CXCL9 and CXCL10 support the exacerbated humoral response in recovered COVID-19 patients who developed acute respiratory distress syndrome by promoting plasma cell differentiation, whereas CXCL9 also induces CD40L and CXCR3 upregulation on T helper c

Four months after COVID-19, patients with prior ARDS and persistent pulmonary sequelae exhibit sustained elevations of anti-SARS-CoV-2 IgG and chemokines CXCL9 and CXCL10. Both chemokines directly enhance B cell differentiation into IgG-secreting plasma cells <i>in vitro</i>, while CXCL9 also increases CD4<sup>+</sup> T cell help, suggesting a mechanistic link between chronic inflammation, increased humoral responses, and long-term lung impairment. Targeting CXCL9/CXCL10-CXCR3 signaling could offer therapeutic potential to mitigate post-COVID pulmonary complications.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-12-04
DOI
https://doi.org/10.3389/fimmu.2025.1684704
Primary Topic
Long-Term Effects of COVID-19
Type
article
Field-Weighted Citation Impact
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article

CXCL9 and CXCL10 support the exacerbated humoral response in recovered COVID-19 patients who developed acute respiratory distress syndrome by promoting plasma cell differentiation, whereas CXCL9 also induces CD40L and CXCR3 upregulation on T helper c

Gonzalo Labarca, Catarina Sepúlveda, Mario Henríquez‐Beltrán, Marco Fraga et al.
Frontiers in Immunology
Long-Term Effects of COVID-19
article

CXCL9 and CXCL10 support the exacerbated humoral response in recovered COVID-19 patients who developed acute respiratory distress syndrome by promoting plasma cell differentiation, whereas CXCL9 also induces CD40L and CXCR3 upregulation on T helper c

Gonzalo Labarca, Catarina Sepúlveda, Mario Henríquez‐Beltrán, Marco Fraga, Luciano Ferrada, Faryd Llerena, Sergio Manuel Rivera Sanhueza, Camilo Cabrera, Liliana Lamperti, Alicia Colombo, Romina Andrea Quiroga, María Inés Barría, Camila Muñoz, Estefanía Nova‐Lamperti, Bárbara Antilef
article en

Abstract

Four months after COVID-19, patients with prior ARDS and persistent pulmonary sequelae exhibit sustained elevations of anti-SARS-CoV-2 IgG and chemokines CXCL9 and CXCL10. Both chemokines directly enhance B cell differentiation into IgG-secreting plasma cells <i>in vitro</i>, while CXCL9 also increases CD4<sup>+</sup> T cell help, suggesting a mechanistic link between chronic inflammation, increased humoral responses, and long-term lung impairment. Targeting CXCL9/CXCL10-CXCR3 signaling could offer therapeutic potential to mitigate post-COVID pulmonary complications.

Frontiers in ImmunologyVol. 16
Brigham and Women's Hospital (US), University of Concepción (CL), Instituto de Salud Carlos III (ES), Hospital Universitari Arnau de Vilanova (ES), San Sebastián University (CL), Universidad Santo Tomás (CL), Universidad Adventista de Chile (CL), Hospital Clínico de la Universidad de Chile (CL), Complejo Asistencial Sótero del Río (CL), Centro de Investigación Biomédica en Red de Cáncer (ES), University of Chile (CL)
European Commission, Universidad de Chile, Agencia Nacional de Investigación y Desarrollo, Instituto de Salud Carlos III
Openalex Percentile: Top 47%
Long-Term Effects of COVID-19
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