Objective:
From the first-generation options available in 1985, tests to detect HIV-1 specific antibodies have increased its sensitivity and specificity. HIV-1 and SARS-CoV-2 surface glycoproteins present a certain degree of homology and shared epitope motifs, which results of relevance as both pandemics coexist. Here, we aimed to evaluate the rate of false-positive HIV serology results among individuals with COVID-19 diagnosis and in vaccinated individuals.
Design:
A retrospective analysis of the samples stored at the Infectious Disease Biobank in Argentina from donors with previous COVID-19 diagnosis or anti-SARS-CoV-2 vaccination.
Methods:
Plasma samples were analyzed using Genscreen Ultra HIV Ag-Ab. In those with a positive result, the following assays were also performed: ELISA lateral flow Determine Early Detect; RecomLine HIV-1 & HIV-2 IgG and Abbott m2000 RealTime PCR for HIV-1 viral load quantification. In all samples, the presence of anti-SARS-CoV-2 IgG antibodies was evaluated by ELISA using the COVIDAR kit. Statistical analysis was done using Pearson's and Fisher's exact chi-squared test; Mann–Whitney and Kruskal–Wallis tests.
Results:
Globally, the false-positive HIV ELISA rate was 1.3% [95% confidence interval (95% CI) 0.66–2.22;
χ
2
= 4.68,
P
= 0.03, when compared with the expected 0.4% false-positive rate]. It increased to 1.4% (95% CI 0.70–2.24,
χ
2
= 5.16,
P
= 0.02) when only samples from individuals with previous COVID-19 diagnosis, and to 1.8% (95% CI 0.91–3.06,
χ
2
= 7.99,
P
= 0.005) when only individuals with detectable IgG SARS-CoV-2 antibodies were considered.
Conclusion:
This higher occurrence of HIV false-positive results among individuals with detectable antibodies against Spike SARS-CoV-2 protein should be dispersed among virology testing settings, health providers, and authorities.