Genetic, Clinical, Epidemiological, and Immunological Profiling of IgG Response Duration after SARS-CoV-2 Infection.
Flávia Póvoa da CostaKevin Matheus Lima de SargesRosilene da SilvaErika Ferreira Dos SantosMatheus Holanda do NascimentoAlice Maciel RodriguesMarcos Henrique Damasceno CantanhedeFabíola Brasil Barbosa RodriguesMaria de Nazaré do Socorro de Almeida VianaMauro de Meira LeiteCamille Ferreira de OliveiraPablo Fabiano Moura das NevesGabriel Dos Santos Pereira NetoMioni Thieli Figueiredo Magalhães de BritoAndréa Luciana Soares da SilvaDaniele Freitas HenriquesJuarez Antonio Simões QuaresmaLuiz Fábio Magno FalcãoMaria Alice Freitas QueirozIzaura Maria Vieira Cayres VallinotoAntonio Carlos Rosário VallinotoGiselle Maria Rachid VianaEduardo José Melo Dos SantosPublished in: International journal of molecular sciences (2024)
The IgG response against SARS-CoV-2 infection can persist for over six months (long response; LR). However, among 30% of those infected, the duration can be as short as three months or less (short response; SR). The present study assembled serological data on the anti-SARS-CoV-2 IgG response duration of two previous studies and integrated these results with the plasmatic cytokine levels and genetic profile of 10 immune-relevant SNPs that were also previously published, along with the plasmatic total IgG, IgA, and IgM levels, allowing for the genetic, clinical, immunological, and epidemiological aspects of the post-COVID-19 IgG response duration to be understood. The SR was associated with previous mild acute COVID-19 and with an SNP (rs2228145) in IL6R related to low gene expression. Additionally, among the SR subgroup, no statistically significant Spearman correlations were observed between the plasma levels of IL-17A and the Th17 regulatory cytokines IFN-γ (rs = 0.2399; p = 0.1043), IL-4 (rs = 0.0273; p = 0.8554), and IL-2 (rs = 0.2204; p = 0.1365), while among the LR subgroup, weaker but statistically significant Spearman correlations were observed between the plasma levels of IL-17A and IFN-γ (rs = 0.3873; p = 0.0016), IL-4 (rs = 0.2671; p = 0.0328), and IL-2 (rs = 0.3959; p = 0.0012). These results suggest that the Th17 response mediated by the IL-6 pathway has a role in the prolonged IgG response to SARS-CoV-2 infection.