发明授权
US06982082B1 Gene therapy by cell specific targeting 失效
通过细胞特异性靶向进行基因治疗

Gene therapy by cell specific targeting
摘要:
This invention is directed to a modified cyclosporin A and to a modified, genetically engineered version of its receptor, cyclophilin. This invention is further directed to a method for treating host versus graft disease following blood marrow transplantation by transfecting stem cells so that after introduction into a patient the stem cells will express the modified cyclophilin, and, as necessary, administer the modified cyclosporin A to the patient.
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