The evolving role of tissue-resident memory T cells in infections and cancer

Author:

Yenyuwadee Sasitorn123ORCID,Sanchez-Trincado Lopez Jose Luis124,Shah Rushil125ORCID,Rosato Pamela C.6,Boussiotis Vassiliki A.127ORCID

Affiliation:

1. Division of Hematology-Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

2. Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

3. Department of Dermatology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

4. Laboratory of Immunomedicine, School of Medicine, Complutense University of Madrid, Ave Complutense S/N, 28040 Madrid, Spain.

5. Cornell University, Ithaca, NY 14850 , USA.

6. The Geisel School of Medicine at Dartmouth, Lebanon, NH 03755, USA.

7. Cancer Center, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

Abstract

Resident memory T cells (T RM ) form a distinct type of T memory cells that stably resides in tissues. T RM form an integral part of the immune sensing network and have the ability to control local immune homeostasis and participate in immune responses mediated by pathogens, cancer, and possibly autoantigens during autoimmunity. T RM express residence gene signatures, functional properties of both memory and effector cells, and remarkable plasticity. T RM have a well-established role in pathogen immunity, whereas their role in antitumor immune responses and immunotherapy is currently evolving. As T RM form the most abundant T memory cell population in nonlymphoid tissues, they are attractive targets for therapeutic exploitation. Here, we provide a concise review of the development and physiological role of CD8 + T RM , their involvement in diseases, and their potential therapeutic exploitation.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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