4.7 Review

Immune responses during COVID-19 infection

Journal

ONCOIMMUNOLOGY
Volume 9, Issue 1, Pages -

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/2162402X.2020.1807836

Keywords

Covid-19; Sars-CoV-2; Coronavirus; immune response; immunity; cellular; humoral

Funding

  1. Dassault Systems
  2. Izipizi
  3. Ligue contre le Cancer (equipe labelisee)
  4. Agence National de la Recherche (ANR) - Projets blancs
  5. ANR under the frame of E-Rare-2, the ERA-Net for Research on Rare Diseases
  6. Association pour la recherche sur le cancer (ARC)
  7. Canceropole Ile-de-France
  8. Chancelerie des universites de Paris (Legs Poix)
  9. Fondation pour la Recherche Medicale (FRM)
  10. European Commission (Horizon 2020: Oncobiome)
  11. European Research Council (ERC)
  12. Institut National du Cancer (INCa)
  13. Inserm (HTE)
  14. Institut Universitaire de France
  15. LeDucq Foundation
  16. LabEx Immuno-Oncology
  17. RHU Torino Lumiere
  18. Seerave Foundation
  19. SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE)
  20. ONCOBIOME H2020 network
  21. SIRIC Cancer Research and Personalized Medicine (CARPEM)
  22. RHU Torino Lumiere [ANR-16-RHUS-0008]
  23. CARE
  24. RHU Lumiere
  25. Ralph Lauren
  26. Malakoff Humanis
  27. Sanofi

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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 thesebetacoronaviruses, 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.

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