CD64-directed microtubule associated protein tau kills leukemic blasts ex vivo

نویسندگان

  • Radoslav Mladenov
  • Dmitrij Hristodorov
  • Christian Cremer
  • Gerrit Gresch
  • Elena Grieger
  • Lea Schenke
  • Diana Klose
  • Manal Amoury
  • Mira Woitok
  • Edgar Jost
  • Tim H. Brümmendorf
  • Rolf Fendel
  • Rainer Fischer
  • Christoph Stein
  • Theo Thepen
  • Stefan Barth
چکیده

Fc gamma receptor I (FcγRI, CD64) is a well-known target antigen for passive immunotherapy against acute myeloid leukemia and chronic myelomonocytic leukemia. We recently reported the preclinical immunotherapeutic potential of microtubule associated protein tau (MAP) against a variety of cancer types including breast carcinoma and Hodgkin's lymphoma. Here we demonstrate that the CD64-directed human cytolytic fusion protein H22(scFv)-MAP kills ex vivo 15-50% of CD64+ leukemic blasts derived from seven myeloid leukemia patients. Furthermore, in contrast to the nonspecific cytostatic agent paclitaxel, H22(scFv)-MAP showed no cytotoxicity towards healthy CD64+ PBMC-derived cells and macrophages. The targeted delivery of this microtubule stabilizing agent therefore offers a promising new strategy for specific treatment of CD64+ leukemia.

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عنوان ژورنال:

دوره 7  شماره 

صفحات  -

تاریخ انتشار 2016