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

Author:

Halsey Taylor M.1ORCID,Thomas Anusha S.2,Hayase Tomo3,Ma Weijie24,Abu-Sbeih Hamzah25,Sun Baohua6,Parra Edwin Roger6,Jiang Zhi-Dong7ORCID,DuPont Herbert L.78ORCID,Sanchez Christopher3,El-Himri Rawan3,Brown Alexandria3,Flores Ivonne3,McDaniel Lauren3,Ortega Turrubiates Miriam3,Hensel Matthew9,Pham Dung3,Watowich Stephanie S.10ORCID,Hayase Eiko3ORCID,Chang Chia-Chi3ORCID,Jenq Robert R.311ORCID,Wang Yinghong2ORCID

Affiliation:

1. Graduate School of Biomedical Sciences, Microbiology and Infectious Diseases, University of Texas MD Anderson Cancer Center UTHealth Houston, Houston, TX 77054, USA.

2. Department of Gastroenterology, Hepatology and Nutrition, University of Texas MD Anderson Cancer Center, Houston, TX 77054, USA.

3. Department of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77054, USA.

4. Department of Hepatobiliary and Pancreatic Surgery, Zhongnan Hospital of Wuhan University, Wuhan, Hubei Province 430071, People’s Republic of China.

5. Department of Internal Medicine, University of Missouri, Kansas City, MO 65211, USA.

6. Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, TX 77054, USA.

7. Center for Infectious Diseases, School of Public Health, University of Texas, Houston, TX 77054, USA.

8. Kelsey Research Foundation, Houston, TX 77005, USA.

9. Middlebury College, Middlebury, VT 05753, USA.

10. Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77054, USA.

11. Department of Stem Cell Transplantation, Division of Cancer Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77054, USA.

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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