Does acute inflammation triggered by infection promote cancer progression?

Chronic infections are associated with cancer incidence and progression in human epidemiological data, but less is known about how such infections might promote cancer progression. Recent data implicate acute infection with common respiratory viruses, such as influenza and SARS-CoV-2, in cancer progression, providing evidence that infection-driven inflammation can promote tumor expansion and dissemination in experimental systems. The resulting acute inflammatory cascade and dynamic immune cell reprogramming can rapidly remodel the tissue microenvironment to favor cancer cell survival, growth, and evasion of immune elimination. However, acute infections can also elicit anti-tumor immune responses. Defining how infections differentially skew immune programs to promote or restrain cancer progression will therefore be essential for developing future strategies to target this disease.

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Publication Details

Journal
PLoS Biology
Published
2026-09-15
DOI
https://doi.org/10.1371/journal.pbio.3003962
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
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article

Does acute inflammation triggered by infection promote cancer progression?

Felipe Valença-Pereira, Mercedes Rincón, Bryan Johnson, James DeGregori
PLoS Biology
Cancer Immunotherapy and Biomarkers
article

Does acute inflammation triggered by infection promote cancer progression?

Felipe Valença-Pereira, Mercedes Rincón, Bryan Johnson, James DeGregori
article en

Abstract

Chronic infections are associated with cancer incidence and progression in human epidemiological data, but less is known about how such infections might promote cancer progression. Recent data implicate acute infection with common respiratory viruses, such as influenza and SARS-CoV-2, in cancer progression, providing evidence that infection-driven inflammation can promote tumor expansion and dissemination in experimental systems. The resulting acute inflammatory cascade and dynamic immune cell reprogramming can rapidly remodel the tissue microenvironment to favor cancer cell survival, growth, and evasion of immune elimination. However, acute infections can also elicit anti-tumor immune responses. Defining how infections differentially skew immune programs to promote or restrain cancer progression will therefore be essential for developing future strategies to target this disease.

PLoS BiologyVol. 24(9)
University of Colorado Anschutz Medical Campus (US)
Good health and well-being
Openalex Percentile: Top 14%
Cancer Immunotherapy and Biomarkers
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