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Preservation of the fecal microbiome is associated with reduced severity of graft-versus-host disease

微生物群 粪便细菌疗法 移植物抗宿主病 生物 寄主(生物学) 粪便 免疫学 疾病 艰难梭菌 内科学 医学 微生物学 生态学 生物信息学 抗生素
作者
Marina Burgos da Silva,Doris M. Ponce,Anqi Dai,Sean M. Devlin,Antonio L. C. Gomes,Gillian Moore,John Slingerland,Roni Shouval,Gabriel K. Armijo,Susan DeWolf,Teng Fei,Annelie Clurman,Emily Fontana,Luigi A. Amoretti,Roberta J. Wright,Hana Andrlová,Oriana Miltiadous,Miguel-Ángel Perales,Ying Taur,Jonathan U. Peled,Marcel R.M. van den Brink
出处
期刊:Blood [Elsevier BV]
卷期号:140 (22): 2385-2397 被引量:36
标识
DOI:10.1182/blood.2021015352
摘要

Abstract Following allogeneic hematopoietic cell transplantation (allo-HCT), the gastrointestinal (GI) tract is frequently affected by acute graft-versus-host disease (aGVHD), the pathophysiology of which is associated with a dysbiotic microbiome. Since microbial composition varies along the length of the GI tract, the authors hypothesized that microbiome features correlate with the pattern of organ involvement after allo-HCT. We evaluated 266 allo-HCT recipients from whom 1303 stool samples were profiled by 16S ribosomal gene sequencing. Patients were classified according to which organs were affected by aGVHD. In the 20 days prior to disease onset, GVHD patients had lower abundances of members of the class Clostridia, lower counts of butyrate producers, and lower ratios of strict-to-facultative (S/F) anaerobic bacteria compared with allograft recipients who were free of GVHD. GI GVHD patients showed significant reduction in microbial diversity preonset. Patients with lower GI aGVHD had lower S/F anaerobe ratios compared with those with isolated upper GI aGVHD. In the 20 days after disease onset, dysbiosis was observed only in GVHD patients with GI involvement, particularly those with lower-tract disease. Importantly, Clostridial and butyrate-producer abundance as well as S/F anaerobe ratio were predictors of longer overall survival; higher abundance of butyrate producers and higher S/F anaerobe ratio were associated with decreased risk of GVHD-related death. These findings suggest that the intestinal microbiome can serve as a biomarker for outcomes of allo-HCT patients with GVHD.
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