Universal Nanovial Screening Enables Functional Discovery of Metabolite-Reactive T‑Cell Receptors for Cancer Therapy

Citradewi Soemardy, Yan-Ruide Li, Yichen Zhu, Xinyuan Shen, Lili Yang, Dino Di Carlo

ACS Nano, April 2026

https://doi.org/10.1021/acsnano.5c22721


Abstract

Unconventional T cells, including mucosal-associated invariant T (MAIT) cells and invariant natural killer T (iNKT) cells, recognize nonpeptide antigens presented by MR1 and CD1d, respectively, and offer unique therapeutic potential. Despite invariant TCRα chains, diversity in TCRβ regions may underlie unique sequence-to-function relationships. Here, we develop a nanovial-based functional screening platform for the high-throughput discovery of TCRs from unconventional T cells present in human blood. By labeling nanovials with MR1 or CD1d molecules and cytokine-capture antibodies, we enable antigen-specific capture, activation, cytokine secretion, and oligobarcode-linked identification. Using secretion-encoded single-cell sequencing, we isolate rare MAIT and iNKT cells and associate their TCR identities with functional phenotypes. All five MAIT TCRs conferred antigen-specific cytokine secretion and cytotoxicity in vitro, with the two tested in vivo demonstrating tumor targeting, intratumoral accumulation, and measurable antitumor activity. Our nanotechnology-enabled “function-first” screen unlocks precision TCR discovery for unconventional T cells and supports the development of therapies targeting aberrant metabolic pathways.

Nanovials functionalized with MR1 or CD1d selectively capture MAIT or iNKT cells, respectively, and reveal increased IFNγ secretion compared with nonspecific anti-CD45 capture.
 

Topics

TCR Discovery, Cell Therapy, Functional Cell Screening

Cell Types

Mucosal-associated invariant T (MAIT) cells, invariant natural killer T (iNKT) cells

Secretion Targets

IFN-γ

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Systematic mapping of emergent transcriptional states in interacting single-cell dyads by Cell-Cell-seq