Abstract

In response to a JE virus attack, infected body cells start secretion of different cytokines and activate innate immune response. Virus starts neuronal invasion by entering into nerve cells and inflecting the central nervous system. It avoids exposure of body’s natural immunity and generates neurotrophic effects. Virus causes acute susceptibility to CNS and establishes encephalitis syndrome that results in very high fatality in children. In survivors, JEV inhibits the growth and proliferation of NCPs and imposes permanent neuronal disorders like cognitive, motor, and behavioral impairments. However, body cells start TCR mediated interactions, to recognize viral antigens with class I MHC complex on specific target cells, and operate mass killing of virus infected cells by increased CTL activity. Thus, both cell mediated and antibody interactions plays a central role in protection against JEV. In the present review article virus generated neurovirulence, antigenicity, and host immune responses are described in detail. More emphasis is given on diagnosis, clinical care, and active immunization with well-designed potential antiflavivirus vaccines. Further, for achieving an elite success against JEV, global eradication strategies are to be needed for making vaccination program more responsible and effective in endemic areas.

Highlights

  • Japanese encephalitis virus (JEV) is an enveloped positive single stranded RNA virus that belongs to genus Flavivirus in the family Flaviviridae

  • The natural cycle of Japanese encephalitis (JE) virus in endemic areas involves presence of water birds and Culex mosquitoes, Culex tritaeniorhynchus, with pigs being involved as an amplifying host and providing a link to humans through their proximity to housing

  • Virus avoids recognition and its elimination from a sequestered defense made by body cells and molecules in operation

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Summary

Introduction

It is a multifunctional protein that assists the virus in neuronal invasion [10] and plays important role in pathogenesis and cellular profusion and acts as a virulence determinant [11,12,13] It shows host immune response and elicits protective immunity in mice [14]; that is why it is used to generate protective antibodies against flavivirus [15,16,17]. Just after inoculation of JE virus in human, it starts replication in Langerhans dendritic, skin cells and migrates to draining lymph nodes [20] At this vary stage viral infection and disjunctive power of body cells and other factors play important role in development of an early immune response. Similar invasion NCPs were made by HIV infection and lead to quiescence in these cells [52, 53]

Flavivirus Generated Immune Responses
Control of Flavivirus Infection
Third Generation Vaccines
Findings
Conclusion
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