Serial transplantation unmasks galectin-9 contribution to tumor immune escape in the MB49 murine model

• Published in: Scientific reports 2021-03, Vol.11 (1), p.5227-5227, Article 5227
• Main Authors: Baloche, Valentin, Rivière, Julie, Tran, Thi Bao Tram, Gelin, Aurore, Bawa, Olivia, Signolle, Nicolas, Diop, M′Boyba Khadija, Dessen, Philippe, Beq, Stéphanie, David, Muriel, Busson, Pierre
• Format: Article
• Language: English
• Subjects: 631/67/327; 631/67/580; 631/67/589/1336; 631/67/70; Ablation; Animal models; Animals; Bladder; Bladder cancer; Cancer; Cell Line, Tumor; Chemokine CXCL10 - genetics; Cloning; CXCL10 protein; Cytokines; Disease Models, Animal; Galectin-9; Galectins - genetics; Genes; Humanities and Social Sciences; Humans; Immune evasion; Immune response; Immunology; Inflammation; Interferon-gamma - genetics; Interferon-gamma - immunology; Life Sciences; Melanoma; Metastasis; Mice; Mice, Nude; multidisciplinary; Science; Science (multidisciplinary); Transplantation; Transplantation, Isogeneic; Tumor Escape - genetics; Tumor Escape - immunology; Tumors; Urinary Bladder Neoplasms - genetics; Urinary Bladder Neoplasms - immunology; Urinary Bladder Neoplasms - pathology; γ-Interferon
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-84270-1

Mechanisms of tumor immune escape are quite diverse and require specific approaches for their exploration in syngeneic tumor models. In several human malignancies, galectin-9 (gal-9) is suspected to contribute to the immune escape. However, in contrast with what has been done for the infiltrating cells, the contribution of gal-9 produced by malignant cells has never been demonstrated in an animal model. Therefore, we derived isogenic clones—either positive or negative for gal-9—from the MB49 murine bladder carcinoma cell line. A progressive and consistent reduction of tumor growth was observed when gal-9-KO cells were subjected to serial transplantations into syngeneic mice. In contrast, tumor growth was unaffected during parallel serial transplantations into nude mice, thus linking tumor inhibition to the enhancement of the immune response against gal-9-KO tumors. This stronger immune response was at least in part explained by changing patterns of response to interferon-γ. One consistent change was a more abundant production of CXCL10, a major inflammatory factor whose production is often induced by interferon-γ. Overall, these observations demonstrate for the first time that serial transplantation into syngeneic mice can be a valuable experimental approach for the exploration of novel mechanisms of tumor immune escape.