T-cell proliferative response to human papillomavirus type 16 peptides: Relationship to cervical intraepithelial neoplasia

被引:40
作者
Nakagawa, M
Stites, DP
Farhat, S
Judd, A
Moscicki, AB
Canchola, AJ
Hilton, JF
Palefsky, JM
机构
[1] UNIV CALIF SAN FRANCISCO,SCH MED,DEPT PEDIAT,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,SCH MED,DEPT STOMATOL,SAN FRANCISCO,CA 94143
[3] UNIV CALIF SAN FRANCISCO,SCH MED,DEPT EPIDEMIOL & BIOSTAT,SAN FRANCISCO,CA 94143
[4] UNIV CALIF SAN FRANCISCO,SCH DENT,SAN FRANCISCO,CA 94143
[5] SRI INT,BIOORGAN CHEM LAB,MENLO PK,CA 94025
关键词
D O I
10.1128/CDLI.3.2.205-210.1996
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The incidence of human papillomavirus (HPV)-related cervical intraepithelial neoplasia (CIN) and cervical cancer is increased with immunodeficiency, but the role of immune response, including cell-mediated immunity, in disease prevention is not well understood. In this study, T-cell proliferative responses to six synthetic peptides with predicted immunogenic determinants from the HPV-16 E4, E6, E7, and L1 open reading frames were analyzed in 22 sexually active women with ne-cv-onset CIN and 65 sexually active women without cervical disease, characterized by cytology, colposcopy, and HPV testing, T-cell proliferative responses were demonstrated to all six HPV-16 peptides. Although not statistically significant, rates of reactivity to E6 (24-45) were higher among sexually active women without disease (26%) than among women with current CIN (7%), as was the overall number of peptides stimulating a response. Women with CIN may not respond to selected HPV antigens as well as women without disease do.
引用
收藏
页码:205 / 210
页数:6
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