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用同基因脊髓和弗氏不完全佐剂免疫的DA大鼠发生的慢性、复发性和脱髓鞘性实验性自身免疫性脑脊髓炎

Protracted, relapsing and demyelinating experimental autoimmune encephalomyelitis in DA rats immunized with syngeneic spinal cord and incomplete Freund's adjuvant.

作者信息

Lorentzen J C, Issazadeh S, Storch M, Mustafa M I, Lassman H, Linington C, Klareskog L, Olsson T

机构信息

Department of Rheumatology; Karolinska Hospital, Karolinska Institute, Stockholm, Sweden.

出版信息

J Neuroimmunol. 1995 Dec 31;63(2):193-205. doi: 10.1016/0165-5728(95)00153-0.

Abstract

Experimental autoimmune encephalomyelitis (EAE) is a model for multiple sclerosis (MS). However, MS is a chronic, relapsing and demyelinating disease, whereas EAE in rats is typically a brief and monophasic disorder showing little demyelination. We demonstrate here that DA rats develop severe, protracted and relapsing EAE (SPR-EAE) after a subcutaneous immunization at the tail base with syngeneic spinal cord and incomplete Freund's adjuvant (IFA). The neurological deficits were accompanied by demyelinating inflammatory lesions in the spinal cord, with infiltrating T lymphocytes and perivascular deposition of immunoglobulins and complement. The induction of SPR-EAE was associated with humoral autoreactivity to myelin oligodendrocyte glycoprotein (MOG) and cellular autoreactivity to the rat myelin basic protein (MBP) peptides 69-87 and 87-101. These two peptides, as well as whole rat MBP, were encephalitogenic. In conclusion, we believe that the presently described demyelinating SPR-EAE represents a useful model for MS.

摘要

实验性自身免疫性脑脊髓炎(EAE)是多发性硬化症(MS)的一种模型。然而,MS是一种慢性、复发性脱髓鞘疾病,而大鼠的EAE通常是一种短暂的单相疾病,几乎没有脱髓鞘表现。我们在此证明,DA大鼠在尾基部皮下注射同基因脊髓和不完全弗氏佐剂(IFA)后会发生严重、迁延性和复发性EAE(SPR-EAE)。神经功能缺损伴有脊髓脱髓鞘性炎性病变,有浸润的T淋巴细胞以及免疫球蛋白和补体的血管周围沉积。SPR-EAE的诱导与针对髓鞘少突胶质细胞糖蛋白(MOG)的体液自身反应性以及针对大鼠髓鞘碱性蛋白(MBP)肽段69-87和87-101的细胞自身反应性有关。这两个肽段以及完整的大鼠MBP都具有致脑炎性。总之,我们认为目前所描述的脱髓鞘性SPR-EAE是一种对MS有用的模型。

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