Antonio Gomes

Dr. Antonio Gomes

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Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 February 2020 in New England Journal of Medicine
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Journal Article
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JPJonathan U. Peled
Jonathan U. Peled
AGAntonio Gomes
Antonio Gomes
SDSean M. Devlin
Sean M. Devlin
ELEric R. Littmann
Eric R. Littmann
YTYing Taur
Ying Taur
MBMarcel R.M. van Den Brink
Marcel R.M. van Den Brink
Relationships between microbiota composition and clinical outcomes after allogeneic hematopoietic-cell transplantation have been described in single-center studies. Geographic variations in the composition of human microbial communities and differences in clinical practices across institutions raise the question of whether these associations are generalizable. The microbiota composition of fecal samples obtained from patients who were undergoing allogeneic hematopoietic-cell transplantation at four centers was profiled by means of 16S ribosomal RNA gene sequencing. In an observational study, we examined associations between microbiota diversity and mortality using Cox proportional-hazards analysis. For stratification of the cohorts into higher- and lower-diversity groups, the median diversity value that was observed at the study center in New York was used. In the analysis of independent cohorts, the New York center was cohort 1, and three centers in Germany, Japan, and North Carolina composed cohort 2. Cohort 1 and subgroups within it were analyzed for additional outcomes, including transplantation-related death. We profiled 8767 fecal samples obtained from 1362 patients undergoing allogeneic hematopoietic-cell transplantation at the four centers. We observed patterns of microbiota disruption characterized by loss of diversity and domination by single taxa. Higher diversity of intestinal microbiota was associated with a lower risk of death in independent cohorts (cohort 1: 104 deaths among 354 patients in the higher-diversity group vs. 136 deaths among 350 patients in the lower-diversity group; adjusted hazard ratio, 0.71; 95% confidence interval [CI], 0.55 to 0.92; cohort 2: 18 deaths among 87 patients in the higher-diversity group vs. 35 deaths among 92 patients in the lower-diversity group; adjusted hazard ratio, 0.49; 95% CI, 0.27 to 0.90). Subgroup analyses identified an association between lower intestinal diversity and higher risks of transplantation-related death and death attributable to graft-versus-host disease. Baseline samples obtained before transplantation already showed evidence of microbiome disruption, and lower diversity before transplantation was associated with poor survival. Patterns of microbiota disruption during allogeneic hematopoietic-cell transplantation were similar across transplantation centers and geographic locations; patterns were characterized by loss of diversity and domination by single taxa. Higher diversity of intestinal microbiota at the time of neutrophil engraftment was associated with lower mortality. (Funded by the National Cancer Institute and others.)

30 October 2020 in Science
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Journal Article
Closed access
HGHao Guo
Hao Guo
WCWei-Chun Chou
Wei-Chun Chou
YLYunjia Lai
Yunjia Lai
KLKaixin Liang
Kaixin Liang
JTJason W. Tam
Jason W. Tam
JTJenny P. Y. Ting
Jenny P. Y. Ting
Radioprotective bacteria: A common symptom of radiation treatment for cancer is gastrointestinal disruption. The damage caused can become so severe and debilitating that it interrupts treatment. Guo et al. noticed that mice surviving experimental radiation exposure had distinctive taxonomic representation in their gut microbiota. A similar correlation was also observed in a small group of human subjects. Further experiments in mice revealed that some strains of bacteria produced high levels of short-chain fatty acids, which seemed to be dampening inflammatory responses and alleviating the damage caused by reactive oxygen species released by the radiation. A metabolomics analysis also implicated a role for tryptophan metabolic pathways in radiation survivorship. Science , this issue p. eaay9097

3 July 2013 in Nature
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JGJames E. Galagan
James E. Galagan
KMKyle Minch
Kyle Minch
MPMatthew Peterson
Matthew Peterson
ALAnna Lyubetskaya
Anna Lyubetskaya
EAElham Azizi
Elham Azizi
GSGary K. Schoolnik
Gary K. Schoolnik

29 November 2019 in Science
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Journal Article
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CSC. K. Stein-Thoeringer
C. K. Stein-Thoeringer
KNK. B. Nichols
K. B. Nichols
ALA. Lazrak
A. Lazrak
MDM. D. Docampo
M. D. Docampo
ASA. E. Slingerland
A. E. Slingerland
MBM. R. M. van Den Brink
M. R. M. van Den Brink
Lactose can fuel GVHD: Allogeneic hematopoietic cell transplantation (allo-HCT) is used to treat certain hematopoietic malignancies, but patients have a risk of developing graft-versus-host disease (GVHD). Stein-Thoeringer et al. performed a large-scale analysis of more than 1300 patients treated with allo-HCT across four clinical centers (see the Perspective by Zitvogel and Kroemer). High levels of bacteria from the Enterococcus genus were associated with greater incidence of GVHD and mortality. Lactose appears to provide a substrate for Enterococcus growth, and patients with a lactose-malabsorption genotype had a greater abundance of Enterococcus. A lactose-free diet limited Enterococcus growth, reduced the severity of GVHD, and improved survival in gnotobiotic mouse models. Science , this issue p. 1143 ; see also p. 1077

1 June 2016 in Current Opinion in Microbiology
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Journal Article
Closed access
NJNathan I Johns
Nathan I Johns
TBTomasz Blazejewski
Tomasz Blazejewski
AGAntonio Gomes
Antonio Gomes
HWHarris H Wang
Harris H Wang

14 March 2022 in Nature Medicine
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Journal Article
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MSMelody Smith
Melody Smith
ADAnqi Dai
Anqi Dai
GGGuido Ghilardi
Guido Ghilardi
KAKimberly V. Amelsberg
Kimberly V. Amelsberg
SDSean M. Devlin
Sean M. Devlin
MRMarco Ruella
Marco Ruella