Yaron Jordan R, Zhang Liqiang, Guo Qiuyun, Burgin Michelle, Schutz Lauren N, Awo Enkidia, Wise Lyn, Krause Kurt L, Ildefonso Cristhian J, Kwiecien Jacek M, Juby Michael, Rahman Masmudur M, Chen Hao, Moyer Richard W, Alcami Antonio, McFadden Grant, Lucas Alexandra R
Center for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Center for Immunotherapy, Vaccines and Virotherapy, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
J Clin Med. 2020 Mar 31;9(4):972. doi: 10.3390/jcm9040972.
Viruses are widely used as a platform for the production of therapeutics. Vaccines containing live, dead and components of viruses, gene therapy vectors and oncolytic viruses are key examples of clinically-approved therapeutic uses for viruses. Despite this, the use of virus-derived proteins as natural sources for immune modulators remains in the early stages of development. Viruses have evolved complex, highly effective approaches for immune evasion. Originally developed for protection against host immune responses, viral immune-modulating proteins are extraordinarily potent, often functioning at picomolar concentrations. These complex viral intracellular parasites have "performed the R&D", developing highly effective immune evasive strategies over millions of years. These proteins provide a new and natural source for immune-modulating therapeutics, similar in many ways to penicillin being developed from mold or streptokinase from bacteria. Virus-derived serine proteinase inhibitors (serpins), chemokine modulating proteins, complement control, inflammasome inhibition, growth factors (e.g., viral vascular endothelial growth factor) and cytokine mimics (e.g., viral interleukin 10) and/or inhibitors (e.g., tumor necrosis factor) have now been identified that target central immunological response pathways. We review here current development of virus-derived immune-modulating biologics with efficacy demonstrated in pre-clinical or clinical studies, focusing on pox and herpesviruses-derived immune-modulating therapeutics.
病毒被广泛用作生产治疗药物的平台。包含活病毒、死病毒和病毒成分的疫苗、基因治疗载体以及溶瘤病毒是临床上已获批准的病毒治疗用途的关键实例。尽管如此,将病毒衍生蛋白用作免疫调节剂的天然来源仍处于开发的早期阶段。病毒已经进化出复杂且高效的免疫逃避方法。病毒免疫调节蛋白最初是为抵御宿主免疫反应而开发的,其效力极强,通常在皮摩尔浓度下起作用。这些复杂的病毒细胞内寄生虫已经“完成了研发”,在数百万年的时间里开发出了高效的免疫逃避策略。这些蛋白为免疫调节治疗提供了一种新的天然来源,在许多方面类似于从霉菌中开发出青霉素或从细菌中开发出链激酶。现已鉴定出病毒衍生的丝氨酸蛋白酶抑制剂(丝氨酸蛋白酶抑制因子)、趋化因子调节蛋白、补体控制蛋白、炎性小体抑制蛋白、生长因子(如病毒血管内皮生长因子)以及细胞因子模拟物(如病毒白细胞介素10)和/或抑制剂(如肿瘤坏死因子),它们靶向中枢免疫反应途径。我们在此综述病毒衍生的免疫调节生物制品在临床前或临床研究中已证明具有疗效的当前开发情况,重点关注痘病毒和疱疹病毒衍生的免疫调节治疗药物。