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通过输注供体白细胞成功治疗早期移植物排斥反应,进一步证明了移植物抗宿主淋巴造血效应。

Successful treatment of incipient graft rejection with donor leukocyte infusions, further proof of a graft versus host lymphohaemopoietic effect.

作者信息

Díez-Martín J L, Gómez-Pineda A, Serrano D, Carrión R, Balsalobre P, Buño I

机构信息

Unidad de Trasplante de Médula Osea, Hosp. G.U. Gregorio Marañón, Doctor Esquerdo 46, 28007 Madrid, Spain.

出版信息

Bone Marrow Transplant. 2004 May;33(10):1037-41. doi: 10.1038/sj.bmt.1704488.

Abstract

Graft rejection is a major cause of treatment failure after T-cell-depleted stem cell transplantation (TCD-SCT) and remains a therapeutic challenge. Donor leukocyte infusions (DLIs) have an efficient graft versus host effect, which has been successfully used to treat recipient relapses. We hypothesized that this effect could be exploited to counteract the host versus graft reactions responsible for graft rejection. We report two adult patients with haematological malignancies who underwent sex-mismatched TCD-SCT from HLA-identical sibling donors. Peripheral blood (PB) counts and bone marrow (BM) cellularity were studied on a serial basis. Sequential chimaerism and minimal residual disease analysis were performed by FISH on PB and BM samples as well as on leukocyte lineages (T and B lymphocytes and myeloid cells) purified from PB using immunomagnetic technology. Both patients were diagnosed with incipient graft rejection 2-3 months after engraftment, based on persistently decreasing PB counts and BM cellularity together with the observation of decreasing mixed chimaerism (increasing percentage of recipient cells), mostly in whole PB and T lymphocytes. Both patients were successfully treated with a single DLI (1 x 10(7) CD3+ cells/kg), thereafter achieving normal PB counts and BM cellularity as well as complete chimaerism. Interestingly, the only side effect observed was mild graft versus host disease that did not require treatment. In conclusion, provided that an early diagnosis is made, the graft versus host lymphohaemopoietic effect harboured by immunocompetent donor cells can be successfully used for the treatment of incipient graft rejection.

摘要

移植物排斥是去T细胞干细胞移植(TCD-SCT)后治疗失败的主要原因,仍然是一个治疗挑战。供体白细胞输注(DLI)具有有效的移植物抗宿主效应,已成功用于治疗受者复发。我们推测这种效应可用于对抗导致移植物排斥的宿主抗移植物反应。我们报告了两名患有血液系统恶性肿瘤的成年患者,他们接受了来自HLA相同同胞供体的性别不匹配的TCD-SCT。连续研究外周血(PB)计数和骨髓(BM)细胞成分。通过荧光原位杂交(FISH)对PB和BM样本以及使用免疫磁技术从PB中纯化的白细胞谱系(T和B淋巴细胞以及髓细胞)进行连续嵌合体分析和微小残留病分析。两名患者在植入后2-3个月均被诊断为早期移植物排斥,依据是PB计数和BM细胞成分持续下降,以及观察到混合嵌合体减少(受者细胞百分比增加),主要发生在全PB和T淋巴细胞中。两名患者均接受单次DLI(1×10⁷ CD3⁺细胞/kg)成功治疗,此后PB计数和BM细胞成分恢复正常,并实现完全嵌合体。有趣的是,观察到的唯一副作用是轻度移植物抗宿主病,无需治疗。总之,只要能早期诊断,有免疫活性的供体细胞所具有的移植物抗宿主淋巴造血效应可成功用于治疗早期移植物排斥。

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