CD28 null CD4 T-cell expansions in autoimmune disease suggest a link with cytomegalovirus infection

F1000Res. 2019 Mar 25:8:F1000 Faculty Rev-327. doi: 10.12688/f1000research.17119.1. eCollection 2019.

Abstract

Immunosenescence is thought to contribute to the increase of autoimmune diseases in older people. Immunosenescence is often associated with the presence of an expanded population of CD4 T cells lacking expression of CD28 (CD28 null). These highly cytotoxic CD4 T cells were isolated from disease-affected tissues in patients with rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, or other chronic inflammatory diseases and their numbers appeared to be linked to disease severity. However, we recently demonstrated that the common herpes virus, cytomegalovirus (CMV), not ageing, is the major driver of this subset of cytotoxic T cells. In this review, we discuss how CMV might potentiate and exacerbate autoimmune disease through the expansion of CD28 null CD4 T cells.

Keywords: CD28 null; autoimmune disease; cytomegalovirus infection; ​​​​​​​CD4 T cell.

Publication types

  • Review

MeSH terms

  • Autoimmune Diseases / complications*
  • Autoimmune Diseases / virology
  • CD28 Antigens
  • CD4-Positive T-Lymphocytes / cytology*
  • Cytomegalovirus Infections / complications*
  • Humans

Substances

  • CD28 Antigens

Grants and funding

The author(s) declared that no grants were involved in supporting this work.