Unknown

Dataset Information

0

Gut microbiome and CAR-T therapy.


ABSTRACT: Considerable progress has been made in cancer therapeutics recently with targeted strategies that are efficacious and less toxic. Immunotherapy and chimeric antigen receptor (CAR) T-cells are increasingly being evaluated in a variety of tumors in the relapsed/refractory as well as frontline disease settings, predominantly in hematologic malignancies (HM). Despite impressive outcomes in select patients, there remains significant heterogeneity in clinical response to CAR T-cells. The gut microbiome has emerged as one of the key host factors that could potentially be modulated to enhance responses to immunotherapy. Several recent human studies receiving immunotherapy showed a significantly superior response and survival in patients with the more diverse gut microbiome. Currently, it is unknown if gut microbiota modulates anti-tumor responses to CAR T-cells. Based on molecular and immunological understanding, we hypothesize that strategically manipulating gut microbiota may enhance responses to CAR T-cells. In this review, we further discuss resistance mechanisms to CAR T-cells in HM, potential approaches to overcome resistance by harnessing gut microbiota and other related novel strategies.

SUBMITTER: Abid MB 

PROVIDER: S-EPMC6862813 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

altmetric image

Publications

Gut microbiome and CAR-T therapy.

Abid Muhammad Bilal MB   Shah Nirav N NN   Maatman Theresa C TC   Hari Parameswaran N PN  

Experimental hematology & oncology 20191119


Considerable progress has been made in cancer therapeutics recently with targeted strategies that are efficacious and less toxic. Immunotherapy and chimeric antigen receptor (CAR) T-cells are increasingly being evaluated in a variety of tumors in the relapsed/refractory as well as frontline disease settings, predominantly in hematologic malignancies (HM). Despite impressive outcomes in select patients, there remains significant heterogeneity in clinical response to CAR T-cells. The gut microbiom  ...[more]

Similar Datasets

| S-EPMC9434490 | biostudies-literature
| S-EPMC9913364 | biostudies-literature
| S-EPMC9461447 | biostudies-literature
| S-EPMC7985695 | biostudies-literature
| S-EPMC6048199 | biostudies-other
2018-11-01 | GSE104871 | GEO
| S-EPMC10448936 | biostudies-literature
| S-EPMC3376388 | biostudies-other
| S-EPMC4732525 | biostudies-other