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将一个外来组织相容性基因导入动脉壁会诱发血管炎。

Transduction of a foreign histocompatibility gene into the arterial wall induces vasculitis.

作者信息

Nabel E G, Plautz G, Nabel G J

机构信息

Howard Hughes Medical Institute, University of Michigan Medical Center, Department of Internal Medicine, Ann Arbor 48109-0650.

出版信息

Proc Natl Acad Sci U S A. 1992 Jun 1;89(11):5157-61. doi: 10.1073/pnas.89.11.5157.

Abstract

Autoimmune vasculitis represents a disease characterized by focal inflammation within arteries at multiple sites in the vasculature. Therapeutic interventions in this disease are empirical and often unsuccessful, and the mechanisms of immune injury are not well-defined. The direct transfer of recombinant genes and their expression in the arterial wall provides an opportunity to explore the pathogenesis and treatment of vascular disease. In this report, an animal model for vasculitis has been developed. Inflammation has been elicited by direct gene transfer of a foreign class I major histocompatibility complex gene, HLA-B7, to specific sites in porcine arteries. Transfer and expression of this recombinant gene was confirmed by a polymerase chain reaction and immunohistochemistry, and cytolytic T cells specific for HLA-B7 were detected. These findings demonstrate that expression of a recombinant gene in the vessel wall can induce a focal immune response and suggest that vessel damage induced by cell-mediated immune injury can initiate vasculitis.

摘要

自身免疫性血管炎是一种以脉管系统中多个部位动脉的局灶性炎症为特征的疾病。该疾病的治疗干预是经验性的,且常常不成功,免疫损伤机制尚不明确。重组基因的直接转移及其在动脉壁中的表达为探索血管疾病的发病机制和治疗提供了契机。在本报告中,已建立了一种血管炎动物模型。通过将外源I类主要组织相容性复合体基因HLA - B7直接基因转移至猪动脉的特定部位引发炎症。通过聚合酶链反应和免疫组织化学证实了该重组基因的转移和表达,并检测到了针对HLA - B7的细胞毒性T细胞。这些发现表明重组基因在血管壁中的表达可诱导局灶性免疫反应,并提示细胞介导的免疫损伤所诱导的血管损伤可引发血管炎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9034/49248/f20baaf746bb/pnas01085-0388-a.jpg

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