| Literature DB >> 32939324 |
Cléa Melenotte1,2,3,4, Aymeric Silvin1, Anne-Gaëlle Goubet1,2,5,6, Imran Lahmar1,2,5,6, Agathe Dubuisson1,2,5,6, Alimuddin Zumla7, Didier Raoult2,3, Mansouria Merad8, Bertrand Gachot1, Clémence Hénon1, Eric Solary1, Michaela Fontenay9, Fabrice André1, Markus Maeurer10,11, Giuseppe Ippolito12, Mauro Piacentini13,14, Fu-Sheng Wang15, Florent Ginhoux16,17,18, Aurélien Marabelle3, Guido Kroemer19,20,21,22,23, Lisa Derosa1,2,5,6, Laurence Zitvogel1,2,5,6,23.
Abstract
Over the past 16 years, three coronaviruses (CoVs), severe acute respiratory syndrome CoV (SARS-CoV) in 2002, Middle East respiratory syndrome CoV (MERS-CoV) in 2012 and 2015, and SARS-CoV-2 in 2020, have been causing severe and fatal human epidemics. The unpredictability of coronavirus disease-19 (COVID-19) poses a major burden on health care and economic systems across the world. This is caused by the paucity of in-depth knowledge of the risk factors for severe COVID-19, insufficient diagnostic tools for the detection of SARS-CoV-2, as well as the absence of specific and effective drug treatments. While protective humoral and cellular immune responses are usually mounted against these betacoronaviruses, immune responses to SARS-CoV2 sometimes derail towards inflammatory tissue damage, leading to rapid admissions to intensive care units. The lack of knowledge on mechanisms that tilt the balance between these two opposite outcomes poses major threats to many ongoing clinical trials dealing with immunostimulatory or immunoregulatory therapeutics. This review will discuss innate and cognate immune responses underlying protective or deleterious immune reactions against these pathogenic coronaviruses.Entities:
Keywords: Coronavirus; Covid-19; Sars-CoV-2; cellular; humoral; immune response; immunity
Year: 2020 PMID: 32939324 PMCID: PMC7480812 DOI: 10.1080/2162402X.2020.1807836
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110