CD21 (Complement Receptor 2) Is the Receptor for Epstein-Barr Virus Entry into T Cells

Author:

Smith Nicholas A.1,Coleman Carrie B.1,Gewurz Benjamin E.234,Rochford Rosemary1

Affiliation:

1. Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, Colorado, USA

2. Division of Infectious Diseases, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA

3. Program in Virology, Harvard Medical School, Boston, Massachusetts, USA

4. Broad Institute of Harvard and MIT, Cambridge, Massachusetts, USA

Abstract

Epstein-Barr virus (EBV) has a well-described tropism for B cells and epithelial cells. Recently, we described the ability of a second strain of EBV, EBV type 2, to infect mature peripheral T cells. Using a neutralizing antibody assay, we determined that EBV uses the viral glycoprotein gp350 and the cellular protein CD21 to gain entry into mature peripheral T cells. CRISPR-Cas9 deletion of CD21 on the Jurkat T-cell line confirmed that CD21 is required for EBV infection. This study has broad implications, as we have defined a function for CD21 on mature peripheral T cells, i.e., as a receptor for EBV. In addition, the requirement for gp350 for T-cell entry has implications for EBV vaccine studies currently targeting the gp350 glycoprotein to prevent EBV-associated diseases.

Funder

HHS | NIH | National Cancer Institute

HHS | NIH | National Institute of Allergy and Infectious Diseases

Burroughs Wellcome Fund

American Cancer Society

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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