CD112 Lactylation Drives Dual Immune Evasion From CD8+ T Cells and NK Cells.

Authors

Zhuoshuo Xu, Xinyu Zhang, Fang Dong, Nenghao Shen, Jun Zhou, Zihan Xi, Zhenghao Wu

Published in

Advanced science (Weinheim, Baden-Wurttemberg, Germany). Pages e78088. Oct 04, 2026. Epub Oct 04, 2026.

Abstract

Current cancer immunotherapy predominantly targets CD8+ T cells, leaving NK cell surveillance largely unaddressed. We report that lactylation of the membrane checkpoint ligand CD112 serves as a convergent mechanism for dual immune escape. In contrast to T cell-centric checkpoints such as PD-L1, CD112 functions as a shared inhibitory ligand for both CD8+ T cells and NK cells through TIGIT/CD112R signaling. Mechanistically, the lactyltransferase AARS2 catalyzes CD112 lactylation at lysine 412 in response to tumor lactate accumulation, competitively blocking the HECT E3 ligase UBE3C to suppress K48/K63-linked ubiquitination and lysosomal degradation. This stabilizes CD112 at the plasma membrane, enabling tumor cells to coordinately evade both adaptive and innate cytotoxic lymphocytes. Disrupting this axis restores dual immune surveillance and suppresses tumor growth. Tumors with high CD112 lactylation and surface enrichment are selectively vulnerable to TIGIT/PD-L1 bispecific antibody blockade and HSV-2 oncolytic virotherapy, nominating CD112 lactylation status as a predictive biomarker for combination immunotherapy.

PMID:
42829916
Bibliographic data and abstract were imported from PubMed on 05 Oct 2026.

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