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Session 168 Poster Abstracts
Malignancies
Session Day and Time: Wednesday, 1-4 pm
Room: Hall B


1023
Cervical Human Papillomavirus Infection in HIV-1-infected Pregnant Women in Zimbabwe
David Hill*1, D Katzenstein1, A Shetty2, C Ley3, J Palefsky4, and Y Maldonado1
1Stanford Univ Sch of Med, Palo Alto, CA, US; 2Wake Forest Univ Baptist Med Ctr, Winston-Salem, NC, US; 3Caradon Consulting, San Carlos, CA, US; and 4Univ of California, San Francisco, US

Background:  Protective human papilloma virus (HPV) immunization and ART are interventions to reduce cervical cancer and the sexual and vertical transmission of HIV. However, the 2 current HPV vaccines are only known to be effective against specific types (16 and 18) of HPV. In Zimbabwe, we surveyed HPV genotypes among HIV+ pregnant women infected with subtype C HIV-1 and assessed cervical HPV infection and HIV-1 virus shedding.

Methods:  HIV-1 (subtype C) -positive pregnant women in Zimbabwe were evaluated for HIV and HPV infection by assays of cervical swab samples. For HPV, real-time polymerase chain reaction (RT-PCR) was performed followed by a generic (“consensus”) HPV probe using DNA hybridization, and positive samples were re-probed for 29 individual HPV types and a probe mixture of 10 types. Cervical HIV RNA was measured by a modified Amplicor RT-PCR of viral particles concentrated from the supernatant and expressed as log copies/ml with a lower limit of detection of 2.29.  

Results:  A total of 119 subjects were enrolled; 5 were excluded from HPV analyses because of insufficient DNA. With the generic probe, 82% (94 of 114) of samples were HPV+. Re-probing identified 27 unique HPV types in 72 women; 58% (66 of 114) had high cancer risk genotypes; HPV 58 in 19 women, followed by HPV 66, found in 14 women. HIV cervical virus was detected in 46 of 52 (88%) of cervical samples tested, with a median cervical virus load of 3.54 log copies/mL. There was no correlation between HIV-1 shedding and the presence of HPV, or specific HPV types in cervical samples.

Conclusions:  A high proportion of HIV+ pregnant women in Zimbabwe shed HIV-1 RNA and carried high risk cervical HPV types associated with increased cervical cancer risk. However, only 16 of 94 (17%) were infected with HPV-16 or -18, types against which current vaccines are known to be protective. These data suggest that current HPV vaccines may not prevent HPV infections or provide protection against the high risk HPV types prevalent among HIV-infected women in Zimbabwe.