• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

针对人类白血病的靶向T细胞疗法:对源自蛋白酶3的肽具有特异性的细胞毒性T淋巴细胞优先裂解人类髓系白血病细胞。

Targeted T-cell therapy for human leukemia: cytotoxic T lymphocytes specific for a peptide derived from proteinase 3 preferentially lyse human myeloid leukemia cells.

作者信息

Molldrem J, Dermime S, Parker K, Jiang Y Z, Mavroudis D, Hensel N, Fukushima P, Barrett A J

机构信息

Bone Marrow Transplant Unit, National Heart, Lung and Blood Institute, Bethesda, MD 20892-1652, USA.

出版信息

Blood. 1996 Oct 1;88(7):2450-7.

PMID:8839835
Abstract

Proteinase 3 is present in high concentration in the primary granules of acute and chronic myeloid leukemia blasts, and may represent a potential T-cell target antigen. We screened proteinase 3 against the binding motif of HLA-A2.1. Based on its high predicted binding, a 9-mer peptide, "PR-1," was synthesized and tested for binding to HLA-A2.1 using the T2 cell line. PR-1 at 100 micrograms/mL significantly increased expression of HLA-A2.1, with median channel of fluorescence increasing from 22 to 294. Binding half-life was determined to be 1,460 minutes by I125-labeled beta 2-microglobulin incorporation. HLA-A2.1+ peripheral blood mononuclear cells from a normal donor were used to generate a T-cell line specific for PR-1. The line demonstrated 85% PR-1-specific lysis at an E:T ratio of 50:1, compared with 20% lysis without PR-1, using T2 cells as targets. It also showed 79% specific lysis to fresh chronic myelogenous leukemia blasts, 54% to fresh acute myelogenous leukemia blasts, and only background lysis (< 20%) to HLA-A2.1+ normal allogeneic marrow cells. The amount of lysis of HLA-A2.1+ myeloid cells was proportional to cytoplasmic proteinase 3 expression. Thus, HLA-A2.1-restricted cytotoxic T cells, raised against a peptide contained in proteinase 3, preferentially lysed fresh human leukemic cells.

摘要

蛋白酶3在急性和慢性髓细胞白血病母细胞的初级颗粒中高浓度存在,可能代表一种潜在的T细胞靶抗原。我们针对HLA - A2.1的结合基序筛选了蛋白酶3。基于其高预测结合能力,合成了一种9聚体肽“PR - 1”,并使用T2细胞系检测其与HLA - A2.1的结合。100微克/毫升的PR - 1显著增加了HLA - A2.1的表达,荧光中位数通道从22增加到294。通过掺入I125标记的β2 -微球蛋白测定结合半衰期为1460分钟。使用来自正常供体的HLA - A2.1 +外周血单个核细胞生成了对PR - 1特异的T细胞系。以T2细胞为靶细胞,在E:T比为50:1时,该细胞系对PR - 1的特异性裂解率为85%,而无PR - 1时裂解率为20%。它对新鲜慢性髓性白血病母细胞的特异性裂解率为79%,对新鲜急性髓性白血病母细胞的特异性裂解率为54%,对HLA - A2.1 +正常同种异体骨髓细胞仅为背景裂解(<20%)。HLA - A2.1 +髓细胞的裂解量与细胞质蛋白酶3的表达成正比。因此,针对蛋白酶3中所含肽产生的HLA - A2.1限制性细胞毒性T细胞优先裂解新鲜的人类白血病细胞。

相似文献

1
Targeted T-cell therapy for human leukemia: cytotoxic T lymphocytes specific for a peptide derived from proteinase 3 preferentially lyse human myeloid leukemia cells.针对人类白血病的靶向T细胞疗法:对源自蛋白酶3的肽具有特异性的细胞毒性T淋巴细胞优先裂解人类髓系白血病细胞。
Blood. 1996 Oct 1;88(7):2450-7.
2
Cytotoxic T lymphocytes specific for a nonpolymorphic proteinase 3 peptide preferentially inhibit chronic myeloid leukemia colony-forming units.对一种非多态性蛋白酶3肽具有特异性的细胞毒性T淋巴细胞优先抑制慢性髓性白血病集落形成单位。
Blood. 1997 Oct 1;90(7):2529-34.
3
A PR1-human leukocyte antigen-A2 tetramer can be used to isolate low-frequency cytotoxic T lymphocytes from healthy donors that selectively lyse chronic myelogenous leukemia.PR1-人白细胞抗原A2四聚体可用于从健康供体中分离出能选择性裂解慢性粒细胞白血病的低频细胞毒性T淋巴细胞。
Cancer Res. 1999 Jun 1;59(11):2675-81.
4
PR1-specific cytotoxic T lymphocytes are relatively frequent in umbilical cord blood and can be effectively expanded to target myeloid leukemia.PR1特异性细胞毒性T淋巴细胞在脐带血中相对常见,并且可以有效地扩增以靶向髓系白血病。
Cytotherapy. 2016 Aug;18(8):995-1001. doi: 10.1016/j.jcyt.2016.05.007.
5
Allorestricted cytotoxic T cells specific for human CD45 show potent antileukemic activity.对人类CD45特异的异体限制性细胞毒性T细胞表现出强大的抗白血病活性。
Blood. 2003 Feb 1;101(3):1007-14. doi: 10.1182/blood-2002-02-0525. Epub 2002 Sep 12.
6
Human cytotoxic T-lymphocyte responses specific for peptides of the wild-type Wilms' tumor gene (WT1 ) product.对野生型肾母细胞瘤基因(WT1)产物的肽具有特异性的人细胞毒性T淋巴细胞反应。
Immunogenetics. 2000 Feb;51(2):99-107. doi: 10.1007/s002510050018.
7
A novel TCR-like CAR with specificity for PR1/HLA-A2 effectively targets myeloid leukemia in vitro when expressed in human adult peripheral blood and cord blood T cells.一种对PR1/HLA - A2具有特异性的新型TCR样嵌合抗原受体(CAR),当在成人外周血和脐带血T细胞中表达时,可在体外有效靶向髓系白血病。
Cytotherapy. 2016 Aug;18(8):985-994. doi: 10.1016/j.jcyt.2016.05.001. Epub 2016 Jun 2.
8
In vitro generation of human cytotoxic T lymphocytes specific for peptides derived from prostate-specific antigen.体外产生对源自前列腺特异性抗原的肽具有特异性的人细胞毒性T淋巴细胞。
J Natl Cancer Inst. 1997 Feb 19;89(4):293-300. doi: 10.1093/jnci/89.4.293.
9
HLA-A2-restricted cytotoxic T lymphocyte epitopes from human hepsin as novel targets for prostate cancer immunotherapy.人组织蛋白酶 H 的 HLA-A2 限制性细胞毒性 T 淋巴细胞表位作为前列腺癌免疫治疗的新靶点。
Scand J Immunol. 2013 Sep;78(3):248-57. doi: 10.1111/sji.12083.
10
Identification and characterization of epitopes of the receptor for hyaluronic acid-mediated motility (RHAMM/CD168) recognized by CD8+ T cells of HLA-A2-positive patients with acute myeloid leukemia.急性髓系白血病HLA - A2阳性患者CD8 + T细胞识别的透明质酸介导的运动受体(RHAMM/CD168)表位的鉴定与表征
Blood. 2005 Aug 1;106(3):938-45. doi: 10.1182/blood-2004-12-4787. Epub 2005 Apr 12.

引用本文的文献

1
CAR-T cell therapy for treatment of acute myeloid leukemia, advances and outcomes.嵌合抗原受体T细胞疗法治疗急性髓系白血病:进展与结果
Mol Ther. 2025 Jun 4;33(6):2441-2453. doi: 10.1016/j.ymthe.2025.03.052. Epub 2025 Apr 2.
2
Hu8F4-CAR T cells with mutated Fc spacer segment improve target specificity and mediate anti-leukemia activity in vivo.Hu8F4-CAR T 细胞具有突变的 Fc 间隔区片段,可提高靶向特异性,并在体内介导抗白血病活性。
Cytotherapy. 2024 Nov;26(11):1331-1340. doi: 10.1016/j.jcyt.2024.06.010. Epub 2024 Jul 3.
3
Hu8F4-CAR T cells with mutated Fc spacer segment improve target-specificity and mediate anti-leukemia activity .
具有突变Fc间隔区片段的Hu8F4嵌合抗原受体T细胞可提高靶向特异性并介导抗白血病活性。
Res Sq. 2024 Feb 19:rs.3.rs-3937972. doi: 10.21203/rs.3.rs-3937972/v1.
4
Estrogen Receptor Mutations as Novel Targets for Immunotherapy in Metastatic Estrogen Receptor-positive Breast Cancer.雌激素受体突变作为转移性雌激素受体阳性乳腺癌免疫治疗的新靶点。
Cancer Res Commun. 2024 Feb 22;4(2):496-504. doi: 10.1158/2767-9764.CRC-23-0244.
5
Vaccines: a promising therapy for myelodysplastic syndrome.疫苗:骨髓增生异常综合征有希望的治疗方法。
J Hematol Oncol. 2024 Jan 8;17(1):4. doi: 10.1186/s13045-023-01523-4.
6
Allogeneic Tumor Antigen-Specific T Cells for Broadly Applicable Adoptive Cell Therapy of Cancer.用于癌症广泛适用的过继性细胞疗法的同种异体肿瘤抗原特异性T细胞
Cancer Treat Res. 2022;183:131-159. doi: 10.1007/978-3-030-96376-7_4.
7
Novel TCR-like CAR-T cells targeting an HLA∗0201-restricted SSX2 epitope display strong activity against acute myeloid leukemia.靶向HLA∗0201限制性SSX2表位的新型TCR样CAR-T细胞对急性髓系白血病显示出强大活性。
Mol Ther Methods Clin Dev. 2021 Oct 1;23:296-306. doi: 10.1016/j.omtm.2021.09.008. eCollection 2021 Dec 10.
8
Trial Watch: Adoptive TCR-Engineered T-Cell Immunotherapy for Acute Myeloid Leukemia.试验观察:过继性T细胞受体工程化T细胞免疫疗法治疗急性髓系白血病
Cancers (Basel). 2021 Sep 8;13(18):4519. doi: 10.3390/cancers13184519.
9
Novel myeloperoxidase-derived HLA-A2-restricted peptides as therapeutic targets against myeloid leukemia.新型髓过氧化物酶衍生的 HLA-A2 限制性肽作为治疗髓性白血病的靶点。
Cytotherapy. 2021 Sep;23(9):793-798. doi: 10.1016/j.jcyt.2021.05.003. Epub 2021 Jun 30.
10
Myelodysplastic syndrome and immunotherapy novel to next in-line treatments.骨髓增生异常综合征和免疫疗法——下一个新兴的治疗方法。
Hum Vaccin Immunother. 2021 Aug 3;17(8):2602-2616. doi: 10.1080/21645515.2021.1898307. Epub 2021 May 3.