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将携带父源Thy-1(+)CD34(+)细胞的胎儿移植用于慢性肉芽肿病。

Transplantation of a fetus with paternal Thy-1(+)CD34(+)cells for chronic granulomatous disease.

作者信息

Muench M O, Rae J, Bárcena A, Leemhuis T, Farrell J, Humeau L, Maxwell-Wiggins J R, Capper J, Mychaliska G B, Albanese C T, Martin T, Tsukamoto A, Curnutte J T, Harrison M R

机构信息

Fetal Treatment Center at the University of California, San Francisco 94143-0793, USA.

出版信息

Bone Marrow Transplant. 2001 Feb;27(4):355-64. doi: 10.1038/sj.bmt.1702798.

Abstract

A fetus diagnosed with X-linked chronic granulomatous disease was transplanted with Thy-1(+)CD34(+) cells of paternal origin. The transplant was performed at 14 weeks gestation by ultrasound guided injection into the peritoneal cavity. The fetus was delivered at 38 weeks gestation after an otherwise uneventful pregnancy. Umbilical cord blood was collected and used to determine the level of peripheral blood chimerism as well as levels of functional engrafted cells. Flow cytometry was used to detect donor leukocytes identified as HLA-A2(-)B7(+) cells, whereas recipient cells were identified as HLA-A2(+)B7(-) cells. No evidence of donor cell engraftment above a level of 0.01% was found. PCR was used to detect HLA-DRB115(+) donor cells among the recipient's HLA-DRB115(-) cells, but no engraftment was seen with a sensitivity of 1:1000. The presence of functional, donor-derived neutrophils was assessed by flow cytometry using two different fluorescent dyes that measure reactive oxygen species generated by the phagocyte NADPH oxidase. No evidence of paternal-derived functional neutrophils above a level of 0.15% was observed. Peripheral blood and bone marrow samples were collected at 6 months of age. Neither sample showed engraftment by HLA typing using both flow cytometry and PCR. Functional phagocytes were also not observed. Furthermore, no indication of immunological tolerance specific for the donor cells was indicated by a mixed lymphocyte reaction assay performed at 6 months of age. While there appears to be no engraftment of the donor stem cells, the transplant caused no harm to the fetus and the child was healthy at 6 months of age. Analyses of fetal tissues, obtained from elective abortions, revealed that CD3(+) T cells and CD56(+)CD3(-) NK cells are present in the liver at 8 weeks gestation and in the blood by 9 weeks gestation. The presence of these lymphocytes may contribute to the lack of donor cell engraftment in the human fetus.

摘要

一名被诊断患有X连锁慢性肉芽肿病的胎儿接受了父源Thy-1(+)CD34(+)细胞移植。移植在妊娠14周时通过超声引导注入腹腔进行。在妊娠38周时,胎儿在孕期其他方面均正常的情况下出生。采集脐带血用于测定外周血嵌合水平以及功能性植入细胞的水平。流式细胞术用于检测被鉴定为HLA-A2(-)B7(+)细胞的供体白细胞,而受体细胞被鉴定为HLA-A2(+)B7(-)细胞。未发现供体细胞植入水平高于0.01%的证据。PCR用于检测受体的HLA-DRB115(-)细胞中HLA-DRB115(+)供体细胞,但未观察到植入,灵敏度为1:1000。使用两种不同的荧光染料通过流式细胞术评估功能性供体来源中性粒细胞的存在,这两种染料用于测量吞噬细胞NADPH氧化酶产生的活性氧。未观察到父源功能性中性粒细胞水平高于0.15%的证据。在6个月大时采集外周血和骨髓样本。通过流式细胞术和PCR进行HLA分型,两个样本均未显示植入。也未观察到功能性吞噬细胞。此外,在6个月大时进行的混合淋巴细胞反应试验未显示对供体细胞有特异性免疫耐受的迹象。虽然似乎没有供体干细胞植入,但移植对胎儿没有造成伤害,孩子在6个月大时健康。对选择性流产获得的胎儿组织进行分析发现,在妊娠8周时肝脏中存在CD3(+)T细胞和CD56(+)CD3(-)NK细胞,在妊娠9周时血液中存在这些细胞。这些淋巴细胞的存在可能导致人类胎儿中供体细胞植入失败。

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