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Microbiota-immune dysregulation in cervical cancer patients from Western Mexico: linking gut dysbiosis and NK cell exhaustion as promising biomarkers.

단면연구 1/5 보강
Frontiers in immunology 2025 Vol.16() p. 1637098
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
환자: cervical cancer (CC), a connection not previously explored
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Our findings suggest that gut dysbiosis may contribute to impaired anti-tumor immunity.

Klimov-Kravtchenko K, Baltazar-Díaz TA, Haramati J, Castaño-Jiménez PA, Solorzano-Ibarra F, Rojas-Diaz JM, Garcia-Barrientos NT, Cruz-Ramos JA, Facundo-Medina CG, Del Toro-Arreola S, Bueno-Topete MR

📝 환자 설명용 한 줄

Alterations in gut microbiota composition have been implicated in various diseases, including cancer.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 연구 설계 cross-sectional

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BibTeX ↓ RIS ↓
APA Klimov-Kravtchenko K, Baltazar-Díaz TA, et al. (2025). Microbiota-immune dysregulation in cervical cancer patients from Western Mexico: linking gut dysbiosis and NK cell exhaustion as promising biomarkers.. Frontiers in immunology, 16, 1637098. https://doi.org/10.3389/fimmu.2025.1637098
MLA Klimov-Kravtchenko K, et al.. "Microbiota-immune dysregulation in cervical cancer patients from Western Mexico: linking gut dysbiosis and NK cell exhaustion as promising biomarkers.." Frontiers in immunology, vol. 16, 2025, pp. 1637098.
PMID 41246357

Abstract

Alterations in gut microbiota composition have been implicated in various diseases, including cancer. Recent evidence suggests that intestinal microbiota may influence the efficacy of immunotherapy. In this study, we investigated the relationship between gut dysbiosis and NK cell exhaustion in Mexican patients with cervical cancer (CC), a connection not previously explored. This cross-sectional study included newly diagnosed CC patients, a separate cohort of post-radio-chemotherapy (RCT) patients, and healthy donors (HD). Fecal microbiota profiles were assessed using 16S rRNA sequencing, while peripheral NK cell immune checkpoint expression was analyzed by multiparametric flow cytometry. CC patients exhibited significant gut dysbiosis, marked by reduced α-diversity, enrichment of pro-inflammatory taxa (-, ), depletion of short-chain fatty acid (SCFA)-producing bacteria (, ), and enrichment of microbial metabolic pathways related to inflammation, oxidative stress, nutrient limitation, and immune suppression. Dysbiosis was more pronounced in patients after RCT, with further enrichment of . In parallel, NK cells displayed a putative exhausted phenotype, with elevated expression and co-expression of PD-1, LAG-3, TIM-3, TIGIT, BTLA, and NKG2A. A dysbiosis score and an NK exhaustion score were developed, revealing a significant positive correlation between microbial imbalance and NK cell exhaustion. Machine learning analysis identified the / ratio and PD-1CD56 NK cells as predictive markers of CC. Moreover, both dysbiosis and NK cell exhaustion markers were significantly associated with reduced patient survival. This is the first study to demonstrate a link between gut microbiota alterations and NK cell exhaustion in CC. Our findings suggest that gut dysbiosis may contribute to impaired anti-tumor immunity. This study supports the rationale for microbiota-targeted interventions as adjunctive strategies in CC, although prospective validation is required.

MeSH Terms

Humans; Dysbiosis; Female; Killer Cells, Natural; Gastrointestinal Microbiome; Uterine Cervical Neoplasms; Middle Aged; Mexico; Adult; Cross-Sectional Studies; Aged; Biomarkers, Tumor; RNA, Ribosomal, 16S; Immune System Exhaustion