Surviving the Rookie Virus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV2): The Immunopathology of a SARS-CoV2 Infection

被引:3
|
作者
Tsai, Sheng Feng [1 ,2 ]
Lu, Kang-Yun [2 ,3 ]
Chuang, Hong-Meng [4 ]
Liu, Ching-Ann [2 ,5 ,6 ]
机构
[1] Natl Chung Hsing Univ, Agr Biotechnol Ctr, Dept Life Sci, Taichung, Taiwan
[2] Buddhist Tzu Chi Med Fdn, Bioinnovat Ctr, Hualien 970, Taiwan
[3] China Med Univ, Grad Inst Basic Med Sci, Taichung, Taiwan
[4] Dev Ctr Biotechnol, Lab Translat Med Off, Taipei, Taiwan
[5] Hualien Tzu Chi Hosp, Dept Med Res, Hualien, Taiwan
[6] Hualien Tzu Chi Hosp, Dept Neurosci Ctr, Hualien, Taiwan
关键词
SARS-CoV2; immunopathology; vaccine; SYNDROME SARS; SAUDI-ARABIA; OUTBREAK; PNEUMONIA; DISEASE;
D O I
10.1177/0963689721993769
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Until July 29th, the number of confirmed coronavirus (COVID-19) cases worldwide has risen to over 16 million, within which 655 k deaths. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) emerges as the 11th global pandemic disease, showing the highest infectivity and lowest infection fatality rate. In this review, we compare the immunopathology among SARS-CoV, Middle East respiratory syndrome coronavirus, and SARS-CoV2. SARS-CoV2 is similar to SARS-CoV; it can cause lymphocytopenia and a rising granulocyte count. Here we point out the human body and concentrated society make for an excellent incubator for virus evolution. Most research energies put into developing the SARS-CoV2 vaccine are trying to block virus infection. Sixty-five percent of severe patients die with multiple organ failure, inflammation, and cytokine storm, which indicates that the patient's immune system maintains functionality. Finding a way to trigger the specific T cell subset and plasmablast in our body is the best shot to get away with SARS-CoV2.
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页数:6
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