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Eliciting protective immune responses against murine myeloma challenge in lymphopenia mice through adoptive transfer of tumor antigen-specific lymphocytes and immunization of tumor vaccine secreting mIL-21

机译:通过过继转移肿瘤抗原特异性淋巴细胞和免疫分泌mIL-21的肿瘤疫苗来增强针对淋巴细胞减少症小鼠抗鼠骨髓瘤攻击的保护性免疫应答

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Previous studies have indicated that the cytokine interleukin (IL)-21 may induce both innate and adaptive immune responses against tumors. The goal of this study was to evaluate a new adoptive immunotherapy strategy that combined lymphocytes from mice immunized with a murine myeloma vaccine secreting murine IL-21 (mIL-21-Sp2/0) in lymphopenic mice induced by cyclophosphamide. The data indicate that effective antitumor immunity was induced in mice receiving syngeneic murine lymphocytes from the mice immunized with the mIL-21-Sp2/0. More importantly, the efficacy against the Sp2/0 cell challenge was enhanced after the lymphocytes were activated and proliferated ex vivo before administration into the lymphopenic mice. We conclude that the adoptive transfer of tumor antigen-specific lymphocytes into mice immunized with mIL-21-Sp2/0 induced protective immune responses against myeloma challenge.
机译:先前的研究表明,细胞因子白介素(IL)-21可能诱导针对肿瘤的先天性和适应性免疫反应。这项研究的目的是评估一种新的过继免疫治疗策略,该策略结合了用环磷酰胺诱导的淋巴细胞减少的小鼠中用分泌骨髓IL-21(mIL-21-Sp2 / 0)的小鼠骨髓瘤疫苗免疫的小鼠的淋巴细胞。数据表明,在接受来自用mIL-21-Sp2 / 0免疫的小鼠的同系鼠淋巴细胞的小鼠中诱导了有效的抗肿瘤免疫。更重要的是,在激活淋巴细胞并给予淋巴细胞减少小鼠之前,离体增殖了淋巴细胞后,增强了针对Sp2 / 0细胞攻击的功效。我们得出的结论是,将肿瘤抗原特异性淋巴细胞过继转移到用mIL-21-Sp2 / 0免疫的小鼠中,可以诱导针对骨髓瘤攻击的保护性免疫应答。

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