Abstract

Dengue virus (DENV) causes dengue fever (DF) and dengue hemorrhagic fever in humans. Some DF patients suddenly develop severe symptoms around the defervescent period. Although the pathogenic mechanism of the severe symptoms has not been fully elucidated, the viremia level in the early phase has been shown to correlate with the disease severity. One of the hypotheses is that a phenomenon called antibody-dependent enhancement (ADE) of infection leads to high level of viremia. To examine the plausibility of this hypothesis, we examined the relationship between in vitro ADE activity and in vivo viral load quantity in six patients with dengue diseases. Blood samples were collected at multiple time points between the acute and defervescent phases, and the balance between neutralizing and enhancing activities against the autologous and prototype viruses was examined. As the antibody levels against DENV were rapidly increased, ADE activity was decreased over time or partially maintained against some viruses at low serum dilution. In addition, positive correlations were observed between ADE activity representing in vitro progeny virus production and viremia levels in patient plasma samples. The measurement of ADE activity in dengue-seropositive samples may help to predict the level of viral load in the subsequent DENV infection.

Highlights

  • Dengue virus (DENV) causes dengue fever (DF) and dengue hemorrhagic fever in humans

  • We previously developed a simple method to detect the balance between the enhancing and neutralizing a­ ctivities[26], and demonstrated that mouse monoclonal Enhancing antibodies (EAbs) and neutralizing antibodies (NAbs) competed over the neutralizing activities in vitro[25,27]

  • Serum samples, which were collected at several time points between the acute and defervescent phases, were subjected to an antibody assay to determine the balance between neutralizing and enhancing activities (NAb/EAb-balance assay) using each autologous virus

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Summary

Introduction

Dengue virus (DENV) causes dengue fever (DF) and dengue hemorrhagic fever in humans. Some DF patients suddenly develop severe symptoms around the defervescent period. The measurement of ADE activity in dengue-seropositive samples may help to predict the level of viral load in the subsequent DENV infection. Antibody-dependent enhancement of infection (ADE) that increases the viremia level has been proposed as one of the pathogenic mechanisms in DHF/DSS17; in the case of ADE the increase occurs by viral internalization via Fc gamma r­ eceptors[18]. A potential relationship between ADE and human disease severity in DENV infection has been ­reported[19] It is still unclear whether in vitro ADE can be used for the prediction in subsequent clinical outcomes. Neutralizing antibodies (NAbs) have a biological function to decrease the viremia level to protect the host from DENV i­nfection[23], while most NAbs show ADE activity at subneutralizing d­ oses[24]. The neutralizing activity of an NAb was reduced in the presence of a sufficient level of an EAb, suggesting that the relative capacity for neutralization might be affected by the balance between NAbs and EAbs

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