Spike-specific circulating T follicular helper cell and cross-neutralizing antibody responses in COVID-19-convalescent individuals
Coronavirus disease 2019 (COVID-19) is caused by infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)1-3 and individuals with COVID-19 have symptoms that can be asymptomatic, mild, moderate or severe4,5. In the early phase of infection, T- and B-cell counts are substantially decreased6,7; however, IgM8-11 and IgG12-14 are detectable within 14 d after symptom onset. In COVID-19-convalescent individuals, spike-specific neutralizing antibodies are variable3,15,16. No specific drug or vaccine is available for COVID-19 at the time of writing; however, patients benefit from treatment with serum from COVID-19-convalescent individuals17,18. Nevertheless, antibody responses and cross-reactivity with other coronaviruses in COVID-19-convalescent individuals are largely unknown. Here, we show that the majority of COVID-19-convalescent individuals maintained SARS-CoV-2 spike S1- and S2-specific antibodies with neutralizing activity against the SARS-CoV-2 pseudotyped virus, and that some of the antibodies cross-neutralized SARS-CoV, Middle East respiratory syndrome coronavirus or both pseudotyped viruses. Convalescent individuals who experienced severe COVID-19 showed higher neutralizing antibody titres, a faster increase in lymphocyte counts and a higher frequency of CXCR3+ T follicular help (TFH) cells compared with COVID-19-convalescent individuals who experienced non-severe disease. Circulating TFH cells were spike specific and functional, and the frequencies of CXCR3+ TFH cells were positively associated with neutralizing antibody titres in COVID-19-convalescent individuals. No individuals had detectable autoantibodies. These findings provide insights into neutralizing antibody responses in COVID-19-convalescent individuals and facilitate the treatment and vaccine development for SARS-CoV-2 infection.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2021 |
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Erschienen: |
2021 |
Enthalten in: |
Zur Gesamtaufnahme - volume:6 |
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Enthalten in: |
Nature microbiology - 6(2021), 1 vom: 16. Jan., Seite 51-58 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Zhang, Jian [VerfasserIn] |
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Links: |
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Themen: |
Antibodies, Neutralizing |
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Anmerkungen: |
Date Completed 13.01.2021 Date Revised 22.04.2022 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1038/s41564-020-00824-5 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM317671782 |
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520 | |a Coronavirus disease 2019 (COVID-19) is caused by infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)1-3 and individuals with COVID-19 have symptoms that can be asymptomatic, mild, moderate or severe4,5. In the early phase of infection, T- and B-cell counts are substantially decreased6,7; however, IgM8-11 and IgG12-14 are detectable within 14 d after symptom onset. In COVID-19-convalescent individuals, spike-specific neutralizing antibodies are variable3,15,16. No specific drug or vaccine is available for COVID-19 at the time of writing; however, patients benefit from treatment with serum from COVID-19-convalescent individuals17,18. Nevertheless, antibody responses and cross-reactivity with other coronaviruses in COVID-19-convalescent individuals are largely unknown. Here, we show that the majority of COVID-19-convalescent individuals maintained SARS-CoV-2 spike S1- and S2-specific antibodies with neutralizing activity against the SARS-CoV-2 pseudotyped virus, and that some of the antibodies cross-neutralized SARS-CoV, Middle East respiratory syndrome coronavirus or both pseudotyped viruses. Convalescent individuals who experienced severe COVID-19 showed higher neutralizing antibody titres, a faster increase in lymphocyte counts and a higher frequency of CXCR3+ T follicular help (TFH) cells compared with COVID-19-convalescent individuals who experienced non-severe disease. Circulating TFH cells were spike specific and functional, and the frequencies of CXCR3+ TFH cells were positively associated with neutralizing antibody titres in COVID-19-convalescent individuals. No individuals had detectable autoantibodies. These findings provide insights into neutralizing antibody responses in COVID-19-convalescent individuals and facilitate the treatment and vaccine development for SARS-CoV-2 infection | ||
650 | 4 | |a Journal Article | |
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700 | 1 | |a Wu, Qian |e verfasserin |4 aut | |
700 | 1 | |a Liu, Ziyan |e verfasserin |4 aut | |
700 | 1 | |a Wang, Qijie |e verfasserin |4 aut | |
700 | 1 | |a Wu, Jiajing |e verfasserin |4 aut | |
700 | 1 | |a Hu, Yabin |e verfasserin |4 aut | |
700 | 1 | |a Bai, Tingting |e verfasserin |4 aut | |
700 | 1 | |a Xie, Ting |e verfasserin |4 aut | |
700 | 1 | |a Huang, Mincheng |e verfasserin |4 aut | |
700 | 1 | |a Wu, Tiantian |e verfasserin |4 aut | |
700 | 1 | |a Peng, Danhong |e verfasserin |4 aut | |
700 | 1 | |a Huang, Weijin |e verfasserin |4 aut | |
700 | 1 | |a Jin, Kun |e verfasserin |4 aut | |
700 | 1 | |a Niu, Ling |e verfasserin |4 aut | |
700 | 1 | |a Guo, Wangyuan |e verfasserin |4 aut | |
700 | 1 | |a Luo, Dixian |e verfasserin |4 aut | |
700 | 1 | |a Lei, Dongzhu |e verfasserin |4 aut | |
700 | 1 | |a Wu, Zhijian |e verfasserin |4 aut | |
700 | 1 | |a Li, Guicheng |e verfasserin |4 aut | |
700 | 1 | |a Huang, Renbin |e verfasserin |4 aut | |
700 | 1 | |a Lin, Yingbiao |e verfasserin |4 aut | |
700 | 1 | |a Xie, Xiangping |e verfasserin |4 aut | |
700 | 1 | |a He, Shuangyan |e verfasserin |4 aut | |
700 | 1 | |a Deng, Yunfan |e verfasserin |4 aut | |
700 | 1 | |a Liu, Jianghua |e verfasserin |4 aut | |
700 | 1 | |a Li, Weilang |e verfasserin |4 aut | |
700 | 1 | |a Lu, Zhongyi |e verfasserin |4 aut | |
700 | 1 | |a Chen, Haifu |e verfasserin |4 aut | |
700 | 1 | |a Zeng, Ting |e verfasserin |4 aut | |
700 | 1 | |a Luo, Qingting |e verfasserin |4 aut | |
700 | 1 | |a Li, Yi-Ping |e verfasserin |4 aut | |
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700 | 1 | |a Liu, Wenpei |e verfasserin |4 aut | |
700 | 1 | |a Qu, Xiaowang |e verfasserin |4 aut | |
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