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髓鞘碱性蛋白在多发性硬化症加重期对白细胞迁移的直接抑制作用

Direct leukocyte migration inhibition by myelin basic protein in exacerbations of multiple sclerosis.

作者信息

Sheremata W, Triller H, Cosgrove J B, Eylar E H

出版信息

Can Med Assoc J. 1977 May 7;116(9):985-8.

Abstract

Studies in 13 normal subjects, 9 patients with multiple sclerosis (MS) within 3 weeks of exacerbation and 16 others 1 to 6 months after onset were carried out for evidence of cell-mediated hypersensitivity to myelin basic protein. Ten patients with stroke and 10 with Guillain-Barré syndrome were studied as additional controls. Peripheral leukocytes obtained by leukapheresis were packed into capillary tubes and allowed to migrate out onto glass in the presence or absence of myelin basic protein. Cells of patients within 3 weeks of an MS episode gave a mean migration index of 68 +/- 9%, and those 1 to 6 months after onset, 93 +/- 21%. For the entire MS group the mean index was 88 +/- 20%, for those with Guillain-Barré, 103 +/- 7%; and for the stroke patients, 107 +/- 11%. Results for the acutely ill MS patients were significant (P less than 0.005). The data are similar to those obtained using the migration inhibition factor assay but show that sensitized lymphocytes also elaborate a second mediator during acute exacerbations of illness. These observations strengthen evidence that sensitization to this potent encephalitogen occurs simultaneously with exacerbations of clinical illness.

摘要

对13名正常受试者、9名多发性硬化症(MS)发作3周内的患者以及16名发病1至6个月后的患者进行了研究,以寻找细胞介导的对髓鞘碱性蛋白超敏反应的证据。另外,对10名中风患者和10名格林-巴利综合征患者进行了研究作为对照。通过白细胞分离术获得的外周血白细胞被装入毛细管中,并在有或没有髓鞘碱性蛋白的情况下使其迁移到玻璃片上。MS发作3周内患者的细胞平均迁移指数为68±9%,发病1至6个月后的患者为93±21%。整个MS组的平均指数为88±20%,格林-巴利综合征患者为103±7%,中风患者为107±11%。急性病MS患者的结果具有显著性(P<0.005)。这些数据与使用迁移抑制因子测定法获得的数据相似,但表明致敏淋巴细胞在疾病急性发作期间还会产生第二种介质。这些观察结果进一步证明,对这种强效脑脊髓炎原的致敏与临床疾病发作同时发生。

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Delayed hypersensitivity in vitro using human peripheral leucocytes.
Transplantation. 1969 Nov;8(5):745-8. doi: 10.1097/00007890-196911000-00036.
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Delayed hypersensitivity to myelin antigen in multiple sclerosis investigated with the leucocyte migration method.
Acta Neurol Scand. 1972;48(2):243-8. doi: 10.1111/j.1600-0404.1972.tb07545.x.
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Leukocyte sensitivity to brain fractions in neurological diseases.
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