Qa-1-Restricted CD8+ T Cells Can Compensate for the Absence of Conventional T Cells during Viral Infection

Cell Rep. 2019 Apr 9;27(2):537-548.e5. doi: 10.1016/j.celrep.2019.03.059.

Abstract

The role of non-classical T cells during viral infection remains poorly understood. Using the well-established murine model of CMV infection (MCMV) and mice deficient in MHC class Ia molecules, we found that non-classical CD8+ T cells robustly expand after MCMV challenge, become highly activated effectors, and are capable of forming durable memory. Interestingly, although these cells are restricted by MHC class Ib molecules, they respond similarly to conventional T cells. Remarkably, when acting as the sole component of the adaptive immune response, non-classical CD8+ T cells are sufficient to protect against MCMV-induced lethality. We also demonstrate that the MHC class Ib molecule Qa-1 (encoded by H2-T23) restricts a large, and critical, portion of this population. These findings reveal a potential adaptation of the host immune response to compensate for viral evasion of classical T cell immunity.

Keywords: CD8(+) T cells; MCMV; Qa-1; cytomegalovirus; infection; viral immunity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / immunology*
  • Cytomegalovirus Infections / immunology
  • Disease Models, Animal
  • Histocompatibility Antigens Class I / immunology*
  • Immunity, Innate
  • Mice
  • Muromegalovirus / immunology
  • T-Lymphocytes / immunology*
  • Virus Diseases / immunology*

Substances

  • Histocompatibility Antigens Class I
  • Q surface antigens