Mucosal-associated invariant T cells recognize a tumor-derived metabolite in the DNA synthesis pathway - Scorecard - MDSpire

Mucosal-associated invariant T cells recognize a tumor-derived metabolite in the DNA synthesis pathway

  • By

  • Yanqi Xue

  • Yuka Yamada

  • Rikako Suzuki

  • Brenda Luong

  • Shotaro Fujii

  • Keisuke Nakata

  • Masatomo Takahashi

  • Yoshihiro Izumi

  • Chihiro Fukui

  • Ryosuke Takasaki

  • Francois Legoux

  • Shinsuke Inuki

  • Daisuke Motooka

  • Emi Ito

  • Bridget L. Stocker

  • Mattie S. M. Timmer

  • Takashi Shimizu

  • Yasumasa Matsuoka

  • Jun’ichi Mano

  • Koji Tamada

  • Makoto Furutani-Seiki

  • Kei Sakamoto

  • Koh-Hei Sonoda

  • Olivier Lantz

  • Sho Yamasaki

  • Kensuke Shibata

  • June 24, 2026

  • 0 min

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Clinical Scorecard: Mucosal-associated invariant T cells detect a metabolite from tumors involved in the DNA synthesis pathway

At a Glance

CategoryDetail
ConditionCancer
Key MechanismsMAIT cells recognize tumor-derived metabolite 5-formyl THF, an intermediate in folate metabolism, leading to TCR-dependent activation.
Target PopulationPatients with cancer
Care SettingCancer immunotherapy research

Key Highlights

  • 5-formyl THF is identified as the first tumor-derived ligand recognized by MAIT cells.
  • Activation of MAIT cells by 5-formyl THF is TCR-dependent.
  • Genetic deletion of Amt impairs MAIT cell activation in tumors.
  • MAIT cell activity can be enhanced by overexpression of Amt in tumors.
  • A human MAIT cell clonotype reactive to 5-formyl THF was identified.

Guideline-Based Recommendations

Diagnosis

    Management

      Monitoring & Follow-up

        Risks

          Patient & Prescribing Data

          Patients with tumors expressing 5-formyl THF

          Understanding the role of MAIT cells in tumor immunity may inform future immunotherapeutic strategies.

          Clinical Best Practices

          • Investigate the role of MAIT cells in tumor microenvironments.
          • Explore the therapeutic potential of targeting MAIT cell activation pathways.

          Related Resources & Content

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