Seroprevalence of anti-SARS-CoV-2 IgG antibodies in HIV-positive and HIV-negative patients in clinical settings in Douala, Cameroon.

Frontiers in epidemiology Pub Date : 2023-08-14 eCollection Date: 2023-01-01 DOI:10.3389/fepid.2023.1212220
Sylvie Kwedi Nolna, Miriam Niba, Cedric Djadda, Palmer Masumbe Netongo
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Abstract

Background: The asymptomatic nature of COVID-19 coupled with differential testing are confounders in the assessment of SARS-CoV-2 incidence among people living with HIV (PLWH). As various comorbidities increase the risk of SARS-CoV-2 infection, it is crucial to assess the potential contribution of HIV to the risk of acquiring COVID-19. Our study aimed to compare the anti-SARS-CoV-2 IgG seroprevalence among people living with and without HIV.

Methods: PLWH were enrolled in the HIV units of two health facilities in Douala, Cameroon. Participants were consecutively enrolled, among which 47 were people living with HIV and 31 were HIV-negative patients. SARS-CoV-2 antibody tests were performed on all participants. Overall, medical consultation was conducted. For HIV-positive participants only, viral load, antiretroviral regimen, duration of HIV infection, and duration of antiretroviral treatment were retrieved from medical records.

Results: We found an overall SARS-CoV-2 IgG seroprevalence of 42.31% within the study population, with a SARS-CoV-2 IgG seroprevalence of 44.6% for PLWH and 38.7% among those without HIV infection; no significant statistical difference was observed. Adjusting for sex, HIV status, and BCG vaccination, the odds of previous SARS-CoV-2 infection were higher among married persons in the study population. Sex, BCG vaccination, and HIV status were not found to be associated with SARS-CoV-2 IgG seropositivity.

Conclusions: Our findings support the lack of association between HIV status and susceptibility to SARS-CoV-2 infection. The ARV regimen, suppressed viral load, and Tenofovir boasted ARV regimen might not affect the body's immune response after exposure to SARS-CoV-2 among PLWH. Thus, if HIV is well treated, the susceptibility to COVID-19 in PLWH would be like that of the general population.

喀麦隆杜阿拉临床环境中HIV阳性和HIV阴性患者抗严重急性呼吸系统综合征冠状病毒2型IgG抗体的血清流行率
新冠肺炎的无症状性质加上差异检测是评估艾滋病毒感染者(PLWH)中SARS-CoV-2发病率的混淆因素。由于各种合并症增加了感染SARS-CoV-2的风险,评估艾滋病毒对感染新冠肺炎风险的潜在贡献至关重要。我们的研究旨在比较HIV感染者和非HIV感染者的抗严重急性呼吸系统综合征冠状病毒2型IgG血清流行率。PLWH被纳入喀麦隆杜阿拉两个卫生机构的HIV单位。参与者连续入选,其中47人为艾滋病毒感染者,31人为艾滋病毒阴性患者。对所有参与者进行了严重急性呼吸系统综合征冠状病毒2型抗体测试。总体而言,进行了医疗咨询。仅对于HIV阳性参与者,从医疗记录中检索病毒载量、抗逆转录病毒疗法、HIV感染持续时间和抗逆转录病毒治疗持续时间。我们发现,在研究人群中,严重急性呼吸系统综合征冠状病毒2型IgG的总血清流行率为42.31%,PLWH的严重急性呼吸系综合征冠状病毒2-型IgG的血清流行率是44.6%,在未感染HIV的人群中是38.7%;没有观察到显著的统计学差异。经性别、HIV状况和BCG疫苗接种调整后,研究人群中已婚人群既往感染严重急性呼吸系统综合征冠状病毒2型的几率更高。性别、BCG疫苗接种和HIV状态与严重急性呼吸系统综合征冠状病毒2型IgG血清阳性无关。我们的研究结果支持HIV状态与严重急性呼吸系统综合征冠状病毒2型感染易感性之间缺乏关联。ARV方案抑制了病毒载量,而Tenofovir吹嘘ARV方案可能不会影响PLWH接触严重急性呼吸系统综合征冠状病毒2型后的身体免疫反应。因此,如果HIV得到很好的治疗,PLWH对新冠肺炎的易感性将与普通人群一样。
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