Development of HPV vaccines for HPV-associated head and neck squamous cell carcinoma

被引:57
作者
Devaraj, K
Gillison, ML
Wu, TC
机构
[1] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
[2] Johns Hopkins Med Inst, Dept Oncol, Baltimore, MD 21205 USA
[3] Johns Hopkins Med Inst, Dept Obstet & Gynecol, Baltimore, MD 21205 USA
[4] Johns Hopkins Med Inst, Dept Med Microbiol & Immunol, Baltimore, MD 21205 USA
关键词
HPV vaccines; head and neck squamous cell carcinoma; immunotherapy; tumor; specific antigens; cytotoxic T-lymphocyte; tumor immunology;
D O I
10.1177/154411130301400505
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
High-risk genotypes of the human papillomavirus ( HPV), particularly HPV type 16, are found in a distinct subset of head and neck squamous cell carcinomas ( HNSCC). Thus, these HPV-associated HNSCC may be prevented or treated by vaccines designed to induce appropriate HPV virus-specific immune responses. Infection by HPV may be prevented by neutralizing antibodies specific for the viral capsid proteins. In clinical trials, vaccines comprised of HPV virus-like particles ( VLPs) have shown great promise as prophylactic HPV vaccines. However, given that capsid proteins are not expressed at detectable levels by infected basal keratinocytes, vaccines with therapeutic potential must target other non-structural viral antigens. Two HPV oncogenic proteins, E6 and E7, are important in the induction and maintenance of cellular transformation and are coexpressed in the majority of HPV-containing carcinomas. Therefore, therapeutic vaccines targeting these proteins may have potential to control HPV-associated malignancies. Various candidate therapeutic HPV vaccines are currently being tested whereby E6 and/or E7 is administered in live vectors, in peptides or protein, in nucleic acid form, as components of chimeric VLPs, or in cell-based vaccines. Encouraging results from experimental vaccination systems in animal models have led to several prophylactic and therapeutic vaccine clinical trials. Should they fulfill their promise, these vaccines may prevent HPV infection or control its potentially life-threatening consequences in humans.
引用
收藏
页码:345 / 362
页数:18
相关论文
共 213 条
[91]   HUMAN-LEUKOCYTE ANTIGEN-A2.1 RESTRICTED CANDIDATE CYTOTOXIC T-LYMPHOCYTE EPITOPES OF HUMAN PAPILLOMAVIRUS TYPE-16 E6-PROTEIN AND E7-PROTEIN IDENTIFIED BY USING THE PROCESSING-DEFECTIVE HUMAN CELL LINE-T2 [J].
KAST, WM ;
BRANDT, RMP ;
DRIJFHOUT, JW ;
MELIEF, CJM .
JOURNAL OF IMMUNOTHERAPY, 1993, 14 (02) :115-120
[92]   Common neutralization epitope in minor capsid protein L2 of human papillomavirus types 16 and 6 [J].
Kawana, K ;
Yoshikawa, H ;
Taketani, Y ;
Yoshiike, K ;
Kanda, T .
JOURNAL OF VIROLOGY, 1999, 73 (07) :6188-6190
[93]   Nasal immunization of mice with peptide having a cross-neutralization epitope on minor capsid protein L2 of human papillomavirus type 16 elicit systemic and mucosal antibodies [J].
Kawana, K ;
Kawana, Y ;
Yoshikawa, H ;
Taketani, Y ;
Yoshiike, K ;
Kanda, T .
VACCINE, 2001, 19 (11-12) :1496-1502
[94]   EFFICIENT SELF-ASSEMBLY OF HUMAN PAPILLOMAVIRUS TYPE-16 L1 AND L1-L2 INTO VIRUS-LIKE PARTICLES [J].
KIRNBAUER, R ;
TAUB, J ;
GREENSTONE, H ;
RODEN, R ;
DURST, M ;
GISSMANN, L ;
LOWY, DR ;
SCHILLER, JT .
JOURNAL OF VIROLOGY, 1993, 67 (12) :6929-6936
[95]   Virus-like particles of bovine papillomavirus type 4 in prophylactic and therapeutic immunization [J].
Kirnbauer, R ;
Chandrachud, LM ;
ONeil, BW ;
Wagner, ER ;
Grindlay, GJ ;
Armstrong, A ;
McGarvie, GM ;
Schiller, JT ;
Lowy, DR ;
Campo, MS .
VIROLOGY, 1996, 219 (01) :37-44
[96]   A controlled trial of a human papillomavirus type 16 vaccine [J].
Koutsky, LA ;
Ault, KA ;
Wheeler, CM ;
Brown, DR ;
Barr, E ;
Alvarez, FB ;
Chiacchierini, LM ;
Jansen, KU .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (21) :1645-1651
[97]   Induction of an antibody response in mice against human papillomavirus (HPV) type 16 after immunization with HPV recombinant Salmonella strains [J].
Krul, MRL ;
Tijhaar, EJ ;
Kleijne, JAFW ;
VanLoon, AM ;
Nievers, MG ;
Schipper, H ;
Geerse, L ;
VanderKolk, M ;
Steerenberg, PA ;
Mooi, FR ;
DenOtter, W .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 1996, 43 (01) :44-48
[98]   Phase IIa safety and immunogenicity of a therapeutic vaccine, TA-GW, in persons with genital warts [J].
Lacey, CJN ;
Thompson, HSG ;
Monteiro, EF ;
O'Neill, T ;
Davies, ML ;
Holding, FP ;
Fallon, RE ;
Roberts, JSC .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (03) :612-618
[99]   GENITAL PAPILLOMAVIRUS INFECTION AND CERVICAL DYSPLASIA - OPPORTUNISTIC COMPLICATIONS OF HIV-INFECTION [J].
LAGA, M ;
ICENOGLE, JP ;
MARSELLA, R ;
MANOKA, AT ;
NZILA, N ;
RYDER, RW ;
VERMUND, SH ;
HEYWARD, WL ;
NELSON, A ;
REEVES, WC .
INTERNATIONAL JOURNAL OF CANCER, 1992, 50 (01) :45-48
[100]   Regression of established human papillomavirus type 16 (HPV-16) immortalized tumors in vivo by vaccinia viruses expressing different forms of HPV-16 E7 correlates with enhanced CD8+ T-cell responses that home to the tumor site [J].
Lamikanra, A ;
Pan, ZK ;
Isaacs, SN ;
Wu, TC ;
Paterson, Y .
JOURNAL OF VIROLOGY, 2001, 75 (20) :9654-9664