Table 1.
Gut microbiota taxa | Model | Immunotherapy | Cancer | Major findings | Author/Year | Ref |
---|---|---|---|---|---|---|
Akkermansia muciniphila | Human and mice | Anti‐PD‐1/PD‐L1 | NSCLC, RCC |
|
Routy et al., 2018 | [47] |
Ruminococcaceae | Human | Anti‐PD‐1/PD‐L1 | GI cancer | Associated with distinct bacterial pathways including fermentation to SCFAs, unsaturated fatty acid biosynthesis, vitamin and starch biosynthesis | Peng et al., 2020 | [48] |
Human | Anti‐CD19 CAR‐T | B cell lymphoma and leukemia | Improve antitumor effects of CAR‐T cell infusion | Smith et al., 2018 | [53] | |
Ruminococcus | Human | Anti‐CD19 CAR‐T | B cell lymphoma and leukemia |
|
Smith et al., 2022 | [54] |
Faecalibacterium | human | Anti‐PD‐1 and Anti‐CTLA‐4 | Melanoma |
|
Gopalakrishnan et al., 2018 | [46] |
Human | Anti‐CD19 CAR‐T | B cell lymphoma and leukemia |
|
Smith et al., 2022 | [54] | |
Bifidobacterium | Mice | Anti‐PD‐1 | Melanoma |
|
Sivan et al., 2015 | [43] |
Bifidobacterium longum | Human | Anti‐PD‐1 | Melanoma |
|
Matson et al., 2018 | [44] |
Prevotella | Human | Anti‐PD‐1/PD‐L1 | GI cancer |
|
Peng et al., 2020 | [48] |
Lachnospiraceae | Human | Anti‐PD‐1/PD‐L1 | GI cancer | Associated with distinct bacterial pathways including fermentation to SCFAs, unsaturated fatty acid biosynthesis, vitamin and starch biosynthesis | Peng et al., 2020 | [48] |
Lachnospiraceae Collinsella aerofaciens |
Human | Anti‐CD19 CAR‐T | B cell malignancies | Improve antitumor effects of CAR‐T cell infusion | Smith et al., 2018 | [53] |
Human | Anti‐PD‐1 | Melanoma |
|
Matson et al., 2018 | [44] | |
Enterococcus faecium | Human | Anti‐PD‐1 | Melanoma |
|
Matson et al., 2018 | [44] |
Oscillospiraceae | Human | Anti‐CD19 CAR‐T | B cell malignancies | Improve antitumor effects of CAR T cell infusion | Smith et al., 2018 | [53] |
Abbreviations: CAR‐T, chimeric antigen receptor T‐cell; CTLA‐4, cytotoxic T lymphocyte‐associated antigen 4; DC, dendritic cell; GI cancer, gastrointestinal cancer; ICI, immune checkpoint inhibitor; NSCLC, nonsmall cell lung cancer; PD‐1, programmed cell death protein 1; PD‐L1, programmed cell death ligand 1; RCC, renal cell cancer; SCFAs, short‐chain fatty acids; TME, tumor microenvironment.