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Mucosal-associated invariant T cells modulate innate immune cells and inhibit colon cancer growth.
Cheng, Olivia J; Lebish, Eric J; Jensen, Owen; Jacenik, Damian; Trivedi, Shubhanshi; Cacioppo, Jackson G; Aubé, Jeffrey; Beswick, Ellen J; Leung, Daniel T.
Affiliation
  • Cheng OJ; Division of Microbiology & Immunology, Department of Pathology, University of Utah, Salt Lake City, Utah, USA.
  • Lebish EJ; Division of Infectious Disease, Department of Internal Medicine, University of Utah, Salt Lake City, Utah, USA.
  • Jensen O; Division of Gastroenterology, Department of Internal Medicine, University of Utah, Salt Lake City, Utah, USA.
  • Jacenik D; Division of Microbiology & Immunology, Department of Pathology, University of Utah, Salt Lake City, Utah, USA.
  • Trivedi S; Division of Infectious Disease, Department of Internal Medicine, University of Utah, Salt Lake City, Utah, USA.
  • Cacioppo JG; Division of Gastroenterology, Department of Internal Medicine, University of Utah, Salt Lake City, Utah, USA.
  • Aubé J; Department of Cytobiochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
  • Beswick EJ; Division of Infectious Disease, Department of Internal Medicine, University of Utah, Salt Lake City, Utah, USA.
  • Leung DT; Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Scand J Immunol ; : e13391, 2024 May 21.
Article in En | MEDLINE | ID: mdl-38773691
ABSTRACT
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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Scand J Immunol Year: 2024 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Scand J Immunol Year: 2024 Document type: Article Affiliation country: Estados Unidos
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