Department of Pediatrics, Duke University Medical Center, Durham, NC 27710, USA.
Clin Immunol. 2010 May;135(2):236-46. doi: 10.1016/j.clim.2010.02.007. Epub 2010 Mar 16.
Thymus transplantation is a promising investigational therapy for infants born with no thymus. Because of the athymia, these infants lack T cell development and have a severe primary immunodeficiency. Although thymic hypoplasia or aplasia is characteristic of DiGeorge anomaly, in "complete" DiGeorge anomaly, there is no detectable thymus as determined by the absence of naive (CD45RA(+), CD62L(+)) T cells. Transplantation of postnatal allogeneic cultured thymus tissue was performed in sixty subjects with complete DiGeorge anomaly who were under the age of 2 years. Recipient survival was over 70%. Naive T cells developed 3-5 months after transplantation. The graft recipients were able to discontinue antibiotic prophylaxis, and immunoglobulin replacement. Immunosuppression was used in a subset of subjects but was discontinued when naive T cells developed. The adverse events have been acceptable with thyroid disease being the most common. Research continues on mechanisms underlying immune reconstitution after thymus transplantation.
胸腺移植是一种有前途的研究性治疗方法,适用于出生时没有胸腺的婴儿。由于无胸腺,这些婴儿缺乏 T 细胞发育,存在严重的原发性免疫缺陷。虽然 DiGeorge 异常的特征是胸腺发育不全或发育不良,但在“完全”DiGeorge 异常中,由于缺乏幼稚(CD45RA(+)、CD62L(+))T 细胞,因此无法检测到胸腺。对 60 名年龄在 2 岁以下的完全 DiGeorge 异常患者进行了同种异体培养胸腺组织的移植。受体存活率超过 70%。移植后 3-5 个月出现幼稚 T 细胞。移植物受者能够停止抗生素预防和免疫球蛋白替代。免疫抑制用于一部分患者,但当幼稚 T 细胞出现时停止使用。不良事件是可以接受的,最常见的是甲状腺疾病。研究仍在继续探讨胸腺移植后免疫重建的机制。