Cytokine conjugation to enhance T cell therapy

Author:

Liu Yutong12ORCID,Adu-Berchie Kwasi12,Brockman Joshua M.12,Pezone Matthew1,Zhang David K.Y.12,Zhou Jingyi3ORCID,Pyrdol Jason W.4,Wang Hua3,Wucherpfennig Kai W.4,Mooney David J.12ORCID

Affiliation:

1. John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138

2. Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, MA 02115

3. Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana and Champaign, IL 61801

4. Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA 02115

Abstract

Adoptive T cell transfer (ACT) therapies suffer from a number of limitations (e.g., poor control of solid tumors), and while combining ACT with cytokine therapy can enhance effectiveness, this also results in significant side effects. Here, we describe a nanotechnology approach to improve the efficacy of ACT therapies by metabolically labeling T cells with unnatural sugar nanoparticles, allowing direct conjugation of antitumor cytokines onto the T cell surface during the manufacturing process. This allows local, concentrated activity of otherwise toxic cytokines. This approach increases T cell infiltration into solid tumors, activates the host immune system toward a Type 1 response, encourages antigen spreading, and improves control of aggressive solid tumors and achieves complete blood cancer regression with otherwise noncurative doses of CAR-T cells. Overall, this method provides an effective and easily integrated approach to the current ACT manufacturing process to increase efficacy in various settings.

Funder

HHS | U.S. Food and Drug Administration

HHS | National Institutes of Health

Universitas Harvardiana | Hansjörg Wyss Institute for Biologically Inspired Engineering, Harvard University

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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