Ectopic activation of the miR-200c–EpCAM axis enhances antitumor T cell responses in models of adoptive cell therapy

Author:

Zhang Minggang1ORCID,Zhao Zeguo12ORCID,Pritykin Yuri3ORCID,Hannum Margaret4,Scott Andrew C.1ORCID,Kuo Fengshen5ORCID,Sanghvi Viraj6ORCID,Chan Timothy A.5,Seshan Venkatraman4,Wendel Hans-Guido6ORCID,Schietinger Andrea1,Sadelain Michel12ORCID,Huse Morgan1ORCID

Affiliation:

1. Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

2. Center for Cell Engineering, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

3. Lewis-Sigler Institute for Integrative Genomics and Computer Science Department, Princeton University, Princeton, NJ 08540, USA.

4. Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

5. Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

6. Cancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

Abstract

Up-regulation of the miR-200c–EpCAM axis promotes the engraftment, persistence, and antitumor activity of transferred T cells in murine models.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

Reference72 articles.

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3. CAR therapy: the CD19 paradigm

4. Mechanisms of resistance to CAR T cell therapy;Shah N. N.;Nat. Rev. Clin. Oncol.,2019

5. CD8+ T Cells: Foot Soldiers of the Immune System

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