Why the study?
What are the distinct roles of human IgG subclasses in the neutralization and enhancement of EV71 infection?
What are the distinct roles of human IgG subclasses in the neutralization and enhancement of EV71 infection?
Different human IgG subclasses have distinct roles in EV71 infection, with IgG1 mediating neutralization and IgG3 causing antibody-dependent enhancement, which is critical for immunotherapy and vaccine design.
IVIG subclass composition may affect EV71 outcomes; leaves open in vivo translation and therapeutic implications.
The emerging human enterovirus 71 (EV71) represents a growing threat to public health, and no vaccine or specific antiviral is currently available. Human intravenous immunoglobulin (IVIG) is clinical used in treating severe EV71 infections. However, the discovery of antibody dependent enhancement (ADE) of EV71 infection illustrates the complex roles of antibody in controlling EV71 infection. In this study, to identify the distinct role of each IgG subclass on neutralization and enhancement of EV71 infection, different lots of pharmaceutical IVIG preparations manufactured from Chinese donors were used for IgG subclass fractionation by pH gradient elution with the protein A-conjugated affinity column. The neutralization and ADE capacities on EV71 infection of each purified IgG subclass were then assayed, respectively. The neutralizing activity of human IVIG is mainly mediated by IgG1 subclass and to less extent by IgG2 subclass. Interestingly, IgG3 fraction did not have neutralizing activity but enhanced EV71 infection in vitro. These results revealed the different roles of human IgG subclasses on EV71 infection, which is of critical importance for the rational design of immunotherapy and vaccines against severe EV71 diseases.
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Cao et al. (2013) studied this question.
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