The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.
Brief Title: IMPAACT P1085: Human Papilloma Virus (HPV) Type-Specific Antibody
Official Title: Duration of Human Papilloma Virus (HPV) Type-Specific Antibody After Administration of Quadrivalent HPV Vaccine (QHPV) to HIV-1 Infected Children Previously Enrolled in IMPAACT P1047
Study ID: NCT01206556
Brief Summary: This study is being done to evaluate how long the immune response from the Human Papilloma Virus (HPV) vaccine you / your child received persists. The immune response occurred after immunization and is what protects you/your child from HPV disease. You / your child received this vaccine as part of an earlier study (P1047). The vaccine is called Human Papillomavirus Vaccine (QHPV Vaccine, also known as GARDASIL®). The study will check to see if the protective effects (called "antibodies") produced by the vaccine have lasted, and for how long these effects will continue to last. You will not be given any medications or vaccines as part of this follow-up study.
Detailed Description: Genital Human Papilloma Virus (HPV) infection is the most common sexually transmitted infection (STI) in the United States and worldwide. Over 50% of sexually active adolescents will become infected with HPV. HPV infection is strongly associated with the development of anogenital dysplasias and invasive cancers. Because HPV is a STI, optimal prevention in women will depend on prevention in their partners as well. Males remain a significant reservoir of HPV and vaccinating them will be essential for rapidly preventing transmission of HPV in the community. P1085 is a sub study of P1047, which investigated the safety and immunogenicity of Quadrivalent HPV (QHPV) in HIV-infected girls and boys, age 7 to \<12 years of age. This study was a placebo-controlled trial that compared a recommended three dose schedule of QHPV in one study arm (Arm A) with an arm that received placebo (Arm B). P1047 has thus far demonstrated that QHPV can be safely administered to human immunodeficiency virus (HIV)-infected boys and girls and will stimulate seroconversion in more than 95% of vaccinees. However, these antibody levels were 30-50% lower than those achieved in children without HIV infection. Since levels of vaccine-induced antibodies decline with time after vaccination, it is uncertain if vaccine-induced immunity will be life-long. This concern is supported by some evidence that naturally acquired HPV-specific antibody might decline to a level that will permit re-infection. Comparative persistence data for HPV-specific antibody is available for 5-6 years after vaccination of almost 1000 children without HIV infection (manufacturer's data, unpublished), but there is no such information available from HIV-infected vaccinees. We seek to determine the long-term durability and kinetics of the vaccine-induced HPV-type-specific antibody and CMI responses in HIV-infected children that were, and are being, immunized in P1047. These subjects are a unique cohort that will allow us to approach this specific clinical issue.
Minimum Age:
Eligible Ages: CHILD, ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Miller Children's Hospital Long Beach (5093), Long Beach, California, United States
USC/Los Angeles County Medical Center NICHD CRS (5048), Los Angeles, California, United States
UCLA-Los Angeles/Brazil AIDS Consortium (LABAC) CR (3601), Los Angeles, California, United States
Univ of California, San Diego (4601), San Diego, California, United States
Univ. of California San Francisco NICHD CRS, San Francisco,, California, United States
Univ. of Colorado Denver NICHD CRS (5052), Aurora, Colorado, United States
Children's National Med. Ctr. Washington DC NICHD CRS (5015), Washington, District of Columbia, United States
South Florida CDC Ft. Lauderdale NICHD CRS (5055), Ft. Lauderdale, Florida, United States
Univ of Miami Pediatric/Perinatal HIV/AIDS (4201), Miami, Florida, United States
Rush University Cook County Hospital NICHD CRS (5083), Chicago, Illinois, United States
Chicago Children's CRS (4001), Chicago, Illinois, United States
Children's Hospital of Boston (5009), Boston, Massachusetts, United States
Boston Medical Center Ped. HIV Program NICHD CRS (5011), Boston, Massachusetts, United States
WNE Maternal Pediatric Adolescent AIDS CRS (7301), Worcester, Massachusetts, United States
Wayne State University/Children's Hospital of Michigan NICHD CRS (5041), Detroit, Michigan, United States
New Jersey Medical School (NJ) (2802), Newark, New Jersey, United States
Bronx-Lebanon Hospital (6901), Bronx, New York, United States
Jacobi Medical Center Bronx (5013), Bronx, New York, United States
New York University NY (5012), New York, New York, United States
Strong Memorial Hospital, University of Rochester NICHD CRS (5057), Rochester, New York, United States
SUNY Stony Brook (5040), Stony Brook, New York, United States
Texas Children's Hosp / Baylor Univ (3801), Houston, Texas, United States
San Juan City Hosp. PR NICHD CRS (5031), San Juan, , Puerto Rico
Name: Myron J Levin, MD
Affiliation: University of Colorado, Denver
Role: STUDY_CHAIR