Surface‐Functionalized Microgels as Artificial Antigen‐Presenting Cells to Regulate Expansion of T Cells

Author:

Lou Junzhe12ORCID,Meyer Charlotte13ORCID,Vitner Einat B.1ORCID,Adu‐Berchie Kwasi12ORCID,Dacus Mason T.12,Bovone Giovanni12,Chen Anqi1,To Tania12,Weitz David A.124,Mooney David J.12ORCID

Affiliation:

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

2. Wyss Institute for Biologically Inspired Engineering Harvard University Boston MA 02215 USA

3. Department of Information Technology and Electrical Engineering ETH Zürich Zürich 8092 Switzerland

4. Department of Physics Harvard University Cambridge MA 02138 USA

Abstract

AbstractArtificial antigen‐presenting cells (aAPCs) are currently used to manufacture T cells for adoptive therapy in cancer treatment, but a readily tunable and modular system can enable both rapid T cell expansion and control over T cell phenotype. Here, it is shown that microgels with tailored surface biochemical properties can serve as aAPCs to mediate T cell activation and expansion. Surface functionalization of microgels is achieved via layer‐by‐layer coating using oppositely charged polymers, forming a thin but dense polymer layer on the surface. This facile and versatile approach is compatible with a variety of coating polymers and allows efficient and flexible surface‐specific conjugation of defined peptides or proteins. The authors demonstrate that tethering appropriate stimulatory ligands on the microgel surface efficiently activates T cells for polyclonal and antigen‐specific expansion. The expansion, phenotype, and functional outcome of primary mouse and human T cells can be regulated by modulating the concentration, ratio, and distribution of stimulatory ligands presented on microgel surfaces as well as the stiffness and viscoelasticity of the microgels.

Funder

National Institutes of Health

Publisher

Wiley

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