Hepatitis B surface antigen loss in individuals with chronic hepatitis B virus and HIV-1 infections in Botswana

被引:1
|
作者
Mpebe, Gorata G. A. [1 ,2 ]
Phinius, Bonolo B. [1 ,3 ]
Mutenga, Sharon [1 ,4 ]
Baruti, Kabo [1 ,2 ]
Bhebhe, Lynnette [1 ]
Choga, Wonderful T. [1 ,3 ]
Jongman, Mosimanegape [1 ,2 ]
Pretorius-Holme, Molly [5 ]
Gaolathe, Tendani [1 ]
Mmalane, Mompati [1 ,5 ]
Shapiro, Roger [1 ,5 ]
Makhema, Joseph [1 ,5 ]
Lockman, Shahin [1 ,5 ]
Moyo, Sikhulile [1 ,3 ,5 ,6 ]
Anderson, Motswedi [1 ]
Gaseitsiwe, Simani [1 ,5 ,7 ]
机构
[1] Univ Botswana, Botswana Harvard AIDS Inst Partnership, Gaborone, Botswana
[2] Univ Botswana, Fac Sci, Biol Sci, Gaborone, Botswana
[3] Univ Botswana, Fac Hlth Sci, Sch Allied Hlth Profess, Gaborone, Botswana
[4] Midlands State Univ, Gweru, Zimbabwe
[5] Harvard TH Chan Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA USA
[6] Univ Pretoria, Sch Hlth Syst & Publ Hlth, Gauteng, South Africa
[7] Botswana Harvard Botswana Harvard AIDS Inst Partne, Private Bag BO 320, Gaborone, Botswana
基金
英国惠康基金; 美国国家卫生研究院;
关键词
antiretroviral therapy; chronic hepatitis B; hepatitis B surface antigen loss; hepatitis B virus; HIV co-infection; COINFECTION; ADULTS;
D O I
10.1097/QAD.0000000000003753
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives: We sought to determine hepatitis B surface antigen (HBsAg) loss and its predictors among people with chronic hepatitis B (CHB) infections and HIV (PWH) in Botswana. Methods: Archived plasma samples from a cohort of PWH in Botswana (20132018) with 3 yearly time-points were used. Samples were screened for HBsAg, immunoglobulin M HBV core antibodies (anti-HBc IgM) and HBV e-antigen (HBeAg) at all time points. HBV deoxyribonucleic acid (DNA) quantification was done at baseline. The Wilcoxon rank-sum was used to compare continuous variables while the chi-squared test and Fishers exact test were used for categorical data wherever appropriate. Logistic regression was used to assess predictors of seroclearance. Results: Of 141 participants with HBsAg-positive serology (HBsAg+) at baseline, 92.2% (131/141) [95% confidence interval (CI) 87.4-96.1] were persistently HBsAg+ at year 1. We report a HBsAg loss of 7.1% (10/141) (95% CI 3.912.6) among participants with negative HBeAg and negative IgM serologies. HBsAg loss was 6.3% (7/111) among antiretroviral therapy (ART)-experienced participants and 10.7% (3/28) (95% CI 0.45.0) in ART-naive participants. Most participants who had positive anti-HBc IgM serology and did not lose HBsAg were on either lamivudine (3TC)-based therapy or non-tenofovir disoproxil fumarate (TDF)-based therapy, except for one participant. The participants also had varying HBeAg status. HBsAg loss was independent of HIV viral load, CD4(+) cell count, age, and sex. Conclusion: We report a HBsAg loss of 6.3% over a 3-year period among ART-experienced CHB participants. Future studies that focus on HBsAg loss in mono-infected patients and the possible correlation between HBeAg status and HBsAg loss are warranted. Copyright (C) 2023 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:153 / 159
页数:7
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