Ten‐year immune persistence and safety of the HPV‐16/18 AS04‐adjuvanted vaccine in females vaccinated at 15–55 years of age
Women remain at risk of human papillomavirus (HPV) infection for most of their lives. The duration of protection against HPV‐16/18 from prophylactic vaccination remains unknown. We investigated the 10‐year immune response and long‐term safety profile of the HPV‐16/18 AS04‐adjuvanted vaccine (AS04‐HP...
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Published in | Cancer medicine (Malden, MA) Vol. 6; no. 11; pp. 2723 - 2731 |
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Main Authors | , , , , , , , , , , |
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John Wiley and Sons Inc
01.11.2017
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Abstract | Women remain at risk of human papillomavirus (HPV) infection for most of their lives. The duration of protection against HPV‐16/18 from prophylactic vaccination remains unknown. We investigated the 10‐year immune response and long‐term safety profile of the HPV‐16/18 AS04‐adjuvanted vaccine (AS04‐HPV‐16/18 vaccine) in females aged between 15 and 55 years at first vaccination. Females who received primary vaccination with three doses of AS04‐HPV‐16/18 vaccine in the primary phase‐III study (NCT00196937) were invited to attend annual evaluations for long‐term immunogenicity and safety. Anti‐HPV‐16/18 antibodies in serum and cervico‐vaginal secretions (CVS) were measured using enzyme‐linked immunosorbent assay (ELISA). Serious adverse events (SAEs) were recorded throughout the follow‐up period. Seropositivity rates for anti‐HPV‐16 remained high (≥96.3%) in all age groups 10 years after first vaccination. It was found that 99.2% of 15–25‐year olds remained seropositive for anti‐HPV‐18 compared to 93.7% and 83.8% of 26–45‐year olds and 45–55‐year olds, respectively. Geometric mean titers (GMT) remained above natural infection levels in all age groups. Anti‐HPV‐16 and anti‐HPV‐18 titers were at least 5.3‐fold and 3.1‐fold higher than titers observed after natural infection, respectively, and were predicted to persist above natural infection levels for ≥30 years in all age groups. At Year 10, anti‐HPV‐16/18 antibody titers in subjects aged 15–25 years remained above plateau levels observed in previous studies. Correlation coefficients for antibody titers in serum and CVS were 0.64 (anti‐HPV‐16) and 0.38 (anti‐HPV‐18). This study concluded that vaccinated females aged 15–55 years elicited sustained immunogenicity with an acceptable safety profile up to 10 years after primary vaccination, suggesting long‐term protection against HPV.
The HPV‐16/18 AS04‐adjuvanted vaccine produced a sustained immune response in women aged 15–55 years at vaccination for up to 10 years, with an acceptable safety profile. Study results suggest that women in age groups not targeted by adolescent immunization and catch‐up programs may still individually benefit from HPV vaccination. |
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AbstractList | Women remain at risk of human papillomavirus (
HPV
) infection for most of their lives. The duration of protection against
HPV
‐16/18 from prophylactic vaccination remains unknown. We investigated the 10‐year immune response and long‐term safety profile of the
HPV
‐16/18
AS
04‐adjuvanted vaccine (
AS
04‐
HPV
‐16/18 vaccine) in females aged between 15 and 55 years at first vaccination. Females who received primary vaccination with three doses of
AS
04‐
HPV
‐16/18 vaccine in the primary phase‐
III
study (
NCT
00196937) were invited to attend annual evaluations for long‐term immunogenicity and safety. Anti‐
HPV
‐16/18 antibodies in serum and cervico‐vaginal secretions (
CVS
) were measured using enzyme‐linked immunosorbent assay (
ELISA
). Serious adverse events (
SAE
s) were recorded throughout the follow‐up period. Seropositivity rates for anti‐
HPV
‐16 remained high (≥96.3%) in all age groups 10 years after first vaccination. It was found that 99.2% of 15–25‐year olds remained seropositive for anti‐
HPV
‐18 compared to 93.7% and 83.8% of 26–45‐year olds and 45–55‐year olds, respectively. Geometric mean titers (
GMT
) remained above natural infection levels in all age groups. Anti‐
HPV
‐16 and anti‐
HPV
‐18 titers were at least 5.3‐fold and 3.1‐fold higher than titers observed after natural infection, respectively, and were predicted to persist above natural infection levels for ≥30 years in all age groups. At Year 10, anti‐
HPV
‐16/18 antibody titers in subjects aged 15–25 years remained above plateau levels observed in previous studies. Correlation coefficients for antibody titers in serum and
CVS
were 0.64 (anti‐
HPV
‐16) and 0.38 (anti‐
HPV
‐18). This study concluded that vaccinated females aged 15–55 years elicited sustained immunogenicity with an acceptable safety profile up to 10 years after primary vaccination, suggesting long‐term protection against
HPV
. Women remain at risk of human papillomavirus (HPV) infection for most of their lives. The duration of protection against HPV-16/18 from prophylactic vaccination remains unknown. We investigated the 10-year immune response and long-term safety profile of the HPV-16/18 AS04-adjuvanted vaccine (AS04-HPV-16/18 vaccine) in females aged between 15 and 55 years at first vaccination. Females who received primary vaccination with three doses of AS04-HPV-16/18 vaccine in the primary phase-III study (NCT00196937) were invited to attend annual evaluations for long-term immunogenicity and safety. Anti-HPV-16/18 antibodies in serum and cervico-vaginal secretions (CVS) were measured using enzyme-linked immunosorbent assay (ELISA). Serious adverse events (SAEs) were recorded throughout the follow-up period. Seropositivity rates for anti-HPV-16 remained high (≥96.3%) in all age groups 10 years after first vaccination. It was found that 99.2% of 15-25-year olds remained seropositive for anti-HPV-18 compared to 93.7% and 83.8% of 26-45-year olds and 45-55-year olds, respectively. Geometric mean titers (GMT) remained above natural infection levels in all age groups. Anti-HPV-16 and anti-HPV-18 titers were at least 5.3-fold and 3.1-fold higher than titers observed after natural infection, respectively, and were predicted to persist above natural infection levels for ≥30 years in all age groups. At Year 10, anti-HPV-16/18 antibody titers in subjects aged 15-25 years remained above plateau levels observed in previous studies. Correlation coefficients for antibody titers in serum and CVS were 0.64 (anti-HPV-16) and 0.38 (anti-HPV-18). This study concluded that vaccinated females aged 15-55 years elicited sustained immunogenicity with an acceptable safety profile up to 10 years after primary vaccination, suggesting long-term protection against HPV.Women remain at risk of human papillomavirus (HPV) infection for most of their lives. The duration of protection against HPV-16/18 from prophylactic vaccination remains unknown. We investigated the 10-year immune response and long-term safety profile of the HPV-16/18 AS04-adjuvanted vaccine (AS04-HPV-16/18 vaccine) in females aged between 15 and 55 years at first vaccination. Females who received primary vaccination with three doses of AS04-HPV-16/18 vaccine in the primary phase-III study (NCT00196937) were invited to attend annual evaluations for long-term immunogenicity and safety. Anti-HPV-16/18 antibodies in serum and cervico-vaginal secretions (CVS) were measured using enzyme-linked immunosorbent assay (ELISA). Serious adverse events (SAEs) were recorded throughout the follow-up period. Seropositivity rates for anti-HPV-16 remained high (≥96.3%) in all age groups 10 years after first vaccination. It was found that 99.2% of 15-25-year olds remained seropositive for anti-HPV-18 compared to 93.7% and 83.8% of 26-45-year olds and 45-55-year olds, respectively. Geometric mean titers (GMT) remained above natural infection levels in all age groups. Anti-HPV-16 and anti-HPV-18 titers were at least 5.3-fold and 3.1-fold higher than titers observed after natural infection, respectively, and were predicted to persist above natural infection levels for ≥30 years in all age groups. At Year 10, anti-HPV-16/18 antibody titers in subjects aged 15-25 years remained above plateau levels observed in previous studies. Correlation coefficients for antibody titers in serum and CVS were 0.64 (anti-HPV-16) and 0.38 (anti-HPV-18). This study concluded that vaccinated females aged 15-55 years elicited sustained immunogenicity with an acceptable safety profile up to 10 years after primary vaccination, suggesting long-term protection against HPV. Women remain at risk of human papillomavirus (HPV) infection for most of their lives. The duration of protection against HPV‐16/18 from prophylactic vaccination remains unknown. We investigated the 10‐year immune response and long‐term safety profile of the HPV‐16/18 AS04‐adjuvanted vaccine (AS04‐HPV‐16/18 vaccine) in females aged between 15 and 55 years at first vaccination. Females who received primary vaccination with three doses of AS04‐HPV‐16/18 vaccine in the primary phase‐III study (NCT00196937) were invited to attend annual evaluations for long‐term immunogenicity and safety. Anti‐HPV‐16/18 antibodies in serum and cervico‐vaginal secretions (CVS) were measured using enzyme‐linked immunosorbent assay (ELISA). Serious adverse events (SAEs) were recorded throughout the follow‐up period. Seropositivity rates for anti‐HPV‐16 remained high (≥96.3%) in all age groups 10 years after first vaccination. It was found that 99.2% of 15–25‐year olds remained seropositive for anti‐HPV‐18 compared to 93.7% and 83.8% of 26–45‐year olds and 45–55‐year olds, respectively. Geometric mean titers (GMT) remained above natural infection levels in all age groups. Anti‐HPV‐16 and anti‐HPV‐18 titers were at least 5.3‐fold and 3.1‐fold higher than titers observed after natural infection, respectively, and were predicted to persist above natural infection levels for ≥30 years in all age groups. At Year 10, anti‐HPV‐16/18 antibody titers in subjects aged 15–25 years remained above plateau levels observed in previous studies. Correlation coefficients for antibody titers in serum and CVS were 0.64 (anti‐HPV‐16) and 0.38 (anti‐HPV‐18). This study concluded that vaccinated females aged 15–55 years elicited sustained immunogenicity with an acceptable safety profile up to 10 years after primary vaccination, suggesting long‐term protection against HPV. The HPV‐16/18 AS04‐adjuvanted vaccine produced a sustained immune response in women aged 15–55 years at vaccination for up to 10 years, with an acceptable safety profile. Study results suggest that women in age groups not targeted by adolescent immunization and catch‐up programs may still individually benefit from HPV vaccination. Women remain at risk of human papillomavirus (HPV) infection for most of their lives. The duration of protection against HPV-16/18 from prophylactic vaccination remains unknown. We investigated the 10-year immune response and long-term safety profile of the HPV-16/18 AS04-adjuvanted vaccine (AS04-HPV-16/18 vaccine) in females aged between 15 and 55 years at first vaccination. Females who received primary vaccination with three doses of AS04-HPV-16/18 vaccine in the primary phase-III study (NCT00196937) were invited to attend annual evaluations for long-term immunogenicity and safety. Anti-HPV-16/18 antibodies in serum and cervico-vaginal secretions (CVS) were measured using enzyme-linked immunosorbent assay (ELISA). Serious adverse events (SAEs) were recorded throughout the follow-up period. Seropositivity rates for anti-HPV-16 remained high (≥96.3%) in all age groups 10 years after first vaccination. It was found that 99.2% of 15-25-year olds remained seropositive for anti-HPV-18 compared to 93.7% and 83.8% of 26-45-year olds and 45-55-year olds, respectively. Geometric mean titers (GMT) remained above natural infection levels in all age groups. Anti-HPV-16 and anti-HPV-18 titers were at least 5.3-fold and 3.1-fold higher than titers observed after natural infection, respectively, and were predicted to persist above natural infection levels for ≥30 years in all age groups. At Year 10, anti-HPV-16/18 antibody titers in subjects aged 15-25 years remained above plateau levels observed in previous studies. Correlation coefficients for antibody titers in serum and CVS were 0.64 (anti-HPV-16) and 0.38 (anti-HPV-18). This study concluded that vaccinated females aged 15-55 years elicited sustained immunogenicity with an acceptable safety profile up to 10 years after primary vaccination, suggesting long-term protection against HPV. |
Author | Galaj, Andrzej Folschweiller, Nicolas Struyf, Frank Schwarz, Tino F. Wysocki, Jacek Spaczynski, Marek Suryakiran, Pemmaraju V. Thomas, Florence Lin, Lan Kaufmann, Andreas M. Poncelet, Sylviane |
AuthorAffiliation | 4 Department of Preventive Medicine Poznan University of Medical Sciences Poznan Poland 8 GSK Wavre Belgium 1 Central Laboratory and Vaccination Centre Klinikum Würzburg Mitte Standort Juliusspital Würzburg Germany 6 GSK Rixensart Belgium 7 GSK Bangalore India 5 Department of Gynecology Charité‐Universitätsmedizin Berlin Berlin Germany 2 NZOZ Vitamed Bydgoszcz Poland 3 Faculty of Medicine and Health Sciences University of Zielona Gora Zielona Gora Poland |
AuthorAffiliation_xml | – name: 3 Faculty of Medicine and Health Sciences University of Zielona Gora Zielona Gora Poland – name: 5 Department of Gynecology Charité‐Universitätsmedizin Berlin Berlin Germany – name: 8 GSK Wavre Belgium – name: 2 NZOZ Vitamed Bydgoszcz Poland – name: 7 GSK Bangalore India – name: 1 Central Laboratory and Vaccination Centre Klinikum Würzburg Mitte Standort Juliusspital Würzburg Germany – name: 4 Department of Preventive Medicine Poznan University of Medical Sciences Poznan Poland – name: 6 GSK Rixensart Belgium |
Author_xml | – sequence: 1 givenname: Tino F. orcidid: 0000-0003-1505-1823 surname: Schwarz fullname: Schwarz, Tino F. email: t.schwarz@juliusspital.de organization: Standort Juliusspital – sequence: 2 givenname: Andrzej surname: Galaj fullname: Galaj, Andrzej organization: NZOZ Vitamed – sequence: 3 givenname: Marek surname: Spaczynski fullname: Spaczynski, Marek organization: University of Zielona Gora – sequence: 4 givenname: Jacek surname: Wysocki fullname: Wysocki, Jacek organization: Poznan University of Medical Sciences – sequence: 5 givenname: Andreas M. surname: Kaufmann fullname: Kaufmann, Andreas M. organization: Charité‐Universitätsmedizin Berlin – sequence: 6 givenname: Sylviane surname: Poncelet fullname: Poncelet, Sylviane organization: GSK – sequence: 7 givenname: Pemmaraju V. surname: Suryakiran fullname: Suryakiran, Pemmaraju V. organization: GSK – sequence: 8 givenname: Nicolas surname: Folschweiller fullname: Folschweiller, Nicolas organization: GSK – sequence: 9 givenname: Florence surname: Thomas fullname: Thomas, Florence organization: GSK – sequence: 10 givenname: Lan surname: Lin fullname: Lin, Lan organization: GSK – sequence: 11 givenname: Frank surname: Struyf fullname: Struyf, Frank organization: GSK |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28984053$$D View this record in MEDLINE/PubMed |
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Keywords | AS04-HPV-16/18 vaccine persistence older women safety |
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Snippet | Women remain at risk of human papillomavirus (HPV) infection for most of their lives. The duration of protection against HPV‐16/18 from prophylactic... Women remain at risk of human papillomavirus (HPV) infection for most of their lives. The duration of protection against HPV-16/18 from prophylactic... Women remain at risk of human papillomavirus ( HPV ) infection for most of their lives. The duration of protection against HPV ‐16/18 from prophylactic... |
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SubjectTerms | Adolescent Adult Antibodies, Viral - analysis Antibodies, Viral - blood AS04‐HPV‐16/18 vaccine Bodily Secretions - immunology Cancer Prevention Cervix Uteri - immunology Female Follow-Up Studies Human papillomavirus 16 - immunology Human papillomavirus 18 - immunology Humans Middle Aged older women Original Research Papillomavirus Infections - prevention & control Papillomavirus Vaccines - adverse effects Papillomavirus Vaccines - immunology persistence safety Uterine Cervical Neoplasms - prevention & control Vaccination - adverse effects Vagina - immunology Young Adult |
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Title | Ten‐year immune persistence and safety of the HPV‐16/18 AS04‐adjuvanted vaccine in females vaccinated at 15–55 years of age |
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