Suppressive effects of the obese tumor microenvironment on CD8 T cell infiltration and effector function

Author:

Dyck Lydia1ORCID,Prendeville Hannah1ORCID,Raverdeau Mathilde1ORCID,Wilk Mieszko M.1ORCID,Loftus Roisin M.1ORCID,Douglas Aaron1ORCID,McCormack Janet2ORCID,Moran Bruce3ORCID,Wilkinson Michael4ORCID,Mills Evanna L.56ORCID,Doughty Michael7ORCID,Fabre Aurelie3ORCID,Heneghan Helen8ORCID,LeRoux Carel8ORCID,Hogan Andrew910ORCID,Chouchani Edward T.56ORCID,O’Shea Donal8ORCID,Brennan Donal411ORCID,Lynch Lydia11213ORCID

Affiliation:

1. School of Biochemistry and Immunology, Trinity College Dublin, Dublin, Ireland

2. Research Pathology Core Facility, Conway Institute, University College Dublin, Dublin, Ireland

3. Department of Pathology, St. Vincent’s University Hospital, Dublin, Ireland

4. University College Dublin Gynaecological Oncology Group, University College Dublin School of Medicine, Mater Misericordiae University Hospital, Dublin, Ireland

5. Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA

6. Department of Cell Biology, Harvard Medical School, Boston, MA

7. Department of Cellular Pathology, Mater Misericordiae University Hospital, Dublin, Ireland

8. School of Medicine, St. Vincent's University Hospital and University College Dublin, Dublin, Ireland

9. Human Health Institute, Department of Biology, Maynooth University, Maynooth, Ireland

10. National Children’s Research Centre, Dublin, Ireland

11. Systems Biology Ireland, School of Medicine, University College Dublin, Dublin, Ireland

12. Brigham and Women’s Hospital, Boston, MA

13. Harvard Medical School, Boston, MA

Abstract

Obesity is one of the leading preventable causes of cancer; however, little is known about the effects of obesity on anti-tumor immunity. Here, we investigated the effects of obesity on CD8 T cells in mouse models and patients with endometrial cancer. Our findings revealed that CD8 T cell infiltration is suppressed in obesity, which was associated with a decrease in chemokine production. Tumor-resident CD8 T cells were also functionally suppressed in obese mice, which was associated with a suppression of amino acid metabolism. Similarly, we found that a high BMI negatively correlated with CD8 infiltration in human endometrial cancer and that weight loss was associated with a complete pathological response in six of nine patients. Moreover, immunotherapy using anti–PD-1 led to tumor rejection in lean and obese mice and partially restored CD8 metabolism and anti-tumor immunity. These findings highlight the suppressive effects of obesity on CD8 T cell anti-tumor immunity, which can partially be reversed by weight loss and/or immunotherapy.

Funder

Irish Research Council

Science Foundation Ireland

European Research Council

Claudia Adams Barr Program

Lavine Family Fund

Pew Charitable Trusts

National Institutes of Health

Cancer Research Institute

UCD Clinical Research Centre

Science Foundation Ireland Precision Oncology Ireland

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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