Galectin-4 potentiates CD8+ T cell immunity by enhancing MHC-I expression on dendritic cells

  • Mol Ther. 2025 Aug 6;33(8):3662-3679. doi: 10.1016/j.ymthe.2025.06.040.
In-Gu Lee  1 Jeonghyeon Lee  1 Hyeong-Rae Kim  1 Younghyun Lim  1 Hye-Won Yu  2 Tae-Hyung Kim  3 Bumsuk Hahm  4 Hyun Ah Kang  1 So-Hee Hong  5 Young-Jin Seo  6
Affiliations
  • 1. Department of Life Science, Chung-Ang University, 84 Heukseok-ro, Dongjak-gu, Seoul 06974, Republic of Korea.
  • 2. Department of Microbiology, College of Medicine, Ewha Womans University, 25 Magokdong-ro 2-gil, Gangseo-gu, Seoul 07804, Republic of Korea.
  • 3. Department of Pathology, School of Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.
  • 4. Departments of Surgery and Molecular Microbiology and Immunology, University of Missouri, Columbia, MO 65212, USA.
  • 5. Department of Microbiology, College of Medicine, Ewha Womans University, 25 Magokdong-ro 2-gil, Gangseo-gu, Seoul 07804, Republic of Korea. Electronic address: [email protected].
  • 6. Department of Life Science, Chung-Ang University, 84 Heukseok-ro, Dongjak-gu, Seoul 06974, Republic of Korea. Electronic address: [email protected].
Abstract

Galectin-4 (Gal-4), a member of the β-galactoside-binding Galectin family, plays a role in various physiological processes, including tumor progression and intestinal disorders. However, its contribution to adaptive immunity remains poorly understood. In this study, Gal-4 is identified as a critical factor for effective generation of CD8+ T cell responses against tumors and viral infections. Gal-4-deficient mice exhibit significantly enhanced tumor growth in syngeneic mouse Cancer models, attributed to impaired CD8+ T cell responses. Similarly, Antiviral CD8+ T cell responses against lymphocytic choriomeningitis virus (LCMV) are profoundly diminished in Gal-4-deficient mice. This is not due to CD8+ T cell-intrinsic defects but instead linked to decreased surface expression of antigen-MHC-I complexes on dendritic cells. Building on these findings, the therapeutic potential of Gal-4 is investigated. Administration of Gal-4 enhances the efficacy of Cancer vaccines and PD-1 blockade Cancer therapy to improve outcomes in tumor-bearing mice. Additionally, systemic administration of Gal-4 markedly amplifies Antiviral CD8+ T cell responses against LCMV. Collectively, these results underscore the pivotal role of Gal-4 in modulating CD8+ T cell immunity and highlight its promise as a therapeutic target for the development of novel immunotherapeutics against Cancer and viral diseases.

Keywords
CD8+ T cells; antitumor immunity; antiviral immunity; dendritic cells; galectin-4.