Fecal microbiota transplant overcomes resistance to anti–PD-1 therapy in melanoma patients

Diwakar Davar(UPMC Hillman Cancer Center), Amiran Dzutsev(National Cancer Institute), John A. McCulloch(National Cancer Institute), Richard R. Rodrigues(Frederick National Laboratory for Cancer Research), Joë-Marc Chauvin(UPMC Hillman Cancer Center), Robert M. Morrison(UPMC Hillman Cancer Center), Richelle DeBlasio(UPMC Hillman Cancer Center), Carmine Menna(UPMC Hillman Cancer Center), Quanquan Ding(UPMC Hillman Cancer Center), Ornella Pagliano(UPMC Hillman Cancer Center), Bochra Zidi(UPMC Hillman Cancer Center), Shuowen Zhang(UPMC Hillman Cancer Center), Jonathan H. Badger(National Cancer Institute), Marie Vétizou(National Cancer Institute), Alicia M. Cole(National Cancer Institute), Miriam R. Fernandes(National Cancer Institute), Stephanie Prescott(National Cancer Institute), Raquel Costa(National Cancer Institute), Ascharya K. Balaji(National Cancer Institute), Andrey Morgun(Oregon State University), Ivan Vujkovic-Cvijin(National Institute of Allergy and Infectious Diseases), Hong Wang(UPMC Hillman Cancer Center), Amir A. Borhani(University of Pittsburgh), Marc Schwartz(University of Pittsburgh), Howard M. Dubner(University of Pittsburgh), S. Ernst(UPMC Hillman Cancer Center), Amy Rose(UPMC Hillman Cancer Center), Yana G. Najjar(UPMC Hillman Cancer Center), Yasmine Belkaid(National Institute of Allergy and Infectious Diseases), John M. Kirkwood(UPMC Hillman Cancer Center), Giorgio Trinchieri(National Cancer Institute), Hassane M. Zarour(University of Pittsburgh)
Science
February 4, 2021
Cited by 1,583Open Access
Full Text

Abstract

New fecal microbiota for cancer patients The composition of the gut microbiome influences the response of cancer patients to immunotherapies. Baruch et al. and Davar et al. report first-in-human clinical trials to test whether fecal microbiota transplantation (FMT) can affect how metastatic melanoma patients respond to anti–PD-1 immunotherapy (see the Perspective by Woelk and Snyder). Both studies observed evidence of clinical benefit in a subset of treated patients. This included increased abundance of taxa previously shown to be associated with response to anti–PD-1, increased CD8 + T cell activation, and decreased frequency of interleukin-8–expressing myeloid cells, which are involved in immunosuppression. These studies provide proof-of-concept evidence for the ability of FMT to affect immunotherapy response in cancer patients. Science , this issue p. 602 , p. 595 ; see also p. 573


Related Papers

No related papers found

Powered by citation graph analysis