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Massive surge of mRNA expression of clonal B-cell receptor in patients with COVID-19

BACKGROUND: Antibody production is one of the primary mechanisms for recovery from coronavirus disease 2019 (COVID-19). It is speculated that massive clonal expansion of B cells, which can produce clinically meaningful neutralizing antibodies, occurs in patients who recover on the timing of acquirin...

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Autores principales: Funakoshi, Yohei, Ohji, Goh, Yakushijin, Kimikazu, Ebisawa, Kei, Arakawa, Yu, Saegusa, Jun, Matsumoto, Hisayuki, Imanishi, Takamitsu, Fukuda, Eriko, Matsutani, Takaji, Mori, Yasuko, Iwata, Kentaro, Minami, Hironobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8352648/
https://www.ncbi.nlm.nih.gov/pubmed/34395931
http://dx.doi.org/10.1016/j.heliyon.2021.e07748
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author Funakoshi, Yohei
Ohji, Goh
Yakushijin, Kimikazu
Ebisawa, Kei
Arakawa, Yu
Saegusa, Jun
Matsumoto, Hisayuki
Imanishi, Takamitsu
Fukuda, Eriko
Matsutani, Takaji
Mori, Yasuko
Iwata, Kentaro
Minami, Hironobu
author_facet Funakoshi, Yohei
Ohji, Goh
Yakushijin, Kimikazu
Ebisawa, Kei
Arakawa, Yu
Saegusa, Jun
Matsumoto, Hisayuki
Imanishi, Takamitsu
Fukuda, Eriko
Matsutani, Takaji
Mori, Yasuko
Iwata, Kentaro
Minami, Hironobu
author_sort Funakoshi, Yohei
collection PubMed
description BACKGROUND: Antibody production is one of the primary mechanisms for recovery from coronavirus disease 2019 (COVID-19). It is speculated that massive clonal expansion of B cells, which can produce clinically meaningful neutralizing antibodies, occurs in patients who recover on the timing of acquiring adaptive immunity. METHODS: To evaluate fluctuations in clonal B cells and the size of the clones, we chronologically assessed the B-cell receptor (BCR) repertoire in three patients with COVID-19 who recovered around 10 days after symptom onset. RESULTS: We focused on the three dominant clonotypes (top 3) in each individual. The percentage frequencies of the top 3 clonotypes increased rapidly and accounted for 27.8 % on day 9 in patient 1, 10.4 % on day 12 in patient 2, and 10.8 % on day 11 in patient 3, respectively. The frequencies of these top 3 clonotypes rapidly decreased as the patients’ clinical symptoms improved. Furthermore, BCR network analysis revealed that accumulation of clusters composed of similar complementarity-determining region 3 (CDR3) sequences were rapidly formed, grew, and reached their maximum size around 10 days after symptom onset. CONCLUSIONS: BCR repertoire analysis revealed that a massive surge of some unique BCRs occurs during the acquisition of adaptive immunity and recovery. The peaks were more prominent than expected. These results provide insight into the important role of BCRs in the recovery from COVID-19 and raise the possibility of developing neutralizing antibodies as COVID-19 immunotherapy.
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spelling pubmed-83526482021-08-10 Massive surge of mRNA expression of clonal B-cell receptor in patients with COVID-19 Funakoshi, Yohei Ohji, Goh Yakushijin, Kimikazu Ebisawa, Kei Arakawa, Yu Saegusa, Jun Matsumoto, Hisayuki Imanishi, Takamitsu Fukuda, Eriko Matsutani, Takaji Mori, Yasuko Iwata, Kentaro Minami, Hironobu Heliyon Research Article BACKGROUND: Antibody production is one of the primary mechanisms for recovery from coronavirus disease 2019 (COVID-19). It is speculated that massive clonal expansion of B cells, which can produce clinically meaningful neutralizing antibodies, occurs in patients who recover on the timing of acquiring adaptive immunity. METHODS: To evaluate fluctuations in clonal B cells and the size of the clones, we chronologically assessed the B-cell receptor (BCR) repertoire in three patients with COVID-19 who recovered around 10 days after symptom onset. RESULTS: We focused on the three dominant clonotypes (top 3) in each individual. The percentage frequencies of the top 3 clonotypes increased rapidly and accounted for 27.8 % on day 9 in patient 1, 10.4 % on day 12 in patient 2, and 10.8 % on day 11 in patient 3, respectively. The frequencies of these top 3 clonotypes rapidly decreased as the patients’ clinical symptoms improved. Furthermore, BCR network analysis revealed that accumulation of clusters composed of similar complementarity-determining region 3 (CDR3) sequences were rapidly formed, grew, and reached their maximum size around 10 days after symptom onset. CONCLUSIONS: BCR repertoire analysis revealed that a massive surge of some unique BCRs occurs during the acquisition of adaptive immunity and recovery. The peaks were more prominent than expected. These results provide insight into the important role of BCRs in the recovery from COVID-19 and raise the possibility of developing neutralizing antibodies as COVID-19 immunotherapy. Elsevier 2021-08-10 /pmc/articles/PMC8352648/ /pubmed/34395931 http://dx.doi.org/10.1016/j.heliyon.2021.e07748 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Funakoshi, Yohei
Ohji, Goh
Yakushijin, Kimikazu
Ebisawa, Kei
Arakawa, Yu
Saegusa, Jun
Matsumoto, Hisayuki
Imanishi, Takamitsu
Fukuda, Eriko
Matsutani, Takaji
Mori, Yasuko
Iwata, Kentaro
Minami, Hironobu
Massive surge of mRNA expression of clonal B-cell receptor in patients with COVID-19
title Massive surge of mRNA expression of clonal B-cell receptor in patients with COVID-19
title_full Massive surge of mRNA expression of clonal B-cell receptor in patients with COVID-19
title_fullStr Massive surge of mRNA expression of clonal B-cell receptor in patients with COVID-19
title_full_unstemmed Massive surge of mRNA expression of clonal B-cell receptor in patients with COVID-19
title_short Massive surge of mRNA expression of clonal B-cell receptor in patients with COVID-19
title_sort massive surge of mrna expression of clonal b-cell receptor in patients with covid-19
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8352648/
https://www.ncbi.nlm.nih.gov/pubmed/34395931
http://dx.doi.org/10.1016/j.heliyon.2021.e07748
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