Vaccine-specific antibody secreting cells are a robust early marker of LAIV-induced B-cell response in ferrets
► Antibody secreting cells are an immunogenicity biomarker of influenza vaccination. ► Sensitive correlate of immunogenicity not impacted by prior influenza exposures. ► Seronegative ferret model simulating immunologically naïve pediatric populations. ► Serpositive older ferret model simulating adul...
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Published in | Vaccine Vol. 30; no. 2; pp. 237 - 246 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier Ltd
05.01.2012
Elsevier Limited |
Subjects | |
Online Access | Get full text |
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Summary: | ► Antibody secreting cells are an immunogenicity biomarker of influenza vaccination. ► Sensitive correlate of immunogenicity not impacted by prior influenza exposures. ► Seronegative ferret model simulating immunologically naïve pediatric populations. ► Serpositive older ferret model simulating adult human populations.
Currently, a robust set of immune correlates for
live
attenuated
influenza
vaccine (LAIV) efficacy in humans has not been fully elucidated. The serum
hem
agglutination
inhibition (HAI) assay has been historically used to measure humoral immune responses to injectable inactivated influenza vaccination. However, serum antibody titers do not reliably reflect the complete mechanism of action of LAIV, which is an intranasally delivered vaccine and is expected to induce local mucosal and cellular immune responses in addition to humoral immune responses. Therefore, we designed a study to evaluate potential immune correlates of LAIV vaccination in the ferret animal model of influenza infection. Ferrets were vaccinated with increasing doses of LAIV and four weeks later challenged with a homologous wild-type (
wt) H1N1 strain. Humoral immune responses measured following LAIV vaccination included HAI, serum antibodies and antibody secreting cells (ASC); and the responses were found to correlate with the dose level of LAIV administered in this model. Protection from
wt virus challenge was determined by measuring inhibition of
wt viral replication in nasal washes and in lung tissue. Results demonstrated that LAIV doses
≥
5.0
log
10 Plaque Forming Units (PFU) elicited vaccine-specific IgG and IgA ASC frequencies and induced complete protection in the lungs. Further, we developed a novel model utilizing seropositive older ferrets to demonstrate that in the background of previous
wt influenza infection LAIV induces a robust vaccine-specific B-cell response even in the absence of serum antibody response, a result that suggests that effector B-cell responses generated by LAIV are not inhibited by prior viral exposure. Finally, we demonstrated that LAIV elicits strain-specific memory B-cell responses that are measurable in a background of
wt influenza infections. Taken together, results from these studies identified the antigen-specific ASC frequency as a useful early biomarker of LAIV-induced B-cell immune response. |
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Bibliography: | http://dx.doi.org/10.1016/j.vaccine.2011.11.001 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 0264-410X 1873-2518 1873-2518 |
DOI: | 10.1016/j.vaccine.2011.11.001 |