Abstract
Few studies on the humoral immune responses in human during natural influenza infection have been reported. Here, we used serum samples from pandemic 2009 H1N1 influenza infected patients to characterize the humoral immune responses to influenza during natural infection in humans. We observed for the first time that the pandemic 2009 H1N1 influenza induced influenza A-specific IgM within days after symptoms onset, whereas the unit of IgG did not changed. The magnitude of influenza A-specific IgM antibodies might have a value in predicting the rate of virus clearance to some degree. However, the newly developed IgM was not associated with hemagglutination inhibition (HI) activities in the same samples but correlated with HI activities of subsequently collected sera which were mediated by IgG antibodies, indicating that IgM was critical for influenza infection and influences subsequent IgG antibody responses. These findings provide new important insights on the human immunity to natural influenza infection.
Highlights
Adaptive humoral immunity is an essential component of immune responses to different microbe infections including influenza
Influenza A-specific IgM and IgG were quantified in samples of 131 pandemic 2009 H1N1 infected patients on the 1st or 2nd day after they were admitted into hospital
We used residual serum samples taken from a HIV cohort study to validate whether Influenza A-specific IgM is a surrogate marker for recent exposure to H1N1 influenza
Summary
Adaptive humoral immunity is an essential component of immune responses to different microbe infections including influenza. Secreted IgM in acute phase of infection plays important role in protection from influenza virus. Both natural IgM produced by B-1 cells in the absence of exposure to virus and antigen induced IgM secreted by B-2 cells after antigen stimulation nonredundantly contribute to immune protection from infection of influenza virus [3]. Most of these data have been collected from mice infection model. No observation intensively monitoring early humoral responses to the pandemic or seasonal influenza infection in humans has been reported
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