COVID-19
Raúl F. Reyes-Huerta, BSc
Graduate Student (Maestría en Ciencias en Inmunología)
Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional
Mexico City, Distrito Federal, Mexico
Rodrigo Cervantes-Díaz, MSc
Universidad Nacional Autónoma de México
Mexico City, Distrito Federal, Mexico
Víctor A. Sosa-Hernandez, MD, MSc
PhD student
Cinvestav IPN
Mexico City, Distrito Federal, Mexico
Jiram Torres-Ruíz, MD, PhD
Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán
Mexico City, Distrito Federal, Mexico
Sandra Romero-Ramírez, MSc
PhD student
Universidad Nacional Autónoma de México
Mexico City, Distrito Federal, Mexico
Mariana Cañez-Hernández, MD
Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional
Mexico City, Distrito Federal, Mexico
Alfredo Pérez-Fragoso, MD
Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán
Mexico City, Distrito Federal, Mexico
José C. Páez-Franco, PhD
Universidad Nacional Autónoma de México
Mexico City, Distrito Federal, Mexico
David E. Meza-Sánchez, PhD
Universidad Nacional Autónoma de México
Mexico City, Distrito Federal, Mexico
Miriam Pescador-Rojas, PhD
Escuela Superior de Cómputo, Instituto Politécnico Nacional
Mexico City, Distrito Federal, Mexico
Víctor Adrián Sosa-Hernández, PhD
School of Engineering and Science, Tecnológico de Monterrey
Mexico City, Distrito Federal, Mexico
Diana Gómez-Martín, MD, PhD
Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán
Mexico City, Distrito Federal, Mexico
José L. Maravillas-Montero, PhD
Universidad Nacional Autónoma de México
Mexico City, Distrito Federal, Mexico
Background: The role of B cells in COVID‐19, beyond the production of specific antibodies against SARS-CoV-2, is still not well understood. Here, we describe the novel landscape of circulating Double Negative (DN) CD27- IgD- B cells in COVID‐19 patients, representing a group of atypical and neglected subpopulations of this cell lineage.
Methods: Using multiparametric flow cytometry, we determined DN B cell subsets (frequencies and absolute numbers) from a cohort of 91 COVID-19 patients, correlated those with cytokines, clinical and laboratory parameters, and segregated them by principal components analysis.
Results: We detected significant increments in the DN2 and DN3 B cell subsets, while we found a relevant decrease in the DN1 B cell subpopulation, according to disease severity and patient outcomes. These DN cell numbers also appeared to correlate with pro or anti-inflammatory signatures respectively and contributed to the segregation of the patients into disease severity groups.
Conclusion: This study provides insights into DN B cell subsets' potential role in immune responses against SARS‐CoV‐2, particularly linked to the severity of COVID‐19.
Supported by CONACyT A3-S-36875 and UNAM-DGAPA-PAPIIT IN212122.