IL-18 Is Involved in Eosinophil-Mediated Tumoricidal Activity against a Colon Carcinoma Cell Line by Upregulating LFA-1 and ICAM-1

嗜酸性粒细胞 细胞毒性T细胞 细胞毒性 细胞培养 细胞粘附分子 细胞粘附 癌症研究 细胞凋亡 免疫学 细胞 生物 细胞生物学 体外 遗传学 哮喘 生物化学
作者
S. Gatault,Marie Delbeke,Virginie Driss,Aurore Sarazin,Arnaud Dendooven,Jean‐Emmanuel Kahn,Guillaume Lefèvre,Moníque Capron
出处
期刊:Journal of Immunology [American Association of Immunologists]
卷期号:195 (5): 2483-2492 被引量:81
标识
DOI:10.4049/jimmunol.1402914
摘要

Abstract Eosinophils are multifunctional leukocytes that are involved in innate and adaptive immune responses through the expression of various receptors and mediators. Previously, we showed that human eosinophils and T cells shared cytotoxic activities against tumor cells that involved the γ-δ TCR and cell–cell contact. In this study, we investigated the molecules involved in eosinophil–tumor cell interactions. Given the role of IL-18 in cell adhesion and in protecting against colon cancer, we evaluated its role in eosinophil-mediated cytotoxicity against Colo-205, a human colon carcinoma cell line. We found that human eosinophils exerted dose- and time-dependent tumoricidal activity against Colo-205 cells. Neutralization of IL-18 significantly reduced eosinophil-mediated Colo-205 apoptosis and inhibited cell–cell adhesion. Moreover, addition of rIL-18 led to upregulation of CD11a and ICAM-1 adhesion molecules, which were involved in the contact between eosinophils and Colo-205 cells. Our results indicated that IL-18 was involved in the eosinophil-mediated death of Colo-205 by facilitating contact between effector and target cells. These data underscored the involvement of an additional mediator in eosinophil-mediated antitumor cytotoxicity. Our findings support existing evidence that eosinophils could play a beneficial role in the context of colon cancer.
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