期刊文献+

基于CAB技术的新型Axl抗体偶联药物——BA3011 被引量:1

New Axl antibody drug conjugate based on CAB technology——BA3011
原文传递
导出
摘要 BA3011(CAB-AXL-ADC)是BioAtla公司开发的新型肿瘤微环境条件性激活的Axl受体靶向抗体偶联药物。其抗体部分通过条件性激活技术(conditionally active biologics,CAB)改造后,能选择性靶向于肿瘤组织的Axl受体。BA3011已获批进行Ⅰ/Ⅱ期临床试验,适应证包括非小细胞肺癌、去势抵抗性前列腺癌和胰腺癌等晚期实体瘤。BA3011是首个进入临床试验的CAB产品,标志着CAB由技术研发阶段跨入产品开发阶段。本文就Axl受体为靶标的药物,CAB技术和BA3011的临床进展情况作一概述。 BA3011(CAB-AXL-ADC) is a novel tumor microenvironment conditionally activated Axl receptortargeting antibody-drug conjugate developed by BioAtla Its antibody part was modified by conditionally active biologies(CAB), which selectively acts on the Axl receptor in tumor tissues. BA3011 has been approved for Phase Ⅰ/Ⅱ clinical trials. The indications include advanced solid tumors. such as non-small cell lung cancer, castration-resistant prostate cancer, and pancreatic cancer. BA3011 is the first CAB product entering clinical trials, indicating CAB technology has matured. Drugs target of Axl receptor, CAB technology and clinical progress of BA3011 were reviewed in this article.
作者 李微 王彦明 肖典 LI Wei;WANG Yan-ming;XIAO Dian(National Engineering and Technology Center of Emergency Prevention and Control Drugs,Chinese PLA Academy of Military Medical Sci-ences,Beijing 100850,China)
出处 《临床药物治疗杂志》 2018年第6期29-31,51,共4页 Clinical Medication Journal
关键词 Axl受体 条件性激活技术 抗体偶联药物 Axl repceptor conditionally active biologics antibody-drug conjugate
  • 相关文献

参考文献4

二级参考文献91

  • 1RESCIGNO J, MANSUKHANI A, BASILICO C. A putative re- ceptor tyrosine kinase with unique structural topology [ J]. Onco- gene,1991,6(10) :1909 - 1913.
  • 2JANSSEN J, SCHULZ A, STEENVOORDEN A, et al. A novel putative tyrosine kinase receptor with oncogenic potential [ J ]. Oncogene,1991,6( 11 ) :2113 - 2120.
  • 3LA1 C, LEMKE G. An extended family of protein-tyrosine kinase genes differentially expressed in the vertebrate nervous system [ J ]. Neuron,1991,6(5):691 -704.
  • 4STITT TN, CONN G, GORE M, et al. The anticoagulation factor protein S and its relative, gas6, are ligands for the tyro 3/Axl family of receptor tyrosine kinases [ J ]. Cell, 1995,80 (4) : 661 - 670.
  • 5CHEN J, CAREY K, GODOWSKI PJ. Identification of Gas6 as a ligand for Mer, a neural cell adhesion molecule related receptor tyrosine kinase implicated in cellular transformation [ J]. Onco- gene, 1997,14 ( 17 ) :2033 - 2039.
  • 6FISHER PW, BRIGHAM-BURKE M, WU SJ, et al. A novel site contributing to growth-arrest-specific gene 6 binding to its re- ceptors as revealed by a human monoclonal antibody [ J]. Bio- chem J,2005,385 ( Pt3 ) :727 - 735.
  • 7NAGATA K, OHASHI K, NAKANO T, et al. Identification of the product of growth arrest-specific gene 6 as a common ligand for axl, sky, and mer receptor tyrosine kinases [ J ]. J Biolog Chem, 1996,271 (47) :30022 - 30027.
  • 8HAFIZI S, DAHLBACK B. Gas6 and protein S. Vitamin K-de- pendent ligands for the Axl receptor tyrosine kinase subfamily[ J]. The FEBS J,2006,273 (23) :5231 - 5244.
  • 9HAFIZI S, DAHLBACK B. Signalling and functional diversity within the Axl subfamily of receptor tyrosine kinases [ J]. Cyto- kine Growth Factor Rev,2006,17 (4) :295 - 304.
  • 10KORSHUNOV VA. Axl-dependent signalling: a clinical update [J]. Clin Sci,2012,122(8):361-368.

共引文献18

同被引文献7

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部