Literature DB >> 26743519

Ebola Virus Altered Innate and Adaptive Immune Response Signalling Pathways: Implications for Novel Therapeutic Approaches.

Anoop Kumar1.   

Abstract

Ebola virus (EBOV) arise attention for their impressive lethality by the poor immune response and high inflammatory reaction in the patients. It causes a severe hemorrhagic fever with case fatality rates of up to 90%. The mechanism underlying this lethal outcome is poorly understood. In 2014, a major outbreak of Ebola virus spread amongst several African countries, including Leone, Sierra, and Guinea. Although infections only occur frequently in Central Africa, but the virus has the potential to spread globally. Presently, there is no vaccine or treatment is available to counteract Ebola virus infections due to poor understanding of its interaction with the immune system. Accumulating evidence indicates that the virus actively alters both innate and adaptive immune responses and triggers harmful inflammatory responses. In the literature, some reports have shown that alteration of immune signaling pathways could be due to the ability of EBOV to interfere with dendritic cells (DCs), which link innate and adaptive immune responses. On the other hand, some reports have demonstrated that EBOV, VP35 proteins act as interferon antagonists. So, how the Ebola virus altered the innate and adaptive immune response signaling pathways is still an open question for the researcher to be explored. Thus, in this review, I try to summarize the mechanisms of the alteration of innate and adaptive immune response signaling pathways by Ebola virus which will be helpful for designing effective drugs or vaccines against this lethal infection. Further, potential targets, current treatment and novel therapeutic approaches have also been discussed.

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Year:  2016        PMID: 26743519     DOI: 10.2174/1871526516666160108114644

Source DB:  PubMed          Journal:  Infect Disord Drug Targets        ISSN: 1871-5265


  3 in total

1.  Therapeutic potential of the heme oxygenase-1 inducer hemin against Ebola virus infection.

Authors:  Hanxia Huang; Krishnamurthy Konduru; Veronica Solovena; Zhao-Hua Zhou; Namita Kumari; Kazuyo Takeda; Sergei Nekhai; Sina Bavari; Gerardo G Kaplan; Kenneth M Yamada; Subhash Dhawan
Journal:  Curr Trends Immunol       Date:  2016

2.  Different features of Vδ2 T and NK cells in fatal and non-fatal human Ebola infections.

Authors:  Eleonora Cimini; Domenico Viola; Mar Cabeza-Cabrerizo; Antonella Romanelli; Nicola Tumino; Alessandra Sacchi; Veronica Bordoni; Rita Casetti; Federica Turchi; Federico Martini; Joseph A Bore; Fara Raymond Koundouno; Sophie Duraffour; Janine Michel; Tobias Holm; Elsa Gayle Zekeng; Lauren Cowley; Isabel Garcia Dorival; Juliane Doerrbecker; Nicole Hetzelt; Jonathan H J Baum; Jasmine Portmann; Roman Wölfel; Martin Gabriel; Osvaldo Miranda; Graciliano Díaz; José E Díaz; Yoel A Fleites; Carlos A Piñeiro; Carlos M Castro; Lamine Koivogui; N'Faly Magassouba; Boubacar Diallo; Paula Ruibal; Lisa Oestereich; David M Wozniak; Anja Lüdtke; Beate Becker-Ziaja; Maria R Capobianchi; Giuseppe Ippolito; Miles W Carroll; Stephan Günther; Antonino Di Caro; César Muñoz-Fontela; Chiara Agrati
Journal:  PLoS Negl Trop Dis       Date:  2017-05-30

Review 3.  Dendritic Cells/Macrophages-Targeting Feature of Ebola Glycoprotein and its Potential as Immunological Facilitator for Antiviral Vaccine Approach.

Authors:  Titus Abiola Olukitibi; Zhujun Ao; Mona Mahmoudi; Gary A Kobinger; Xiaojian Yao
Journal:  Microorganisms       Date:  2019-09-29
  3 in total

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