Impact of Baseline Covariates on the Immunogenicity of a Quadrivalent (Types 6, 11, 16, and 18) Human Papillomavirus Virus-Like-Particle Vaccine
Background.The quadrivalent (types 6, 11, 16, and 18) human papillomavirus (HPV) L1 virus-like-particle vaccine was 95%–100% effective in preventing cervical and genital disease related to HPV-6, -11, -16, and -18. Vaccine efficacy is thought to be mediated by humoral immunity. Here, we analyze the...
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Published in | The Journal of infectious diseases Vol. 196; no. 8; pp. 1153 - 1162 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
The University of Chicago Press
15.10.2007
University of Chicago Press |
Subjects | |
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Abstract | Background.The quadrivalent (types 6, 11, 16, and 18) human papillomavirus (HPV) L1 virus-like-particle vaccine was 95%–100% effective in preventing cervical and genital disease related to HPV-6, -11, -16, and -18. Vaccine efficacy is thought to be mediated by humoral immunity. Here, we analyze the effect of the baseline characteristics of subjects on vaccine-induced immune responses. Methods.Immunogenicity data from 12,343 subjects 9–26 years old randomized to quadrivalent HPV vaccine or placebo in phase 2/3 studies were analyzed. Covariates examined were day 1 HPV serostatus, age, race/ethnicity, region of residence, lactation status, hormonal contraceptive usage, smoking status, Pap test diagnosis, immunosuppressant or anti-inflammatory agent use, and number of sex partners. Anti-HPV responses were summarized as serum anti-HPV-6, -11, -16, or -18 geometric mean titers 1 month after dose 3. Results.Age at vaccination initiation was inversely proportional to the vaccine-induced anti-HPV response. Vaccination of subpopulations of subjects who were seropositive at day 1 to a vaccine HPV type resulted in more robust anti-HPV responses to that type, compared with those in subjects who were seronegative at baseline. Anti-HPV responses were comparable among the remaining demographic subgroups. Conclusions.The immunogenicity of quadrivalent HPV vaccine was comparable among subjects with differing baseline characteristics. These data support vaccination with quadrivalent HPV vaccine across a broad range of baseline subject characteristics. |
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AbstractList | Background. The quadrivalent (types 6, 11, 16, and 18) human papillomavirus (HPV) L1 virus-like-particle vaccine was 95%-100% effective in preventing cervical and genital disease related to HPV-6, -11, -16, and -18. Vaccine efficacy is thought to be mediated by humoral immunity. Here, we analyze the effect of the baseline characteristics of subjects on vaccine-induced immune responses. Methods. Immunogenicity data from 12,343 subjects 9-26 years old randomized to quadrivalent HPV vaccine or placebo in phase 2/3 studies were analyzed. Covariates examined were day 1 HPV serostatus, age, race/ethnicity, region of residence, lactation status, hormonal contraceptive usage, smoking status, Pap test diagnosis, immunosuppressant or anti-inflammatory agent use, and number of sex partners. Anti-HPV responses were summarized as serum anti-HPV-6, -11, -16, or -18 geometric mean titers 1 month after dose 3. Results. Age at vaccination initiation was inversely proportional to the vaccine-induced anti-HPV response. Vaccination of subpopulations of subjects who were seropositive at day 1 to a vaccine HPV type resulted in more robust anti-HPV responses to that type, compared with those in subjects who were seronegative at baseline. Anti-HPV responses were comparable among the remaining demographic subgroups. Conclusions. The immunogenicity of quadrivalent HPV vaccine was comparable among subjects with differing baseline characteristics. These data support vaccination with quadrivalent HPV vaccine across a broad range of baseline subject characteristics. The quadrivalent (types 6, 11, 16, and 18) human papillomavirus (HPV) L1 virus-like-particle vaccine was 95%-100% effective in preventing cervical and genital disease related to HPV-6, -11, -16, and -18. Vaccine efficacy is thought to be mediated by humoral immunity. Here, we analyze the effect of the baseline characteristics of subjects on vaccine-induced immune responses. Immunogenicity data from 12,343 subjects 9-26 years old randomized to quadrivalent HPV vaccine or placebo in phase 2/3 studies were analyzed. Covariates examined were day 1 HPV serostatus, age, race/ethnicity, region of residence, lactation status, hormonal contraceptive usage, smoking status, Pap test diagnosis, immunosuppressant or anti-inflammatory agent use, and number of sex partners. Anti-HPV responses were summarized as serum anti-HPV-6, -11, -16, or -18 geometric mean titers 1 month after dose 3. Age at vaccination initiation was inversely proportional to the vaccine-induced anti-HPV response. Vaccination of subpopulations of subjects who were seropositive at day 1 to a vaccine HPV type resulted in more robust anti-HPV responses to that type, compared with those in subjects who were seronegative at baseline. Anti-HPV responses were comparable among the remaining demographic subgroups. The immunogenicity of quadrivalent HPV vaccine was comparable among subjects with differing baseline characteristics. These data support vaccination with quadrivalent HPV vaccine across a broad range of baseline subject characteristics. The quadrivalent (types 6, 11, 16, and 18) human papillomavirus (HPV) L1 virus-like-particle vaccine was 95%-100% effective in preventing cervical and genital disease related to HPV-6, -11, -16, and -18. Vaccine efficacy is thought to be mediated by humoral immunity. Here, we analyze the effect of the baseline characteristics of subjects on vaccine-induced immune responses.BACKGROUNDThe quadrivalent (types 6, 11, 16, and 18) human papillomavirus (HPV) L1 virus-like-particle vaccine was 95%-100% effective in preventing cervical and genital disease related to HPV-6, -11, -16, and -18. Vaccine efficacy is thought to be mediated by humoral immunity. Here, we analyze the effect of the baseline characteristics of subjects on vaccine-induced immune responses.Immunogenicity data from 12,343 subjects 9-26 years old randomized to quadrivalent HPV vaccine or placebo in phase 2/3 studies were analyzed. Covariates examined were day 1 HPV serostatus, age, race/ethnicity, region of residence, lactation status, hormonal contraceptive usage, smoking status, Pap test diagnosis, immunosuppressant or anti-inflammatory agent use, and number of sex partners. Anti-HPV responses were summarized as serum anti-HPV-6, -11, -16, or -18 geometric mean titers 1 month after dose 3.METHODSImmunogenicity data from 12,343 subjects 9-26 years old randomized to quadrivalent HPV vaccine or placebo in phase 2/3 studies were analyzed. Covariates examined were day 1 HPV serostatus, age, race/ethnicity, region of residence, lactation status, hormonal contraceptive usage, smoking status, Pap test diagnosis, immunosuppressant or anti-inflammatory agent use, and number of sex partners. Anti-HPV responses were summarized as serum anti-HPV-6, -11, -16, or -18 geometric mean titers 1 month after dose 3.Age at vaccination initiation was inversely proportional to the vaccine-induced anti-HPV response. Vaccination of subpopulations of subjects who were seropositive at day 1 to a vaccine HPV type resulted in more robust anti-HPV responses to that type, compared with those in subjects who were seronegative at baseline. Anti-HPV responses were comparable among the remaining demographic subgroups.RESULTSAge at vaccination initiation was inversely proportional to the vaccine-induced anti-HPV response. Vaccination of subpopulations of subjects who were seropositive at day 1 to a vaccine HPV type resulted in more robust anti-HPV responses to that type, compared with those in subjects who were seronegative at baseline. Anti-HPV responses were comparable among the remaining demographic subgroups.The immunogenicity of quadrivalent HPV vaccine was comparable among subjects with differing baseline characteristics. These data support vaccination with quadrivalent HPV vaccine across a broad range of baseline subject characteristics.CONCLUSIONSThe immunogenicity of quadrivalent HPV vaccine was comparable among subjects with differing baseline characteristics. These data support vaccination with quadrivalent HPV vaccine across a broad range of baseline subject characteristics. |
Author | Golm, Greg McCarroll, Kathleen Barr, Eliav Esser, Mark T. Radley, David Giuliano, Anna R. Villa, Luisa Vuocolo, Scott C. Nolan, Terry Lazcano-Ponce, Eduardo Marchant, Colin Yu, Jimmy |
Author_xml | – sequence: 1 givenname: Anna R. surname: Giuliano fullname: Giuliano, Anna R. email: Anna.Giuliano@moffitt.org organization: H. Lee Moffitt Cancer Center, Tampa, Florida – sequence: 2 givenname: Eduardo surname: Lazcano-Ponce fullname: Lazcano-Ponce, Eduardo organization: National Institute of Public Health, Cuernavaca, Mexico – sequence: 3 givenname: Luisa surname: Villa fullname: Villa, Luisa organization: Ludwig Institute for Cancer Research, Sao Paulo, Brazil – sequence: 4 givenname: Terry surname: Nolan fullname: Nolan, Terry organization: University of Melbourne, Department of Public Health, and Murdoch Children's Research Institute, Melbourne, Australia – sequence: 5 givenname: Colin surname: Marchant fullname: Marchant, Colin organization: Boston University Medical Center, Boston, Massachusetts – sequence: 6 givenname: David surname: Radley fullname: Radley, David organization: Merck & Company, Inc., West Point, Pennsylvania – sequence: 7 givenname: Greg surname: Golm fullname: Golm, Greg organization: Merck & Company, Inc., West Point, Pennsylvania – sequence: 8 givenname: Kathleen surname: McCarroll fullname: McCarroll, Kathleen organization: Merck & Company, Inc., West Point, Pennsylvania – sequence: 9 givenname: Jimmy surname: Yu fullname: Yu, Jimmy organization: Merck & Company, Inc., West Point, Pennsylvania – sequence: 10 givenname: Mark T. surname: Esser fullname: Esser, Mark T. organization: Merck & Company, Inc., West Point, Pennsylvania – sequence: 11 givenname: Scott C. surname: Vuocolo fullname: Vuocolo, Scott C. organization: Merck & Company, Inc., West Point, Pennsylvania – sequence: 12 givenname: Eliav surname: Barr fullname: Barr, Eliav organization: Merck & Company, Inc., West Point, Pennsylvania |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/17955433$$D View this record in MEDLINE/PubMed |
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Snippet | Background.The quadrivalent (types 6, 11, 16, and 18) human papillomavirus (HPV) L1 virus-like-particle vaccine was 95%–100% effective in preventing cervical... Background. The quadrivalent (types 6, 11, 16, and 18) human papillomavirus (HPV) L1 virus-like-particle vaccine was 95%-100% effective in preventing cervical... The quadrivalent (types 6, 11, 16, and 18) human papillomavirus (HPV) L1 virus-like-particle vaccine was 95%-100% effective in preventing cervical and genital... |
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SubjectTerms | Adolescent Adult Alphapapillomavirus - classification Alphapapillomavirus - immunology Antibodies Antibody Formation Child Cigarette smoking Double-Blind Method Female Human papillomavirus Human papillomavirus 16 Human papillomavirus 6 Humans Immune response Infections Male Papillomavirus Infections - immunology Papillomavirus Infections - prevention & control Papillomavirus Vaccines - immunology Placebos Preventive medicine Sexually Transmitted Diseases, Viral - immunology Sexually Transmitted Diseases, Viral - prevention & control Treatment Outcome Vaccination Viruses |
Title | Impact of Baseline Covariates on the Immunogenicity of a Quadrivalent (Types 6, 11, 16, and 18) Human Papillomavirus Virus-Like-Particle Vaccine |
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