key: cord-0950791-dr7zikd5
authors: Gudipati, Smitha; Lee, Monica; Scott, Megan; Yaphe, Sean; Huisting, Joanne; Yared, Nicholas; Brar, Indira; Markowitz, Norman
title: The seroprevalence of COVID-19 in patients living with HIV in metropolitan Detroit
date: 2022-03-25
journal: Int J STD AIDS
DOI: 10.1177/09564624221076629
sha: 38bec5f2d4d1dfa32692945c20053b26af751e8f
doc_id: 950791
cord_uid: dr7zikd5

BACKGROUND: COVID-19, a novel respiratory illness caused by SARS-CoV-2, has become a global pandemic. As of December 2020, 4.8% of the 941 people living with HIV in our Ryan White clinic have tested polymerase chain reaction positive for SARS-CoV-2. The aim of our study was to estimate the seroprevalence of COVID-19 in our Ryan White people living with HIV, irrespective of known past infection. METHODS: We conducted a cross-sectional study that recruited people living with HIV in the Ryan White program at Henry Ford Hospital in Detroit, Michigan, from September 2020 through May 2021. All Ryan White patients were offered participation during clinic visits. After informed consent, patients completed a survey, and had blood sampled for SARS-CoV-2 antibody testing. RESULTS: Of the 529 individuals who completed the written survey, 504 participants were tested for SARS-CoV-2 antibody and 52 people living with HIV were COVID-19 immunoglobulin (Ig) G positive resulting in a seroprevalence of 10.3%. Among 36 persons with PCR-confirmed COVID-19, 52.8% were IgG negative. Inclusion of PCR positive but IgG-negative people living with HIV yields a COVID-19 infection prevalence of 14.1%. CONCLUSIONS: These findings suggest that passive public health-based antibody surveillance in people living with HIV significantly underestimates past infection.

COVID-19, a novel respiratory illness caused by SARS-CoV-2, was first reported in December 2019 among patients with pneumonia in Wuhan, Hubei Province, China, and has now become a global pandemic. 1 The risk of acquisition of COVID-19 and outcome of infection for people living with HIV is not precisely known (personal communication from Jim Kent). [2] [3] [4] [5] As of December 2020, 4.8% of the 941 people living with HIV in our Ryan White clinic have tested polymerase chain reaction (PCR) positive for SARS-CoV-2 and 6/45 persons have died (13.3%). However, reported cases do not account for all SARS-CoV-2 infections, as an unknown proportion is not ascertained through passive public health reporting. Detection of SARS-CoV-2 antibodies can be used to estimate SARS-CoV-2 infection in asymptomatic or mildly symptomatic individuals and as a tool to estimate prevalence in populations. 2, 3 The aim of our study was to estimate the seroprevalence of COVID-19 in our Ryan White people living with HIV, irrespective of known past infection.

We conducted a cross-sectional study that recruited people living with HIV in the Ryan White program at Henry Ford Hospital in Detroit, Michigan. A survey and antibody testing were performed from September 2020 through May 2021. All Ryan White patients were offered participation during clinic visits if they had not already received a dosage of any COVID-19 vaccine. After informed consent, patients completed a survey (Figure 1 ), and had blood sampled for SARS-CoV-2 antibody testing using the Beckman Coulter Access SARS-CoV-2 Immunoglobulin (Ig) G assay (Brea, CA), an FDA-approved qualitative assay which detects IgG antibodies to the receptor-binding domain of the spike protein. 6 Patients' electronic medical records were reviewed for demographic and clinical information. Continuous variables were analyzed using a two-sample Wilcoxon test. A nonparametric test was used as the data was not normally distributed. Count variables were analyzed using chisquared tests of Fisher's exact tests if the sample size was low. Past medical histories were analyzed as the condition versus all others. A p-value less than .05 was considered to indicate significance. The study was approved by the Henry Ford Health System Institutional Review Board IRB approval number 14190-01. Written consent was 

The seroprevalence of 10.3% that we report in our study of SARS-CoV-2 in people living with HIV in our Ryan White program was about 2-fold higher than the number of reported cases by positive SARS-CoV-2 PCR in the same population. Estimating past infection by serology would have underestimated infection, given the absence of antibodies at the time of the serological testing in those with documented PCR-positive infection and those with possible infection who were never tested. The inclusion of PCRpositive but IgG-negative people living with HIV yields an infection prevalence of 14.1%. In comparison, a study among healthcare workers and first responders in Detroit found a seroprevalence of 6.9%. 7 The seroprevalence of SARS-CoV-2 in people living with HIV is an emerging topic. One study from San Francisco found that the seroprevalence of SARS-CoV-2 among people living with HIV was about 2 times lower compared to the population without HIV. This finding was attributed to a greater caution and sheltering in place among people living with HIV. 4 Another small study in Italy attempted to estimate the seroprevalence of people living with HIV in Umbria. They screened 270 asymptomatic people living with HIV, and found 5.4% had SARS-CoV-2 IgG antibodies. 8 Another study from Thailand revealed that there were no cases of COVID-19 in people living with HIV despite a high prevalence of HIV infection in this area. 9 The seroprevalence appears to be low in people living with HIV compared to our people living with HIV population; this suggests that the impact of health disparities on the Ryan White patients likely increases the chance of acquisition of COVID-19. 10 It is of interest that 19 participants, previously diagnosed with COVID-19 by PCR, either lost their antibodies or never made antibodies; thus, nearly 53% of people living with HIV were IgG-negative at a mean of 203 days after PCR diagnosis, while 47% were IgG positive at a mean of 139 days. This bespeaks of antibody loss over time from infection. Although other studies have shown that persistent immunity lasts for at least 6-8 months, 5, 11, 12 the duration of protection from reinfection and adverse outcome remains unknown. Although there has been a rapid decline in SARS-CoV-2 antibodies reported in the immunocompromised population, 5, 13, 14 all participants in our study had CD4 cell counts above 200 cell/μl and had suppressed HIV viral loads, suggesting some degree of immune competence. Age and diabetes mellitus type II were found to be associated with acquisition of COVID-19 IgG. Older age and comorbidities have been previously reported to be associated with an increased risk of hospitalization and mortality in patients infected with SARS-CoV-2. 15, 16 Nevertheless, the absence of SARS-CoV-2 antibodies in the majority of people living with HIV less than 1 year post-infection supports the potential for reinfection and the potential need for a sequential immunization strategy. 17 Our study had a few limitations. We were unable to determine IgG status on 25 patients who completed our survey due to indeterminate test results or failure to have testing performed. Additionally, surveys were answered subjectively, and the number of confirmed SARS-CoV-2 cases was relatively low.

In conclusion, our findings illustrate that the seroprevalence of 10.3% in our Ryan White people living with HIV population is consistent with what has been reported in the literature but significantly underestimates past infection. In order to better understand the penetration of COVID-19 into the people living with HIV community, a greater understanding of the dynamics of the antibody response to COVID-19 and the duration of protective immunity is needed.

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by the Health Resources Service Administration Ryan White HIV/AIDS program [grant number C20066].

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We would like to thank our Ryan White patients who participated in this study as well as Jim Kent, STI epidemiologist at Michigan Department of Health and Human Services, for conducting our incidence of PCR testing in this population.

Smitha Gudipati  https://orcid.org/0000-0002-0760-8268 Sean Yaphe  https://orcid.org/0000-0001-8799-4703