Haider Asifa S, Lowes Michelle A, Gardner Humphrey, Bandaru Raj, Darabi Kamruz, Chamian Francesca, Kikuchi Toyoko, Gilleaudeau Patricia, Whalen Mary S, Cardinale Irma, Novitskaya Inna, Krueger James G
Laboratory for Investigative Dermatology, Rockefeller University, New York, NY 10021, USA.
J Immunol. 2007 Jun 1;178(11):7442-9. doi: 10.4049/jimmunol.178.11.7442.
Alefacept is an LFA3-Ig fusion protein that binds to CD2 and is thought to inhibit T cell activation by antagonism of CD2 signaling or by lysis of CD2(+) cells. Alefacept is potential future therapeutic for organ transplant recipients or graft-vs-host disease and is an approved therapeutic for psoriasis vulgaris, which is a T cell-mediated inflammatory disease. However, alefacept improves psoriasis in only approximately 50% of patients treated for 12 wk. We studied the immunologic effects of alefacept in a group of psoriasis patients during treatment. We found that T cells, especially CD8(+) T cells, were rapidly decreased in the peripheral circulation. Decreases in circulating T cells were not associated with induced apoptosis. Unexpectedly, in addition to suppression of inflammatory genes, we found a marked induction of mRNAs for STAT1, IL-8, and monokine induced by IFN-gamma during the first day of treatment in PBMC. We confirmed the agonistic effects of alefacept in PBMC in vitro, which were similar to CD3/CD28 ligation on T cells. These data establish that alefacept activates gene expression programs in leukocytes and suggest that its therapeutic action may be as a mixed agonist/antagonist. Furthermore, responding patients to alefacept treatment show unique patterns of gene modulation. Whereas alefacept down-regulated TCRs CD3D and CD2 in responders, nonresponders reveal a higher expression of T cell activation genes such as CD69 in pretreatment PBMC. These finding suggest a potential basis for categorizing responders vs nonresponders at an early time point in treatment or before treatment of a broad range of proinflammatory diseases. This study 1) establishes alefacept as a novel CD2 agonist molecule for induction of leukocyte activation genes (prior work proposed its mechanism as a CD2 antagonist) and 2) that differential activation of genes may categorize clinical responders to this agent, critical for cost-effective use of this drug.
阿法赛特是一种LFA3-Ig融合蛋白,它与CD2结合,被认为可通过拮抗CD2信号传导或裂解CD2(+)细胞来抑制T细胞活化。阿法赛特对器官移植受者或移植物抗宿主病可能具有未来治疗潜力,它是寻常型银屑病(一种T细胞介导的炎症性疾病)的已获批治疗药物。然而,阿法赛特仅能使约50%接受12周治疗的患者的银屑病病情得到改善。我们研究了阿法赛特在一组银屑病患者治疗期间的免疫效应。我们发现外周循环中的T细胞,尤其是CD8(+) T细胞迅速减少。循环T细胞的减少与诱导凋亡无关。出乎意料的是,除了抑制炎症基因外,我们还发现在治疗的第一天,外周血单核细胞中STAT1、IL-8和干扰素-γ诱导的单核因子的mRNA显著上调。我们在体外证实了阿法赛特在外周血单核细胞中的激动作用,这与T细胞上的CD3/CD28连接相似。这些数据表明阿法赛特可激活白细胞中的基因表达程序,并提示其治疗作用可能是作为一种混合激动剂/拮抗剂。此外,对阿法赛特治疗有反应的患者表现出独特的基因调节模式。在有反应者中,阿法赛特下调了TCRs CD3D和CD2,而无反应者在治疗前的外周血单核细胞中显示出较高的T细胞活化基因如CD69的表达。这些发现提示了在治疗早期或在广泛的促炎疾病治疗前对有反应者与无反应者进行分类的潜在依据。本研究1) 将阿法赛特确立为一种新型的诱导白细胞活化基因的CD2激动剂分子(先前的研究认为其机制是作为一种CD2拮抗剂),2) 基因的差异激活可能对该药物的临床反应者进行分类,这对于该药物的成本效益使用至关重要。