Antoniou A V, el-Sady H, Butter C, Turk J L
J Neuroimmunol. 1987 May;15(1):57-71. doi: 10.1016/0165-5728(87)90006-3.
Cryostat sections of spinal cord of guinea pigs with chronic relapsing experimental allergic encephalomyelitis (CREAE) were stained with monoclonal antibodies recognising a Strain 13-specific Ia epitope, a non-strain-specific Ia antigen and an 'activated' macrophage determinant. It was found that both Ia antigens and the 'activated' macrophage determinant, observed on infiltrating cells within both perivascular and meningeal compartments, appeared to be modulated during the course of CREAE. This correlated with the neurological symptoms of the disease. Blood vessels and 'glial' cells expressed both Ia determinants. 'Glial' cells also expressed the 'activated' macrophage antigen. These antigens were modulated with the course of the disease.
对患有慢性复发性实验性变应性脑脊髓炎(CREAE)的豚鼠脊髓进行冷冻切片,用识别13型特异性Ia表位、非菌株特异性Ia抗原和“活化”巨噬细胞决定簇的单克隆抗体进行染色。结果发现,在血管周围和脑膜间隙内浸润细胞上观察到的Ia抗原和“活化”巨噬细胞决定簇,在CREAE病程中似乎都受到调节。这与该疾病的神经症状相关。血管和“神经胶质”细胞表达两种Ia决定簇。“神经胶质”细胞也表达“活化”巨噬细胞抗原。这些抗原随疾病进程而受到调节。