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

Erscheinungsjahr:

2021

Erschienen:

2021

Enthalten in:

Zur Gesamtaufnahme - volume:6

Enthalten in:

Nature microbiology - 6(2021), 1 vom: 16. Jan., Seite 51-58

Sprache:

Englisch

Beteiligte Personen:

Zhang, Jian [VerfasserIn]
Wu, Qian [VerfasserIn]
Liu, Ziyan [VerfasserIn]
Wang, Qijie [VerfasserIn]
Wu, Jiajing [VerfasserIn]
Hu, Yabin [VerfasserIn]
Bai, Tingting [VerfasserIn]
Xie, Ting [VerfasserIn]
Huang, Mincheng [VerfasserIn]
Wu, Tiantian [VerfasserIn]
Peng, Danhong [VerfasserIn]
Huang, Weijin [VerfasserIn]
Jin, Kun [VerfasserIn]
Niu, Ling [VerfasserIn]
Guo, Wangyuan [VerfasserIn]
Luo, Dixian [VerfasserIn]
Lei, Dongzhu [VerfasserIn]
Wu, Zhijian [VerfasserIn]
Li, Guicheng [VerfasserIn]
Huang, Renbin [VerfasserIn]
Lin, Yingbiao [VerfasserIn]
Xie, Xiangping [VerfasserIn]
He, Shuangyan [VerfasserIn]
Deng, Yunfan [VerfasserIn]
Liu, Jianghua [VerfasserIn]
Li, Weilang [VerfasserIn]
Lu, Zhongyi [VerfasserIn]
Chen, Haifu [VerfasserIn]
Zeng, Ting [VerfasserIn]
Luo, Qingting [VerfasserIn]
Li, Yi-Ping [VerfasserIn]
Wang, Youchun [VerfasserIn]
Liu, Wenpei [VerfasserIn]
Qu, Xiaowang [VerfasserIn]

Links:

Volltext

Themen:

Antibodies, Neutralizing
Antibodies, Viral
Broadly Neutralizing Antibodies
CXCR3 protein, human
Journal Article
Receptors, CXCR3
Research Support, Non-U.S. Gov't

Anmerkungen:

Date Completed 13.01.2021

Date Revised 22.04.2022

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1038/s41564-020-00824-5

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM317671782