Microbiome alteration via fecal microbiota transplantation is effective for refractory immune checkpoint inhibitor–induced colitis

Taylor M. Halsey(The University of Texas MD Anderson Cancer Center), Anusha Shirwaikar Thomas(The University of Texas MD Anderson Cancer Center), Tomo Hayase(The University of Texas MD Anderson Cancer Center), Weijie Ma(The University of Texas MD Anderson Cancer Center), Hamzah Abu‐Sbeih(The University of Texas MD Anderson Cancer Center), Baohua Sun(The University of Texas MD Anderson Cancer Center), Edwin R. Parra(The University of Texas MD Anderson Cancer Center), Zhi‐Dong Jiang(Texas Center for Infectious Disease), Herbert L. DuPont(Texas Center for Infectious Disease), Christopher A. Sanchez(The University of Texas MD Anderson Cancer Center), Rawan K. El-Himri(The University of Texas MD Anderson Cancer Center), Alexandria Brown(The University of Texas MD Anderson Cancer Center), Ivonne I. Flores(The University of Texas MD Anderson Cancer Center), Lauren McDaniel(The University of Texas MD Anderson Cancer Center), Miriam Ortega Turrubiates(The University of Texas MD Anderson Cancer Center), Matthew Hensel(Middlebury College), Dung Pham(The University of Texas MD Anderson Cancer Center), Stephanie S. Watowich(The University of Texas MD Anderson Cancer Center), Eiko Hayase(The University of Texas MD Anderson Cancer Center), Chia‐Chi Chang(The University of Texas MD Anderson Cancer Center), Robert R. Jenq(The University of Texas MD Anderson Cancer Center), Yinghong Wang(The University of Texas MD Anderson Cancer Center)
Science Translational Medicine
June 14, 2023
Cited by 135Open Access
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Abstract

Immune checkpoint inhibitors (ICIs) target advanced malignancies with high efficacy but also predispose patients to immune-related adverse events like immune-mediated colitis (IMC). Given the association between gut bacteria with response to ICI therapy and subsequent IMC, fecal microbiota transplantation (FMT) represents a feasible way to manipulate microbial composition in patients, with a potential benefit for IMC. Here, we present a large case series of 12 patients with refractory IMC who underwent FMT from healthy donors as salvage therapy. All 12 patients had grade 3 or 4 ICI-related diarrhea or colitis that failed to respond to standard first-line (corticosteroids) and second-line immunosuppression (infliximab or vedolizumab). Ten patients (83%) achieved symptom improvement after FMT, and three patients (25%) required repeat FMT, two of whom had no subsequent response. At the end of the study, 92% achieved IMC clinical remission. 16 S rRNA sequencing of patient stool samples revealed that compositional differences between FMT donors and patients with IMC before FMT were associated with a complete response after FMT. Comparison of pre- and post-FMT stool samples in patients with complete responses showed significant increases in alpha diversity and increases in the abundances of Collinsella and Bifidobacterium , which were depleted in FMT responders before FMT. Histologically evaluable complete response patients also had decreases in select immune cells , including CD8 + T cells, in the colon after FMT when compared with non-complete response patients ( n = 4). This study validates FMT as an effective treatment strategy for IMC and gives insights into the microbial signatures that may play a critical role in FMT response.


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