TY - JOUR
T1 - Role of the Microbiome and Diet for Response to Cancer Checkpoint Immunotherapy
T2 - A Narrative Review of Clinical Trials
AU - Gamrath, Lone
AU - Pedersen, Tobias Bruun
AU - Møller, Martin Vad
AU - Volmer, Lone Marie
AU - Holst-Christensen, Linda
AU - Vestermark, Lene Weber
AU - Donskov, Frede
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2025/1
Y1 - 2025/1
N2 - Purpose of Review: The advent of checkpoint immunotherapy has dramatically changed the outcomes for patients with cancer. However, a considerable number of patients have little or no response to therapy. We review recent findings on the connection between the gut microbiota and the immune system, exploring whether this link could enhance the effectiveness of immunotherapy. Recent Findings: Clinical studies have reported specific types of bacteria in larger quantities at baseline in responders than in non-responders, especially Akkermansia mucinifila, Ruminococcaceae, Faecalibacterium, and Lachnospiraceae. Following the consumption of a high-fiber diet, bacteria in the gut ferment dietary fiber to short-chain fatty acids (SCFAs), like acetate, propionate, and butyrate. Some of the SCFAs nurture intestinal epithelial cells, and some enter the bloodstream. Here SCFAs can activate DC8 + cytotoxic T-cells to induce cancer cell death. High fiber intake in the diet was associated with a reduced risk of progression or death during checkpoint immunotherapy. Recent findings demonstrate that high-fiber plant-based diets such as the Mediterranean Diet positively influence the gut microbiota whereas antibiotics and proton pump inhibitors can negatively influence outcomes of cancer immunotherapy by changing the gut microbiota. Summary : This narrative review provides evidence of an association between types of bacteria and their metabolites and favorable responses to checkpoint immunotherapy. Prospective clinical trials are needed to determine if diet interventions can improve treatment outcomes.
AB - Purpose of Review: The advent of checkpoint immunotherapy has dramatically changed the outcomes for patients with cancer. However, a considerable number of patients have little or no response to therapy. We review recent findings on the connection between the gut microbiota and the immune system, exploring whether this link could enhance the effectiveness of immunotherapy. Recent Findings: Clinical studies have reported specific types of bacteria in larger quantities at baseline in responders than in non-responders, especially Akkermansia mucinifila, Ruminococcaceae, Faecalibacterium, and Lachnospiraceae. Following the consumption of a high-fiber diet, bacteria in the gut ferment dietary fiber to short-chain fatty acids (SCFAs), like acetate, propionate, and butyrate. Some of the SCFAs nurture intestinal epithelial cells, and some enter the bloodstream. Here SCFAs can activate DC8 + cytotoxic T-cells to induce cancer cell death. High fiber intake in the diet was associated with a reduced risk of progression or death during checkpoint immunotherapy. Recent findings demonstrate that high-fiber plant-based diets such as the Mediterranean Diet positively influence the gut microbiota whereas antibiotics and proton pump inhibitors can negatively influence outcomes of cancer immunotherapy by changing the gut microbiota. Summary : This narrative review provides evidence of an association between types of bacteria and their metabolites and favorable responses to checkpoint immunotherapy. Prospective clinical trials are needed to determine if diet interventions can improve treatment outcomes.
KW - Cancer Immunotherapy
KW - Dietary fiber
KW - Gut Microbiota
KW - Mediterranean Diet
KW - Short-chain Fatty Acids
KW - Immunotherapy/methods
KW - Dietary Fiber/therapeutic use
KW - Immune Checkpoint Inhibitors/therapeutic use
KW - Humans
KW - Gastrointestinal Microbiome
KW - Clinical Trials as Topic
KW - Diet
KW - Neoplasms/immunology
U2 - 10.1007/s11912-024-01622-6
DO - 10.1007/s11912-024-01622-6
M3 - Journal article
C2 - 39753816
AN - SCOPUS:85214111141
SN - 1523-3790
VL - 27
SP - 45
EP - 58
JO - Current Oncology Reports
JF - Current Oncology Reports
ER -