Preferential Small Intestine Homing and Persistence of CD8 T Cells in Rhesus Macaques Achieved by Molecularly Engineered Expression of CCR9 and Reduced Ex Vivo Manipulation

Author:

Trivett Matthew T.1,Burke James D.1,Deleage Claire1,Coren Lori V.1,Hill Brenna J.1,Jain Sumiti1,Barsov Eugene V.1,Breed Matthew W.2,Kramer Joshua A.2,Del Prete Gregory Q.1,Lifson Jeffrey D.1,Swanstrom Adrienne E.1ORCID,Ott David E.1

Affiliation:

1. AIDS and Cancer Virus Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA

2. Laboratory Animal Science Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA

Abstract

A doptive c ell t ransfer (ACT) of T cells engineered with antigen-specific effector properties can deliver targeted immune responses against malignancies and infectious diseases. Current T-cell-based therapeutic ACT relies on circulatory distribution to deliver engineered T cells to their targets, an approach which has proven effective for some leukemias but provided only limited efficacy against solid tumors. Here, engineered expression of the CCR9 homing receptor redirected CD8 T cells to the small intestine in rhesus macaque ACT experiments. Targeted homing of engineered T-cell immunotherapies holds promise to increase the effectiveness of adoptively transferred cells in both experimental and clinical settings.

Funder

HHS | NIH | National Cancer Institute

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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