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患有类马凡氏综合征表型和深部皮肤溃疡男孩的HLA I类和CD1a分子表达缺陷

Defective expression of HLA class I and CD1a molecules in boy with Marfan-like phenotype and deep skin ulcers.

作者信息

Plebani A, Monafo V, Cattaneo R, Carella G, Brugnoni D, Facchetti F, Battocchio S, Meini A, Notarangelo L D, Duse M, Ugazio A G

机构信息

Department of Pediatrics, Institute G. Gaslini, University of Genova, Italy.

出版信息

J Am Acad Dermatol. 1996 Nov;35(5 Pt 2):814-8. doi: 10.1016/s0190-9622(96)90091-2.

Abstract

We report the case of a boy with low expression of HLA class I molecules on peripheral blood mononuclear cells, which is associated with immunodeficiency. The patient, who had a Marfan-like phenotype, had chronic deep skin ulcers and sinobronchiectasis. Immunohistologic examination of the ulcerated skin showed a dense perivascular infiltrate composed of normal mature lymphocytes and macrophages. All cells in the infiltrate showed an apparently normal expression of HLA class I molecules, but intraepidermal dendritic Langerhans' cells were negative for CD1a, an antigen that is a highly specific marker for these cells and is abundantly expressed in some self-healing forms of cutaneous lesions. It is therefore speculated that a defective expression of CD1a molecules can contribute to the chronic persistence of deep skin ulcers, which have already been reported in association with defective expression of HLA class I molecules.

摘要

我们报告了一例外周血单个核细胞上HLA I类分子表达低下的男孩病例,这与免疫缺陷相关。该患者具有马凡氏综合征样表型,患有慢性深部皮肤溃疡和鼻窦支气管扩张。对溃疡皮肤进行免疫组织学检查显示,血管周围有由正常成熟淋巴细胞和巨噬细胞组成的密集浸润。浸润中的所有细胞HLA I类分子表达明显正常,但表皮内树突状朗格汉斯细胞CD1a呈阴性,CD1a是这些细胞的高度特异性标志物,在某些皮肤病变的自愈形式中大量表达。因此推测,CD1a分子表达缺陷可能导致深部皮肤溃疡的慢性持续存在,此前已有报道称深部皮肤溃疡与HLA I类分子表达缺陷有关。

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