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Immune response to the hepatitis B vaccine among HIV-infected adults in Uganda.
Seremba, E; Ocama, P; Ssekitoleko, R; Mayanja-Kizza, H; Adams, S V; Orem, J; Katabira, E; Reynolds, S J; Nabatanzi, R; Casper, C; Phipps, W.
Affiliation
  • Seremba E; School of Medicine, Makerere University College of Health Sciences, Kampala, Uganda. Electronic address: eseremba@gmail.com.
  • Ocama P; School of Medicine, Makerere University College of Health Sciences, Kampala, Uganda.
  • Ssekitoleko R; School of Medicine, Makerere University College of Health Sciences, Kampala, Uganda.
  • Mayanja-Kizza H; School of Medicine, Makerere University College of Health Sciences, Kampala, Uganda.
  • Adams SV; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Orem J; Uganda Cancer Institute, Kampala, Uganda.
  • Katabira E; School of Medicine, Makerere University College of Health Sciences, Kampala, Uganda.
  • Reynolds SJ; Johns Hopkins University School of Medicine, USA; Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Nabatanzi R; School of Biomedical Sciences, Makerere University College of Health Sciences, Kampala, Uganda.
  • Casper C; Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Infectious Disease Research Institute Seattle, WA, USA; University of Washington, Seattle, WA, USA.
  • Phipps W; Fred Hutchinson Cancer Research Center, Seattle, WA, USA; University of Washington, Seattle, WA, USA.
Vaccine ; 39(8): 1265-1271, 2021 02 22.
Article in En | MEDLINE | ID: mdl-33516601
ABSTRACT

BACKGROUND:

Co-infection with hepatitis B virus (HBV) and human immunodeficiency virus (HIV) is common in sub-Saharan Africa (SSA) and can rapidly progress to cirrhosis and hepatocellular carcinoma. Recent data demonstrate ongoing HBV transmission among HIV-infected adults in SSA, suggesting that complications of HIV/HBV co-infection could be prevented with HBV vaccination. Because HBV vaccine efficacy is poorly understood among HIV-infected persons in SSA, we sought to characterize the humoral response to the HBV vaccine in HIV-seropositive Ugandan adults.

METHODS:

We enrolled HIV-infected adults in Kampala, Uganda without serologic evidence of prior HBV infection. Three HBV vaccine doses were administered at 0, 1 and 6 months. Anti-HBs levels were measured 4 weeks after the third vaccine dose. "Response" to vaccination was defined as anti-HBs levels ≥ 10 IU/L and "high response" as ≥ 100 IU/L. Regression analysis was used to determine predictors of response.

RESULTS:

Of 251 HIV-positive adults screened, 132 (53%) had no prior HBV infection or immunity and were enrolled. Most participants were women [89 (67%)]; median (IQR) age was 32 years (27-41), and 68 (52%) had received antiretroviral therapy (ART) for > 3 months. Median (IQR) CD4 count was 426 (261-583), and 64 (94%) of the 68 receiving ART had undetectable plasma HIV RNA. Overall, 117 (92%) participants seroconverted to the vaccine (anti-HBs ≥ 10 IU/L), with 109 (86%) participants having high-level response (anti-HBs ≥ 100 IU/L). In multivariate analysis, only baseline CD4 > 200 cells/mm3 was associated with response [OR = 6.97 (1.34-34.71), p = 0.02] and high-level response [OR = 4.25 (1.15-15.69)], p = 0.03].

CONCLUSION:

HBV vaccination was effective in eliciting a protective humoral response, particularly among those with higher CD4 counts. Half of the screened patients did not have immunity to HBV infection, suggesting a large at-risk population for HBV infection among HIV-positive adults in Uganda. Our findings support including HBV vaccination as part of routine care among HIV-positive adults.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: HIV Infections / Hepatitis B Vaccines / Immunity, Humoral / Hepatitis B Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Africa Language: En Journal: Vaccine Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: HIV Infections / Hepatitis B Vaccines / Immunity, Humoral / Hepatitis B Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Africa Language: En Journal: Vaccine Year: 2021 Document type: Article