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443 COVID19 disease severity influences the expression of markers of durability in memory B cells

OBJECTIVES/GOALS: Studies have shown that SARS-CoV-2 specific memory B cells can be maintained at least a year after exposure. However, reports show an altered B cell response during infection in severe COVID-19 cases. This study aims to describe the B cell response during COVID-19 convalescence wit...

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Autores principales: Reyes, Raphael, Clarke, Kathleen, Cantwell, Angelene M., Catano, Gabriel, Tragus, Robin E., Patterson, Thomas F., Bol, Sebastiaan, Bunnik, Evelien M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209140/
http://dx.doi.org/10.1017/cts.2022.259
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author Reyes, Raphael
Clarke, Kathleen
Cantwell, Angelene M.
Catano, Gabriel
Tragus, Robin E.
Patterson, Thomas F.
Bol, Sebastiaan
Bunnik, Evelien M
author_facet Reyes, Raphael
Clarke, Kathleen
Cantwell, Angelene M.
Catano, Gabriel
Tragus, Robin E.
Patterson, Thomas F.
Bol, Sebastiaan
Bunnik, Evelien M
author_sort Reyes, Raphael
collection PubMed
description OBJECTIVES/GOALS: Studies have shown that SARS-CoV-2 specific memory B cells can be maintained at least a year after exposure. However, reports show an altered B cell response during infection in severe COVID-19 cases. This study aims to describe the B cell response during COVID-19 convalescence with a focus on signatures that contribute to durable and robust immunity. METHODS/STUDY POPULATION: Our study cohort consisted of individuals who had recovered from non-severe (hospitalized) or severe (hospitalized and requiring invasive mechanical ventilation) COVID-19. In our comparative analysis, samples from both groups were carefully matched to fall within 4-5 weeks post-symptom onset. We also performed a longitudinal analysis of non-severe patients with sampling ending 5 months post-symptom onset. Using high parameter flow cytometry, we characterized the phenotype of memory B cells using 19 distinct cell markers and fluorescently labeled probes to identify B cells reactive with SARS-CoV-2 spike and receptor-binding domain protein. Additionally, serum collected from individuals was used to quantify antibody titers. RESULTS/ANTICIPATED RESULTS: The frequency of spike-specific B cells and serum antibody titers were similar between severe and non-severe groups. However, we observed that individuals recovered from severe COVID-19 have a significantly reduced frequency of spike specific IgG+ memory B cells expressing Tbet and FcRL5 (markers associated with long lived immunity). In the non-severe patients, we observed IgG+Tbet+ B cells targeting the spike protein peak at 2-3 weeks post-symptom onset, decrease by almost fifty percent 4-5 weeks post-symptom onset, and return to baseline 5 months post-symptom onset. Our study also validated previous findings of a short-lived primary response of IgM+ B cells targeting the spike protein. DISCUSSION/SIGNIFICANCE: Our findings highlight potential implications for long-term immunity against re-infection or severity of the resulting disease in patients with severe COVID-19. Further investigation will be necessary to determine whether the maintenance of immunological protection is hindered in patients who overcame severe COVID-19.
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spelling pubmed-92091402022-07-01 443 COVID19 disease severity influences the expression of markers of durability in memory B cells Reyes, Raphael Clarke, Kathleen Cantwell, Angelene M. Catano, Gabriel Tragus, Robin E. Patterson, Thomas F. Bol, Sebastiaan Bunnik, Evelien M J Clin Transl Sci Valued Approaches OBJECTIVES/GOALS: Studies have shown that SARS-CoV-2 specific memory B cells can be maintained at least a year after exposure. However, reports show an altered B cell response during infection in severe COVID-19 cases. This study aims to describe the B cell response during COVID-19 convalescence with a focus on signatures that contribute to durable and robust immunity. METHODS/STUDY POPULATION: Our study cohort consisted of individuals who had recovered from non-severe (hospitalized) or severe (hospitalized and requiring invasive mechanical ventilation) COVID-19. In our comparative analysis, samples from both groups were carefully matched to fall within 4-5 weeks post-symptom onset. We also performed a longitudinal analysis of non-severe patients with sampling ending 5 months post-symptom onset. Using high parameter flow cytometry, we characterized the phenotype of memory B cells using 19 distinct cell markers and fluorescently labeled probes to identify B cells reactive with SARS-CoV-2 spike and receptor-binding domain protein. Additionally, serum collected from individuals was used to quantify antibody titers. RESULTS/ANTICIPATED RESULTS: The frequency of spike-specific B cells and serum antibody titers were similar between severe and non-severe groups. However, we observed that individuals recovered from severe COVID-19 have a significantly reduced frequency of spike specific IgG+ memory B cells expressing Tbet and FcRL5 (markers associated with long lived immunity). In the non-severe patients, we observed IgG+Tbet+ B cells targeting the spike protein peak at 2-3 weeks post-symptom onset, decrease by almost fifty percent 4-5 weeks post-symptom onset, and return to baseline 5 months post-symptom onset. Our study also validated previous findings of a short-lived primary response of IgM+ B cells targeting the spike protein. DISCUSSION/SIGNIFICANCE: Our findings highlight potential implications for long-term immunity against re-infection or severity of the resulting disease in patients with severe COVID-19. Further investigation will be necessary to determine whether the maintenance of immunological protection is hindered in patients who overcame severe COVID-19. Cambridge University Press 2022-04-19 /pmc/articles/PMC9209140/ http://dx.doi.org/10.1017/cts.2022.259 Text en © The Association for Clinical and Translational Science 2022 https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is unaltered and is properly cited. The written permission of Cambridge University Press must be obtained for commercial re-use or in order to create a derivative work.
spellingShingle Valued Approaches
Reyes, Raphael
Clarke, Kathleen
Cantwell, Angelene M.
Catano, Gabriel
Tragus, Robin E.
Patterson, Thomas F.
Bol, Sebastiaan
Bunnik, Evelien M
443 COVID19 disease severity influences the expression of markers of durability in memory B cells
title 443 COVID19 disease severity influences the expression of markers of durability in memory B cells
title_full 443 COVID19 disease severity influences the expression of markers of durability in memory B cells
title_fullStr 443 COVID19 disease severity influences the expression of markers of durability in memory B cells
title_full_unstemmed 443 COVID19 disease severity influences the expression of markers of durability in memory B cells
title_short 443 COVID19 disease severity influences the expression of markers of durability in memory B cells
title_sort 443 covid19 disease severity influences the expression of markers of durability in memory b cells
topic Valued Approaches
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209140/
http://dx.doi.org/10.1017/cts.2022.259
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