Nicholson Emma, Peggs Karl S
Department of Haematology, University College London Hospital, London, NW1 2BU, UK.
Immunotherapy. 2015;7(2):135-46. doi: 10.2217/imt.14.99.
Adoptive transfer of T cells specific for viral pathogens offers an attractive method for hastening immune reconstitution and protective immunity in patients following stem cell transplantation. The largest experience to date has been in the context of treatment or prevention of cytomegalovirus or Epstein-Barr virus. A number of technical hurdles have now been overcome allowing consideration of more widespread application of products compliant with Good Manufacturing Practice regulations, and of the development of commercialization pathways for these products. This review summarizes progress to date and highlights some of the areas that remain problematic and that require further innovation and evaluation before more widespread adoption is considered.
过继转移针对病毒病原体的T细胞为加速干细胞移植患者的免疫重建和保护性免疫提供了一种有吸引力的方法。迄今为止,最大规模的经验是在治疗或预防巨细胞病毒或EB病毒方面。现在已经克服了一些技术障碍,使得可以考虑更广泛地应用符合药品生产质量管理规范(GMP)的产品,并为这些产品开发商业化途径。本综述总结了迄今为止的进展,并强调了一些仍然存在问题的领域,在考虑更广泛采用之前,这些领域需要进一步创新和评估。