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教授宽容:庞贝病酶替代治疗的新方法。

Teaching tolerance: New approaches to enzyme replacement therapy for Pompe disease.

机构信息

EpiVax, Inc., Providence, RI, USA.

出版信息

Hum Vaccin Immunother. 2012 Oct;8(10):1459-64. doi: 10.4161/hv.21405. Epub 2012 Oct 1.

Abstract

Babies born with Pompe disease require life-long treatment with enzyme-replacement therapy (ERT). Despite the human origin of the therapy, recombinant human lysosomal acid α glucosidase (GAA, rhGAA), ERT unfortunately leads to the development of high titers of anti-rhGAA antibody, decreased effectiveness of ERT, and a fatal outcome for a significant number of children who have Pompe disease. The severity of disease, anti-drug antibody (ADA) development, and the consequences thereof are directly related to the degree of the enzyme deficiency. Babies born with a complete deficiency GAA are said to have cross-reactive immunologic material (CRIM)-negative Pompe disease and are highly likely to develop GAA ADA. Less frequently, GAA ADA develop in CRIM-positive individuals. Currently, GAA-ADA sero-positive babies are treated with a combination of immunosuppressive drugs to induce immunological tolerance to ERT, but the long-term effect of these regimens is unknown. Alternative approaches that might redirect the immune response toward antigen-specific tolerance without immunosuppressive agents are needed. Methods leading to the induction of antigen-specific regulatory T cells (Tregs), using peptides such as Tregitopes (T regulatory cell epitopes) are under consideration for the future treatment of CRIM-negative Pompe disease. Tregitopes are natural T cell epitopes derived from immunoglobulin G (IgG) that cause the expansion and activation of regulatory T cells (Treg). Teaching the immune system to tolerate GAA by co-delivering GAA with Tregitope peptides might dramatically improve the lives of CRIM-negative babies and could be applied to other enzyme replacement therapies to which ADA have been induced.

摘要

患有庞贝病的婴儿需要终身接受酶替代疗法(ERT)治疗。尽管这种疗法来源于人类,但重组人溶酶体酸性α-葡萄糖苷酶(GAA,rhGAA),不幸的是,ERT 会导致抗 rhGAA 抗体的产生,降低 ERT 的效果,导致相当数量患有庞贝病的儿童死亡。疾病的严重程度、抗药物抗体(ADA)的发展及其后果与酶缺乏的程度直接相关。出生时完全缺乏 GAA 的婴儿被称为具有交叉反应免疫物质(CRIM)阴性的庞贝病,并且极有可能产生 GAA ADA。较少见的情况下,CRIM 阳性个体也会产生 GAA ADA。目前,GAA-ADA 血清阳性的婴儿接受免疫抑制药物联合治疗,以诱导对 ERT 的免疫耐受,但这些方案的长期效果尚不清楚。需要寻找替代方法,这些方法可能会在不使用免疫抑制剂的情况下将免疫反应重新导向抗原特异性耐受。未来可能会考虑使用 Tregitopes(调节性 T 细胞表位)等肽类诱导抗原特异性调节性 T 细胞(Treg)的方法来治疗 CRIM 阴性的庞贝病。Tregitopes 是源自免疫球蛋白 G(IgG)的天然 T 细胞表位,可引起调节性 T 细胞(Treg)的扩增和激活。通过与 Tregitope 肽共递呈 GAA,教导免疫系统耐受 GAA,可能会极大地改善 CRIM 阴性婴儿的生活,并可应用于其他已诱导产生 ADA 的酶替代疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f98/3660767/25b4de0101bf/hvi-8-1459-g1.jpg

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