scholarly journals Regulation of hepatic innate immunity by hepatitis C virus

2013 ◽  
Vol 19 (7) ◽  
pp. 879-888 ◽  
Author(s):  
Stacy M Horner ◽  
Michael Gale

Cytokine ◽  
2011 ◽  
Vol 56 (1) ◽  
pp. 49 ◽  
Author(s):  
Emmanuel Thomas ◽  
Veronica D. Gonzalez ◽  
Qisheng Li ◽  
Ankit A. Modi ◽  
Lorenzo Uccellini ◽  
...  


2012 ◽  
Vol 7 (1) ◽  
Author(s):  
Luigi Buonaguro ◽  
Annacarmen Petrizzo ◽  
Maria Lina Tornesello ◽  
Franco M Buonaguro




10.2741/3579 ◽  
2009 ◽  
Vol 14 (1) ◽  
pp. 4950 ◽  
Author(s):  
Deborah, R. Taylor


Vaccines ◽  
2020 ◽  
Vol 8 (2) ◽  
pp. 313
Author(s):  
Daniel Sepulveda-Crespo ◽  
Salvador Resino ◽  
Isidoro Martinez

Despite successful treatments, hepatitis C virus (HCV) infections continue to be a significant world health problem. High treatment costs, the high number of undiagnosed individuals, and the difficulty to access to treatment, particularly in marginalized susceptible populations, make it improbable to achieve the global control of the virus in the absence of an effective preventive vaccine. Current vaccine development is mostly focused on weakly immunogenic subunits, such as surface glycoproteins or non-structural proteins, in the case of HCV. Adjuvants are critical components of vaccine formulations that increase immunogenic performance. As we learn more information about how adjuvants work, it is becoming clear that proper stimulation of innate immunity is crucial to achieving a successful immunization. Several hepatic cell types participate in the early innate immune response and the subsequent inflammation and activation of the adaptive response, principally hepatocytes, and antigen-presenting cells (Kupffer cells, and dendritic cells). Innate pattern recognition receptors on these cells, mainly toll-like receptors, are targets for new promising adjuvants. Moreover, complex adjuvants that stimulate different components of the innate immunity are showing encouraging results and are being incorporated in current vaccines. Recent studies on HCV-vaccine adjuvants have shown that the induction of a strong T- and B-cell immune response might be enhanced by choosing the right adjuvant.



2016 ◽  
Vol 90 (15) ◽  
pp. 6832-6845 ◽  
Author(s):  
Binbin Xue ◽  
Darong Yang ◽  
Jingjing Wang ◽  
Yan Xu ◽  
Xiaohong Wang ◽  
...  

ABSTRACTInterferons (IFNs) restrict various kinds of viral infection via induction of hundreds of IFN-stimulated genes (ISGs), while the functions of the majority of ISGs are broadly unclear. Here, we show that a high-IFN-inducible gene, ISG12a (also known as IFI27), exhibits a nonapoptotic antiviral effect on hepatitis C virus (HCV) infection. Viral NS5A protein is targeted specifically by ISG12a, which mediates NS5A degradation via a ubiquitination-dependent proteasomal pathway. K374R mutation in NS5A domain III abrogates ISG12a-induced ubiquitination and degradation of NS5A. S-phase kinase-associated protein 2 (SKP2) is identified as an ubiquitin E3 ligase for NS5A. ISG12a functions as a crucial adaptor that promotes SKP2 to interact with and degrade viral protein. Moreover, the antiviral effect of ISG12a is dependent on the E3 ligase activity of SKP2. These findings uncover an intriguing mechanism by which ISG12a restricts viral infection and provide clues for understanding the actions of innate immunity.IMPORTANCEUpon virus invasion, IFNs induce numerous ISGs to control viral spread, while the functions of the majority of ISGs are broadly unclear. The present study shows a novel antiviral mechanism of ISGs and elucidated that ISG12a recruits an E3 ligase, SKP2, for ubiquitination and degradation of viral protein and restricts viral infection. These findings provide important insights into exploring the working principles of innate immunity.



2014 ◽  
Vol 3 (1) ◽  
pp. 204-214 ◽  
Author(s):  
Xiaoling Zhou ◽  
Pingnan Sun ◽  
Baltasar Lucendo-Villarin ◽  
Allan G.N. Angus ◽  
Dagmara Szkolnicka ◽  
...  


2006 ◽  
Vol 16 (5) ◽  
pp. 311-327 ◽  
Author(s):  
Ting Zhang ◽  
Yuan Li ◽  
Wen-Zhe Ho


Sign in / Sign up

Export Citation Format

Share Document