Vandevyver C, Buyse I, Philippaerts L, Ghabanbasani Z, Medaer R, Carton H, Cassiman J J, Raus J
Department of Immunology/Biotechnology, Dr. L. Willems-Instituut, Diepenbeek, Belgium.
J Neuroimmunol. 1994 Jun;52(1):25-32. doi: 10.1016/0165-5728(94)90158-9.
There are compelling data to indicate that the susceptibility to multiple sclerosis (MS) is inherited, at least in part. Particular HLA genotypes may be associated with MS and recently also polymorphisms in the T-cell receptor (TCR) genes have been reported to correlate with the disease; however, these data have been difficult to confirm. We investigated the TCRA and TCRB chain genes of HLA-typed Belgian CP MS patients employing four DNA restriction fragment length polymorphisms (RFLPs) detected with TCR constant (TCRAC1, TCRBC2) and variable (TCRBV8, TCRBV11) gene segments. Similar frequencies in patients and controls were observed for all RFLPs studied. Although the HLA DR2 genotype was significantly associated with MS, no interactive effects were seen with MS, DR2, TCRAC1, TCRBC2 and TCRBV alleles. We conclude that, while a clear association with HLA DR2 is observed, little convincing evidence exists for an association of CP MS with RFLPs of the TCRA or TCRB chain genes.
有确凿的数据表明,多发性硬化症(MS)的易感性至少部分是可遗传的。特定的人类白细胞抗原(HLA)基因型可能与MS相关,最近也有报道称T细胞受体(TCR)基因的多态性与该疾病相关;然而,这些数据很难得到证实。我们利用通过TCR恒定区(TCRAC1、TCRBC2)和可变区(TCRBV8、TCRBV11)基因片段检测到的四种DNA限制性片段长度多态性(RFLP),对HLA分型的比利时慢性进展型MS患者的TCRA和TCRB链基因进行了研究。在所研究的所有RFLP中,患者和对照组的频率相似。虽然HLA DR2基因型与MS显著相关,但未观察到MS、DR2、TCRAC1、TCRBC2和TCRBV等位基因之间的交互作用。我们得出结论,虽然观察到与HLA DR2有明确关联,但几乎没有令人信服的证据表明慢性进展型MS与TCRA或TCRB链基因的RFLP有关联。