Acod1 expression in cancer cells promotes immune evasion through the generation of inhibitory peptides

Targeting programmed cell death protein 1 (PD-1) is an important component of many immune checkpoint blockade (ICB) therapeutic approaches. However, ICB is not an efficacious strategy in a variety of cancer types, in part due to immunosuppressive metabolites in the tumor microenvironment. Here, we f...

Full description

Saved in:
Bibliographic Details
Published in:Cell reports (Cambridge) Vol. 43; no. 4; p. 113984
Main Authors: Schofield, James H., Longo, Joseph, Sheldon, Ryan D., Albano, Emma, Ellis, Abigail E., Hawk, Mark A., Murphy, Sean, Duong, Loan, Rahmy, Sharif, Lu, Xin, Jones, Russell G., Schafer, Zachary T.
Format: Journal Article
Language:English
Published: United States Elsevier Inc 23-04-2024
Elsevier
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Targeting programmed cell death protein 1 (PD-1) is an important component of many immune checkpoint blockade (ICB) therapeutic approaches. However, ICB is not an efficacious strategy in a variety of cancer types, in part due to immunosuppressive metabolites in the tumor microenvironment. Here, we find that αPD-1-resistant cancer cells produce abundant itaconate (ITA) due to enhanced levels of aconitate decarboxylase (Acod1). Acod1 has an important role in the resistance to αPD-1, as decreasing Acod1 levels in αPD-1-resistant cancer cells can sensitize tumors to αPD-1 therapy. Mechanistically, cancer cells with high Acod1 inhibit the proliferation of naive CD8+ T cells through the secretion of inhibitory factors. Surprisingly, inhibition of CD8+ T cell proliferation is not dependent on the secretion of ITA but is instead a consequence of the release of small inhibitory peptides. Our study suggests that strategies to counter the activity of Acod1 in cancer cells may sensitize tumors to ICB therapy. [Display omitted] •Cancerous epithelial cells can express Acod1 and produce itaconate•Acod1 loss in αPD-1-resistant tumors resensitizes them to therapy•Acod1hi cells inhibit naive CD8+ T cell activation independent of itaconate•Acod1hi cells suppress T cells by secreting inhibitory peptides Schofield et al. report that cancer cells upregulate Acod1 as a survival strategy in response to αPD-1 therapy. Acod1hi cancer cells secrete inhibitory peptides that block the activation of naive CD8+ T cells. Loss of Acod1 resensitizes resistant tumors to αPD-1 ICB.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
AUTHOR CONTRIBUTIONS
J.H.S., J.L., R.D.S., E.A., A.E.E., and M.A.H. conducted experiments, analyzed data, and interpreted results. S.M., L.D., S.R., and X.L. generated the PRs and PRp cell lines and assisted with isolation of T cells from mice. J.L., R.D.S., A.E.E., and R.G.J. were responsible for MS-based analysis. X.L., R.G.J., and Z.T.S. provided funding and supervision for the project. J.H.S. and Z.T.S. were responsible for conception/design of the project and wrote the manuscript with feedback from all other authors. Z.T.S. was responsible for overall study supervision.
ISSN:2211-1247
2211-1247
DOI:10.1016/j.celrep.2024.113984