CD8 + T Cell Exhaustion in Cancer
A paradigm shift in the understanding of the exhausted CD8 T cell (T ) lineage is underway. Originally thought to be a uniform population that progressively loses effector function in response to persistent antigen, single-cell analysis has now revealed that CD8 T is composed of multiple interconnec...
Saved in:
Published in | Frontiers in immunology Vol. 12; p. 715234 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
20.07.2021
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | A paradigm shift in the understanding of the exhausted CD8
T cell (T
) lineage is underway. Originally thought to be a uniform population that progressively loses effector function in response to persistent antigen, single-cell analysis has now revealed that CD8
T
is composed of multiple interconnected subpopulations. The heterogeneity within the CD8
T
lineage is comprised of immune checkpoint blockade (ICB) permissive and refractory subsets termed stem-like and terminally differentiated cells, respectively. These populations occupy distinct peripheral and intratumoral niches and are characterized by transcriptional processes that govern transitions between cell states. This review presents key findings in the field to construct an updated view of the spatial, transcriptional, and functional heterogeneity of anti-tumoral CD8
T
. These emerging insights broadly call for (re-)focusing cancer immunotherapies to center on the driver mechanism(s) underlying the CD8
T
developmental continuum aimed at stabilizing functional subsets. |
---|---|
Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 Edited by: Vandana Kalia, University of Washington, United States This article was submitted to Immunological Memory, a section of the journal Frontiers in Immunology Reviewed by: Sang-Jun Ha, Yonsei University, South Korea; Jianxun J. Song, Texas A&M Health Science Center, United States |
ISSN: | 1664-3224 1664-3224 |
DOI: | 10.3389/fimmu.2021.715234 |