학술논문

AIDS Malignancy Consortium 054: Safety and Immunogenicity of the Quadrivalent Vaccine in Indian Women Living With HIV
Document Type
article
Source
JAIDS Journal of Acquired Immune Deficiency Syndromes. 87(2)
Subject
Vaccine Related
Immunization
Sexually Transmitted Infections
Prevention
HPV and/or Cervical Cancer Vaccines
HIV/AIDS
Infectious Diseases
Cervical Cancer
Clinical Research
Cancer
3.4 Vaccines
Prevention of disease and conditions
and promotion of well-being
Infection
Good Health and Well Being
Adult
Antibodies
Viral
Female
HIV Infections
Human Papillomavirus Recombinant Vaccine Quadrivalent
Types 6
11
16
18
Human papillomavirus 16
Human papillomavirus 18
Humans
India
Papillomavirus Infections
Pilot Projects
Uterine Cervical Neoplasms
Vaccination
Viral Load
Young Adult
Indian
women living with HIV
human papillomavirus
vaccination
quadrivalent HPV vaccine
cervical cancer
Clinical Sciences
Public Health and Health Services
Virology
Language
Abstract
BackgroundHuman papillomavirus (HPV)-associated cervical cancer is a leading cause of death among Indian women. Indian women living with HIV (WLWH) may be at especially high risk. The quadrivalent HPV (qHPV) vaccine is effective in prevention of initial infection with HPV-6/11/16/18 in HIV-negative women. Little is known about previous exposure to HPV-6/11/16/18, safety, and immunogenicity of qHPV in Indian WLWH.MethodologyOne hundred fifty WLWH with different CD4 levels and HIV viral load (VL) were vaccinated at 0/2/6 months at CART-CRS-IDMC, Chennai, India. Serology was performed at weeks 0, 28, and 52 for HPV-6/11/16/18 using a competitive Luminex immunoassay and for HPV-16/18 using a pseudovirion-based neutralization assay.ResultsMean age was 30.8 years (range, 19-44 years). 71/87/73/81% of women were naive (sero-negative and DNA-negative) to HPV-6/11/16/18 at baseline, respectively. Among per-protocol women naive to HPV-6/11/16/18 at baseline, 100/99/99/90%, respectively, seroconverted at week 28 and 95/96/98/71% were sero-positive at week 52, respectively. Pseudovirion-based neutralization assay identified more seroconversion to HPV-18 than competitive Luminex immunoassay. There were no significant differences in the proportion seroconverting by baseline or nadir CD4 or HIV VL; however, there was a trend for increased proportion seroconverting to HPV-18 among women with higher baseline CD4 level (P = 0.052). There were no qHPV-related serious adverse events and no change in CD4 level or HIV VL among women on ART.ConclusionsqHPV vaccine was safe and immunogenic in Indian WLWH. A high proportion were naive to HPV-6/11/16/18 and may benefit from vaccination although many were married and several years post-initiation of sexual activity.