Your browser doesn't support javascript.
Impaired Cellular Immunity to SARS-CoV-2 in Severe COVID-19 Patients.
Ni, Ling; Cheng, Meng-Li; Feng, Yu; Zhao, Hui; Liu, Jingyuan; Ye, Fang; Ye, Qing; Zhu, Gengzhen; Li, Xiaoli; Wang, Pengzhi; Shao, Jing; Deng, Yong-Qiang; Wei, Peng; Chen, Fang; Qin, Cheng-Feng; Wang, Guoqing; Li, Fan; Zeng, Hui; Dong, Chen.
  • Ni L; Institute for Immunology and School of Medicine, Tsinghua University, Beijing, China.
  • Cheng ML; Center for Human Disease Immuno-monitoring, Beijing Friendship Hospital, Beijing, China.
  • Feng Y; College of Basic Medical Science, Jilin University, Changchun, China.
  • Zhao H; Department of Virology, State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing, China.
  • Liu J; Institute for Immunology and School of Medicine, Tsinghua University, Beijing, China.
  • Ye F; Department of Virology, State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing, China.
  • Ye Q; Beijing Ditan Hospital, Capital Medical University, and Beijing Key Laboratory of Emerging Infectious Diseases, Beijing, China.
  • Zhu G; Department of Hematology, Chui Yang Liu Hospital Affiliated to Tsinghua University, Beijing, China.
  • Li X; Department of Virology, State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing, China.
  • Wang P; Institute for Immunology and School of Medicine, Tsinghua University, Beijing, China.
  • Shao J; Institute for Immunology and School of Medicine, Tsinghua University, Beijing, China.
  • Deng YQ; Institute for Immunology and School of Medicine, Tsinghua University, Beijing, China.
  • Wei P; Institute for Immunology and School of Medicine, Tsinghua University, Beijing, China.
  • Chen F; Department of Virology, State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing, China.
  • Qin CF; Institute for Immunology and School of Medicine, Tsinghua University, Beijing, China.
  • Wang G; Department of Cardiology, Chui Yang Liu Hospital Affiliated to Tsinghua University, Beijing, China.
  • Li F; Department of Virology, State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing, China.
  • Zeng H; College of Basic Medical Science, Jilin University, Changchun, China.
  • Dong C; College of Basic Medical Science, Jilin University, Changchun, China.
Front Immunol ; 12: 603563, 2021.
Article in English | MEDLINE | ID: covidwho-1090415
Preprint
This scientific journal article is probably based on a previously available preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
See preprint
ABSTRACT
The high infection rate and rapid spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) make it a world-wide pandemic. Individuals infected by the virus exhibited different degrees of symptoms, and most convalescent individuals have been shown to develop both cellular and humoral immune responses. However, virus-specific adaptive immune responses in severe patients during acute phase have not been thoroughly studied. Here, we found that in a group of COVID-19 patients with acute respiratory distress syndrome (ARDS) during hospitalization, most of them mounted SARS-CoV-2-specific antibody responses, including neutralizing antibodies. However, compared to healthy controls, the percentages and absolute numbers of both NK cells and CD8+ T cells were significantly reduced, with decreased IFNγ expression in CD4+ T cells in peripheral blood from severe patients. Most notably, their peripheral blood lymphocytes failed in producing IFNγ against viral proteins. Thus, severe COVID-19 patients at acute infection stage developed SARS-CoV-2-specific antibody responses but were impaired in cellular immunity, which emphasizes on the role of cellular immunity in COVID-19.
Subject(s)
Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / Killer Cells, Natural / CD4-Positive T-Lymphocytes / CD8-Positive T-Lymphocytes / SARS-CoV-2 / COVID-19 Limits: Female / Humans / Male / Middle aged Language: English Journal: Front Immunol Year: 2021 Document Type: Article Affiliation country: Fimmu.2021.603563

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / Killer Cells, Natural / CD4-Positive T-Lymphocytes / CD8-Positive T-Lymphocytes / SARS-CoV-2 / COVID-19 Limits: Female / Humans / Male / Middle aged Language: English Journal: Front Immunol Year: 2021 Document Type: Article Affiliation country: Fimmu.2021.603563