Association of cutaneous anergy with human papillomavirus and cervical neoplasia in HIV-seropositive and seronegative women

被引:7
|
作者
Harris, Tiffany G. [1 ]
Burk, Robert D. [1 ]
Xue, Xiaonan [1 ]
Anastos, Kathryn [1 ]
Minkoff, Howard [1 ]
Massad, L. Stewart [1 ]
Young, Mary A. [1 ]
Levine, Alexandra M. [1 ]
Gange, Stephen J. [1 ]
Watts, D. Heather [1 ]
Palefsky, Joel M. [1 ]
Strickler, Howard D. [1 ]
机构
[1] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10461 USA
关键词
anergy; CD4 T-lymphocyte count; cellular immunity; HIV; human papillornavirus;
D O I
10.1097/QAD.0b013e3282c3a945
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: Cutaneous anergy testing evaluates delayed type hypersensitivity responses and is, in essence, an in-vivo measure of cell-mediated immune function at an epithelial surface. This study assessed the relationship of anergy test results with cervical infection by human papillomavirus (HPV) and cervical neoplasia in HIV-seropositive and seronegative women. Methods: HIV-seropositive (n=1029) and HIV-seronegative (n=272) women enrolled in a long-term cohort study were followed semi-annually with HPV-DNA testing and cytology. Anergy was defined as unresponsiveness to Candida albicans, tetanus toxoid, and mumps antigen. Results: Anergy was associated with the prevalent detection of squamous intraepithelial lesions [SIL; adjusted odds ratio 1.70; 95% confidence interval (CI) 1.16-2.48] in multivariable logistic regression models, and with the incident detection of oncogenic HPV (adjusted hazard ratio 1.24; 95% CI 0.99-1.56) in multivariable Cox regression models. These models adjusted for HIV infection, combined CD4 T-cell and HIV-RNA strata (13 separate strata to control optimally for their interactive effects), as well as other variables. Conclusion: Cutaneous anergy testing may measure aspects of local cellular immune function in epithelial tissues that are important for the control of HPV and development of SIL, and that in HIV-seropositive women are not fully accounted for by circulating CD4 T-cell counts and HIV-RNA levels. (C) 2007 Lippincott Williams & Wilkins.
引用
收藏
页码:1933 / 1941
页数:9
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