The effects of intestinal tract bacterial diversity on mortality following allogeneic hematopoietic stem cell transplantation

被引:658
作者
Taur, Ying [1 ,2 ,3 ]
Jenq, Robert R. [2 ,3 ,4 ]
Perales, Miguel-Angel [3 ,4 ]
Littmann, Eric R. [1 ]
Morjaria, Sejal [1 ]
Ling, Lilan [2 ]
No, Daniel [2 ]
Gobourne, Asia [2 ]
Viale, Agnes [5 ]
Dahi, Parastoo B. [3 ,4 ]
Ponce, Doris M. [3 ,4 ]
Barker, Juliet N. [3 ,4 ]
Giralt, Sergio [3 ,4 ]
van den Brink, Marcel [3 ,4 ,6 ]
Pamer, Eric G. [1 ,2 ,3 ,6 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Infect Dis Serv, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Lucille Castori Ctr Microbes Inflammat & Canc, New York, NY 10065 USA
[3] Weill Cornell Med Coll, New York, NY USA
[4] Mem Sloan Kettering Canc Ctr, Dept Med, Adult Bone Marrow Transplant Serv, New York, NY 10065 USA
[5] Sloan Kettering Inst, Genom Core Lab, New York, NY USA
[6] Sloan Kettering Inst, Program Immunol, New York, NY USA
基金
美国国家卫生研究院;
关键词
VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; INFLAMMATORY-BOWEL-DISEASE; CORD COLITIS SYNDROME; CLOSTRIDIUM-DIFFICILE; COLONIZATION RESISTANCE; GUT MICROBIOME; RECIPIENTS; MICE; SUPPRESSION;
D O I
10.1182/blood-2014-02-554725
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Highly diverse bacterial populations inhabit the gastrointestinal tract and modulate host inflammation and promote immune tolerance. In allogeneic hematopoietic stem cell transplantation (allo-HSCT), the gastrointestinal mucosa is damaged, and colonizing bacteria are impacted, leading to an impaired intestinal microbiota with reduced diversity. We examined the impact of intestinal diversity on subsequent mortality outcomes following transplantation. Fecal specimens were collected from 80 recipients of allo-HSCT at the time of stem cell engraftment. Bacterial 16S rRNA gene sequences were characterized, and microbial diversity was estimated using the inverse Simpson index. Subjects were classified into high, intermediate, and low diversity groups and assessed for differences in outcomes. Mortality outcomes were significantly worse in patients with lower intestinal diversity; overall survival at 3 years was 36%, 60%, and 67% for low, intermediate, and high diversity groups, respectively (P=.019, log-rank test). Low diversity showed a strong effect on mortality after multivariate adjustment for other clinical predictors (transplant related mortality: adjusted hazard ratio, 5.25; P=.014). In conclusion, the diversity of the intestinal microbiota at engraftment is an independent predictor of mortality in allo-HSCT recipients. These results indicate that the intestinal microbiota may be an important factor in the success or failure in allo-HSCT.
引用
收藏
页码:1174 / 1182
页数:9
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