过继免疫疗法治疗异基因造血干细胞移植后白血病复发

Beverley M. Kerr , Andy Kang-Wei Hsu , Kathryn L. Jones , Alison M. Rice
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引用次数: 0

摘要

急性白血病患者在造血干细胞移植(HSCT)后复发预后差,治疗选择很少。一种专门针对白血病的免疫治疗方法可以治疗和预防这些复发,从而提高这些患者的生存率。最近,一些潜在的白血病抗原靶点已被描述。这些包括过度表达的正常抗原,如survivin,由易位和突变引起的白血病特异性靶标,以及造血受限的次要组织相容性抗原,如HA-1和HA-2。大量的实验数据表明,靶向这些抗原的细胞毒性T细胞可以在体外产生。抗原呈递和T细胞活化扩增效果的进一步提高,将促进这些T细胞作为HSCT术后复发患者的治疗策略的临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adoptive immunotherapy to treat leukemic relapse following allogeneic hematopoietic stem cell transplantation

Acute leukemia patients who relapse after haematopoetic stem cell transplantation (HSCT) have poor prognosis with few therapeutic options. An immunotherapeutic approach that specifically targets the leukemia to treat and prevent these relapses could improve survival rates for these patients. Recently a number of potential antigenic targets for leukemia have been described. These include over-expressed normal antigens such as survivin, leukemia-specific targets resulting from translocations and mutations and hematopoietic-restricted minor histocompatibility antigens such as HA-1 and HA-2. Considerable experimental data indicates that cytotoxic T cells targeting these antigens can be generated in vitro. Further improvements in the efficacy of antigen presentation and T cell activation and expansion will facilitate the clinical application of these T cells as a therapeutic strategy for patients who are likely to relapse after HSCT.

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