作者
Elena J. Orlando,Xia Han,Catherine Tribouley,Patricia A. Wood,Rebecca J. Leary,Markus Riester,John E. Levine,Muna Qayed,Stephan A. Grupp,Michael Boyer,Barbara De Moerloose,Eneida R. Nemecek,Henrique Bittencourt,Hidefumi Hiramatsu,Jochen Buechner,Stella M. Davies,Michael R. Verneris,Kevin T. Nguyen,Jennifer L. Brogdon,Hans Bitter,Michael Morrissey,Piotr Pierog,Serafino Pantano,Jeffrey A. Engelman,Wendy Winckler
摘要
We identified genetic mutations in CD19 and loss of heterozygosity at the time of CD19- relapse to chimeric antigen receptor (CAR) therapy. The mutations are present in the vast majority of resistant tumor cells and are predicted to lead to a truncated protein with a nonfunctional or absent transmembrane domain and consequently to a loss of surface antigen. This irreversible loss of CD19 advocates for an alternative targeting or combination CAR approach.