Kiefer R, Dangond F, Mueller M, Toyka K V, Hafler D A, Hartung H P
Klinik und Poliklinik für Neurologie, Westfälische Wilhelms-Universität, Albert-Schweitzer- Strasse 33, D-48129 Münster, Germany.
J Neurol Neurosurg Psychiatry. 2000 Sep;69(3):362-8. doi: 10.1136/jnnp.69.3.362.
To define the role of the costimulatory molecules B7-1 and B7-2 in inflammatory disorders of the peripheral nervous system. B7 molecules are essential for effective antigen presentation and may determine the differentiation of T cells into a Th-1 or Th-2 phenotype, thus modulating immune response and disease course.
Forty nine sural nerve biopsies from patients with neuroborreliosis, Guillain-Barré syndrome (GBS), chronic inflammatory demyelinating polyneuropathy (CIDP), CIDP variants and hereditary neuropathies, and those with no detectable abnormality were investigated. The expression of B7-1 and B7-2 mRNA and protein was investigated by polymerase chain reaction (PCR) and immunocytochemistry.
B7-1 mRNA was strongly upregulated in both cases of neuroborreliosis, in two cases of GBS and one case of variant CIDP. Moderate to low levels were detected in the remaining GBS and CIDP biopsies and were rarely found in a non-inflammatory control group consisting of hereditary neuropathy and normal nerves. At the immunocytochemical level, strong expression of B7-1 protein was found in both neuroborreliosis cases, and moderate or low expression in six of eight GBS cases and seven of 17 CIDP cases investigated, whereas only one of five non-inflammatory control nerves showed staining, which was very weak. In neuroborreliosis, B7-1 protein was found very pronounced in epineurial infiltrates, whereas in GBS and CIDP, labelling was predominantly endoneurial and localised to putative macrophages. B7-2 mRNA and protein were expressed only at low levels in neuroborreliosis and selected autoimmune neuropathy cases, and were essentially absent from non-inflammatory controls.
B7 molecules are expressed in the peripheral nervous system and regulated during disease, and their presence in macrophages underlines the putative function of endoneurial macrophages as local antigen presenting cells in the immunopathology of peripheral nerve. B7-1 rather than B7-2 is preferentially upregulated, possibly promoting the induction of a Th-1-type T cell response within the nerve.
确定共刺激分子B7-1和B7-2在周围神经系统炎性疾病中的作用。B7分子对于有效的抗原呈递至关重要,并且可能决定T细胞分化为Th-1或Th-2表型,从而调节免疫反应和疾病进程。
对49例来自患有神经莱姆病、格林-巴利综合征(GBS)、慢性炎性脱髓鞘性多发性神经病(CIDP)、CIDP变异型和遗传性神经病患者以及无明显异常患者的腓肠神经活检标本进行研究。通过聚合酶链反应(PCR)和免疫细胞化学研究B7-1和B7-2 mRNA及蛋白的表达。
在两例神经莱姆病、两例GBS和一例CIDP变异型病例中,B7-1 mRNA强烈上调。在其余的GBS和CIDP活检标本中检测到中度至低度水平,而在由遗传性神经病和正常神经组成的非炎性对照组中很少发现。在免疫细胞化学水平上,在两例神经莱姆病病例中均发现B7-1蛋白强烈表达,在八例GBS病例中的六例以及17例CIDP病例中的七例中发现中度或低度表达,而在五例非炎性对照神经中只有一例显示染色,且非常微弱。在神经莱姆病中,B7-1蛋白在神经外膜浸润中非常明显,而在GBS和CIDP中,标记主要在内神经,定位于假定的巨噬细胞。B7-2 mRNA和蛋白在神经莱姆病和选定的自身免疫性神经病病例中仅低水平表达,在非炎性对照中基本不存在。
B7分子在周围神经系统中表达并在疾病过程中受到调节,它们在巨噬细胞中的存在强调了内神经巨噬细胞作为周围神经免疫病理学中局部抗原呈递细胞的假定功能。B7-1而非B7-2优先上调,可能促进神经内Th-1型T细胞反应的诱导。