Beyersdorf N, Hanke T, Kerkau T, Hünig T
Institute for Virology and Immunobiology, University of Würzburg, Versbacherstr. 7, 97078 Würzburg, Germany.
Ann Rheum Dis. 2005 Nov;64 Suppl 4(Suppl 4):iv91-5. doi: 10.1136/ard.2005.042564.
This paper reviews the existing evidence regarding the use of superagonistic anti-CD28 antibodies (CD28 superagonists) for therapeutic manipulation of regulatory T cells (T(reg) cells). The molecular properties of superagonistic anti-CD28 antibodies allow the generation of a strong activating signal in mature T cells, including T(reg) cells, without additional stimulation of the T cell receptor complex. CD28 superagonist administration in vivo leads to the preferential expansion and strong activation of naturally occurring CD4+CD25+CTLA-4+FoxP3+ T(reg) cells over conventional T cells. In animal models, both prophylactic and therapeutic administration of a CD28 superagonist prevented or at least greatly mitigated clinical symptoms and induced remission. Adoptive transfer experiments have further shown that CD28 superagonists mediate protection by expansion and activation of CD4+CD25+ T(reg) cells. Therefore, superagonistic anti-CD28 antibodies offer a promising novel treatment option for human autoimmune diseases and the first clinical trials are eagerly awaited.
本文综述了关于使用超激动性抗CD28抗体(CD28超激动剂)对调节性T细胞(Treg细胞)进行治疗性调控的现有证据。超激动性抗CD28抗体的分子特性能够在成熟T细胞(包括Treg细胞)中产生强烈的激活信号,而无需额外刺激T细胞受体复合物。在体内施用CD28超激动剂会导致天然存在的CD4+CD25+CTLA-4+FoxP3+Treg细胞相较于传统T细胞优先扩增并被强烈激活。在动物模型中,预防性和治疗性施用CD28超激动剂均可预防或至少极大地减轻临床症状并诱导缓解。过继性转移实验进一步表明,CD28超激动剂通过扩增和激活CD4+CD25+Treg细胞介导保护作用。因此,超激动性抗CD28抗体为人类自身免疫性疾病提供了一种有前景的新型治疗选择,人们急切期待着首批临床试验的结果。