Heslop Helen E, Leen Ann M
1Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, The Methodist Hospital, Houston, TX.
Hematology Am Soc Hematol Educ Program. 2013;2013:342-7. doi: 10.1182/asheducation-2013.1.342.
Viral infections remain a major cause of morbidity in patients with immunodeficiency, such as recipients of hemopoietic stem cell transplantation. Adoptive transfer of donor-derived virus-specific cytotoxic T lymphocytes is a strategy to restore virus-specific immunity to prevent or treat viral diseases and has been tested in the clinical setting for more than 20 years. Several different groups have used expanded virus-specific T-cell products specific for one or multiple viruses to both reconstitute antiviral immunity after transplantation and to treat active viral infections. Response rates are encouraging, although resistance has been seen when the infused cell population has had restricted specificity or has targeted antigens expressed in donor-infected but not virally infected recipient cells. The goal of current trials is to make this approach more broadly applicable using more rapidly available products from the donor, such as directly selected or briefly expanded cells or closely matched banked cells.
病毒感染仍然是免疫缺陷患者发病的主要原因,例如造血干细胞移植受者。供体来源的病毒特异性细胞毒性T淋巴细胞的过继转移是恢复病毒特异性免疫以预防或治疗病毒性疾病的一种策略,并且已经在临床环境中进行了20多年的测试。几个不同的研究小组使用针对一种或多种病毒的扩增的病毒特异性T细胞产品,在移植后重建抗病毒免疫力并治疗活动性病毒感染。尽管当输注的细胞群体具有受限的特异性或靶向供体感染而非病毒感染的受体细胞中表达的抗原时会出现耐药性,但反应率令人鼓舞。当前试验的目标是使用来自供体的更快速可用的产品,例如直接选择或短暂扩增的细胞或紧密匹配的库细胞,使这种方法更广泛地适用。