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DFS70/LEDGFp75: An Enigmatic Autoantigen at the Interface between Autoimmunity AIDS and Cancer

机译:DFS70 / LEDGFp75:在自身免疫艾滋病和癌症之间的交界处的一种神秘的自身抗原

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摘要

Clinical and diagnostic laboratories often encounter patient sera containing antinuclear antibodies (ANAs) that produce a nuclear dense fine speckled immunofluorescence pattern on HEp-2 cells. These autoantibodies usually target the dense fine speckled protein of 70 kDa (DFS70), commonly known as lens epithelium-derived growth factor p75 (LEDGFp75). Anti-DFS70/LEDGFp75 autoantibodies have recently attracted much interest because of their relatively common occurrence in sera from patients with positive ANA tests with no clinical evidence of systemic autoimmune rheumatic disease (SARD). Their presence has been documented primarily in patients with diverse non-SARD inflammatory conditions and “apparently healthy” individuals. While there is circumstantial evidence that depending on the context these autoantibodies could play protective, pathogenic, or sensor roles, their significance remains elusive. DFS70/LEDGFp75 has emerged during the past decade as a stress transcription co-activator relevant to HIV integration, cancer, and inflammation. It is not clear, however, what makes this protein the target of such a common autoantibody response. We suggest that a better understanding of DFS70/LEDGFp75 biology is key to elucidating the significance of its associated autoantibodies. Here, we discuss briefly our current understanding of this enigmatic autoantigen and potential scenarios leading to its targeting by the immune system.
机译:临床和诊断实验室经常会遇到含有抗核抗体(ANA)的患者血清,这些抗体会在HEp-2细胞上产生核密集的斑点状免疫荧光图谱。这些自身抗体通常靶向70 kDa的致密斑点蛋白(DFS70),通常被称为晶状体上皮来源的生长因子p75(LEDGFp75)。抗DFS70 / LEDGFp75自身抗体近来引起了人们的极大兴趣,因为它们在ANA测试阳性且没有系统性自身免疫性风湿病(SARD)临床证据的患者血清中相对常见。主要在患有各种非SARD炎性疾病的患者和“显然健康”的患者中发现了它们的存在。尽管有间接证据表明,根据上下文的不同,这些自身抗体可能起保护性,致病性或传感器性作用,但其重要性仍然难以捉摸。在过去的十年中,DFS70 / LEDGFp75成为与HIV整合,癌症和炎症相关的应激转录共激活因子。然而,尚不清楚什么使这种蛋白质成为这种常见自身抗体反应的靶标。我们建议更好地了解DFS70 / LEDGFp75生物学是阐明其相关自身抗体的重要性的关键。在这里,我们简短地讨论了我们目前对这种神秘的自身抗原的了解以及可能导致其被免疫系统靶向的潜在情况。

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