• 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

Treatment of human B-cell precursor leukemia in SCID mice by using a combination of the anti-CD19 immunotoxin B43-PAP with the standard chemotherapeutic drugs vincristine, methylprednisolone, and L-asparaginase.

作者信息

Ek O, Gaynon P, Zeren T, Chelstrom L M, Myers D E, Uckun F M

机构信息

Biotherapy Program, University of Minnesota, Minneapolis, USA.

出版信息

Leuk Lymphoma. 1998 Sep;31(1-2):143-9. doi: 10.3109/10428199809057594.

DOI:10.3109/10428199809057594
PMID:9720724
Abstract

We have compared the antileukemic activity of the investigational biotherapeutic agent B43-PAP to the antileukemic activities of the standard chemotherapeutic drugs vincristine (VCR), methylprednisolone (PDN), L-asparaginase (L-ASP) as single agents as well as in a 3-drug combination regimen ("VPL") using a SCID mouse model of human B-cell precursor (BCP) acute lymphoblastic leukemia (ALL). When mice (N = 95) were challenged with 1 x 10(6) NALM-6 leukemia cells, all of them died of disseminated leukemia with a median event-free survival (EFS) of 47 +/- 6 days. B43-PAP was more active than VCR, PDN, or L-ASP and the two-drug combinations VCR + B43-PAP, PDN + B43-PAP, or L-ASP + B43-PAP were not significantly more active than B43-PAP. The 120 days EFS outcome results were 46 +/- 13% for B43-PAP (Median EFS = 92 +/- 22 days), 0 +/- 0% for VCR (Median EFS = 49 +/- 1 days), 40 +/- 22% for PDN (Median EFS = 100 +/- 20 days), 0 +/- 0% for L-ASP (Median EFS = 41 +/- 1 days), 60 +/- 22% for VCR + B43-PAP (Median EFS = >120 days), 60 +/- 22% for PDN + B43-PAP (Median EFS = >120 days), and 50 +/- 25% for L-ASP + B43-PAP (Median EFS = 93 +/- 27 days), When mice (N = 61) were challenged with 5 x 10(6) NALM-6 cells, all of them rapidly died of disseminated leukemia with a median EFS of 37 +/- 3 days. The 3-drug combination "VPL" (Median EFS = 75 +/- 23 days) was slightly less active than B43-PAP (Median EFS = 84 +/- 19 days) (P = 0.09). Notably, the combination of "VPL" with B43-PAP (i.e., VPLB) resulted in 100% survival. By comparison, the combination of "VPL" with daunorubicin (i.e., VPLD) (Median EFS = 69 +/- 31 days) was not more active than VPL. To our knowledge, this preclinical study is the first to demonstrate the feasibility and superb antileukemic activity of immunochemotherapy using anti-CD19 immunotoxin in combination with the standard 3-drug combination "VPL" against BCP ALL.

摘要

相似文献

1
Treatment of human B-cell precursor leukemia in SCID mice by using a combination of the anti-CD19 immunotoxin B43-PAP with the standard chemotherapeutic drugs vincristine, methylprednisolone, and L-asparaginase.
Leuk Lymphoma. 1998 Sep;31(1-2):143-9. doi: 10.3109/10428199809057594.
2
Effective immunochemotherapy of CALLA+C mu+ human pre-B acute lymphoblastic leukemia in mice with severe combined immunodeficiency using B43 (anti-CD19) pokeweed antiviral protein immunotoxin plus cyclophosphamide.使用B43(抗CD19)商陆抗病毒蛋白免疫毒素联合环磷酰胺对严重联合免疫缺陷小鼠体内的CALLA+Cμ+人前B急性淋巴细胞白血病进行有效的免疫化学疗法。
Blood. 1992 Jun 15;79(12):3116-29.
3
In vivo efficacy of B43 (anti-CD19)-pokeweed antiviral protein immunotoxin against human pre-B cell acute lymphoblastic leukemia in mice with severe combined immunodeficiency.B43(抗CD19)-商陆抗病毒蛋白免疫毒素对重症联合免疫缺陷小鼠体内人前B细胞急性淋巴细胞白血病的疗效
Blood. 1992 May 1;79(9):2201-14.
4
Effective immunochemotherapy of human t(4;11) leukemia in mice with severe combined immunodeficiency (SCID) using B43 (anti-CD19)-pokeweed antiviral protein immunotoxin plus cyclophosphamide.使用B43(抗CD19)-商陆抗病毒蛋白免疫毒素联合环磷酰胺对重症联合免疫缺陷(SCID)小鼠体内的人t(4;11)白血病进行有效的免疫化学治疗。
Leukemia. 1993 Feb;7(2):290-7.
5
Combined therapeutic efficacy of the thymidylate synthase inhibitor ZD1694 (Tomudex) and the immunotoxin B43(anti-CD19)-PAP in a SCID mouse model of human B-lineage acute lymphoblastic leukemia.
Leuk Lymphoma. 1998 Feb;28(5-6):509-14. doi: 10.3109/10428199809058358.
6
Evaluation of temozolomide in a SCID mouse model of human B-cell precursor leukemia.替莫唑胺在人B细胞前体白血病SCID小鼠模型中的评估
Leuk Lymphoma. 1999 Apr;33(3-4):289-93. doi: 10.3109/10428199909058428.
7
Treatment of human B-cell precursor leukemia in SCID mice using a combination of the investigational biotherapeutic agent B43-PAP with cytosine arabinoside.使用研究性生物治疗药物B43-PAP与阿糖胞苷联合治疗重症联合免疫缺陷(SCID)小鼠的人B细胞前体白血病。
Clin Cancer Res. 1996 Sep;2(9):1533-42.
8
Feasibility Study of a Novel Experimental Induction Protocol Combining B43-PAP (Anti-CD19) Immunotoxin With Standard Induction Chemotherapy in Children and Adolescents With Relapsed B-Lineage ALL: A Report From the Children's Oncology Group.儿童肿瘤研究组报告:一种将B43-PAP(抗CD19)免疫毒素与标准诱导化疗相结合的新型实验诱导方案用于复发B系急性淋巴细胞白血病儿童和青少年的可行性研究
J Immunother. 2015 Sep;38(7):299-305. doi: 10.1097/CJI.0000000000000088.
9
Toxicity profile of the investigational new biotherapeutic agent, B43 (anti-CD19)-pokeweed antiviral protein immunotoxin.
Leuk Lymphoma. 1996 Jun;22(1-2):61-70, follow.186, color plate II-V. doi: 10.3109/10428199609051729.
10
In vitro and in vivo antileukemic activity of B43-pokeweed antiviral protein against radiation-resistant human B-cell precursor leukemia cells.B43-商陆抗病毒蛋白对辐射抗性人B细胞前体白血病细胞的体外和体内抗白血病活性
Blood. 1995 Dec 1;86(11):4228-33.

引用本文的文献

1
Immunotoxins constructed with ribosome-inactivating proteins and their enhancers: a lethal cocktail with tumor specific efficacy.免疫毒素由核糖体失活蛋白及其增强子构建:具有肿瘤特异性疗效的致命鸡尾酒。
Curr Pharm Des. 2014;20(42):6584-643. doi: 10.2174/1381612820666140826153913.
2
The anti-CD19 antibody-drug conjugate SAR3419 prevents hematolymphoid relapse postinduction therapy in preclinical models of pediatric acute lymphoblastic leukemia.抗 CD19 抗体药物偶联物 SAR3419 可预防儿科急性淋巴细胞白血病诱导治疗后血液和淋巴系统的复发。
Clin Cancer Res. 2013 Apr 1;19(7):1795-805. doi: 10.1158/1078-0432.CCR-12-3613. Epub 2013 Feb 20.
3
Pharmacokinetic modeling of an induction regimen for in vivo combined testing of novel drugs against pediatric acute lymphoblastic leukemia xenografts.
新型药物抗小儿急性淋巴细胞白血病异种移植物体内联合检测诱导方案的药代动力学模型建立。
PLoS One. 2012;7(3):e33894. doi: 10.1371/journal.pone.0033894. Epub 2012 Mar 29.
4
Novel molecular and cellular therapeutic targets in acute lymphoblastic leukemia and lymphoproliferative disease.急性淋巴细胞白血病和淋巴增殖性疾病中的新型分子与细胞治疗靶点。
Immunol Res. 2008;42(1-3):84-105. doi: 10.1007/s12026-008-8038-9.
5
The mTOR inhibitor CCI-779 induces apoptosis and inhibits growth in preclinical models of primary adult human ALL.mTOR抑制剂CCI-779在原发性成人人类急性淋巴细胞白血病的临床前模型中可诱导细胞凋亡并抑制生长。
Blood. 2006 Feb 1;107(3):1149-55. doi: 10.1182/blood-2005-05-1935. Epub 2005 Sep 29.