van Gelder M, Kinwel-Bohré E P, van Bekkum D W
Department of Immunopathology, Institute of Applied Radiobiology and Immunology-TNO, Rijswijk, The Netherlands.
Bone Marrow Transplant. 1993 Mar;11(3):233-41.
Experimental allergic encephalomyelitis (EAE) was induced in Buffalo rats by immunization with syngeneic spinal cord homogenate in complete adjuvant. EAE, an autoimmune disease of the central nervous system (CNS), is regarded as a model for multiple sclerosis. When severe paresis had developed, rats were treated with high-dose total body irradiation (TBI) and transplanted with syngeneic BM from healthy donors. Nine Gy TBI followed by syngeneic BMT greatly accelerated recovery of paresis compared with untreated controls. In 6-33% of the treated animals a relapse of EAE was observed shortly after treatment. Reimmunization 20 days after treatment, resulted in a relapse in 12-44% of the rats. Employing the maximally tolerated dose of TBI (10 Gy) did not significantly alter the incidence of spontaneous or induced relapses. Furthermore, it was shown that irradiation of the CNS only was not sufficient for the induction of complete regression of paresis. The origin of the cells responsible for these relapses is discussed, as is the importance of reimmunization in evaluating the effect of treatment of experimental autoimmune disease.
通过用完全弗氏佐剂中的同基因脊髓匀浆免疫布法罗大鼠诱导实验性自身免疫性脑脊髓炎(EAE)。EAE是一种中枢神经系统(CNS)的自身免疫性疾病,被视为多发性硬化症的模型。当出现严重麻痹时,大鼠接受大剂量全身照射(TBI),并移植来自健康供体的同基因骨髓。与未治疗的对照组相比,9 Gy TBI后进行同基因骨髓移植(BMT)极大地加速了麻痹的恢复。在6% - 33%的治疗动物中,治疗后不久观察到EAE复发。治疗后20天再次免疫,12% - 44%的大鼠出现复发。采用最大耐受剂量的TBI(10 Gy)并未显著改变自发或诱导复发的发生率。此外,研究表明仅对中枢神经系统进行照射不足以诱导麻痹完全消退。文中讨论了导致这些复发的细胞来源,以及再次免疫在评估实验性自身免疫性疾病治疗效果中的重要性。