工程化机械敏感 MSC 实现跨瘤种的合成放射诊疗靶向
Engineered mechanosensitive MSCs enable synthetic radiotheranostic targeting across tumor types.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Race-Related Differences in Sipuleucel-T Response among Men with Metastatic Castrate-Resistant Prostate Cancer.
Race-Related Differences in Sipuleucel-T Response among Men with Metastatic Castrate-Resistant Prostate Cancer.
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Sipuleucel-T 是一种靶向前列腺酸性磷酸酶 (PAP) 的自体细胞免疫疗法,可用于治疗无症状或轻微症状的转移性去势抵抗性前列腺癌 (mCRPC) 男性患者。在这项单臂、两队列、多中心临床研究中,探索了 mCRPC 男性患者对 sipuleucel-T 免疫应答的潜在种族差异。获取患者血样以评估治疗前后的血清细胞因子、体液应答和细胞免疫标志物。评估基线累积产品参数(总有核细胞和 CD54+ 细胞计数以及 CD54 上调)。通过 ELISA 定量针对免疫原 PA2024、靶抗原 PAP、前列腺特异性膜抗原 (PSMA) 和前列腺特异性抗原 (PSA) 的 IgM 滴度。通过 ELISpots 测定细胞毒性 T 淋巴细胞活性,通过 Luminex 测定细胞因子和趋化因子浓度。29 名非裔美国人 (AA) 男性和 28 名非非裔美国人 (non-AA) 男性 mCRPC 患者接受了 sipuleucel-T 治疗。non-AA 男性的基线总有核细胞计数、CD54+ 细胞计数、CD54 表达和累积产品参数更高。尽管 AA 男性的 PSA 基线水平更高,但治疗前后针对 PA2024、PAP、PSA 和 PSMA 的 IgM 抗体和 IFNγ ELISpots 应答均无种族差异。AA 男性在治疗前和/或治疗后,CD4+ 和 CD8+ T 细胞上共刺激受体 ICOS 的表达,以及 Th1 细胞因子粒细胞-巨噬细胞集落刺激因子和趋化因子 CCL4 和 CCL5 的水平显著更高。尽管总生存期无差异,但两种族间 PSA 较基线的变化存在显著差异。数据表明,在mCRPC的AA和非AA男性中,sipuleucel-T治疗前后的血液免疫相关指标存在差异。意义:我们在转移性去势抵抗性前列腺癌(mCRPC)非裔美国患者中sipuleucel-T治疗前后发现CD4+和CD8+ T细胞上共刺激受体ICOS表达更高的新发现,提示CD4+和CD8+ T细胞活化。数据表明,sipuleucel-T前后这些及其他免疫相关指标中观察到的种族差异值得进一步研究,以加深我们对非裔美国男性及其他mCRPC男性免疫系统的理解。
UNLABELLED: Sipuleucel-T is an autologous cellular immunotherapy that targets prostatic acid phosphatase (PAP) and is available for treatment of men with asymptomatic or minimally symptomatic metastatic castration-resistant prostate cancer (mCRPC). In this single-arm, two-cohort, multicenter clinical study, potential racial differences in immune responses to sipuleucel-T in men with mCRPC were explored. Patients' blood samples were obtained to assess serum cytokines, humoral responses, and cellular immunity markers before and after treatment. Baseline cumulative product parameters (total nucleated and CD54+ cell counts and CD54 upregulation) were evaluated. IgM titers against the immunogen PA2024, the target antigen PAP, prostate-specific membrane antigen (PSMA) and prostate-specific antigen (PSA) were quantified by ELISA. Cytotoxic T-lymphocyte activity was determined by ELISpots, and cytokine and chemokine concentrations were determined by Luminex. Twenty-nine African American (AA) men and 28 non-African American (non-AA) men with mCRPC received sipuleucel-T. Baseline total nucleated cell count, CD54+ cell count, CD54 expression, and cumulative product parameters were higher in non-AA men.
Although PSA baseline levels were higher in AA men, there were no racial differences in IgM antibody and IFNγ ELISpots responses against PA2024, PAP, PSA, and PSMA before and after treatment. Expression of co-stimulatory receptor ICOS on CD4+ and CD8+ T cells, and the levels of Th1 cytokine granulocyte-macrophage colony-stimulating factor and chemokines CCL4 and CCL5, were significantly higher in AA men before and/or after treatment. Despite no difference in the overall survival, PSA changes from baseline were significantly different between the two races.
The data suggest that immune correlates in blood differ in AA and non-AA men with mCRPC pre- and post-sipuleucel-T. SIGNIFICANCE: Our novel findings of higher expression of co-stimulatory receptor ICOS on CD4+ and CD8+ T cells in African American patients with metastatic castrate-resistant prostate cancer (mCRPC) prior and post-sipuleucel-T suggest activation of CD4+ and CD8+ T cells.
The data indicate that racial differences observed in these and other immune correlates before and after sipuleucel-T warrant additional investigation to further our understanding of the immune system in African American men and other men with mCRPC.
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