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Intracerebroventricular and Intravascular Injection of Viral Particles and Fluorescent Microbeads into the Neonatal Brain
Published on: July 24, 2016
The neonatal Fc receptor (FcRn): Guardian or Trojan Horse in viral infection?
Lei Na1, Yang Zheng1, Jian-Bo Yang1
1College of Animal Husbandry and Veterinary Medicine, Jiangsu Vocational College of Agriculture and Forestry, Jurong, China.
Insights
The neonatal Fc receptor (FcRn) is crucial for immune defenses but can be exploited by viruses. This review explores how viruses use FcRn for infection and suggests therapeutic strategies targeting this receptor.
Area of Science:
- Immunology
- Virology
- Molecular Biology
Background:
- The neonatal Fc receptor (FcRn) is essential for transferring maternal immunoglobulin G (IgG) to neonates, supporting antimicrobial defenses.
- FcRn regulates IgG and albumin homeostasis, prolonging their circulation time through pH-dependent recycling.
- FcRn facilitates antibody transcytosis across cellular barriers, vital for humoral immunity.
Purpose of the Study:
- To comprehensively review the dual roles of FcRn in viral infections.
- To elucidate how various viruses exploit FcRn to promote infection.
- To summarize molecular mechanisms of FcRn-mediated proviral processes.
Main Methods:
- Literature review of studies on FcRn and viral infections.
- Analysis of molecular mechanisms of FcRn exploitation by viruses.
- Identification of therapeutic strategies targeting FcRn.
Main Results:
- FcRn plays a dual role, aiding immune defenses but also facilitating viral infections.
- Viruses utilize FcRn for processes like viral uncoating and transcytosis.
- Antibody-dependent enhancement (ADE) of infection is a key FcRn-mediated proviral mechanism.
Conclusions:
- Viruses strategically exploit FcRn's natural functions for their own replication and spread.
- Understanding these molecular mechanisms is key to developing novel antiviral therapies.
- Targeting FcRn presents a promising strategy to inhibit viral replication and enhance immune responses.
Abstract:
The neonatal Fc receptor (FcRn), well-known for mediating the transfer of maternal immunoglobulin G (IgG) to neonates, plays a critical role in neonatal antimicrobial defenses. Furthermore, FcRn regulates IgG and albumin homeostasis via pH-dependent recycling pathways, thereby prolonging their plasma half-life in circulation. FcRn also enables bidirectional transcytosis of antibodies across cellular barriers, a function essential for maintaining humoral immunity. However, recent studies have demonstrated that some viruses exploit FcRn to facilitate viral infection, underscoring its dual role in the viral lifecycle. This review aims to comprehensively discuss the dual functions of FcRn during viral infections, with particular focus on how diverse viruses utilize FcRn to promote infection. Here, we summarize the molecular mechanisms underlying FcRn-mediated proviral processes, including viral uncoating, transcytosis, and antibody-dependent enhancement (ADE) of infection. Finally, we propose potential therapeutic strategies targeting FcRn to inhibit viral replication.
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