Wraith D C
Department of Pathology and Microbiology, Bristol University School of Medical Sciences, UK.
Int Arch Allergy Immunol. 1995 Dec;108(4):355-9. doi: 10.1159/000237182.
Current drug-based therapies for autoimmune and allergic conditions are non-specific and often associated with severe side effects. Recent advances in our knowledge of how T cells see antigens points to an improved strategy. T lymphocytes recognise processed forms of antigen which can be mimicked by synthetic peptides designed and built in the laboratory. It is clear from recent work that these synthetic peptides, when given systemically in solution, induce a state of hyporesponsiveness in naive T cells thereby specifically preventing a subsequent immune response. Moreover systemic administration of soluble peptides can inhibit ongoing immune responses. Taken together this new information offers great promise for future development of antigen-based drugs for the treatment of autoimmune and allergic diseases.
目前用于自身免疫性疾病和过敏性疾病的药物疗法缺乏特异性,且常常伴有严重的副作用。我们对T细胞识别抗原方式的最新认识为改进治疗策略指明了方向。T淋巴细胞识别经过加工的抗原形式,而这些形式可以被在实验室设计和合成的肽所模拟。近期研究表明,这些合成肽在溶液中全身给药时,可诱导初始T细胞进入低反应状态,从而特异性地预防后续免疫反应。此外,可溶性肽的全身给药可抑制正在进行的免疫反应。综合来看,这些新信息为基于抗原的药物治疗自身免疫性疾病和过敏性疾病的未来发展带来了巨大希望。