Tolerogenic dendritic cell therapy – causal treatment of autoimmune diseases

U. Švajger, M. Jeras
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Abstract

Background: Dendritic cells (DCs) are considered as primary carriers of antigenic (Ag) information in the human body. This information is later presented to Ag-specific T lymphocytes in various ways that can be either immunostimulating or immunosuppressive. The latter depends on the activation status of DCs, in which way the DCs display extreme plasticity in terms of their function. Tolerogenic DCs, which are characterized by extensive immunosuppressive properties, can induce the generation of regulatory T lymphocytes or cause T-cell anergy. In the last two decades, considerable evidence has accumulated using animal models, which points to safety and efficacy of DC application in terms of treating immune-mediated diseases. Immuntherapy using DCs is nowadays becoming a clinical reality. At present, a clinical study using autologous DCs derived from human monocytes and treated ex vivo to induce their immunosuppressive potential, with the aim to treat autoimmune type 1 diabetes, is registered within NIH (National Institutes of Health). Conclusion: The review discusses the characteristics of DCs, suitable for use in cellular therapy of autoimmune diseases, their role in such therapies and the way in which such cells can be generated in the laboratory. Therapy of autoimmune diseases using tolerogenic DCs represents an outstanding potential, however the major obstacles lay in the way of proper preparation of cellular products, where all procedures should follow the strict demands of good manufacturing practice (GMP).
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耐受性树突状细胞疗法-自身免疫性疾病的因果治疗
背景:树突状细胞(dc)被认为是人体抗原(Ag)信息的主要载体。这些信息随后以免疫刺激或免疫抑制的各种方式呈现给ag特异性T淋巴细胞。后者取决于DCs的激活状态,在这种情况下,DCs在其功能方面表现出极大的可塑性。耐受性dc具有广泛的免疫抑制特性,可诱导调节性T淋巴细胞的产生或引起T细胞能量。在过去的二十年中,通过动物模型积累了大量证据,这些证据表明DC在治疗免疫介导性疾病方面的安全性和有效性。利用树突状细胞进行免疫治疗已成为临床现实。目前,一项临床研究已在美国国立卫生研究院(NIH)注册,该研究使用来自人类单核细胞的自体dc,并在体外处理以诱导其免疫抑制潜力,目的是治疗自身免疫性1型糖尿病。结论:本文综述了适合自身免疫性疾病细胞治疗的树突状细胞的特点,它们在这种治疗中的作用以及在实验室中产生这种细胞的方法。使用耐受性dc治疗自身免疫性疾病具有突出的潜力,但主要障碍在于细胞产品的适当制备方式,其中所有程序都应严格遵守良好生产规范(GMP)的要求。
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来源期刊
CiteScore
0.30
自引率
0.00%
发文量
65
审稿时长
4-8 weeks
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