Abramsky T O, Teitelbaum D, Arnon R
Eur J Immunol. 1977 Apr;7(4):213-7. doi: 10.1002/eji.1830070405.
Experimental allergic neuritis (EAN) in the peripheral nervous system, without involvement of the central nervous system, was produced in laboratory animals by the injection of a basic neuritogenic protein, P1L, purified from human peripheral nerves. The animals manifested a positive skin test with P1L, and their lymphocytes were found to be transformed in vitro in the presence of this protein several days before the appearance of the clinical signs. Passive transfer of the disease was performed with lymph node cells from donor guinea pigs immunized with P1L protein. EAN, the experimental model for the human disease Guillaain-Barré syndrome, was shown to be a transient disease and could be suppressed by the administration of hydrocortisone.
通过注射从人周围神经中纯化的碱性神经原性蛋白P1L,在实验动物中诱发了仅累及周围神经系统而不累及中枢神经系统的实验性变应性神经炎(EAN)。这些动物对P1L呈现阳性皮肤试验,并且在临床症状出现前数天,发现它们的淋巴细胞在该蛋白存在的情况下于体外发生转化。用经P1L蛋白免疫的供体豚鼠的淋巴结细胞进行疾病的被动转移。EAN作为人类吉兰-巴雷综合征的实验模型,被证明是一种自限性疾病,并且可以通过给予氢化可的松来抑制。