Immune characterization of a Colombian family cluster with SARS-CoV-2 infection

Introduction: Immunological markers have been described during COVID-19 and persist after recovery. These immune markers are associated with clinical features among SARSCoV- 2 infected individuals. Nevertheless, studies reporting a comprehensive analysis of the immune changes occurring during SARS-C...

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Autores:
Aguilar Jiménez, Wbeimar
Flórez Álvarez, Lizdany
Rincón, Daniel S.
Marín Palma, Damariz
Sanchez Martinez, Alexandra
Martínez Moreno, Jahnnyer
Zapata Cardona, María Isabel
Loaiza Durán, John Darío
Cardenas, Constanza
Guzman, Fanny
Velilla Hernandez, Paula Andrea
Taborda, Natalia Andrea
Zapata Builes, Wildeman
Hernández López, Juan Carlos
Diaz, Francisco Javier
Rugeles López, María Teresa
Tipo de recurso:
Article of investigation
Fecha de publicación:
2021
Institución:
Universidad Cooperativa de Colombia
Repositorio:
Repositorio UCC
Idioma:
OAI Identifier:
oai:repository.ucc.edu.co:20.500.12494/43606
Acceso en línea:
https://hdl.handle.net/20.500.12494/43606
Palabra clave:
Coronavirus infections
Inflammation
Killer cells, natural
T-lymphocytes
Antibodies
Neutralizing
Coronavirus infections
Inflammation
Killer cells, natural
T-lymphocytes
Antibodies
Neutralizing
Rights
openAccess
License
Atribución
Description
Summary:Introduction: Immunological markers have been described during COVID-19 and persist after recovery. These immune markers are associated with clinical features among SARSCoV- 2 infected individuals. Nevertheless, studies reporting a comprehensive analysis of the immune changes occurring during SARS-CoV-2 infection are still limited. Objective: To evaluate the production of proinflammatory cytokines, the antibody response, and the phenotype and function of NK cells and T cells in a Colombian family cluster with SARS-CoV-2 infection. Materials and methods: Proinflammatory cytokines were evaluated by RT-PCR and ELISA. The frequency, phenotype, and function of NK cells (cocultures with K562 cells) and T-cells (stimulated with spike/RdRp peptides) were assessed by flow cytometry. Anti-SARS-CoV-2 antibodies were determined using indirect immunofluorescence and plaque reduction neutralization assay. Results: During COVID-19, we observed a high proinflammatory-cytokine production and a reduced CD56bright-NK cell and cytotoxic response. Compared with healthy controls, infected individuals had a higher frequency of dysfunctional CD8+ T cells CD38+HLA-DR-. During the acute phase, CD8+ T cells stimulated with viral peptides exhibited a monofunctional response characterized by high IL-10 production. However, during recovery, we observed a bifunctional response characterized by the co-expression of CD107a and granzyme B or perforin. Conclusion: Although the proinflammatory response is a hallmark of SARS-CoV-2 infection, other phenotypic and functional alterations in NK cells and CD8+ T cells could be associated with the outcome of COVID-19. However, additional studies are required to understand these alterations and to guide future immunotherapy strategies.