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近期发病的多发性硬化症中活化的γ/δ T细胞的克隆性扩增。

Clonal expansions of activated gamma/delta T cells in recent-onset multiple sclerosis.

作者信息

Shimonkevitz R, Colburn C, Burnham J A, Murray R S, Kotzin B L

机构信息

Rocky Mountain Multiple Sclerosis Center, Englewood, CO 80110.

出版信息

Proc Natl Acad Sci U S A. 1993 Feb 1;90(3):923-7. doi: 10.1073/pnas.90.3.923.

DOI:10.1073/pnas.90.3.923
PMID:8430106
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC45782/
Abstract

Multiple sclerosis (MS) is a chronic disease characterized by focal demyelination of the white matter of the brain and spinal cord. Central nervous system damage appears to be mediated by infiltrating T lymphocytes and macrophages, and a central role for autoreactive CD4+ T cells has been proposed. However, the initial immune events that lead to the chronic process of MS remain unidentified. We now present evidence that a subset of T lymphocytes bearing gamma/delta T-cell antigen receptors has been activated in patients with recent-onset disease. Cells recovered from the cerebrospinal fluid of subjects with MS were cultured for short periods of time in medium supplemented with T-cell growth factors. Expansions of V delta 1 and V delta 2 T-cell receptor-bearing lymphocytes were found only in cell populations obtained from subjects with recent-onset disease. Similar populations were not expanded in subjects with chronic MS or other neurological diseases. Junctional region sequencing showed the expanded gamma/delta T cells to be oligoclonal in nature, suggestive of specific stimulation by antigen. These results reveal a fundamental difference in the immunopathogenesis of acute vs. chronic disease and provide additional insight into the autoimmune nature of MS.

摘要

多发性硬化症(MS)是一种以脑和脊髓白质局灶性脱髓鞘为特征的慢性疾病。中枢神经系统损伤似乎是由浸润的T淋巴细胞和巨噬细胞介导的,并且有人提出自身反应性CD4 + T细胞起核心作用。然而,导致MS慢性病程的初始免疫事件仍未明确。我们现在提供证据表明,在近期发病的患者中,携带γ/δ T细胞抗原受体的一部分T淋巴细胞已被激活。从MS患者的脑脊液中回收的细胞在补充有T细胞生长因子的培养基中短期培养。仅在从近期发病患者获得的细胞群体中发现了携带Vδ1和Vδ2 T细胞受体的淋巴细胞扩增。在慢性MS患者或其他神经系统疾病患者中,类似的细胞群体未扩增。连接区测序显示扩增的γ/δ T细胞本质上是寡克隆的,提示受抗原有特异性刺激。这些结果揭示了急性与慢性疾病免疫发病机制的根本差异,并为MS的自身免疫性质提供了更多见解。