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T细胞受体肽疗法治疗实验性自身免疫性脑脊髓炎和多发性硬化症。

T-cell receptor peptide therapy in EAE and MS.

作者信息

Vandenbark A A, Bourdette D N, Whitham R, Chou Y K, Hashim G A, Offner H

机构信息

V.A. Medical Center, Portland, OR 97201.

出版信息

Clin Exp Rheumatol. 1993 Mar-Apr;11 Suppl 8:S51-3.

PMID:7686833
Abstract

Synthetic peptides corresponding to germline TCR V beta 8.2 sequences overexpressed by Lewis rat encephalitogenic T cells are effective in the prevention and treatment of autoimmune encephalomyelitis (EAE). In evaluating optimal conditions for identifying disease-relevant target V beta genes, we found that the biased expression of V beta 8.2 was most pronounced in the CNS among activated, IL-2 responsive T cells, but was weakly reflected in the cerebrospinal fluid. Evaluation of basic protein reactive T cells from patients with multiple sclerosis revealed biased expression of V beta 5.2 and to a lesser degree, V beta 6.1. Treatment of 11 MS patients with synthetic TCR V beta 5.2 and V beta 6.1 CDR2 peptides boosted the frequency of anti-TCR reactive T cells in a majority of patients, without compromising recall immunity or causing side effects. TCR peptides may be useful in the treatment of human autoimmune diseases, providing that disease-relevant V genes can be identified.

摘要

与刘易斯大鼠致脑炎性T细胞过度表达的种系TCR Vβ8.2序列相对应的合成肽在自身免疫性脑脊髓炎(EAE)的预防和治疗中有效。在评估鉴定疾病相关靶Vβ基因的最佳条件时,我们发现Vβ8.2的偏向性表达在活化的、对IL-2有反应的T细胞中在中枢神经系统最为明显,但在脑脊液中反映较弱。对多发性硬化症患者的碱性蛋白反应性T细胞的评估显示Vβ5.2有偏向性表达,Vβ6.1的偏向性表达程度较轻。用合成的TCR Vβ5.2和Vβ6.1 CDR2肽治疗11例MS患者,在大多数患者中提高了抗TCR反应性T细胞的频率,而不损害回忆免疫或引起副作用。只要能鉴定出与疾病相关的V基因,TCR肽可能对人类自身免疫性疾病的治疗有用。

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