Anti-NK antibodies injected into recipient mice enhance engraftment and chimerism after allogeneic transplantation of fetal liver stem cells.

Thymus Pub Date : 1997-01-01
J Chargui, M J Moya, K Sanhadji, N Blanc-Brunat, J L Touraine
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Abstract

Natural killer (NK) cells have been shown to play a role in the phenomenon of resistance to transplantation of allogeneic stem cells. To explore and prevent such resistance, we treated severe combined immunodeficiency mice (SCID) with anti-NK antibodies and analysed the improved engraftment of stem cells induced by this treatment. Two groups of nine SCID mice (H-2d) were compared: group A received two injections of anti-asialo GM1 rabbit antibodies (anti-NK) on days 1 and 4; group B received two injections of normal rabbit serum. All mice were injected intravenously with 7 x 10(6) fetal liver cells from B6 mice (H-2b) on day 2. One month after fetal liver cell transplantation, all mice from group A demonstrated engraftment and chimerism; at this time, donor cells accounted for more than 50% of peripheral blood mononuclear cells (PBMC). In contrast, in group B, only one mouse had 26% of donor cells among PBMC and all other mice had less than 10%. At two months, results were virtually identical in group A (over 72% of donor cells among PBMC from all mice) and slightly improved in group B (0-38% of donor cells). After the third month and continuously until the 12th month, the stability of chimerism was established in group A (over 55% of donor cells in 7 of the 9 mice) but had virtually disappeared in group B (0-2% of donor cells in all mice). Tissue analysis demonstrated the improved reconstitution of the thymus and the spleen in mice from group A. The proliferative responses of spleen cells to phytomitogens were significantly higher in all mice from group A than in any mouse from group B. Skin allografts from a third party (H-2k) were rejected within 10 days by group A mice but not by group B mice, one year after fetal liver cell transplantation. On the whole, anti-NK antibodies were able to improve engraftment, chimerism and stability of allogeneic stem cell transplants.

受体小鼠体内注射抗nk抗体可增强异体胚胎肝干细胞移植后的植入和嵌合。
自然杀伤(NK)细胞已被证明在异基因干细胞移植抵抗现象中发挥作用。为了探索和预防这种耐药性,我们用抗nk抗体治疗严重联合免疫缺陷小鼠(SCID),并分析了这种治疗对干细胞移植的改善作用。比较两组9只SCID小鼠(H-2d): A组分别于第1、4天注射2次抗亚麻黄GM1兔抗体(抗nk);B组注射正常兔血清2次。第2天,所有小鼠静脉注射7 × 10(6)个来自B6小鼠(H-2b)的胎儿肝细胞。胚胎肝细胞移植1个月后,A组小鼠均出现移植嵌合现象;此时供体细胞占外周血单个核细胞(PBMC)的50%以上。相比之下,在B组中,只有一只小鼠在PBMC中有26%的供体细胞,其他所有小鼠的供体细胞都低于10%。两个月后,A组的结果几乎相同(来自所有小鼠的PBMC中超过72%的供体细胞),B组略有改善(0-38%的供体细胞)。第3个月后并持续到第12个月,A组的嵌合稳定(9只小鼠中有7只小鼠的供体细胞超过55%),而B组的嵌合几乎消失(所有小鼠的供体细胞为0-2%)。组织分析表明,A组小鼠胸腺和脾脏的重建得到改善。A组小鼠脾脏细胞对植物滋生原的增殖反应明显高于B组小鼠。在胎儿肝细胞移植一年后,来自第三方(H-2k)的同种异体皮肤在10天内被A组小鼠排斥,而B组小鼠没有。总的来说,抗nk抗体能够改善同种异体干细胞移植的着床性、嵌合性和稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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