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自体髓鞘肽耦联细胞诱导的抗原特异性耐受:多发性硬化的 1 期临床试验。

Antigen-specific tolerance by autologous myelin peptide-coupled cells: a phase 1 trial in multiple sclerosis.

机构信息

Institute for Neuroimmunology and Clinical MS Research, Center for Molecular Neurobiology, 20251 Hamburg, Germany.

出版信息

Sci Transl Med. 2013 Jun 5;5(188):188ra75. doi: 10.1126/scitranslmed.3006168.

Abstract

Multiple sclerosis (MS) is a devastating inflammatory disease of the brain and spinal cord that is thought to result from an autoimmune attack directed against antigens in the central nervous system. The aim of this first-in-man trial was to assess the feasibility, safety, and tolerability of a tolerization regimen in MS patients that uses a single infusion of autologous peripheral blood mononuclear cells chemically coupled with seven myelin peptides (MOG1-20, MOG35-55, MBP13-32, MBP83-99, MBP111-129, MBP146-170, and PLP139-154). An open-label, single-center, dose-escalation study was performed in seven relapsing-remitting and two secondary progressive MS patients who were off-treatment for standard therapies. All patients had to show T cell reactivity against at least one of the myelin peptides used in the trial. Neurological, magnetic resonance imaging, laboratory, and immunological examinations were performed to assess the safety, tolerability, and in vivo mechanisms of action of this regimen. Administration of antigen-coupled cells was feasible, had a favorable safety profile, and was well tolerated in MS patients. Patients receiving the higher doses (>1 × 10(9)) of peptide-coupled cells had a decrease in antigen-specific T cell responses after peptide-coupled cell therapy. In summary, this first-in-man clinical trial of autologous peptide-coupled cells in MS patients establishes the feasibility and indicates good tolerability and safety of this therapeutic approach.

摘要

多发性硬化症 (MS) 是一种破坏性的脑和脊髓炎症性疾病,被认为是由针对中枢神经系统抗原的自身免疫攻击引起的。这项首次人体试验的目的是评估在 MS 患者中使用一种单次输注自体外周血单核细胞与七种髓鞘肽(MOG1-20、MOG35-55、MBP13-32、MBP83-99、MBP111-129、MBP146-170 和 PLP139-154)化学偶联的耐受方案的可行性、安全性和耐受性。在七名缓解-复发型和两名继发进展型 MS 患者中进行了开放性、单中心、剂量递增研究,这些患者已停止标准治疗。所有患者都必须表现出针对试验中使用的至少一种髓鞘肽的 T 细胞反应。进行了神经学、磁共振成像、实验室和免疫学检查,以评估该方案的安全性、耐受性和体内作用机制。在 MS 患者中,抗原偶联细胞的给药是可行的,具有良好的安全性,并且耐受良好。接受更高剂量 (>1 × 10(9)) 肽偶联细胞的患者在肽偶联细胞治疗后抗原特异性 T 细胞反应下降。总之,这项首次在 MS 患者中进行的自体肽偶联细胞的临床试验确立了这种治疗方法的可行性,并表明了这种治疗方法的良好耐受性和安全性。

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