Long-term changes in the phenotype and cytokine production of monocytes in COVID-19 recovered and vaccinated individuals.
Yekaterina O OstapchukAnzhelika V LushovaSofia A KanNurshat AbdollaAikyn KaliRaikhan TleulievaAnastassiya V PerfilyevaYuliya V PerfilyevaPublished in: Infection and immunity (2024)
Monocytes play a crucial role in the immune response against pathogens. Here, we sought to determine COVID-19 and the vaccine Gam-COVID-Vac induce long-term changes in the phenotype and cytokine production of circulating monocytes. Monocytes were purified from peripheral blood mononuclear cells of healthy donors who had not had COVID-19 or vaccination, who had received two doses of Gam-COVID-Vac, and who had mild/moderate COVID-19 in the last 6 months and evaluated by flow cytometry. To investigate the effect of SARS-CoV-2 proteins, monocytes were cultured for 2 days with or without stimulation with recombinant SARS-CoV-2 S1 and N peptides. Monocytes obtained from vaccinated and recovered individuals showed increased basal expression of HLA-DR, CD63, CXCR2, and TLR7. We also observed an increased frequency of CD63 + classical monocytes in both groups, as well as an increased frequency of HLA-DR + non-classical monocytes in the COVID-19-recovered group compared to the control group. Monocytes from vaccinated and recovered donors produced higher basal levels of IL-6, IL-1β, and TNF-α cytokines. Ex vivo stimulation with SARS-CoV-2 antigens induced increased expression of HLA-DR and TLR7 on monocytes obtained from the control group. The challenge with SARS-CoV-2 antigens had no effect on the production of IL-6, IL-1β, and TNF-α cytokines by monocytes. The acquired data offer compelling evidence of enduring alterations in both the phenotype and functional status of circulating monocytes subsequent to vaccination with Gam-COVID-Vac and mild/moderate COVID-19 infection. At least some of these changes appear to be a consequence of exposure to SARS-CoV-2 S1 and N antigens.
Keyphrases
- sars cov
- dendritic cells
- respiratory syndrome coronavirus
- coronavirus disease
- peripheral blood
- immune response
- toll like receptor
- flow cytometry
- inflammatory response
- rheumatoid arthritis
- poor prognosis
- machine learning
- big data
- endothelial cells
- high intensity
- high glucose
- binding protein
- editorial comment
- electronic health record
- multidrug resistant
- kidney transplantation
- stress induced
- drug induced