Linington C, Izumo S, Suzuki M, Uyemura K, Meyermann R, Wekerle H
J Immunol. 1984 Oct;133(4):1946-50.
A rat T cell line of the "helper" phenotype (W3/25-positive, OX 8-negative) has been derived from Lewis rats inoculated with P2 protein isolated from bovine PNS myelin. The line LiP2/A is exquisitely specific for P2 protein, exhibiting no reactivity to bovine basic protein or to PPD. In addition to responding strongly to the intact P2 protein, the line cells show some response to a synthetic peptide containing the neuritogenic amino acid sequence of P2 protein (SP-B, residues 66-78). Intravenous inoculation of naive rats with as few as 10(4) activated LiP2/A cells leads to the onset of mild clinical signs of experimental allergic neuritis. Higher doses of cells lead to more severe clinical disease. Histologic examination of clinically ill animals confirmed the disease as EAN. The pathologic lesions were confined to the PNS and spared the central nervous system. The lesions consisted of marked perivascular cuffs and infiltrates of inflammatory cells associated with marked degenerative changes--demyelination and some axonal degeneration.
一种具有“辅助性”表型(W3/25阳性,OX 8阴性)的大鼠T细胞系,是从接种了从牛周围神经髓磷脂中分离出的P2蛋白的Lewis大鼠中获得的。LiP2/A细胞系对P2蛋白具有高度特异性,对牛碱性蛋白或PPD无反应。除了对完整的P2蛋白有强烈反应外,该细胞系细胞对含有P2蛋白神经生成氨基酸序列的合成肽(SP-B,第66 - 78位氨基酸残基)也有一些反应。给未致敏的大鼠静脉注射低至10⁴个活化的LiP2/A细胞,会导致实验性变应性神经炎出现轻微的临床症状。更高剂量的细胞会导致更严重的临床疾病。对出现临床症状动物的组织学检查证实该疾病为实验性变应性神经炎。病理病变局限于周围神经系统,中枢神经系统未受累。病变包括明显的血管周围套袖状浸润以及伴有明显退行性改变(脱髓鞘和一些轴突变性)的炎性细胞浸润。