The γδ T cells dual function and crosstalk with intestinal flora in treating colorectal cancer is a promising area of study

Int Immunopharmacol. 2023 Oct:123:110733. doi: 10.1016/j.intimp.2023.110733. Epub 2023 Aug 12.

Abstract

The occurrence of colorectal cancer (CRC) is highly prevalent and severely affects human health, with the third-greatest occurrence and the second-greatest rate of death globally. Current CRC treatments, including surgery, radiotherapy, and chemotherapy, do not significantly improve CRC patients' survival rate and quality of life, so it is essential to develop new treatment strategies. Adoptive cell therapy and other immunotherapy came into being. Currently, there has been an especially significant emphasis on γδ T cells as being the primary recipient of adoptive cell therapy. The present investigation found that γδ T cells possess the capability to trigger cytotoxicity in CRC cells, secrete cytokines, recruit immune cells for the purpose of destroying cancer cells, and inhibit the progress of CRC indirectly. Nevertheless, It is possible for γδ T cells to initiate a storm of inflammatory factors and inhibit the immune response to promote the advancement of CRC. This review demonstrates a close association between the γδ T cell initiation pathway and their close association with the intestinal flora. It has been observed that the intestinal flora performs a vital function in facilitating the stimulation and functioning of γδ T cells. The tumor-fighting effect is mainly regulated by desulphurizing Vibrio and lactic acid bacteria. In contrast, the regulation of tumor-promoting impact is closely related to Clostridia and ETBF. This review systematically combs γδ T cell dual function and their relationship to intestinal flora, which offers a conceptual framework for the γδ T cell application for CRC therapies.

Keywords: Anti-tumor function; Colorectal cancer; Intestinal flora; Tumor-promoting function; γδ T cell.

Publication types

  • Review

MeSH terms

  • Colorectal Neoplasms* / therapy
  • Gastrointestinal Microbiome*
  • Humans
  • Immunotherapy
  • Quality of Life
  • Receptors, Antigen, T-Cell, gamma-delta / metabolism

Substances

  • Receptors, Antigen, T-Cell, gamma-delta