首页> 美国卫生研究院文献>EBioMedicine >Epitope-Specific Immunotherapy Targeting CD4-Positive T Cells in Celiac Disease: Safety Pharmacokinetics and Effects on Intestinal Histology and Plasma Cytokines with Escalating Dose Regimens of Nexvax2 in a Randomized Double-Blind Placebo-Controlled Phase 1 Study
【2h】

Epitope-Specific Immunotherapy Targeting CD4-Positive T Cells in Celiac Disease: Safety Pharmacokinetics and Effects on Intestinal Histology and Plasma Cytokines with Escalating Dose Regimens of Nexvax2 in a Randomized Double-Blind Placebo-Controlled Phase 1 Study

机译:针对乳糜泻中CD4阳性T细胞的针对抗原决定簇的特定免疫疗法:安全性药代动力学以及对Nexvax2剂量剂量递增的肠道组织学和血浆细胞因子的影响涉及一项随机双盲安慰剂对照的1期研究

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

BackgroundNexvax2® is a novel, peptide-based, epitope-specific immunotherapy intended to be administered by regular injections at dose levels that increase the threshold for clinical reactivity to natural exposure to gluten and ultimately restore tolerance to gluten in patients with celiac disease. Celiac disease patients administered fixed intradermal doses of Nexvax2 become unresponsive to the HLA-DQ2·5-restricted gluten epitopes in Nexvax2, but gastrointestinal symptoms and cytokine release mimicking gluten exposure, that accompany the first dose, limit the maximum tolerated dose to 150 μg. Our aim was to test whether stepwise dose escalation attenuated the first dose effect of Nexvax2 in celiac disease patients.
机译:背景Nexvax2®是一种新型的,基于肽的,表位特异性的免疫疗法,旨在通过常规注射给药,其剂量水平可提高对自然暴露于麸质的临床反应性的阈值,并最终恢复乳糜泻患者对麸质的耐受性。腹腔疾病患者使用固定剂量的Nexvax2皮内注射后,对Nexvax2中受HLA-DQ2·5限制的面筋表位无反应,但胃肠道症状和细胞因子的释放模仿了面筋的暴露,在第一剂量时,最大耐受剂量被限制为150μg。我们的目的是测试逐步剂量增加是否会减轻Nexvax2在腹腔疾病患者中的首剂作用。

著录项

相似文献

  • 外文文献
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号