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Coxsackievirus A16 capsid protein (main antigens: VP1, VP2, VP3, VP4) (CVA16 antigen (less commonly VP1, VP2, VP3, VP4 for individual proteins))

Target
CVA16 antigen (less commonly VP1, VP2, VP3, VP4 for individual proteins)
Molecular classification
Viral protein, Structural protein (Virus capsid protein), Other
01

Overview

Coxsackievirus A16 antigen generally refers to the structural proteins forming the viral capsid, principally VP1, VP2, VP3, and VP4, which display multiple conformational and sequence-defined epitopes recognized by the immune system. These antigens are the primary targets of neutralizing antibodies induced by infection or vaccination, playing a crucial role in the prevention of viral entry into host cells. Coxsackievirus A16 antigens are under investigation as both diagnostic markers (for serology) and as candidates for vaccine development and antibody-based therapies aimed at preventing or treating hand, foot and mouth disease. These proteins mediate viral attachment and uncoating by interacting with cellular receptors, most notably heparan sulfate (attachment) and SCARB2 (uncoating), and are associated with viral pathogenesis in young children[2][3][1]. **Note:** - "Coxsackievirus A16 antigen" is not a unique gene/protein but a collective descriptor of antigenic viral proteins, mainly the capsid proteins[2][4]. For structured data, VP1 is the single most commonly used antigen for neutralizing antibody response and diagnostics[2].

Other names
CVA16 capsid antigenCVA16 structural proteinCoxsackievirus A16 VP1/VP2/VP3/VP4CVA16 virus-like particle (when used as immunogen/vaccine)
02

Mechanism of action

Neutralizing antibodies block viral entry by: - Inhibiting attachment to host receptor heparan sulfate - Interfering with uncoating by blocking interaction with SCARB2 receptor

03

Biological functions

Viral entry (mediates attachment and uncoating via interaction with host cell receptors)Elicitation of antibody-mediated immune response (major target of neutralizing antibodies)
04

Disease associations

Infection (target in vaccine development for hand, foot and mouth disease)
05

Safety considerations

Possibility of viral antigenic variation leading to evasion of immunityNo currently licensed vaccine
06

Interacting drugs

Monoclonal antibodies 9B5 and 8C4 (experimental)

1 more in the full profile.

07

Biomarkers

Presence of anti-CVA16 IgG/IgM (indicative of infection or vaccine response)

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