<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Spencer CN</submitter><funding>Cancer Research UK</funding><funding>NIAID NIH HHS</funding><funding>NIEHS NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>1632-1640</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8970537</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>374(6575)</volume><pubmed_abstract>Gut bacteria modulate the response to immune checkpoint blockade (ICB) treatment in cancer, but the effect of diet and supplements on this interaction is not well studied. We assessed fecal microbiota profiles, dietary habits, and commercially available probiotic supplement use in melanoma patients and performed parallel preclinical studies. Higher dietary fiber was associated with significantly improved progression-free survival in 128 patients on ICB, with the most pronounced benefit observed in patients with sufficient dietary fiber intake and no probiotic use. Findings were recapitulated in preclinical models, which demonstrated impaired treatment response to anti–programmed cell death 1 (anti–PD-1)–based therapy in mice receiving a low-fiber diet or probiotics, with a lower frequency of interferon-γ–positive cytotoxic T cells in the tumor microenvironment. Together, these data have clinical implications for patients receiving ICB for cancer.</pubmed_abstract><journal>Science (New York, N.Y.)</journal><pubmed_title>Dietary fiber and probiotics influence the gut microbiome and melanoma immunotherapy response.</pubmed_title><pmcid>PMC8970537</pmcid><funding_grant_id>R01 AI133822</funding_grant_id><funding_grant_id>P50 CA221703</funding_grant_id><funding_grant_id>R25 CA203650</funding_grant_id><funding_grant_id>U54 CA224070</funding_grant_id><funding_grant_id>F32 CA260769</funding_grant_id><funding_grant_id>P30 ES030285</funding_grant_id><funding_grant_id>T32 CA009599</funding_grant_id><funding_grant_id>R01 CA219896</funding_grant_id><funding_grant_id>P30 CA013696</funding_grant_id><funding_grant_id>R01 AI143886</funding_grant_id><funding_grant_id>27140</funding_grant_id><funding_grant_id>P30 CA016672</funding_grant_id><funding_grant_id>R56 AI109294</funding_grant_id><funding_grant_id>R01 HL124112</funding_grant_id><funding_grant_id>R01 AI109294</funding_grant_id><pubmed_authors>McCulloch JA</pubmed_authors><pubmed_authors>Wong MC</pubmed_authors><pubmed_authors>Lee JE</pubmed_authors><pubmed_authors>Anang NAS</pubmed_authors><pubmed_authors>Gaudreau PO</pubmed_authors><pubmed_authors>Day CP</pubmed_authors><pubmed_authors>Simon J</pubmed_authors><pubmed_authors>Nelson KC</pubmed_authors><pubmed_authors>Wong MK</pubmed_authors><pubmed_authors>Morgun A</pubmed_authors><pubmed_authors>Helmink BA</pubmed_authors><pubmed_authors>Wargo JA</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Wani K</pubmed_authors><pubmed_authors>Nezi L</pubmed_authors><pubmed_authors>Arora R</pubmed_authors><pubmed_authors>Cogdill AP</pubmed_authors><pubmed_authors>Petrosino JF</pubmed_authors><pubmed_authors>Trinchieri G</pubmed_authors><pubmed_authors>Spencer CN</pubmed_authors><pubmed_authors>Duncan S</pubmed_authors><pubmed_authors>Straussman R</pubmed_authors><pubmed_authors>Amaria RN</pubmed_authors><pubmed_authors>Patel SP</pubmed_authors><pubmed_authors>Hoffman KL</pubmed_authors><pubmed_authors>Sharma P</pubmed_authors><pubmed_authors>Pazdrak B</pubmed_authors><pubmed_authors>Huttenhower C</pubmed_authors><pubmed_authors>Khan MAW</pubmed_authors><pubmed_authors>Lochmann BS</pubmed_authors><pubmed_authors>Haydu LE</pubmed_authors><pubmed_authors>Daniel CR</pubmed_authors><pubmed_authors>Ross MI</pubmed_authors><pubmed_authors>Jamal MA</pubmed_authors><pubmed_authors>Tetzlaff MT</pubmed_authors><pubmed_authors>Perez-Guijarro E</pubmed_authors><pubmed_authors>Hu J</pubmed_authors><pubmed_authors>Vetizou M</pubmed_authors><pubmed_authors>Medik YB</pubmed_authors><pubmed_authors>Davies MA</pubmed_authors><pubmed_authors>Ajami NJ</pubmed_authors><pubmed_authors>Kahn LM</pubmed_authors><pubmed_authors>McQuade JL</pubmed_authors><pubmed_authors>Badger JH</pubmed_authors><pubmed_authors>Lazar AJ</pubmed_authors><pubmed_authors>Rodrigues RR</pubmed_authors><pubmed_authors>Szczepaniak-Sloane RA</pubmed_authors><pubmed_authors>Peterson CB</pubmed_authors><pubmed_authors>Roszik J</pubmed_authors><pubmed_authors>Johnson S</pubmed_authors><pubmed_authors>Toker J</pubmed_authors><pubmed_authors>Dang M</pubmed_authors><pubmed_authors>Zheng J</pubmed_authors><pubmed_authors>Malke JC</pubmed_authors><pubmed_authors>Andrews MC</pubmed_authors><pubmed_authors>Diab A</pubmed_authors><pubmed_authors>Woodman SE</pubmed_authors><pubmed_authors>Jensen V</pubmed_authors><pubmed_authors>Zobniw CM</pubmed_authors><pubmed_authors>White MG</pubmed_authors><pubmed_authors>Kim YS</pubmed_authors><pubmed_authors>Burton EM</pubmed_authors><pubmed_authors>Allison JP</pubmed_authors><pubmed_authors>Futreal PA</pubmed_authors><pubmed_authors>Watowich SS</pubmed_authors><pubmed_authors>Baruch EN</pubmed_authors><pubmed_authors>Schneider S</pubmed_authors><pubmed_authors>Cohen L</pubmed_authors><pubmed_authors>Merlino G</pubmed_authors><pubmed_authors>Sirmans E</pubmed_authors><pubmed_authors>Morad G</pubmed_authors><pubmed_authors>Gershenwald JE</pubmed_authors><pubmed_authors>Jenq RR</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Yan Y</pubmed_authors><pubmed_authors>Tawbi HA</pubmed_authors><pubmed_authors>Gopalakrishnan V</pubmed_authors><pubmed_authors>Clise-Dwyer K</pubmed_authors><pubmed_authors>Anderson J</pubmed_authors><pubmed_authors>Harris AL</pubmed_authors><pubmed_authors>Chapman T</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Hudgens CW</pubmed_authors><pubmed_authors>Hwu P</pubmed_authors><pubmed_authors>Posada E</pubmed_authors><pubmed_authors>Garrett WS</pubmed_authors><pubmed_authors>Samuels Y</pubmed_authors><pubmed_authors>Glitza IC</pubmed_authors><pubmed_authors>Rodgers T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dietary fiber and probiotics influence the gut microbiome and melanoma immunotherapy response.</name><description>Gut bacteria modulate the response to immune checkpoint blockade (ICB) treatment in cancer, but the effect of diet and supplements on this interaction is not well studied. We assessed fecal microbiota profiles, dietary habits, and commercially available probiotic supplement use in melanoma patients and performed parallel preclinical studies. Higher dietary fiber was associated with significantly improved progression-free survival in 128 patients on ICB, with the most pronounced benefit observed in patients with sufficient dietary fiber intake and no probiotic use. Findings were recapitulated in preclinical models, which demonstrated impaired treatment response to anti–programmed cell death 1 (anti–PD-1)–based therapy in mice receiving a low-fiber diet or probiotics, with a lower frequency of interferon-γ–positive cytotoxic T cells in the tumor microenvironment. Together, these data have clinical implications for patients receiving ICB for cancer.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Dec</publication><modification>2026-05-31T21:01:09.886Z</modification><creation>2025-02-19T04:21:59.333Z</creation></dates><accession>S-EPMC8970537</accession><cross_references><pubmed>34941392</pubmed><doi>10.1126/science.aaz7015</doi></cross_references></HashMap>