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Atypical Hepatitis B Virus Serology Profile-Hepatitis B Surface Antigen-Positive/Hepatitis B Core Antibody-Negative-In Hepatitis B Virus/HIV Coinfected Individuals in Botswana
被引:3
|作者:
Phinius, Bonolo B.
[1
,2
]
Anderson, Motswedi
[1
]
Mokomane, Margaret
[2
]
Gobe, Irene
[2
]
Choga, Wonderful T.
[1
,2
]
Ratsoma, Tsholofelo
[1
]
Phakedi, Basetsana
[1
]
Mpebe, Gorata
[1
]
Ditshwanelo, Doreen
[1
]
Musonda, Rosemary
[1
]
Makhema, Joseph
[1
,3
]
Moyo, Sikhulile
[1
,2
,3
,4
]
Gaseitsiwe, Simani
[1
,3
]
机构:
[1] Botswana Harvard AIDS Inst Partnership, Private Bag BO 320, Gaborone, Botswana
[2] Univ Botswana, Fac Hlth Sci, Sch Allied Hlth Profess, Private Bag UB 0022, Gaborone, Botswana
[3] Harvard T H Chan Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[4] Univ Pretoria, Sch Hlth Syst & Publ Hlth, Private Bag X20, ZA-0028 Pretoria, South Africa
来源:
VIRUSES-BASEL
|
2023年
/
15卷
/
07期
基金:
英国惠康基金;
美国国家卫生研究院;
关键词:
hepatitis B surface antigen (HBsAg);
hepatitis B core antibodies (anti-HBc);
HBV;
HIV;
Botswana;
Africa;
INFECTED PATIENTS;
HBC;
PREVALENCE;
D O I:
10.3390/v15071544
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
(1) Background: Hepatitis B core antibodies (anti-HBc) are a marker of hepatitis B virus (HBV) exposure; hence, a normal HBV serology profile is characterized by HBV surface antigen (HBsAg) and anti-HBc positivity. However, atypical HBV serologies occur, and we aimed to determine the prevalence of an atypical profile (HBsAg+/anti-HBc-) in a cohort of people with HIV-1 (PWH) in Botswana. (2) Methods: Plasma samples from an HIV-1 cohort in Botswana (2013-2018) were used. The samples were screened for HBsAg and anti-HBc. Next-generation sequencing was performed using the GridION platform. The Wilcoxon rank-sum test and Chi-squared tests were used for the comparison of continuous and categorical variables, respectively. (3) Results: HBsAg+/anti-HBc- prevalence was 13.7% (95% CI 10.1-18.4) (36/263). HBsAg+/anti-HBc- participants were significantly younger (p < 0.001), female (p = 0.02) and ART-naive (p = 0.04) and had a detectable HIV viral load (p = 0.02). There was no statistically significant difference in the number of mutations observed in participants with HBsAg+/anti-HBc- vs. those with HBsAg+/anti-HBc+ serology. (4) Conclusions: We report a high HBsAg+/anti-HBc- atypical serology profile prevalence among PWH in Botswana. We caution against HBV-testing algorithms that consider only anti-HBc+ samples for HBsAg testing, as they are likely to underestimate HBV prevalence. Studies to elucidate the mechanisms and implications of this profile are warranted.
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