Immune response to the hepatitis B vaccine among HIV-infected adults in Uganda

被引:7
作者
Seremba, E. [1 ]
Ocama, P. [1 ]
Ssekitoleko, R. [1 ]
Mayanja-Kizza, H. [1 ]
Adams, S., V [2 ]
Orem, J. [3 ]
Katabira, E. [1 ]
Reynolds, S. J. [4 ,5 ]
Nabatanzi, R. [6 ]
Casper, C. [2 ,7 ,8 ]
Phipps, W. [2 ,8 ]
机构
[1] Makerere Univ, Sch Med, Coll Hlth Sci, Kampala, Uganda
[2] Fred Hutchinson Canc Res Ctr, 1124 Columbia St, Seattle, WA 98104 USA
[3] Uganda Canc Inst, Kampala, Uganda
[4] Johns Hopkins Univ, Sch Med, Baltimore, MD 21218 USA
[5] NIAID, Div Intramural Res, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[6] Makerere Univ, Sch Biomed Sci, Coll Hlth Sci, Kampala, Uganda
[7] Infect Dis Res Inst, Seattle, WA USA
[8] Univ Washington, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
Immune response; Hepatitis B vaccine; HIV seropositive adults; Sub-Saharan Africa;
D O I
10.1016/j.vaccine.2021.01.043
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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. (C) 2021 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1265 / 1271
页数:7
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