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Antibody-dependent enhancement and neutralization against CVB4 investigated in vitro and in silico through an agent-based model.
Morvan, Corentin; Nekoua, Magloire Pandoua; Debuysschere, Cyril; Alidjinou, Enagnon Kazali; Hober, Didier.
Afiliación
  • Morvan C; Laboratoire de Virologie ULR3610, Univ Lille et CHU Lille, Lille, France.
  • Nekoua MP; Laboratoire de Virologie ULR3610, Univ Lille et CHU Lille, Lille, France.
  • Debuysschere C; Laboratoire de Virologie ULR3610, Univ Lille et CHU Lille, Lille, France.
  • Alidjinou EK; Laboratoire de Virologie ULR3610, Univ Lille et CHU Lille, Lille, France.
  • Hober D; Laboratoire de Virologie ULR3610, Univ Lille et CHU Lille, Lille, France.
J Med Virol ; 96(1): e29399, 2024 01.
Article en En | MEDLINE | ID: mdl-38235792
ABSTRACT
The infection with coxsackievirus B4 (CVB4) can be enhanced in vitro by antibodies directed against the viral capsid protein VP4. In peripheral blood mononuclear cells, antibody-dependent enhancement (ADE) of CVB4 infection leads to the production of interferon alpha (IFN-α). To investigate ADE of CVB4-induced production of IFN-α, an agent-based model was constructed with enhancing and neutralizing antibodies. The model recapitulates viral neutralization and ADE in silico. The enhancing and neutralizing activities of serum samples were evaluated in vitro to confront the model predictions with experimental results. Increasing the incubation time of CVB4 with serum samples improves virus neutralization in silico as well as in vitro. It also results in ADE at lower antibody numbers in silico, which is confirmed in vitro with IFN-α production at lower serum concentrations. Furthermore, incubation of CVB4 with serum at a low temperature does not induce IFN-α production in vitro. Thus, taken together our results suggest that enhancing antibodies bind cryptic epitopes, more accessible with longer incubation time and at higher temperature due to changes in capsid conformation, consistent with previous results indicating that enhancing antibodies are anti-VP4 antibodies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Leucocitos Mononucleares / Enterovirus Humano B Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Med Virol Año: 2024 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Leucocitos Mononucleares / Enterovirus Humano B Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Med Virol Año: 2024 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos