Targeting TMED4 enhances CD8 + T cell function and CAR T cell efficacy in solid tumors through the IRE1α-autophagy axis
- Huizi Wang
- Licai Shi
- Ke Jiang
- Shuyao Wu
- Zhenyan Jiang
- Yuexiao Tao
- Jia Li
- Xin Li
- Jiamin Liu
- Jun Ni
- Emily Jiatong Wu
- Sophia Jiaxin Wu
- Guang Chen
- Ming Qin
- Lin Xu
- Chu-Hu Lai
- Alexandra Aicher
- Youqiong Ye
- Christopher Heeschen
- Yu J. Cao
- Xuefeng Wu
2026-06-12
Endoplasmic reticulum stress (ERS) and autophagy regulate tumor-infiltrating T cell function and exhaustion, but the underlying mechanisms remain unclear. Here, we identified the ERS-related transmembrane protein TMED4 (transmembrane emp24 domain-containing 4) as a critical regulator of CD8 + T cell antitumor immunity. Tmed4 deletion in T cells enhanced antitumor responses by promoting CD8 + T proliferation, infiltration, and killing capacity, while reducing terminal exhaustion. Mechanistically, Tmed4 deficiency hyperactivated the inositol-requiring enzyme 1α (IRE1α)–X-box binding protein 1 (XBP1) axis and induced autophagy flux in an IRE1α-dependent manner. Genetic deletion of Ern1 (IRE1α) or Becn1 (Beclin1) impaired the antitumor effects of Tmed4 deficiency, underscoring the role of ERS and autophagy in CD8 + T cell function. Moreover, Tmed4 -deficient chimeric antigen receptor T cells (CAR T cells) displayed improved antitumor immunity. Pharmacological inhibition of Tmed4 using antisense oligonucleotide also enhanced CD8 + T cell–mediated tumor control. In summary, our study reveals that TMED4 governs CD8 + T cell effector function and limits terminal exhaustion through IRE1α-driven autophagy, establishing TMED4 as a promising immunotherapeutic target for improving CAR T cell efficacy.