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首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Induction of Immune Response after Allogeneic Wilms' Tumor 1 Dendritic Cell Vaccination and Donor Lymphocyte Infusion in Patients with Hematologic Malignancies and Post-Transplantation Relapse
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Induction of Immune Response after Allogeneic Wilms' Tumor 1 Dendritic Cell Vaccination and Donor Lymphocyte Infusion in Patients with Hematologic Malignancies and Post-Transplantation Relapse

机译:血液系统恶性肿瘤和移植后复发的同种异体肿瘤瘤1树突状细胞疫苗接种和供体淋巴细胞输注后免疫反应的诱导。

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摘要

Relapse of hematologic malignancies is the primary cause of treatment failure after allogeneic hematopoietic stem cell transplantation (HCT). Treatment for post-HCT relapse using donor lymphocyte infusion (DLI) has limited utility, particularly in the setting of acute leukemia, and can result in the development of graft versus-host disease (GVHD). The Wilms' tumor 1 (WTI) gene product is a tumor-associated antigen that is expressed in acute leukemia and other hematologic malignancies, with limited expression in normal tissues. In this pilot trial, we assessed safety and feasibility of a WTI peptide-loaded donor-derived dendritic cell (DC) vaccine given with DLI designed to enhance and direct the graft-versus-leukemia effect. Secondary objectives were to evaluate immunologic and clinical responses. A total of 5 subjects, median age 17 years (range, 9 to 19 years), with post-HCT relapse were enrolled. Disease subtypes included acute lymphoblastic leukemia (n =3), acute myelogenous leukemia (n = 1), and Hodgkin lymphoma (n=1). Successful vaccine production was feasible from all donors. DC vaccination and DLI were well tolerated. One recipient developed grade 1 skin GVHD not requiring systemic therapy. The most common adverse events included grade 1 reversible pain and pruritus at the vaccine injection and delayed-type hypersensitivity (DTH) skin testing sites. There were no grade 3 or higher adverse events related to the research. Immune responses consisted of ELISpot response in 3 recipients and positive DTH tests to WTI peptide cocktail in 2 subjects. Our study provides 1 of the first attempts to apply tumor-specific vaccine therapy to the allogeneic setting. Preliminary results show the DC-based vaccination is safe and feasible after allogeneic HCT, with a suggestion that this approach can be used to sensitize the repopulated allogeneic-donor immune system to WT1. Future directions may include testing of vaccination strategies in the early post-transplantation setting for relapse prevention. Published by Elsevier Inc. on behalf of the American Society for Blood and Marrow Transplantation.
机译:血液恶性肿瘤的复发是同种异体造血干细胞移植(HCT)后治疗失败的主要原因。使用供体淋巴细胞输注(DLI)治疗HCT后复发的用途有限,尤其是在急性白血病的情况下,并且可能导致发生移植物抗宿主病(GVHD)。 Wilms'肿瘤1(WTI)基因产物是一种与肿瘤相关的抗原,在急性白血病和其他血液系统恶性肿瘤中表达,在正常组织中表达有限。在该试验性试验中,我们评估了带有DLI的WTI肽加载的供体来源的树突状细胞(DC)疫苗的安全性和可行性,该疫苗旨在增强和指导移植物抗白血病作用。次要目标是评估免疫和临床反应。总共招募了5名受试者,中位年龄17岁(9至19岁),且HCT后复发。疾病亚型包括急性淋巴细胞白血病(n = 3),急性骨髓性白血病(n = 1)和霍奇金淋巴瘤(n = 1)。所有捐助者都可以成功生产疫苗。 DC疫苗接种和DLI耐受性良好。一位接受者开发出不需要系统治疗的1级皮肤GVHD。最常见的不良事件包括疫苗注射和延迟型超敏反应(DTH)皮肤测试部位的1级可逆性疼痛和瘙痒。没有与该研究相关的3级或更高的不良事件。免疫反应包括3位接受者的ELISpot反应和2位受试者对WTI肽混合物的DTH阳性试验。我们的研究提供了将肿瘤特异性疫苗疗法应用于同种异体环境的首次尝试之一。初步结果表明,异基因HCT后基于DC的疫苗接种是安全可行的,这表明该方法可用于使重新填充的异基因供体免疫系统对WT1敏感。未来的方向可能包括在移植后的早期阶段测试疫苗接种策略以预防复发。由Elsevier Inc.代表美国血液和骨髓移植学会出版。

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