The quantity, function and anti-tumor effect of Mucosal associated invariant T cells in patients with bladder cancer

Int Immunopharmacol. 2024 May 30:133:111892. doi: 10.1016/j.intimp.2024.111892. Epub 2024 Apr 24.

Abstract

Background: Bladder cancer (BC), a prevalent malignancy in the urinary system, often poses challenges for effective treatment. Immunotherapy, harnessing the immune system, has exhibited promise in early-stage clinical trials. Mucosal associated invariant T (MAIT) cells, a subset of immune cells implicated in various diseases, including certain cancer, have yet to be explored in BC patients. We aimed to investigate the quantity, function, and anti-tumor effects of MAIT cells in BC patients.

Methods: A total of 75 newly diagnosed BC patients and 183 healthy volunteers were included. Blood samples were collected and analyzed to evaluate the quantity and function of MAIT cells. Surgical resection provided BC tissues for further analysis, and the clinical features of BC tumors were collected and their relationship with MAIT cells was explored.

Results: MAIT cells were identified in both healthy individuals and BC patients. The proportion of MAIT cells in the peripheral blood of BC patients did not significantly differ from that of healthy controls. However, the study revealed a correlation between the proportion of IFN-γ producing MAIT cells and tumor number and invasion in BC patients. Furthermore, MAIT cells exhibited cytotoxic effects on BC cells in vitro and in vivo.

Conclusions: This study sheds light on the role of MAIT cells in BC. While the quantity of MAIT cells showed no significant change in BC patients, their functional attributes and association with tumor characteristics suggest their potential as an immunotherapy target in BC treatment.

Keywords: Anti-tumor; Bladder cancer; IFN-γ; Mucosa associated constant T cells.

MeSH terms

  • Adult
  • Aged
  • Animals
  • Cell Line, Tumor
  • Cytotoxicity, Immunologic
  • Female
  • Humans
  • Immunotherapy / methods
  • Interferon-gamma / metabolism
  • Male
  • Mice
  • Middle Aged
  • Mucosal-Associated Invariant T Cells* / immunology
  • Urinary Bladder Neoplasms* / immunology
  • Urinary Bladder Neoplasms* / pathology
  • Urinary Bladder Neoplasms* / therapy

Substances

  • Interferon-gamma