...
首页> 外文期刊>Clinical immunology: The official journal of the Clinical Immunology Society >Autologous attenuated T-cell vaccine (Tovaxin) dose escalation in multiple sclerosis relapsing-remitting and secondary progressive patients nonresponsive to approved immunomodulatory therapies.
【24h】

Autologous attenuated T-cell vaccine (Tovaxin) dose escalation in multiple sclerosis relapsing-remitting and secondary progressive patients nonresponsive to approved immunomodulatory therapies.

机译:对批准的免疫调节疗法无反应的多发性硬化症复发和继发进行性患者中的自体减毒T细胞疫苗(Tovaxin)剂量递增。

获取原文
获取原文并翻译 | 示例

摘要

An open-label dose escalation study of T-cell vaccination in multiple sclerosis patients was conducted using attenuated myelin reactive T-cells (MRTC) selected with six myelin peptides, two each from MBP, PLP and MOG. The dose range of subcutaneous injections given at weeks 0, 4, 12 and 20 was 6-9E6, 30-45E6 and 60-90E6 irradiated MRTC. Assessments were over 52 weeks for MRTC levels, EDSS, MSIS-29, brain MRI and relapses. The 30-45E6 dose was the most effective with reductions in MRTC ranging from 92.4% at week 5 to 64.8% at week 52. The reduction in relapses compared to baseline for the M-ITT and evaluable per-protocol analyses were 63.5%, and 85.0% at week 52. The MRI lesions were stable while there was an improvement trend in the EDSS and MSIS-29 physical subscore following the second injection. Adverse events were mild to moderate in intensity with mild injection site reactions occurring with increasing dosage. The mid-dose was selected for further clinical development studies because of the rapid depletion of peripheral blood MRTC and a trend for improvements in clinical outcomes following immunization.
机译:在多发性硬化症患者中,使用减毒的髓鞘反应性T细胞(MRTC)进行了一项公开标记的剂量递增研究,研究对象是从6种髓鞘肽中选择的,它们分别来自MBP,PLP和MOG,其中两种。在第0、4、12和20周时皮下注射的剂量范围是6-9E6、30-45E6和60-90E6辐照的MRTC。对MRTC水平,EDSS,MSIS-29,脑MRI和复发的评估超过52周。 30-45E6剂量最有效,MRTC的降低范围从第5周的92.4%降至第52周的64.8%。与基线相比,M-ITT和按方案评估的复发率降低了63.5%,并且第52周时为85.0%。第二次注射后,MRI病变稳定,而EDSS和MSIS-29物理评分得到改善。不良事件的强度为轻度至中度,随着剂量的增加会发生轻度的注射部位反应。由于外周血MRTC的快速耗竭以及免疫后临床结局有改善的趋势,因此选择了中等剂量进行进一步的临床开发研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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