Cellular immune responses to HPV-18, -31, and -53 in healthy volunteers immunized with recombinant HPV-16 L1 virus-like particles

被引:46
作者
Pinto, Ligia A.
Viscidi, Raphael
Harro, Clayton D.
Kemp, Troy J.
Garcia-Pineres, Alfonso J.
Trivett, Matthew
Demuth, Franklin
Lowy, Douglas R.
Schiller, John T.
Berzofsky, Jay A.
Hildesheim, Allan
机构
[1] NCI, HPV Immunol Lab, SAIC Frederick, Frederick, MD 21702 USA
[2] Johns Hopkins Univ, Baltimore, MD 21218 USA
[3] Informat Management Serv Inc, Silver Spring, MD USA
[4] NCI, Cellular Oncol Lab, NIH, Bethesda, MD 20892 USA
[5] NCI, Vaccine Branch, NIH, Bethesda, MD 20892 USA
[6] NIH, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
关键词
T cells; cytokines; vaccination; infectious diseases;
D O I
10.1016/j.virol.2006.06.021
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human papillomavirus-like particles (HPV VLP) are candidate vaccines that have shown to be efficacious in reducing infection and inducing robust antiviral immunity. Neutralizing antibodies generated by vaccination are largely type-specific, but little is known about the type-specificity of cellular immune responses to VLP vaccination. To determine whether vaccination with HPV-16 L1VLP induces cellular immunity to heterologous HPV types (HPV-18, HPV-31, and HPV-53), we examined proliferative and cytokine responses in vaccine (n=11) and placebo (n=5) recipients. Increased proliferative and cytokine responses to heterologous types were observed postvaccination in some individuals. The proportion of women responding to heterologous types postvaccination (36%-55%) was lower than that observed in response to HPV-16 (73%). Response to HPV-16 VLP predicted response to other types. The strongest correlations in response were observed between HPV-16 and HPV-31, consistent with their phylogenetic relatedness. In summary, PBMC from HPV-16 VLP vaccine recipients can respond to L1VLP from heterologous HPV types, suggesting the presence of conserved T cell epitopes. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:451 / 462
页数:12
相关论文
共 43 条
[21]  
3.0.CO
[22]  
2-6
[23]   Epidemiologic classification of human papillomavirus types associated with cervical cancer [J].
Muñoz, N ;
Bosch, FX ;
de Sanjosé, S ;
Herrero, R ;
Castellsagué, X ;
Shah, KV ;
Snijders, PJF ;
Meijer, CJLM .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (06) :518-527
[24]   Reactivity of human sera in a sensitive, high-throughput pseudovirus-based papillomavirus neutralization assay for HPV16 and HPV18 [J].
Pastrana, DV ;
Buck, CB ;
Pang, YYS ;
Thompson, CD ;
Castle, PE ;
FitzGerald, PC ;
Kjaer, SK ;
Lowy, DR ;
Schiller, JT .
VIROLOGY, 2004, 321 (02) :205-216
[25]   Cellular immune responses to human papillomavirus (HPV)-16 L1 in healthy volunteers immunized with recombinant HPV-16 L1 virus-like particles [J].
Pinto, LA ;
Edwards, J ;
Castle, PE ;
Harro, CD ;
Lowy, DR ;
Schiller, JT ;
Wallace, D ;
Kopp, W ;
Adelsberger, JW ;
Baseler, MW ;
Berzofsky, JA ;
Hildesheim, A .
JOURNAL OF INFECTIOUS DISEASES, 2003, 188 (02) :327-338
[26]   In vitro generation and type-specific neutralization of a human papillomavirus type 16 virion pseudotype [J].
Roden, RBS ;
Greenstone, HL ;
Kirnbauer, R ;
Booy, FP ;
Jessie, J ;
Lowy, DR ;
Schiller, JT .
JOURNAL OF VIROLOGY, 1996, 70 (09) :5875-5883
[27]   Assessment of the serological relatedness of genital human papillomaviruses by hemagglutination inhibition [J].
Roden, RBS ;
Hubbert, NL ;
Kirnbauer, R ;
Christensen, ND ;
Lowy, DR ;
Schiller, JT .
JOURNAL OF VIROLOGY, 1996, 70 (05) :3298-3301
[28]   Human dendritic cells are activated by chimeric human papillomavirus type-16 virus-like particles and induce epitope-specific human T cell responses in vitro [J].
Rudolf, MP ;
Fausch, SC ;
Da Silva, DM ;
Kast, WM .
JOURNAL OF IMMUNOLOGY, 2001, 166 (10) :5917-5924
[29]   CROSS-REACTIVITIES IN MEMORY CYTOTOXIC T-LYMPHOCYTE RECOGNITION OF HETEROLOGOUS VIRUSES [J].
SELIN, LK ;
NAHILL, SR ;
WELSH, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (06) :1933-1943
[30]   CD4 T-cell memory [J].
Stockinger, B ;
Kassiotis, G ;
Bourgeois, C .
SEMINARS IN IMMUNOLOGY, 2004, 16 (05) :295-303