Muller Sylviane, Monneaux Fanny, Schall Nicolas, Rashkov Rasho K, Oparanov Boycho A, Wiesel Philippe, Geiger Jean-Marie, Zimmer Robert
CNRS, Institut de Biologie Moléculaire et Cellulaire, Strasbourg, France.
Arthritis Rheum. 2008 Dec;58(12):3873-83. doi: 10.1002/art.24027.
To assess the safety, tolerability, and efficacy of spliceosomal peptide P140 (IPP-201101; sequence 131-151 of the U1-70K protein phosphorylated at Ser140), which is recognized by lupus CD4+ T cells, in the treatment of patients with systemic lupus erythematosus (SLE).
An open-label, dose-escalation phase II study was conducted in two centers in Bulgaria. Twenty patients (2 male and 18 female) with moderately active SLE received 3 subcutaneous (SC) administrations of a clinical batch of P140 peptide at 2-week intervals. Clinical evaluation was performed using approved scales. A panel of autoantibodies, including antinuclear antibodies, antibodies to extractable nuclear antigens (U1 RNP, SmD1, Ro/SSA, La/SSB), and antibodies to double-stranded DNA (anti-dsDNA), chromatin, cardiolipin, and peptides of the U1-70K protein, was tested by enzyme-linked immunosorbent assay (ELISA). The plasma levels of C-reactive protein, total Ig, IgG, IgG subclasses, IgM, IgA, and IgE, and of the cytokines interleukin-2 and tumor necrosis factor alpha were measured by ELISA and nephelometry.
IgG anti-dsDNA antibody levels decreased by at least 20% in 7 of 10 patients who received 3 x 200 microg IPP-201101 (group 1), but only in 1 patient in the group receiving 3 x 1,000 microg IPP-201101 (group 2). Physician's global assessment of disease activity scores and scores on the SLE Disease Activity Index were significantly decreased in group 1. The changes occurred progressively in the population of responders, increased in magnitude during the treatment period, and were sustained. No clinical or biologic adverse effects were observed in the individuals, except for some local irritation at the highest concentration.
IPP-201101 was found to be safe and well tolerated by subjects. Three SC doses of IPP-201101 at 200 microg significantly improved the clinical and biologic status of lupus patients.
评估狼疮CD4+ T细胞识别的剪接体肽P140(IPP-201101;丝氨酸140磷酸化的U1-70K蛋白的第131-151位序列)治疗系统性红斑狼疮(SLE)患者的安全性、耐受性和疗效。
在保加利亚的两个中心进行了一项开放标签、剂量递增的II期研究。20例中度活动期SLE患者(2例男性和18例女性)每2周接受3次皮下注射临床批次的P140肽。使用批准的量表进行临床评估。通过酶联免疫吸附测定(ELISA)检测一组自身抗体,包括抗核抗体、可提取核抗原抗体(U1 RNP、SmD1、Ro/SSA、La/SSB)以及双链DNA抗体(抗dsDNA)、染色质、心磷脂和U1-70K蛋白肽段的抗体。通过ELISA和散射比浊法测量血浆中C反应蛋白、总免疫球蛋白、IgG、IgG亚类、IgM、IgA和IgE以及细胞因子白细胞介素-2和肿瘤坏死因子α的水平。
在接受3×200μg IPP-201101的10例患者中的7例(第1组),IgG抗dsDNA抗体水平至少降低了20%,但在接受3×1000μg IPP-201101的组(第2组)中仅1例患者出现这种情况。第1组医生对疾病活动评分和SLE疾病活动指数评分显著降低。这些变化在反应者群体中逐渐发生,在治疗期间幅度增加,并持续存在。除了最高浓度时出现一些局部刺激外,未观察到个体有临床或生物学不良反应。
发现IPP-201101对受试者安全且耐受性良好。200μg的3次皮下注射IPP-201101显著改善了狼疮患者的临床和生物学状态。