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梅迪 - 维斯纳病毒聚合酶肽对21.5 kDa髓鞘碱性蛋白肽的模拟并不导致绵羊脑炎的发病机制。

Mimicry of a 21.5 kDa myelin basic protein peptide by a Maedi Visna virus polymerase peptide does not contribute to the pathogenesis of encephalitis in sheep.

作者信息

Davies J M, Watt N J, Torsteinsdottir S, Carnegie P R

机构信息

Biotechnology Programme, School of Biological and Environmental Sciences, Murdoch University, Perth, WA, Australia.

出版信息

Vet Immunol Immunopathol. 1996 Dec;55(1-3):127-39. doi: 10.1016/s0165-2427(96)05619-x.

Abstract

Epitope mimicry is the theory that an infectious agent such as a virus causes pathological effects via mimicry of host proteins and thus elicits a cross-reactive immune response to host tissues. Weise and Carnegie (1988) found a region of sequence similarity between the pol gene of the Maedi Visna virus (MVV), which induces demyelinating encephalitis in sheep, and myelin basic protein (MBP), which is known to induce experimental allergic encephalitis (EAE) in laboratory animals. In this study, cross-reactions between sera raised in sheep against synthetic peptides of MVV (TGKIPWILLPGR) and 21.5 kDa MBP (SGKVPWLKPGR) were demonstrated using enzyme-linked immunosorbant assay (ELISA) and thin layer chromatography (TLC) immunoprobing. The antibody responses of MVV-infected sheep were investigated using ELISA against the peptides, and MBP protein, immunoprobing of the peptides on TLC plates and Western blotting against MBP. Slight significant reactions to the 21.5 kDa MBP peptide (P < 0.001) and to a lesser extent sheep MBP (P < 0.004) were detected in ELISA. The MBP peptide evoked stronger responses from more sera than the MVV peptide on immunoprobed TLC plates. On the Western blots, eight of the 23 sheep with Visna had serum reactivity to MBP. This slight reaction to MBP in MVV-infected sheep is of interest because of the immune responses to MBP evident in multiple sclerosis and EAE, but its relevance in Visna is limited since no correlation with disease severity was observed. The cell-mediated immune responses of MVV-infected sheep against similar peptides was assessed. The peptides did not stimulate proliferation of peripheral blood lymphocytes of MVV-infected sheep. Since the MVV peptide was not recognised by antibodies or T lymphocytes from MVV-infected and encephalic sheep, it was concluded that epitope mimicry of this 21.5 kDa MBP peptide by the similar MVV pol peptide was not contributing to the immunopathogensis of Visna. The slight antibody response to MBP and the MBP peptide can be attributed to by-stander effects of the immunopathology of MVV-induced encephalitis.

摘要

表位模拟是一种理论,即病毒等感染因子通过模拟宿主蛋白引发病理效应,从而引发对宿主组织的交叉反应性免疫应答。魏泽和卡内基(1988年)发现,在引起绵羊脱髓鞘性脑炎的梅迪-维斯纳病毒(MVV)的pol基因与已知在实验动物中引发实验性变应性脑脊髓炎(EAE)的髓鞘碱性蛋白(MBP)之间存在一个序列相似区域。在本研究中,利用酶联免疫吸附测定(ELISA)和薄层色谱(TLC)免疫印迹法,证实了绵羊体内针对MVV合成肽(TGKIPWILLPGR)和21.5 kDa MBP(SGKVPWLKPGR)产生的血清之间的交叉反应。使用ELISA针对这些肽以及MBP蛋白研究了感染MVV的绵羊的抗体反应,在TLC板上对肽进行免疫印迹,并针对MBP进行蛋白质印迹分析。在ELISA中检测到对21.5 kDa MBP肽有轻微的显著反应(P < 0.001),对绵羊MBP的反应程度较小(P < 0.004)。在免疫印迹的TLC板上,MBP肽比MVV肽能从更多血清中引发更强的反应。在蛋白质印迹分析中,23只患有维斯纳病的绵羊中有8只的血清对MBP有反应性。MVV感染的绵羊对MBP的这种轻微反应令人感兴趣,因为在多发性硬化症和EAE中对MBP的免疫反应很明显,但它在维斯纳病中的相关性有限,因为未观察到与疾病严重程度的相关性。评估了MVV感染的绵羊针对类似肽的细胞介导免疫反应。这些肽未刺激MVV感染的绵羊外周血淋巴细胞的增殖。由于MVV肽未被感染MVV的绵羊和患脑病的绵羊的抗体或T淋巴细胞识别,因此得出结论,相似的MVV pol肽对这种21.5 kDa MBP肽的表位模拟并不导致维斯纳病的免疫发病机制。对MBP和MBP肽的轻微抗体反应可归因于MVV诱导的脑炎免疫病理的旁观者效应。

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