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WT1 肽疫苗治疗血液系统恶性肿瘤:从 CTL 表位鉴定到包括治愈策略在内的临床研究最新进展。

Wilms' Tumor Gene 1 (WT1) Peptide Vaccine Therapy for Hematological Malignancies: From CTL Epitope Identification to Recent Progress in Clinical Studies Including a Cure-Oriented Strategy.

机构信息

Department of Cancer Stem Cell Biology, Osaka University Graduate School of Medicine, Suita, Japan.

出版信息

Oncol Res Treat. 2017;40(11):682-690. doi: 10.1159/000481353. Epub 2017 Oct 18.

DOI:10.1159/000481353
PMID:29041012
Abstract

The identification of human Wilms' tumor gene 1 (WT1) protein-derived cytotoxic T lymphocyte (CTL) epitopes and the in vivo efficacy of WT1 peptide-based immunotherapy in a mouse model were reported in 2000. This successful basic research led to clinical studies of a WT1 peptide vaccine, and a positive impact on clinical response was first demonstrated in 2003 in the form of a reduction in blast cells of vaccine-treated patients with myelodysplastic syndromes (MDS). Since then, data on WT1 peptide vaccine-treated patients with immunological and/or clinical response have been accumulated. MDS and acute myeloid leukemia were the major target diseases to provide proof of concept for the therapeutic potential of the WT1 peptide vaccine. WT1 vaccination-induced clinical responses or usefulness were also shown for chronic myeloid leukemia, multiple myeloma, and acute lymphoblastic leukemia, as well as various types of solid cancers. Non-Hodgkin's lymphoma and myeloproliferative neoplasms may also be target diseases because of their WT1 expression. Of note, recent clinical studies have demonstrated that patients with hematological malignancies who have minimal residual disease after chemotherapy or allogeneic hematopoietic stem cell transplantation may be cured by WT1 peptide vaccination. Further enhancement of the efficacy and usefulness of the WT1 peptide vaccine is expected.

摘要

2000 年报道了人类肾母细胞瘤 1 基因(WT1)蛋白衍生的细胞毒性 T 淋巴细胞(CTL)表位的鉴定,以及 WT1 肽免疫疗法在小鼠模型中的体内疗效。这项成功的基础研究导致了 WT1 肽疫苗的临床研究,2003 年首次证明了 WT1 肽疫苗在骨髓增生异常综合征(MDS)患者中的疗效,表现为疫苗治疗组患者原始细胞减少。此后,积累了 WT1 肽疫苗治疗具有免疫和/或临床反应患者的数据。MDS 和急性髓系白血病是主要的目标疾病,为 WT1 肽疫苗的治疗潜力提供了概念验证。WT1 疫苗接种诱导的临床反应或有效性也在慢性髓系白血病、多发性骨髓瘤和急性淋巴细胞白血病以及各种类型的实体瘤中得到证实。非霍奇金淋巴瘤和骨髓增生性肿瘤也可能是目标疾病,因为它们表达 WT1。值得注意的是,最近的临床研究表明,化疗或异基因造血干细胞移植后有微小残留病的血液系统恶性肿瘤患者可能通过 WT1 肽疫苗接种治愈。预计 WT1 肽疫苗的疗效和有效性将进一步提高。

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