Prolonged Evolution of Virus-Specific Memory T Cell Immunity after Severe Avian Influenza A (H7N9) Virus Infection

Author:

Zhao Min12,Chen Junbo3,Tan Shuguang1,Dong Tao4,Jiang Hui5,Zheng Jiandong5,Quan Chuansong6,Liao Qiaohong5,Zhang Hangjie6,Wang Xiling3,Wang Qianli3,Bi Yuhai1,Liu Fengfeng5,Feng Luzhao5,Horby Peter W.7,Klenerman Paul8,Gao George F.126,Liu William J.6,Yu Hongjie35

Affiliation:

1. Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing, China

2. CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China

3. School of Public Health, Fudan University, Key Laboratory of Public Health Safety, Ministry of Education, Shanghai, China

4. Medical Research Council Human Immunology Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom

5. Division of Infectious Disease, Key Laboratory of Surveillance and Early-Warning on Infectious Disease, Chinese Center for Disease Control and Prevention, Beijing, China

6. NHC Key Laboratory of Medical Virology and Viral Diseases, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China

7. Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom

8. Peter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom

Abstract

Avian influenza A H7N9 virus remains a major threat to public health. However, no previous studies have determined the characteristics and dynamics of virus-specific T cell immune memory in patients who have recovered from H7N9 infection. Our findings showed that establishment of H7N9-specific T cell memory after H7N9 infection was prolonged in older and severely affected patients. Severely ill patients mounted lower T cell responses in the first 4 months after infection, while T cell responses tended to increase over time in older and severely ill patients. Higher levels of antigen-specific CD8 + T cells expressing the lung-homing marker CD49a were detected at 6 to 8 months after infection. Our results indicated a long-term impact of H7N9 infection on virus-specific memory T cells. These findings advance our understanding of the dynamics of virus-specific memory T cell immunity after H7N9 infection, which is relevant to the development of T cell-based universal influenza vaccines.

Funder

HHS | National Institutes of Health

National Natural Science Foundation of China

DH | National Institute for Health Research

National Science and Technology Major Project of Control and Prevention for AIDS, Viral Hepatitis, and Other Major Infectious Diseases

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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