Secondary Logo

Journal Logo

Institutional members access full text with Ovid®

Cervical human papillomavirus infection and cervical intraepithelial neoplasia in women positive for human immunodeficiency virus in the era of highly active antiretroviral therapy

Palefsky, Joel M.

Cancer in AIDS

Purpose of review Human papillomavirus (HPV) has been strongly implicated in the pathogenesis of cervical intraepithelial neoplasia (CIN) and cervical cancer. Women who are positive for the human immunodeficiency virus (HIV) have been shown to be at increased risk for cervicovaginal HPV infection and CIN, and cervical cancer is an acquired immunodeficiency syndrome–defining illness. The purpose of this review is to summarize recent studies of cervical HPV infection and CIN in HIV-positive women and to describe the effect of highly active antiretroviral therapy (HAART) on the course of CIN.

Relevant findings HIV-positive women have a higher prevalence of cervical HPV infection than HIV-negative women, and HPV infection is more persistent in the HIV-positive population. The incidence of high-grade CIN is increased in HIV-positive women. HAART has not been shown to affect HPV detection, and data on its effect on the natural history of CIN are mixed. Some studies show no effect of HAART on the natural history of CIN, and others show a statistically significant but modest beneficial effect.

Summary Cervical HPV infection and CIN are clearly increased in HIV-positive women when compared with risk-matched HIV-negative women. HAART appears to have limited ability to clear HPV infection and induce regression of CIN in HIV-positive women. Combined with the high prevalence of cervical HPV infection and CIN, current data suggest that CIN should be aggressively sought and treated in HIV-positive women, including those who have responded well to HAART with good HIV viral load suppression and increasing CD4+ levels.

Department of Medicine, University of California, San Francisco, San Francisco, California, USA

Correspondence to Joel Palefsky MD, CM, FRCP, C 505 Parnassus Ave, Room M1202, Box 0126, UCSF San Francisco, CA 94143, USA


Sources of support: R01 CA 54053, R01 CA/AI 88739, MO1 RR00079. Data in this article were also derived in part from studies carried out in the General Clinical Research Centers, University of California, San Francisco with funds provided by the Division of Research Resources 5 M01-RR-00079, U.S. Public Health Service.

© 2003 Lippincott Williams & Wilkins, Inc.