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弗氏完全佐剂在肠道病毒感染小鼠模型中的抗病毒作用证据。

Evidence for Anti-Viral Effects of Complete Freund's Adjuvant in the Mouse Model of Enterovirus Infection.

作者信息

Gangaplara Arunakumar, Massilamany Chandirasegaran, Lasrado Ninaad, Steffen David, Reddy Jay

机构信息

School of Veterinary Medicine and Biomedical Sciences, University of Nebraska-Lincoln, Lincoln, NE 68583, USA.

Laboratory of Early Sickle Mortality Prevention, Cellular and Molecular Therapeutics Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Vaccines (Basel). 2020 Jul 7;8(3):364. doi: 10.3390/vaccines8030364.

Abstract

Group B coxsackieviruses (CVBs) belonging to the genus, and contain six serotypes that induce various diseases, whose occurrence may involve the mediation of more than one serotype. We recently identified immunogenic epitopes within coxsackieviruses B3 (CVB3) viral protein 1 that induce anti-viral T cell responses in mouse models of CVB infections. In our investigations to determine the protective responses of the viral epitopes, we unexpectedly noted that animals immunized with complete Freund's adjuvant (CFA) alone and later challenged with CVB3 were completely protected against myocarditis. Similarly, the pancreatitis-inducing ability of CVB3 was remarkably reduced to only 10% in the CFA group as opposed to 73.3% in the control group that received no CFA. Additionally, no mortalities were noted in the CFA group, whereas 40% of control animals died during the course of 21 days post-infection with CVB3. Taken together, our data suggest that the adjuvant effects of CFA may be sufficient for protection against CVB infections. These observations may provide new insights into our understanding of the occurrence of viral infections.

摘要

B组柯萨奇病毒(CVB)属于该属,包含六种血清型,可引发多种疾病,其发病可能涉及不止一种血清型的介导。我们最近在柯萨奇病毒B3(CVB3)病毒蛋白1中鉴定出免疫原性表位,这些表位在CVB感染的小鼠模型中可诱导抗病毒T细胞反应。在我们确定病毒表位保护性反应的研究中,我们意外地注意到,仅用完全弗氏佐剂(CFA)免疫、随后用CVB3攻击的动物对心肌炎具有完全的抵抗力。同样,CVB3诱导胰腺炎的能力在CFA组中显著降低至仅10%,而未接受CFA的对照组中这一比例为73.3%。此外,CFA组未观察到死亡情况,而40%的对照动物在感染CVB3后的21天内死亡。综合来看,我们的数据表明CFA的佐剂效应可能足以预防CVB感染。这些观察结果可能为我们理解病毒感染的发生提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec3/7563290/224988f59c0c/vaccines-08-00364-g001.jpg

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