自体造血干细胞移植可逆转系统性硬化症患者的皮肤纤维化,但不改变皮肤血管密度

T. Daikeler , E. Kump , M. Stern , T. Hügle , A. Hij , P. Haeuserman , D. Farge
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引用次数: 11

摘要

造血干细胞移植(HSCT)通过重置免疫系统提高严重系统性硬化症(SSc)患者的生存率。我们研究了造血干细胞移植如何作用于关键的SSc皮肤病理表现(纤维化和血管化)。平均每位患者3次皮肤穿刺活检(范围2-6)分析了13例患者(5例女性)在HSCT之前和之后96个月的严重弥漫性SSc。对四层皮肤的纤维化进行半定量分级,然后计算总体纤维化评分。内皮抗原(CD31, VE-cadherin和vWF)免疫染色后,评估真皮浅层和深层的血管数量和直径。HSCT患者的中位年龄为47岁(24-64岁)。在HSCT后9个月(6-36个月)的第一次随访中,总体改良罗德曼皮肤评分中位数从24降至10 (P = 0.003),组织学皮肤评分也是如此(P = 0.03)。改良罗德曼皮肤评分与纤维化评分呈正相关(r = 0.589, P <0.001)。造血干细胞移植后血管密度无明显变化,内皮标志物的表达也无明显变化。虽然能改善SSc患者的皮肤纤维化,但在皮肤活检中,HSCT不能改变血管密度。
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Autologous hematopoietic stem cell transplantation reverses skin fibrosis but does not change skin vessel density in patients with systemic sclerosis

Hematopoetic stem cell transplantation (HSCT) improves survival in patients with severe systemic sclerosis (SSc) by resetting the immune system. We studied how HSCT acts on the key SSc skin pathology findings (fibrosis and vascularization). In mean, 3 skin punch biopsies per patient (range 2–6) were analyzed from 13 patients (5 females) with severe diffuse SSc before and up to 96 months after HSCT. Fibrosis of the four skin layers was graded semi-quantitatively and an overall fibrosis score was then calculated. Vessel numbers and calibers were assessed in the superficial and deeper dermis after immune-staining for endothelial antigens (CD31, VE-cadherin and vWF). The median age of patients at HSCT was 47 (24–64) years. The overall median modified Rodnan skin score decreased from 24 to 10 (P = 0.003) at first follow-up within a median of 9 (6–36) months after HSCT as did the histological skin score (P = 0.03). The modified Rodnan skin score and the fibrosis score correlated positively (r = 0.589, P < 0.001). The vessels density did not significantly change after HSCT nor did the expression of the tested endothelial markers. Although improving skin fibrosis in patients with SSc, HSCT does not alter vessel density within skin biopsies.

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来源期刊
Pathologie-biologie
Pathologie-biologie 医学-病理学
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审稿时长
6-12 weeks
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