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Phytogalactolipids activate humoral immunity against colorectal cancer.

Authors :
Lin HH
Wu YS
Jian TY
Liao JY
Chang MT
Shyur LF
Lin YL
Source :
Journal of experimental & clinical cancer research : CR [J Exp Clin Cancer Res] 2023 Apr 21; Vol. 42 (1), pp. 95. Date of Electronic Publication: 2023 Apr 21.
Publication Year :
2023

Abstract

Background: Colorectal cancer (CRC) is the third most lethal cancer in the world, and its incidence is steadily rising. In this study, we investigated the induction of humoral immunity by a phytogalactolipid enriched fraction (CRA) derived from the medicinal plant Crassocephalum rabens (Benth.) S. Moore to combat CRC.<br />Methods: Immunocompetent BALB/c mice were used to evaluate CRA's therapeutic effects in CRC. The phenotypes of B cell subsets in splenocytes and tumors from the CRA-treated mice were isolated and analyzed by flow cytometry. The titers, isotypes, specificity, antigen recognition, and cytotoxic activity of CRA-induced anti-tumor antibodies were determined. The mechanisms of CRA on B cell differentiation were determined by cell-based analyses, including co-cultural with T cells, cytokine analysis, gene expression by qPCR, and protein expression by western blotting.<br />Results: CRA efficiently inhibited tumor growth in colorectal tumor-bearing allograft mice. CRA treatment attracted an abundance of B cells into the tumor consequently enhancing the anti-tumor antibodies in sera and inducing a class-switch. CRA-induced antisera (designated CRA antisera) specifically recognized surface antigens on the plasma membrane of cancer cells. CRA antisera induced cytotoxicity including antibody-dependent cell cytotoxicity, phagocytosis, and complement-dependent cytotoxicity. CRA interacted with IL-6 receptor to activate STAT3 and cMaf, resulting in T cell secretion of IL-21, which, in turn induced B cell differentiation through the IL-21R/STAT3/Blimp-1 pathway.<br />Conclusions: CRA regulated T cell activity resulting in B cell activation and triggering of anti-tumor antibodies to impede CRC progression.<br /> (© 2023. The Author(s).)

Details

Language :
English
ISSN :
1756-9966
Volume :
42
Issue :
1
Database :
MEDLINE
Journal :
Journal of experimental & clinical cancer research : CR
Publication Type :
Academic Journal
Accession number :
37081540
Full Text :
https://doi.org/10.1186/s13046-023-02660-x