Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Crit Rev Immunol. 2021;41(2):101-106. doi: 10.1615/CritRevImmunol.2021037614.
Harnessing natural killer (NK) cell activity, either endogenous NK or NK-cell-based therapy, is in the forefront development for many tumor types. There are compelling clinical evidence demonstrating the significant relevance of loss of NK cell activity with prostate cancer (PCa) disease progression to the lethal phenotype, metastatic castration-resistant PCa (mCRPC). Given that mCRPC is generally regarded as a "cold" tumor and has only elicited marginal response to immune checkpoint blockade therapy to revive CD8 T cell activity, NK cell targeted therapy may present a viable opportunity not only to directly target mCRPC and also to "fire up" the cold mCRPC tumor. However, current efforts on harnessing NK cell activity for treating mCRPC is very limited with only one open NK-cell-based clinical trial. This minireview will present the clinical significance of NK cell activity in controlling metastatic PCa and provide perspectives on harnessing NK cell activity for treating mCRPC.
利用自然杀伤 (NK) 细胞活性,无论是内源性 NK 细胞还是基于 NK 细胞的治疗,都是许多肿瘤类型的前沿发展方向。有令人信服的临床证据表明,NK 细胞活性的丧失与前列腺癌 (PCa) 疾病进展到致命表型、转移性去势抵抗性 PCa (mCRPC) 之间存在显著相关性。鉴于 mCRPC 通常被认为是一种“冷”肿瘤,并且对免疫检查点阻断疗法仅引起微弱的反应以恢复 CD8 T 细胞活性,NK 细胞靶向治疗不仅可能提供直接针对 mCRPC 的机会,而且还可能“激发”冷 mCRPC 肿瘤。然而,目前利用 NK 细胞活性治疗 mCRPC 的努力非常有限,只有一项开放的基于 NK 细胞的临床试验。这篇迷你综述将介绍 NK 细胞活性在控制转移性 PCa 中的临床意义,并就利用 NK 细胞活性治疗 mCRPC 提供观点。