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Protection and antibody levels 35 years after primary series with hepatitis B vaccine and response to a booster dose.
Bruce, Michael G; Bruden, Dana; Hurlburt, Debby; Morris, Julie; Bressler, Sara; Thompson, Gail; Lecy, Danielle; Rudolph, Karen; Bulkow, Lisa; Hennessy, Thomas; Simons, Brenna C; Weng, Mark K; Nelson, Noele; McMahon, Brian J.
Afiliação
  • Bruce MG; Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska, USA.
  • Bruden D; Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska, USA.
  • Hurlburt D; Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska, USA.
  • Morris J; Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska, USA.
  • Bressler S; Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska, USA.
  • Thompson G; Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska, USA.
  • Lecy D; Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska, USA.
  • Rudolph K; Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska, USA.
  • Bulkow L; Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska, USA.
  • Hennessy T; Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska, USA.
  • Simons BC; Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska, USA.
  • Weng MK; Epidemiology and Surveillance Branch, Division of Viral Hepatitis, National Center for HIV/AIDS, Viral Hepatitis, Sexually Transmitted Disease, and Tuberculosis Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • Nelson N; Epidemiology and Surveillance Branch, Division of Viral Hepatitis, National Center for HIV/AIDS, Viral Hepatitis, Sexually Transmitted Disease, and Tuberculosis Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • McMahon BJ; Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Arctic Investigations Program, Centers for Disease Control and Prevention, Anchorage, Alaska, USA.
Hepatology ; 76(4): 1180-1189, 2022 10.
Article em En | MEDLINE | ID: mdl-35320592
ABSTRACT
BACKGROUND AND

AIMS:

The duration of protection from hepatitis B vaccination in children and adults is not known. In 1981, we used three doses of plasma-derived hepatitis B vaccine to immunize a cohort of 1578 Alaska Native adults and children from 15 Alaska communities who were ≥6 months old. APPROACH AND

RESULTS:

We tested persons for antibody to hepatitis B surface antigen (anti-HBs) levels 35 years after receiving the primary series. Those with levels <10 mIU/ml received one booster dose of recombinant hepatitis B vaccine 2-4 weeks later and were then evaluated on the basis of anti-HBs measurements 30 days postbooster. Among the 320 recruited, 112 persons had not participated in the 22- or 30-year follow-up study (group 1), and 208 persons had participated but were not given an HBV booster dose (group 2). Among the 112 persons in group 1 who responded to the original primary series, 53 (47.3%) had an anti-HBs level ≥10 mIU/ml. Among group 1, 73.7% (28 of 38) of persons available for a booster dose responded to it with an anti-HBs level ≥10 mIU/ml at 30 days. Initial anti-HBs level after the primary series was correlated with higher anti-HBs levels at 35 years. Among 8 persons who tested positive for antibody to hepatitis B core antigen, none tested positive for HBsAg or HBV DNA.

CONCLUSIONS:

Based on anti-HBs level ≥10 mIU/ml at 35 years and a 73.7% booster dose response, we estimate that 86% of participants had evidence of protection 35 years later. Booster doses are not needed in the general population at this time.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas contra Hepatite B / Hepatite B Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas contra Hepatite B / Hepatite B Idioma: En Ano de publicação: 2022 Tipo de documento: Article