PD-1 regulates CD8+ T cell tissue resident memory differentiation and function following influenza infection 2260210

S Samuel Markson (Harvard Medical School) J Jossef Osborn (Harvard Medical School) K Kelly Burke (Dana Farber Cancer Institute) A Amalia Luthen (Harvard Medical School) A Annette Gleiberman (Harvard Medical School) L Louise Groton (Harvard Medical School) N Naomi Goldman (Harvard Medical School) P Peter Fatouros (Harvard Medical School) M Mei-An Nolan (Harvard Medical School) T Thao Nguyen J Jaclyn Walsh (Harvard Medical School) A Arlene Sharpe (Harvard Medical School)

Abstract

Abstract Introduction In addition to its established role in T cell exhaustion, PD-1 is also upregulated in CD8+ tissue-resident memory (TRM) cells. Methods Here, we examine the cell-intrinsic contributions of PD-1 to CD8+ TRM cell generation and function during influenza infection by comparing wild-type (WT) and PD-1 knockout (KO) antigen-specific CD8+ T cells. Results Transcriptional and epigenetic profiling of these populations reveals early and persistent changes in transcriptional regulation and fate decisions. Conclusion Our findings provide new insight into how PD-1 signaling influences the differentiation and function of CD8+ T cells. Funding Source This work was supported by funding from AbbVie. Topic Categories Computational and Systems Immunology (COMP)

Article Details

Volume / Issue Vol. 215, Issue Supplement_1
Published August 01, 2026
ISSN 0022-1767
Publisher American Association of Immunologists

Authors (12)

S

Samuel Markson

Harvard Medical School

J

Jossef Osborn

Harvard Medical School

K

Kelly Burke

Dana Farber Cancer Institute

A

Amalia Luthen

Harvard Medical School

A

Annette Gleiberman

Harvard Medical School

L

Louise Groton

Harvard Medical School

N

Naomi Goldman

Harvard Medical School

P

Peter Fatouros

Harvard Medical School

M

Mei-An Nolan

Harvard Medical School

T

Thao Nguyen

J

Jaclyn Walsh

Harvard Medical School

A

Arlene Sharpe

Harvard Medical School