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Identification of novel leukemia associated antigen which may useful for immunotherapy of leukemia patients

Identification of novel leukemia associated antigen which may useful for immunotherapy of leukemia patients
新型白血病相关抗原的鉴定可用于白血病患者的免疫治疗
批准号:
15590997
负责人:
FURUKAWA Tatsuo
金额:
$2.24万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2004

项目摘要

项目成果

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相关文献

中文摘要
翻译
1.通过重组表达克隆(SEREX)方法的抗原血清学鉴定已经成功地鉴定了许多引起体液免疫应答的肿瘤抗原。在本研究中,我们定义了一种新的抗原,引起白血病患者的体液免疫反应,并在白血病细胞中过表达。Apg-1可诱导白血病患者产生体液免疫应答,有望成为白血病抗原特异性免疫治疗的新靶点。2.采用体外转录mRNA电穿孔基因转染技术,建立了负载抗原的DC激活的CTL细胞株。然而,我们没有检测到这种活化的T细胞对白血病细胞系的任何细胞毒活性。3.随后,我们通过计算机计算鉴定了Apg-1编码的四个具有HLA-A24结合基序的9聚体肽。其中一种多肽能有效地杀伤同时表达Apg-1和HLA-A_(24)的白血病细胞系。我们的结果提示Apg-1抗原可能是白血病相关抗原之一。
英文摘要
1.Serological identification of antigens by the recombinant expression cloning (SEREX) method has successfully identified many tumor antigens that elicit humoral immune response. In the present study, we defined a novel antigen that elicited humoral immune response in patients with leukemia and that was overexpressed in leukemia cells. Apg-1 can elicit humoral immune responses in leukemia patients and might be potential novel targets for antigen-specific immunotherapy for leukemia.2.Using in vitro transcripted mRNA electroporation gene delivery, we developed CTL line activated by the antigen loading DC. However, we could not detect any cytotoxic activity in this activated T cells for leukemic cell line.3.Thereafter, we identified four 9-mer peptides with HLA-A24-binding motifs encoded by Apg-1 using computer calculation. Of these, one peptide developed efficiently effector cells which lysed leukemic cell line expressing both Apg-1 and HLA-A24.Our results indicate that Apg-1 antigen may be one of leukemia associated antigens.
期刊论文(9)
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科研奖励(0)
会议论文
DOI: 10.1385/mo:20:4:335
发表时间: 2003
期刊: Medical Oncology
影响因子: 3.4
作者: [Masuhiro Takahashi;M. Narita;F. Ayres;Naoko Satoh;T. Abe;Toshio Yanao;T. Furukawa;K. Toba;T. Hirohashi;Y. Aizawa]
通讯作者: Masuhiro Takahashi;M. Narita;F. Ayres;Naoko Satoh;T. Abe;Toshio Yanao;T. Furukawa;K. Toba;T. Hirohashi;Y. Aizawa
The effects of STI571 on antigen presentation of dendritic cells generated from patients with chronic myelogenous leukemia
STI571对慢性粒细胞白血病患者产生的树突状细胞抗原呈递的影响
DOI: --
发表时间: 2003
期刊: Hematol Oncol 21
影响因子: --
作者: [Sato N]
通讯作者: Sato N
Human dendritic cells mediate anti-tumor activity against hematopoietic tumor cells without direct contact and Fas/FasL killing pathway.
人树突状细胞介导针对造血肿瘤细胞的抗肿瘤活性,无需直接接触和Fas/FasL杀伤途径。
DOI: --
发表时间: 2004
期刊: Oncol Rep 11
影响因子: --
作者: [広松雄治, Sato N, 広松雄治, Ayres FM]
通讯作者: Ayres FM
High-dose cytosine arabinoside and etoposide with total body irradiation as a preparatory regimen for allogeneic hematopoietic stem-cell transplantation in patients with acute lymphoblastic leukemia.
大剂量阿糖胞苷和依托泊苷全身照射作为急性淋巴细胞白血病患者异基因造血干细胞移植的准备方案。
DOI: --
发表时间: 2004
期刊: Bone Marrow Transplant 34
影响因子: --
作者: [Sato N]
通讯作者: Sato N
Analysis of the novel gene identified using a SEREX method in the senrm of bone marrow failure patients
  • 批准号:
    18591048
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $2.49万
  • 财政年份:
    2006
  • 负责人:
    FURUKAWA Tatsuo
  • 依托单位:
The effects of hematopoietic cytokines, and the changes of transcriptional factors during the proliferation, differentiation, and maturation of basophilic and eosinophilic progenitors
  • 批准号:
    09671102
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $1.92万
  • 财政年份:
    1997
  • 负责人:
    FURUKAWA Tatsuo
  • 依托单位:
Involvement of neuropeptides and amino acids in central regulation of blood pressure.
  • 批准号:
    63480121
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
  • 资助金额:
    $3.2万
  • 财政年份:
    1988
  • 负责人:
    FURUKAWA Tatsuo
  • 依托单位:
Role of neuropeptides and neuroamino acids in central regulation of blood pressure
  • 批准号:
    59480123
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
  • 资助金额:
    $4.1万
  • 财政年份:
    1984
  • 负责人:
    FURUKAWA Tatsuo
  • 依托单位:
国内基金
海外基金
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  • 批准号:
    MS25H310003
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
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  • 批准号:
    2025JJ50652
  • 项目类别:
    省市级项目
  • 资助金额:
    --
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    2025
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    吴伟民
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CD4+ CTL通过杀伤抗原呈递细胞减轻放射性脑损伤的作用及机制研究
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  • 项目类别:
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  • 资助金额:
    15.0万元
  • 批准年份:
    2024
  • 负责人:
    石中山
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E3泛素连接酶Ctl-b通过DBC1/SIRT1轴调控小胶质细胞NLRP3炎性小体在老年PND中的作用及机制研究
  • 批准号:
    --
  • 项目类别:
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  • 批准年份:
    2024
  • 负责人:
    陈勇
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