Martinez Elisa C, Garg Ravendra, Shrivastava Pratima, Gomis Susantha, van Drunen Littel-van den Hurk Sylvia
Department of Microbiology and Immunology, College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, 107 Wiggins Road, S7N 5E5, Canada; Vaccine and Infectious Disease Organization-International Vaccine Centre (VIDO-InterVac), University of Saskatchewan, Saskatoon, Saskatchewan, 120 Veterinary Road, S7N 5E3, Canada.
Vaccine and Infectious Disease Organization-International Vaccine Centre (VIDO-InterVac), University of Saskatchewan, Saskatoon, Saskatchewan, 120 Veterinary Road, S7N 5E3, Canada.
Antiviral Res. 2016 Nov;135:108-119. doi: 10.1016/j.antiviral.2016.10.008. Epub 2016 Oct 19.
Respiratory syncytial virus (RSV) is the leading cause of acute lower respiratory tract infections in infants and young children. There are no licensed RSV vaccines available, and the few treatment options for high-risk individuals are either extremely costly or cause severe side effects and toxicity. Immunomodulation mediated by a novel formulation consisting of the toll-like receptor 3 agonist poly(I:C), an innate defense regulator peptide and a polyphosphazene (P-I-P) was evaluated in the context of lethal infection with pneumonia virus of mice (PVM). Intranasal delivery of a single dose of P-I-P protected adult mice against PVM when given 24 h prior to challenge. These animals experienced minimal weight loss, no clinical disease, 100% survival, and reduced lung pathology. Similar clinical outcomes were observed in mice treated up to 3 days prior to infection. P-I-P pre-treatment induced early mRNA and protein expression of key chemokine and cytokine genes, reduced the recruitment of neutrophils and eosinophils, decreased virus titers in the lungs, and modulated the delayed exacerbated nature of PVM disease without any short-term side effects. On day 14 post-infection, P-I-P-treated mice were confirmed to be PVM-free. These results demonstrate the capacity of this formulation to prevent PVM and possibly other viral respiratory infections.
呼吸道合胞病毒(RSV)是婴幼儿急性下呼吸道感染的主要病因。目前尚无获得许可的RSV疫苗,针对高危个体的治疗选择很少,要么极其昂贵,要么会导致严重的副作用和毒性。在小鼠肺炎病毒(PVM)致死性感染的背景下,评估了由Toll样受体3激动剂聚肌胞苷酸(poly(I:C))、一种先天性防御调节肽和一种聚磷腈(P-I-P)组成的新型制剂介导的免疫调节作用。在攻击前24小时经鼻给予单剂量的P-I-P可保护成年小鼠免受PVM感染。这些动物体重减轻极少,无临床疾病,存活率达100%,肺部病理学改变减轻。在感染前长达3天接受治疗的小鼠中也观察到了类似的临床结果。P-I-P预处理可诱导关键趋化因子和细胞因子基因的早期mRNA和蛋白表达,减少中性粒细胞和嗜酸性粒细胞的募集,降低肺部病毒滴度,并调节PVM疾病的延迟加剧特性,且无任何短期副作用。在感染后第14天,经P-I-P治疗的小鼠被证实无PVM。这些结果证明了该制剂预防PVM及可能的其他病毒性呼吸道感染的能力。