Hvas J, Oksenberg J R, Fernando R, Steinman L, Bernard C C
Neuroimmunology Laboratory, La Trobe University, Bundoora, Victoria, Australia.
J Neuroimmunol. 1993 Jul;46(1-2):225-34. doi: 10.1016/0165-5728(93)90253-u.
The identification of activated T cells in the brains of patients with multiple sclerosis (MS) suggests that these cells are critical in the pathogenesis of this disease. Recently we have used the PCR method to analyse rearrangements of V alpha and V beta genes of the T cell receptor (TCR) in samples of MS and control brains. The results of these studies showed that TCR V gene usage in MS brains may be restricted and in particular that V beta genes may be preferentially rearranged in certain HLA haplotypes associated with susceptibility to MS. In view of the recent evidence that T lymphocytes bearing the gamma delta chains may have autoreactive potential, we have assessed whether or not such TCR-bearing lymphocytes were also present in chronic MS lesions. TCR V gamma and V delta were analysed by the PCR method using a panel of V gamma and V delta primers paired with C gamma or C delta primers in 12 MS brains, as well as in brain samples of ten normal post-mortem cases and three neurological controls. TCR V gamma-C gamma and V delta-C delta rearrangements were confirmed using Southern blotting and hybridisation of the PCR products with specific C gamma and C delta probes. Only one to four rearranged TCR V gamma and V delta transcripts were detected in each of the 23 brain samples obtained from 12 MS patients, with the majority of gamma delta T cells expressing the V gamma 2 and V delta 2 chains. In marked contrast, V gamma and V delta transcripts could only be found in one of the ten non-neurological control brains analysed. To assess the clonality of V gamma 2 and V delta 2 T cell receptor chains in the brain samples of MS patients, we have sequenced the junctional regions of the TCR V gamma-N-J gamma-C gamma and V delta-N-D delta-N-J delta-C delta segments amplified from brain tissues, CSF and spleens of two MS patients and from the spleen of two control subjects. The sequence analysis obtained so far shows no compelling evidence of an MS specific expansion of one or more clones expressing particular types of gamma delta T cell receptors. In contrast, a clonal expansion of a different population of TCR gamma delta-bearing T cells was found in the spleen of both an MS patient and one of the control individuals.(ABSTRACT TRUNCATED AT 400 WORDS)
在多发性硬化症(MS)患者大脑中发现活化的T细胞,这表明这些细胞在该疾病的发病机制中至关重要。最近,我们使用聚合酶链反应(PCR)方法分析了MS患者和对照者大脑样本中T细胞受体(TCR)的Vα和Vβ基因重排情况。这些研究结果显示,MS患者大脑中TCR V基因的使用可能受到限制,特别是Vβ基因可能在某些与MS易感性相关的HLA单倍型中优先重排。鉴于最近有证据表明携带γδ链的T淋巴细胞可能具有自身反应性潜力,我们评估了此类携带TCR的淋巴细胞是否也存在于慢性MS病变中。使用一组Vγ和Vδ引物与Cγ或Cδ引物配对,通过PCR方法对12例MS患者大脑以及10例正常尸检病例和3例神经疾病对照者的大脑样本中的TCR Vγ和Vδ进行了分析。通过Southern印迹法以及用特异性Cγ和Cδ探针与PCR产物杂交,证实了TCR Vγ-Cγ和Vδ-Cδ重排。在从12例MS患者获取的23个大脑样本中,每个样本仅检测到1至4种重排的TCR Vγ和Vδ转录本,大多数γδ T细胞表达Vγ2和Vδ2链。与之形成显著对比的是,在分析的10个非神经疾病对照大脑中,仅在其中1个大脑中发现了Vγ和Vδ转录本。为了评估MS患者大脑样本中Vγ2和Vδ2 T细胞受体链的克隆性,我们对从2例MS患者的脑组织、脑脊液和脾脏以及2例对照者的脾脏中扩增出的TCR Vγ-N-Jγ-Cγ和Vδ-N-Dδ-N-Jδ-Cδ片段的连接区进行了测序。目前获得的序列分析结果没有显示出表达特定类型γδ T细胞受体的一个或多个克隆存在MS特异性扩增的有力证据。相反,在1例MS患者和1例对照者的脾脏中均发现了不同群体的携带TCRγδ的T细胞的克隆性扩增。(摘要截选至400字)