NLRC5/MHC class I transactivator: A key target for immune escape by SARS‐CoV‐2

Author:

Zhu Baohui1,Ouda Ryota1,Kasuga Yusuke1,de Figueiredo Paul234,Kobayashi Koichi S.156ORCID

Affiliation:

1. Department of Immunology Hokkaido University Graduate School of Medicine Sapporo Hokkaido Japan

2. Christopher S Bond Life Sciences Center University of Missouri Columbia Missouri USA

3. Department of Molecular Microbiology and Immunology, School of Medicine University of Missouri Columbia Missouri USA

4. Department of Veterinary Pathobiology University of Missouri Columbia Missouri USA

5. Institute for Vaccine Research and Development (IVReD) Hokkaido University Sapporo Hokkaido Japan

6. Department of Microbial Pathogenesis and Immunology Texas A&M Health Science Center Bryan Texas USA

Abstract

AbstractAntigen presentation to CD8+ T cells by MHC class I molecules is essential for host defense against viral infections. Various mechanisms have evolved in multiple viruses to escape immune surveillance and defense to support viral proliferation in host cells. Through in vitro SARS‐CoV‐2 infection studies and analysis of COVID‐19 patient samples, we found that SARS‐CoV‐2 suppresses the induction of the MHC class I pathway by inhibiting the expression and function of NLRC5, a major transcriptional regulator of MHC class I genes. In this review, we discuss the molecular mechanisms for suppression of the MHC class I pathway and clinical implications for COVID‐19.

Funder

Hitachi Global Foundation

Japan Agency for Medical Research and Development

China Scholarship Council

SENSHIN Medical Research Foundation

Kobayashi International Scholarship Foundation

Japan Society for the Promotion of Science

Japan Science and Technology Agency

Takeda Science Foundation

Publisher

Wiley

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