Mucosal-associated invariant T cells modulate innate immune cells and inhibit colon cancer growth.
Olivia J ChengEric J LebishOwen JensenDamian JacenikShubhanshi TrivediJackson G CacioppoJeffrey AubeEllen J BeswickDaniel T LeungPublished in: Scandinavian journal of immunology (2024)
Mucosal-associated invariant T (MAIT) cells are innate-like T cells that can be activated by microbial antigens and cytokines and are abundant in mucosal tissues including the colon. MAIT cells have cytotoxic and pro-inflammatory functions and have potentials for use as adoptive cell therapy. However, studies into their anti-cancer activity, including their role in colon cancer, are limited. Using an animal model of colon cancer, we showed that peritumoral injection of in vivo-expanded MAIT cells into RAG1 -/- mice with MC38-derived tumours inhibits tumour growth compared to control. Multiplex cytokine analyses showed that tumours from the MAIT cell-treated group have higher expression of markers for eosinophil-activating cytokines, suggesting a potential association between eosinophil recruitment and tumour inhibition. In a human peripheral leukocyte co-culture model, we showed that leukocytes stimulated with MAIT ligand showed an increase in eotaxin-1 production and activation of eosinophils, associated with increased cancer cell killing. In conclusion, we showed that MAIT cells have a protective role in a murine colon cancer model, associated with modulation of the immune response to cancer, potentially involving eosinophil-associated mechanisms. Our results highlight the potential of MAIT cells for non-donor restricted colon cancer immunotherapy.
Keyphrases
- induced apoptosis
- cell cycle arrest
- cell therapy
- gene expression
- endoplasmic reticulum stress
- immune response
- signaling pathway
- type diabetes
- squamous cell carcinoma
- microbial community
- oxidative stress
- cell death
- adipose tissue
- cell proliferation
- bone marrow
- high fat diet induced
- innate immune
- newly diagnosed
- ultrasound guided
- induced pluripotent stem cells