工程减毒活疫苗:老狗学新把戏。

IF 4.7 Q2 IMMUNOLOGY Journal of Translational Autoimmunity Pub Date : 2023-01-01 DOI:10.1016/j.jtauto.2023.100198
Julia Plocica , Fengguang Guo , Jugal Kishore Das , Koichi S. Kobayashi , Thomas A. Ficht , Robert C. Alaniz , Jianxun Song , Paul de Figueiredo
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引用次数: 1

摘要

类风湿性关节炎和1型糖尿病等自身免疫性疾病是越来越常见的全球问题。对此类疾病患病率增加和传统治疗方案疗效有限的担忧,需要新的疗法来应对这些挑战。自身免疫性疾病的严重程度和微生态失调是相互关联的。尽管益生菌已被确定为一种重新平衡微生物组和抑制自身免疫症状的疗法,但这些微生物往往缺乏非共生细菌中发现的一些有利品质。通过衰减和基因操作,这些非共生细菌已被改造成重组形式,提供了能够解决RA和T1D中发现的免疫失衡的可塑性平台。这些细菌已被改造以表达已知抑制自身免疫的有价值的基因产物,如抗炎细胞因子、自身抗原和合成微生物代谢产物的酶。这篇综述将强调该领域的当前和新兴趋势,并讨论如何将其用于预防和控制自身免疫性疾病。
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Engineering live attenuated vaccines: Old dogs learning new tricks

Autoimmune diseases such as rheumatoid arthritis and type 1 diabetes are increasingly common global problems. Concerns about increases in the prevalence of such diseases and the limited efficacy of conventional treatment regimens necessitates new therapies to address these challenges. Autoimmune disease severity and dysbiosis are interconnected. Although probiotics have been established as a therapy to rebalance the microbiome and suppress autoimmune symptoms, these microbes tend to lack a number of advantageous qualities found in non-commensal bacteria. Through attenuation and genetic manipulation, these non-commensal bacteria have been engineered into recombinant forms that offer malleable platforms capable of addressing the immune imbalances found in RA and T1D. Such bacteria have been engineered to express valuable gene products known to suppress autoimmunity such as anti-inflammatory cytokines, autoantigens, and enzymes synthesizing microbial metabolites. This review will highlight current and emerging trends in the field and discuss how they may be used to prevent and control autoimmune diseases.

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来源期刊
Journal of Translational Autoimmunity
Journal of Translational Autoimmunity Medicine-Immunology and Allergy
CiteScore
7.80
自引率
2.60%
发文量
33
审稿时长
55 days
期刊最新文献
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