Intratumoral bacteria are immunosuppressive and promote immunotherapy resistance in head and neck squamous cell carcinoma

Despite the promise of immune checkpoint blockade (ICB) in head and neck squamous cell carcinoma (HNSCC), mediators of response are poorly understood. To address this, here we analyzed oropharyngeal HNSCCs treated with neoadjuvant durvalumab (anti-PDL1) alone or in combination with tremelimumab (anti-CTLA4) from the CIAO clinical trial ( NCT03144778 ). We found that only the total abundance of intratumoral bacteria predicted ICB response, which was validated in multiple independent cohorts. High intratumoral bacteria abundance was associated with an immunosuppressive tumor microenvironment, characterized by an accumulation of neutrophils coupled with depletion of T cells and other adaptive immune cells. Experimental elevation or reduction in intratumoral bacteria abundance in orthotopic models of HNSCC in female mice recapitulated immunological associations observed in participant tumors. Increasing intratumoral bacteria abundance was sufficient to induce resistance to anti-PDL1 ICB, irrespective of bacterial species tested. Together, these findings demonstrate that high intratumoral bacteria abundance is a key suppressor of antitumor immunity and promotes immunotherapy resistance.

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Publication Details

Journal
Nature Cancer
Published
2026-01-02
DOI
https://doi.org/10.1038/s43018-025-01067-1
Citations
7
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
169.37
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article

Intratumoral bacteria are immunosuppressive and promote immunotherapy resistance in head and neck squamous cell carcinoma

Travis Kerr, Tyler Alban, Laura Noël‐Romas, Andrew G. Sikora et al.
7 citations
Nature Cancer
Cancer Immunotherapy and Biomarkers
169.37
article

Intratumoral bacteria are immunosuppressive and promote immunotherapy resistance in head and neck squamous cell carcinoma

Travis Kerr, Tyler Alban, Laura Noël‐Romas, Andrew G. Sikora, Akeem Santos, Christian Jobin, Apollo Stacy, Daniel J. McGrail, Neil D. Gross, Natalie L. Silver, Mohammed Dwidar, Jessica Altemus, Hannah Simmons, Rekha Garg, Jin Dai, Shwetha V. Kumar, Tim Chan, Rehan Akbani, David J. H. Shih, Elias J. Sayour, Adam Burgener, Renata Ferrarotto, Vladimir Makarov
article en
7 citations

Abstract

Despite the promise of immune checkpoint blockade (ICB) in head and neck squamous cell carcinoma (HNSCC), mediators of response are poorly understood. To address this, here we analyzed oropharyngeal HNSCCs treated with neoadjuvant durvalumab (anti-PDL1) alone or in combination with tremelimumab (anti-CTLA4) from the CIAO clinical trial ( NCT03144778 ). We found that only the total abundance of intratumoral bacteria predicted ICB response, which was validated in multiple independent cohorts. High intratumoral bacteria abundance was associated with an immunosuppressive tumor microenvironment, characterized by an accumulation of neutrophils coupled with depletion of T cells and other adaptive immune cells. Experimental elevation or reduction in intratumoral bacteria abundance in orthotopic models of HNSCC in female mice recapitulated immunological associations observed in participant tumors. Increasing intratumoral bacteria abundance was sufficient to induce resistance to anti-PDL1 ICB, irrespective of bacterial species tested. Together, these findings demonstrate that high intratumoral bacteria abundance is a key suppressor of antitumor immunity and promotes immunotherapy resistance.

Nature CancerVol. 7(1)
Cleveland Clinic (US), Karolinska University Hospital (SE), The University of Texas MD Anderson Cancer Center (US), University of Miami (US), Karolinska Institutet (SE), University of Florida (US), Cleveland Clinic Lerner College of Medicine (US), Center for Global Health (US), University of Manitoba (CA), Case Western Reserve University (US), University of Hong Kong (HK)
Openalex Percentile: Top 0%
Cancer Immunotherapy and Biomarkers
169.37
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