Salgaller M L, Lodge P A, McLean J G, Tjoa B A, Loftus D J, Ragde H, Kenny G M, Rogers M, Boynton A L, Murphy G P
Northwest Biotherapeutics, L.L.C., Pacific Northwest Cancer Foundation, Seattle, Washington 98125, USA.
Prostate. 1998 May;35(2):144-51. doi: 10.1002/(sici)1097-0045(19980501)35:2<144::aid-pros8>3.0.co;2-j.
In this paper we describe our program for the immune monitoring of phase II participants given dendritic cell (DC)/prostate-specific membrane antigen (PSMA)-based immunotherapy, and we also present some initial findings.
Phase II subjects received six administrations of autologous dendritic cells exogenously pulsed with two peptides derived from PSMA. Prior to the initial infusion, and following each treatment, peripheral blood mononuclear cells (PBMC) were collected for the generation of dendritic cells as well as for comprehensive immune monitoring.
Thus far, an increase in PSMA-peptide-specific as well as overall cellular reactivity has been observed in several patients receiving DC plus PSM-P1 and -P2, as measured by delayed-type hypersensitivity (DTH) test and enzyme-linked immunosorbant assay (ELISA).
Our initial observations using an ELISA and DTH test indicate that we are enhancing cellular immunity in prostate cancer patients following infusion with DC plus PSMA-derived peptides. Several methods are underway to comprehensively monitor both cell-mediated and humoral immune responsiveness, including: determining anti-PSMA serum antibody titers, testing immunogen-restricted responder-cell proliferation and cytotoxicity, assessing aberrations in signal transduction, antigen processing, and presentation, and measuring soluble factors that may promote tumor outgrowth.
在本文中,我们描述了针对接受基于树突状细胞(DC)/前列腺特异性膜抗原(PSMA)免疫疗法的II期参与者的免疫监测计划,并展示了一些初步研究结果。
II期受试者接受了六次用两种源自PSMA的肽进行外源性脉冲处理的自体树突状细胞给药。在首次输注前以及每次治疗后,收集外周血单核细胞(PBMC)用于生成树突状细胞以及进行全面的免疫监测。
到目前为止,通过迟发型超敏反应(DTH)试验和酶联免疫吸附测定(ELISA)测量,在几名接受DC加PSM - P1和 - P2治疗的患者中观察到PSMA肽特异性以及总体细胞反应性增加。
我们使用ELISA和DTH试验的初步观察结果表明,在向前列腺癌患者输注DC加PSMA衍生肽后,我们正在增强其细胞免疫力。目前正在采用多种方法全面监测细胞介导和体液免疫反应性,包括:测定抗PSMA血清抗体滴度、检测免疫原限制的反应细胞增殖和细胞毒性、评估信号转导、抗原加工和呈递中的异常情况,以及测量可能促进肿瘤生长的可溶性因子。