Two sides of the same coin: Protective versus pathogenic CD4+ resident memory T cells

Anna E. Oja, René A. W. van Lier, Pleun Hombrink

Research output: Contribution to journalArticleAcademicpeer-review

11 Citations (Scopus)

Abstract

The ability of the adaptive immune system to form memory is key to providing protection against secondary infections. Resident memory T cells (TRM) are specialized T cell populations that reside within tissue sites where they await reencounter with their cognate antigen. TRM are distinct from circulating memory cells, including central and effector memory T cells, both functionally and transcriptionally. Since the discovery of TRM, most research has focused on CD8+ TRM, despite that CD4+ TRM are also abundant in most tissues. In the past few years, more evidence has emerged that CD4+ TRM can contribute both protective and pathogenic roles in disease. A complexity inherent to the CD4+ TRM field is the ability of CD4+ T cells to polarize into a multitude of distinct subsets and recognize not only viruses and intracellular bacteria but also extracellular bacteria, fungi, and parasites. In this review, we outline the key features of CD4+ TRM in health and disease, including their contributions to protection against SARS-CoV-2 and potential contributions to immunopathology associated with COVID-19.
Original languageEnglish
Article numberabf9393
Pages (from-to)eabf9393
JournalScience immunology
Volume7
Issue number70
DOIs
Publication statusPublished - 8 Apr 2022

Cite this