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Antibody-dependent cellular cytotoxicity response to SARS-CoV-2 in COVID-19 patients.
Yu, Yuanling; Wang, Meiyu; Zhang, Xiaoai; Li, Shufen; Lu, Qingbin; Zeng, Haolong; Hou, Hongyan; Li, Hao; Zhang, Mengyi; Jiang, Fei; Wu, Jiajing; Ding, Ruxia; Zhou, Zehua; Liu, Min; Si, Weixue; Zhu, Tao; Li, Hangwen; Ma, Jie; Gu, Yuanyuan; She, Guangbiao; Li, Xiaokun; Zhang, Yulan; Peng, Ke; Huang, Weijin; Liu, Wei; Wang, Youchun.
  • Yu Y; Division of HIV/AIDS and Sex-transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing, China.
  • Wang M; Division of HIV/AIDS and Sex-transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing, China.
  • Zhang X; Graduate School of Peking Union Medical College, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.
  • Li S; State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, China.
  • Lu Q; State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Zeng H; Department of Laboratorial Science and Technology, School of Public Health, Peking University, Beijing, China.
  • Hou H; Department of Laboratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
  • Li H; Department of Laboratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
  • Zhang M; State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, China.
  • Jiang F; Division of HIV/AIDS and Sex-transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing, China.
  • Wu J; Division of HIV/AIDS and Sex-transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing, China.
  • Ding R; Division of HIV/AIDS and Sex-transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing, China.
  • Zhou Z; Division of HIV/AIDS and Sex-transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing, China.
  • Liu M; Division of HIV/AIDS and Sex-transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing, China.
  • Si W; Sinovac Biotech Co., Ltd, Beijing, China.
  • Zhu T; Cansino Biotech Incorporation, Tianjin, China.
  • Li H; Cansino Biotech Incorporation, Tianjin, China.
  • Ma J; Stemirna Therapeutics, Ltd, Shanghai, China.
  • Gu Y; Stemirna Therapeutics, Ltd, Shanghai, China.
  • She G; Stemirna Therapeutics, Ltd, Shanghai, China.
  • Li X; Anhui Zhifeilongcom Biopharmaceutical Co., Ltd, Hefei, China.
  • Zhang Y; State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, China.
  • Peng K; State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Huang W; State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Liu W; University of Chinese Academy of Sciences, Beijing, China.
  • Wang Y; Division of HIV/AIDS and Sex-transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing, China. huangweijin@nifdc.org.cn.
Signal Transduct Target Ther ; 6(1): 346, 2021 09 24.
Article en En | MEDLINE | ID: mdl-34561414
Antibody-dependent cellular cytotoxicity (ADCC) responses to viral infection are a form of antibody regulated immune responses mediated through the Fc fragment. Whether severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) triggered ADCC responses contributes to COVID-19 disease development is currently not well understood. To understand the potential correlation between ADCC responses and COVID-19 disease development, we analyzed the ADCC activity and neutralizing antibody response in 255 individuals ranging from asymptomatic to fatal infections over 1 year post disease. ADCC was elicited by 10 days post-infection, peaked by 11-20 days, and remained detectable until 400 days post-infection. In general, patients with severe disease had higher ADCC activities. Notably, patients who had severe disease and recovered had higher ADCC activities than patients who had severe disease and deceased. Importantly, ADCC activities were mediated by a diversity of epitopes in SARS-COV-2-infected mice and induced to comparable levels against SARS-CoV-2 variants of concern (VOCs) (B.1.1.7, B.1.351, and P.1) as that against the D614G mutant in human patients and vaccinated mice. Our study indicates anti-SARS-CoV-2 ADCC as a major trait of COVID-19 patients with various conditions, which can be applied to estimate the extra-neutralization level against COVID-19, especially lethal COVID-19.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anticuerpos Neutralizantes / SARS-CoV-2 / COVID-19 / Anticuerpos Antivirales / Citotoxicidad Celular Dependiente de Anticuerpos Límite: Adult / Aged / Animals / Female / Humans / Male / Middle aged Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anticuerpos Neutralizantes / SARS-CoV-2 / COVID-19 / Anticuerpos Antivirales / Citotoxicidad Celular Dependiente de Anticuerpos Límite: Adult / Aged / Animals / Female / Humans / Male / Middle aged Idioma: En Año: 2021 Tipo del documento: Article