Faecalibacterium
cellular organisms|Bacteria|Bacillati|Bacillota|Clostridia|Eubacteriales|Oscillospiraceae
MCA-BAC-000028
TaxID: 216851
| Rank: genus
Biology & Ecology
Biology
Gram Statusunknown
Oxygen Toleranceobligate anaerobe
Key Traits
- butyrate-producing
Ecology
Primary Nichesgut
Reservoirhuman
Clinical Profile
Pathobiont
yes
no
context dependent
unknown
Clinical Rolesprotective commensal
Typical Specimenstool
Risk Contextsmelanoma patients receiving immune checkpoint inhibitor therapy (ICB)
Clinical Associations:
E2
E3 — Strong human clinical evidence
E2 — Moderate human evidence
E1 — Limited / preliminary
Faecalibacterium genus relative abundance was significantly higher in anti-PD-1 responders versus non-responders in a newly recruited independent cohort of 132 metastatic melanoma patients (n=87 responders, n=45 non-responders; p=0.018 by Wilcoxon rank sum test), supporting its role as a gut microbiota marker of immunotherapy response.
PMID:
34941392
E2
E3 — Strong human clinical evidence
E2 — Moderate human evidence
E1 — Limited / preliminary
In melanoma patients treated with ICB (n=123), Faecalibacterium genus abundance was numerically higher in patients reporting sufficient dietary fiber intake (≥20 g/day) and no probiotic use — the subgroup with significantly longer progression-free survival (median PFS not reached versus 13 months, P=0.015 vs. all other groups) — though the Faecalibacterium difference per se did not reach statistical significance due to small group size (n=22 in optimal group).
PMID:
34941392
E2
E3 — Strong human clinical evidence
E2 — Moderate human evidence
E1 — Limited / preliminary
Faecalibacterium genus was significantly enriched in anti-PD-1 responders versus non-responders in the gut microbiome of 43 metastatic melanoma patients (30R, 13NR; FDR-adjusted pairwise comparisons and LEfSe; p<0.01), establishing the original human evidence for genus-level enrichment as a marker of immunotherapy response.
PMID:
29097493
E2
E3 — Strong human clinical evidence
E2 — Moderate human evidence
E1 — Limited / preliminary
High Faecalibacterium abundance (above median) was associated with significantly prolonged progression-free survival compared to low abundance in 39 anti-PD-1-treated metastatic melanoma patients (p=0.03; multivariate Cox HR=2.95, 95% CI 1.31–7.29), identifying it as an independent gut microbiome predictor of immunotherapy outcome.
PMID:
29097493
D000082082
Immune Checkpoint Inhibitors
D008545
Melanoma
D000077982
Progression-Free Survival
H00038
Melanoma
E2
E3 — Strong human clinical evidence
E2 — Moderate human evidence
E1 — Limited / preliminary
Faecalibacterium genus abundance was significantly positively correlated with CD8+ T cell density in pre-treatment tumors of melanoma patients on anti-PD-1 therapy (r²=0.42, p<0.01; n=15 matched tumor-microbiome samples), linking gut microbiome composition to intratumoral anti-tumor immunity.
PMID:
29097493
D000069196
Gastrointestinal Microbiome
D000082082
Immune Checkpoint Inhibitors
D008545
Melanoma
H00038
Melanoma
Last reviewed: 2026-04-03
Evidence Timeline
Related Taxa
Shared Niche = same body site
Shared Risk = same vulnerable population
ⓘ