基-二(3-乙基苯并噻唑啉-6-磺酸溶液(roche)中显影10分钟(viscidi等,2005)。在elisa读板器(bio-rad,benchmarkplus)中测量405nm处的吸光度(a405)。中和测定:如先前所述进行乳头瘤病毒假病毒粒子的体外中和测定(pastrana等,2004),使用溶于二乙醇胺中的对硝基苯磷酸盐(sigma,st.louis,mo)测定澄清上清液中分泌的碱性磷酸酶的活性,并在405nm处测量吸光度(a405)。用于制备假病毒粒子的构建物和详细操作步骤可在互联网上找到(home.ccr.cancer.gov/lco/。效价定义为引起a405减少50%的最高稀释度的倒数,效价<50视为不显著。动物研究:根据约翰霍普金斯动物饲养和使用委员会以及动物伦理委员会(iaec,inida)的政策和批准进行研究。以两周为间隔、用所示佐剂中25μg抗原(或化学合成制备的hpv16l217-36肽(sigma))对balb/c小鼠(ncifrederick)接种三次,每组5只动物。在最后一次免疫两周后,由尾静脉放血获得血液样品。在第1、28、42、60和76天时用300μgl2多肽(最初在完全弗氏佐剂中,随后在不完全弗氏佐剂中)接种兔。在第1、21、35和56天时用12或30μg的gardasiltm进行接种。最终加强一周后给兔放血。皮肤hpv攻击:用电动剃刀剃去经麻醉balb/c小鼠腹侧躯干的一小片毛发,同时留心不伤到上皮。通过将3×109个假病毒粒子颗粒(100ng)(其含有10μl0.6%羧甲基纤维素中的pyluc)施加到经剃毛的皮肤上进行攻击。三天后,再次麻醉小鼠,注射萤光素(100μl,7mg/ml),利用ivis200生物发光成像系统(xenogen,cranbury,nj)获得它们10分钟的图像。利用livingimage2.20软件(xenogen)分析含病毒接种位点的大小相等区域,通过用缺少l2的非感染性hpv假病毒粒子攻击来测定生物发光背景。统计方法:通过带有boneferroni比较的单因素anova(graphpadprism,版本4),比较小鼠模型中各组之间的效价和感染水平。以下部分对应于母案申请的原始权利要求书:1.分离的多肽组合物,其包含来自感染性生物之至少两种分离物的至少两种同源性免疫原性肽,其中第一免疫原性肽与来自感染性生物之第二分离物的第二同源性免疫原性肽有效偶联。2.项1的多肽,其中所述免疫原性肽被构建为线性排列。3.项1的多肽,其中所述免疫原性肽通过接头部分有效偶联。4.项1的多肽,其中所述多肽是融合蛋白。5.项4的多肽,其中所述融合蛋白包含偶联免疫原性肽的肽接头。6.项1的多肽,其中所述感染性生物是性传播生物。7.项6的多肽,其中所述性传播生物选自乳头瘤病毒(pv)、巨细胞病毒(cmv)、疱疹病毒、乙型肝炎病毒、人免疫缺陷病毒(hiv/aids)、卡波西氏肉瘤相关疱疹病毒(kshv/hhv8)、软下疳嗜血杆菌(haemophilusducreyi)、腹股沟肉芽肿(granulomainguinale)、肉芽肿鞘杆菌(calymmatobacteriumgranulomatis)、淋病奈瑟菌(neisseriagonorrhoeae)、沙眼衣原体(chlamydiatrachomatis)、解尿素支原体(ureaplasmaurealyticum)、人型支原体(mycoplasmahominis)、金黄色葡萄球菌或梅毒螺旋体(treponemapallidum)。8.项1的多肽,其中所述感染性生物是乳头瘤病毒。9.项8的多肽,其中所述乳头瘤病毒是选自α、β、γ、δ、ε、ζ、η、θ、ι、κ、λ、μ、ν、ξ、o或π乳头瘤病毒的乳头瘤病毒属成员。10.项8的所述多肽,其中所述感染性生物是人乳头瘤病毒(hpv)。11.项10的多肽,其中所述hpv是皮肤hpv。12.项10的多肽,其中所述hpv是粘膜高风险hpv。13.项1的多肽,其中免疫原性肽是选自如下一种或多种的免疫原性hpv肽:hpv1,hpv2,hpv3,hpv4,hpv5,hpv6,hpv7,hpv8,hpv9,hpv10,hpv11,hpv12,hpv13,hpv14,hpv15,hpv16,hpv17,hpv18,hpv19,hpv20,hpv21,hpv22,hpv23,hpv24,hpv25,hpv26,hpv27,hpv28,hpv29,hpv30,hpv31,hpv32,hpv33,hpv34,hpv35,hpv36,hpv37,hpv38,hpv39,hpv40,hpv41,hpv42,hpv43,hpv44,hpv45,hpv46,hpv47,hpv48,hpv49,hpv50,hpv51,hpv52,hpv53,hpv54,hpv55,hpv56,hpv57,hpv58,hpv59,hpv60,hpv61,hpv62,hpv63,hpv64,hpv65,hpv66,hpv67,hpv68,hpv69,hpv70,hpv71,hpv72,hpv73,hpv74,hpv75,hpv76,hpv77,hpv78,hpv79,hpv80,hpv81,hpv82,hpv83,hpv84,hpv85,hpv86,hpv87,hpv88,hpv89,hpv90,hpv91,hpv92,hpv93,hpv94,hpv95,hpv96,hpv97,hpv98,hpv99或hpv100多肽。14.项1的多肽,其中免疫原性肽选自如下一种或多种多肽:hpv1、hpv2、hpv5、hpv6、hpv8、hpv11、hpv16、hpv18、hpv31、hpv33、hpv35、hpv39、hpv45、hpv51、hpv52、hpv56、hpv58、hpv59、hpv68、hpv73或hpv82多肽。15.项1的多肽,其中免疫原性肽选自如下一种或多种多肽:hpv6、hpv16、hpv18、hpv31、hpv39、hpv51、hpv56和/或hpv73多肽。16.项1的多肽,其中免疫原性肽选自hpv1、hpv5、hpv6、hpv16和/或hpv18多肽。17.项1的多肽,其中免疫原性肽选自hpv6、hpv16或hpv18多肽中的一种或多种。18.项13的多肽,其中免疫原性hpv肽是hpvl2多肽区段。19.项13的多肽,其中所述hpvl2肽区段对应于seqidno:1的13-45、17-36、1-88、11-88或11-200位氨基酸位置。20.项18的多肽,其中至少一种hpvl2肽是hpv16l2肽。21.项18的多肽,其中至少一种hpvl2肽是hpv18l2肽。22.项18的多肽,其中至少一种hpvl2肽是hpv6l2肽。23.项18的多肽,其中至少一种hpvl2肽是hpv45l2肽。24.项18的多肽,其包含至少3、4、5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、21、22或更多种免疫原性肽。25.项18的多肽,其包含至少3种免疫原性肽。26.项18的多肽,其包含至少5种免疫原性肽。27.项18的多肽,其包含至少20种免疫原性肽。28.项25的多肽,其中至少一种hpvl2肽是hpv16l2肽。29.项25的多肽,其中至少一种hpvl2肽是hpv18l2肽。30.项25的多肽,其中至少一种hpvl2肽是hpv6l2肽。31.项25的多肽,其中至少一种hpvl2肽是hpv45l2肽。32.项25的多肽,其中第一hpvl2肽是hpv16l2肽,第二hpvl2肽是hpv18l2肽。33.项25的多肽,其中第一hpvl2肽是hpv16l2肽,第二hpvl2肽是hpv6l2肽。34.项25的多肽,其中第一hpvl2肽是hpv18l2肽,第二hpvl2肽是hpv6l2肽。35.项25的多肽,其中第一hpvl2肽是hpv16l2肽,第二hpvl2肽是hpv18l2肽,第三hpvl2肽是hpv6l2肽。36.项18的多肽,其中所述hpvl2肽具有选自seqidno:71-92和/或seqidno:94-106和/或seqidno:110-112的氨基酸序列。37.项1的多肽,其中所述hpvl2肽包含与seqidno:93或seqidno:107或seqidno:108或seqidno:109或seqidno:113或seqidno:114的氨基酸序列具有至少60%同一性的氨基酸序列。38.项1的多肽,其中所述hpvl2肽包含与seqidno:93或seqidno:107或seqidno:108或seqidno:109或seqidno:113或seqidno:114的氨基酸序列具有至少70%同一性的氨基酸序列。39.项1的多肽,其中所述hpvl2肽包含与seqidno:93或seqidno:107或seqidno:108或seqidno:109或seqidno:113或seqidno:114的氨基酸序列具有至少80%同一性的氨基酸序列。40.项1的多肽,其中所述hpvl2肽包含seqidno:93或seqidno:107或seqidno:108或seqidno:109或seqidno:113或seqidno:114的氨基酸序列。41.项18的多肽,其还包含非hpvl2肽。42.项41的多肽,其中所述非hpvl2肽是hpvl1肽或hpvl1蛋白质。43.项41的所述多肽,其中所述非hpvl2肽是th活化表位、载体蛋白质或佐剂。44.包含项1之多肽的药盒。45.编码项1之多肽的核酸。46.包含项1之多肽的颗粒组合物。47.项46的颗粒组合物,其中所述颗粒是病毒颗粒。48.项46的颗粒组合物,其中所述颗粒是病毒样颗粒。49.项46的颗粒组合物,其中所述颗粒是病毒衣壳。50.诱导针对乳头瘤病毒之免疫应答的方法,其包括施用有效量的项8之分离多肽。51.项50的方法,其中所述免疫应答是体液免疫应答。52.预防乳头瘤病毒感染的方法,其包括施用有效量的项8之多肽。53.包含项1之多型组合物的药盒。54.包含与项1之组合物结合的抗体的药盒。参考文献以下参考文献通过引用具体并入本文,其提供了补充本文描述的示范性方法或其它细节。美国专利3,791,932美国专利4,174,384美国专利3,949,064美国专利4,608,251美国专利4,601,903美国专利4,599,231美国专利4,599,230美国专利4,596,792美国专利4,578,770美国专利4,751,180美国专利4,935,233美国专利4,965,195美国专利4,968,607美国专利5,700,910美国专利6,448,070美国专利6,110,466美国专利6,171,591美国专利6,651,655美国专利6,814,971美国专利5,084,269美国专利6,656,462美国专利7,425,438美国专利7,416,846美国专利7,416,732美国专利7,407,807美国专利7,374,767美国专利7,201,908美国专利7,189,513美国专利7,288,258美国专利公开2003/0223938美国专利公开2004/0033585美国专利公开2004/0258698美国专利公开2005/0048082美国专利公开2006/0035853美国专利公开2007/0041999美国专利公开2008/0145375alphsetal.,proc.natl.acad.sci.usa,105(15):5850-5,2008.bachmannandzinkernagel,annu.rev.immunol.,15:235-70,1997.bakeretal.,biophys.j.,60:1445-1456,1991.barrandtamms,clin.i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