The Network aims to promote multi-disciplinary approaches to address challenging vaccine-related questions. This page contains a curated list of publications that highlight high-impact and collaborative approaches.

Citation

BibTex format

@article{de:2017:10.1016/j.jim.2017.06.008,
author = {de, Silva TI and Gould, V and Mohammed, NI and Cope, A and Meijer, A and Zutt, I and Reimerink, J and Kampmann, B and Hoschler, K and Zambon, M and Tregoning, JS},
doi = {10.1016/j.jim.2017.06.008},
journal = {Journal of Immunological Methods},
pages = {1--6},
title = {Comparison of mucosal lining fluid sampling methods and influenza-specific IgA detection assays for use in human studies of influenza immunity},
url = {http://dx.doi.org/10.1016/j.jim.2017.06.008},
volume = {449},
year = {2017}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - We need greater understanding of the mechanisms underlying protection against influenza virus to develop more effective vaccines. To do this, we need better, more reproducible methods of sampling the nasal mucosa. The aim of the current study was to compare levels of influenza virus A subtype-specific IgA collected using three different methods of nasal sampling. Samples were collected from healthy adult volunteers before and after LAIV immunization by nasal wash, flocked swabs and Synthetic Absorptive Matrix (SAM) strips. Influenza A virus subtype-specific IgA levels were measured by haemagglutinin binding ELISA or haemagglutinin binding microarray and the functional response was assessed by microneutralization. Nasosorption using SAM strips lead to the recovery of a more concentrated sample of material, with a significantly higher level of total and influenza H1-specific IgA. However, an equivalent percentage of specific IgA was observed with all sampling methods when normalized to the total IgA. Responses measured using a recently developed antibody microarray platform, which allows evaluation of binding to multiple influenza strains simultaneously with small sample volumes, were compared to ELISA. There was a good correlation between ELISA and microarray values. Material recovered from SAM strips was weakly neutralizing when used in an in vitro assay, with a modest correlation between the level of IgA measured by ELISA and neutralization, but a greater correlation between microarray-measured IgA and neutralizing activity. In conclusion we have tested three different methods of nasal sampling and show that flocked swabs and novel SAM strips are appropriate alternatives to traditional nasal washes for assessment of mucosal influenza humoral immunity.
AU - de,Silva TI
AU - Gould,V
AU - Mohammed,NI
AU - Cope,A
AU - Meijer,A
AU - Zutt,I
AU - Reimerink,J
AU - Kampmann,B
AU - Hoschler,K
AU - Zambon,M
AU - Tregoning,JS
DO - 10.1016/j.jim.2017.06.008
EP - 6
PY - 2017///
SN - 0022-1759
SP - 1
TI - Comparison of mucosal lining fluid sampling methods and influenza-specific IgA detection assays for use in human studies of influenza immunity
T2 - Journal of Immunological Methods
UR - http://dx.doi.org/10.1016/j.jim.2017.06.008
UR - https://www.ncbi.nlm.nih.gov/pubmed/28647455
UR - http://hdl.handle.net/10044/1/50096
VL - 449
ER -