γδ T 细胞调节小细胞肺癌中的抗肿瘤免疫
γδ T cells modulate anti-tumor immunity in small cell lung cancer.
我们的发现表明,活化的γδ T细胞可能是SCLC治疗的有价值靶点。
英文原题:A dendritic cell vaccine for both vaccination and neoantigen-reactive T cell preparation for cancer immunotherapy in mice.
我们提出了一种制备NRTs的方法,该方法提高了ACT疗效,并为个性化免疫疗法的设计铺平了道路。
使用新抗原特异性 T 细胞的过继细胞转移(ACT)是一种有效的免疫治疗策略。然而,新抗原特异性 T 细胞难以分离,限制了 ACT 的临床应用。在此,我们提出了一种在负载肿瘤裂解物的树突状细胞(DC)疫苗免疫后制备用于 ACT 的新抗原反应性 T 细胞(NRT)的方法。我们表明,该 DC 疫苗不仅在体内在荷肺癌小鼠中诱导新抗原反应性免疫应答,而且在体外促进 NRT 细胞的制备。将 NRT 作为联合疗法过继转移至 DC 疫苗免疫的 LL/2 荷瘤小鼠中,可使输注的 NRT 浸润,以及新抗原反应性、非 ACT/NRT T 细胞富集到肿瘤微环境中,这些新抗原反应性 T 细胞受体的功能在体外得到验证。总之,我们提出了一种制备 NRT 的方法,可提高 ACT 疗效,并为个性化免疫疗法的设计铺平道路。
Adoptive cell transfer (ACT) using neoantigen-specific T cells is an effective immunotherapeutic strategy. However, the difficult isolation of neoantigen-specific T cells limits the clinical application of ACT. Here, we propose a method to prepare neoantigen-reactive T cells (NRT) for ACT following immunization with a tumor lysate-loaded dendritic cell (DC) vaccine. We show that the DC vaccine not only induces a neoantigen-reactive immune response in lung cancer-bearing mice in vivo, but also facilitate NRT cell preparation in vitro. Adoptive transfer of the NRTs as combinatorial therapy into DC vaccine-immunized, LL/2 tumor-bearing mice allows infiltration of the infused NRTs, as well as the enrichment of neoantigen reactive, non-ACT/NRT T cells into the tumor microenvironment with the function of these neoantigen-reactive T-cell receptors validated in vitro. In summary, we propose a method for preparing NRTs that increases ACT efficacy and paves the way to the design of personalized immunotherapies.
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