A stable, engineered TL1A ligand co-stimulates T cells via specific binding to DR3

Author:

Zwolak Adam,Chan Szeman Ruby,Harvilla Paul,Mahady Sally,Armstrong Anthony A.,Luistro Leopoldo,Tamot Ninkka,Yamada Douglas,Derebe Mehabaw,Pomerantz Steven,Chiu Mark,Ganesan Rajkumar,Chowdhury Partha

Abstract

AbstractTL1A (TNFSF15) is a TNF superfamily ligand which can bind the TNFRSF member death receptor 3 (DR3) on T cells and the soluble decoy receptor DcR3. Engagement of DR3 on CD4+ or CD8+ effector T cells by TL1A induces downstream signaling, leading to proliferation and an increase in secretion of inflammatory cytokines. We designed a stable recombinant TL1A molecule that (1) displays high monodispersity and stability, (2) displays the ability to activate T cells in vitro and in vivo, and (3) lacks binding to DcR3 while retaining functional activity via DR3. Together these results suggest the TL1A ligand can be amenable to therapeutic development on its own or paired with a tumor-targeting moiety.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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