CLIN CANCER RES:Sipuleucel-T诱导的抗原特异性CD8亚型与患者总生存有关

2018-10-22 MedSci MedSci原创

IMPACT试验结果表明,接受sipuleucel-T治疗的患者与对照患者相比中位总生存期(OS)延长为4.1个月。因此Sipuleucel-T被FDA批准用于治疗转移性去势抵抗性前列腺癌(mCRPC)。尽管sipuleucel-T的有效性已经得到证明,但其机制仍未完全阐明。CLIN CANCER RES近期发表了一篇文章,研究这一问题。

IMPACT试验结果表明,接受sipuleucel-T治疗的患者与对照患者相比中位总生存期(OS)延长为4.1个月。因此Sipuleucel-T被FDA批准用于治疗转移性去势抵抗性前列腺癌(mCRPC)。尽管sipuleucel-T的有效性已经得到证明,但其机制仍未完全阐明。CLIN CANCER RES近期发表了一篇文章,研究这一问题。

作者评估了三个sipuleucel-T试验的患者样本对免疫原PA2024和靶标抗原前列腺酸性磷酸酶(PAP)的外周细胞学免疫应答。为了评估细胞毒性T淋巴细胞(CTL)活性,作者检测了接受sipuleucel-T治疗的患者和健康志愿者样品中PAP-或PA2024-特异性CD8+T细胞的表面CD107a的表达。研究结果表明,在sipuleucel-T治疗后观察到PA2024特异性CD4+(P = 0.030)和CD8+(P = 0.052)T细胞增殖增加,与PAP相比出现更强的PA2024特异性反应。在sipuleucel-T治疗后的第6周和第26周,PAP-和PA2024-CTL活性(CD107a阳性)显着增加。在sipuleucel-T治疗后26周,OS与PA2024 CTL活性有关。治疗26周PA2024-CTL活性升高OS改善有关,而PA2024反应与26周PAP反应有关。

文章最后认为,该研究首次报道了由sipuleucel-T治疗引起的PAP特异性CD8+T细胞反应。PA2024特异性CTL活性的增加与PAP特异性CTL活性增加以及OS改善相关。

原始出处:

Emmanuel S. AntonarakisEric J. et al. Antigen-Specific CD8 Lytic Phenotype Induced by Sipuleucel-T in Hormone-Sensitive or Castration-Resistant Prostate Cancer and Association with Overall Survival. CLIN CANCER RES. October 2018 doi: 10.1158/1078-0432.CCR-18-0638

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