Yuan Jianda, Ku Geoffrey Y, Gallardo Humilidad F, Orlandi Francesca, Manukian Gregor, Rasalan Teresa S, Xu Yinyan, Li Hao, Vyas Shachi, Mu Zhenyu, Chapman Paul B, Krown Susan E, Panageas Katherine, Terzulli Stephanie L, Old Lloyd J, Houghton Alan N, Wolchok Jedd D
Ludwig Center for Cancer Immunotherapy, Immunology Program, Sloan-Kettering Institute, New York, NY, USA.
Cancer Immun. 2009 Jun 5;9:5.
A differentiation antigen commonly expressed on melanoma cells, gp100 is the target of infiltrating T cells. We conducted a phase I randomized cross-over trial of melanoma patients with either xenogeneic (mouse) or human gp100 plasmid DNA injected intramuscularly at three dosages (100, 500 or 1,500 microg) every three weeks for three doses. After the first three injections, patients were then immunized three times with gp100 from the other species. Peripheral blood samples were analyzed at various time points following 10-day culture with gp100 peptides using multi-parametric flow cytometry. A total of 19 patients were enrolled, with 18 assessable for immune function and survival. 14 (74%) were male, with a median age of 56 years (range, 20-82). All patients had no evidence of disease; 10 (53%) had stage III disease, 3 each (16%) had stage IIB and IV disease, 2 (11%) had choroidal and 1 (5%) had anal mucosal involvement. With a median follow-up of 30 months, median progression-free survival (PFS) is 44 months. Median survival is not reached. There was no grade 3/4 toxicity; the most common grade 1/2 toxicity was an injection site reaction in 12 patients (63%, all grade 1). Five patients developed CD8+ cells binding gp100(280-288) HLA-A2-restricted tetramer. One patient had an increase in CD8+ IFN-gamma+ cells. This xenogeneic immunization strategy was safe and associated with minimal toxicity. There was also evidence of immune response.
糖蛋白100(gp100)是一种通常在黑色素瘤细胞上表达的分化抗原,是浸润性T细胞的靶标。我们对黑色素瘤患者进行了一项I期随机交叉试验,以三种剂量(100、500或1500微克)每三周肌肉注射一次异种(小鼠)或人gp100质粒DNA,共注射三剂。在前三次注射后,患者再用来自另一种物种的gp100免疫三次。在使用gp100肽进行10天培养后的不同时间点,使用多参数流式细胞术分析外周血样本。共招募了19名患者,其中18名可评估免疫功能和生存情况。14名(74%)为男性,中位年龄为56岁(范围20 - 82岁)。所有患者均无疾病证据;10名(53%)为III期疾病,各有3名(16%)为IIB期和IV期疾病,2名(11%)有脉络膜受累,1名(5%)有肛门黏膜受累。中位随访30个月,中位无进展生存期(PFS)为44个月。中位生存期未达到。没有3/4级毒性;最常见的1/2级毒性是12名患者(63%,均为1级)出现注射部位反应。5名患者产生了结合gp100(280 - 288)HLA - A2限制性四聚体的CD8 + 细胞。1名患者的CD8 + IFN - γ + 细胞增加。这种异种免疫策略是安全的,且毒性极小。也有免疫反应的证据。
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