Kenderian Saad S, June Carl H, Gill Saar
Center for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA, USA.
Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.
Methods Mol Biol. 2017;1633:267-276. doi: 10.1007/978-1-4939-7142-8_17.
Adoptive transfer of genetically engineered T cells can lead to profound and durable responses in patients with hematologic malignancies, generating enormous enthusiasm among scientists, clinicians, patients, and biotechnology companies. The success of adoptive cellular immunotherapy depends upon the ability to manufacture good quality T cells. We discuss here the methodologies and reagents that are used to generate T cells for the preclinical study of chimeric antigen receptor T cell therapy for acute myeloid leukemia (AML).
过继转移基因工程改造的T细胞可使血液系统恶性肿瘤患者产生深刻且持久的反应,在科学家、临床医生、患者和生物技术公司中引发了极大的热情。过继性细胞免疫疗法的成功取决于生产高质量T细胞的能力。我们在此讨论用于生成T细胞的方法和试剂,这些T细胞用于急性髓系白血病(AML)嵌合抗原受体T细胞疗法的临床前研究。
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