Use of saliva to monitor meningococcal vaccine responses: proposing a threshold in saliva as surrogate of protection

Abstract Background Mucosal antibodies against capsular polysaccharides offer protection against acquisition and carriage of encapsulated bacteria like Neisseria meningitidis serogroup C. Measurements of salivary antibodies as replacement for blood testing has important (cost-effective) advantages,...

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Main Authors: Mariëtte B. van Ravenhorst, Fiona R. M. van der Klis, Debbie M. van Rooijen, Elisabeth A. M. Sanders, Guy A. M. Berbers
Format: Article
Language:English
Published: BMC 2019-01-01
Series:BMC Medical Research Methodology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12874-018-0650-3
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spelling doaj-d54d63fe938d448eac288dc5066b07352020-11-25T01:51:06ZengBMCBMC Medical Research Methodology1471-22882019-01-011911810.1186/s12874-018-0650-3Use of saliva to monitor meningococcal vaccine responses: proposing a threshold in saliva as surrogate of protectionMariëtte B. van Ravenhorst0Fiona R. M. van der Klis1Debbie M. van Rooijen2Elisabeth A. M. Sanders3Guy A. M. Berbers4Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM)Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM)Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM)Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM)Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM)Abstract Background Mucosal antibodies against capsular polysaccharides offer protection against acquisition and carriage of encapsulated bacteria like Neisseria meningitidis serogroup C. Measurements of salivary antibodies as replacement for blood testing has important (cost-effective) advantages, particular in studies that assess the impact of large-scale vaccination or in populations in which blood sampling is difficult. This study aimed to estimate a threshold for meningococcal IgG salivary antibody levels to discriminate between unprotected and protected vaccinated individuals. Methods MenA-, MenC-, MenW- and MenY-polysaccharide (PS) specific IgG levels in serum and saliva from participants in a meningococcal vaccination study were measured using the fluorescent-bead-based multiplex immunoassay. Functional antibody titers in serum against the four serogroups were measured with serum bactericidal assay using rabbit complement (rSBA). A threshold for salivary IgG was determined by analysis of ROC curves using a serum rSBA titer ≥128 as correlate of protection. The area under the curve (AUC) was calculated to quantify the accuracy of the salivary test and was considered adequate when ≥0.80. The optimal cut-off was considered adequate when salivary IgG cut-off levels provided specificity of ≥90%. True positive rate (sensitivity), positive predictive value, and negative predictive value were calculated to explore the possible use of salivary antibody levels as a surrogate of protection. Results The best ROC curve (AUC of 0.95) was obtained for MenC, with an estimated minimum threshold of MenC-PS specific salivary IgG ≥3.54 ng/mL as surrogate of protection. An adequate AUC (> 0.80) was also observed for MenW and MenY with an estimated minimal threshold of 2.00 and 1.82 ng/mL, respectively. When applying these thresholds, all (100%) samples collected 1 month and 1 year after the (booster) meningococcal vaccination, that were defined as protective in the saliva test for MenC, MenW and MenY, corresponded with concomitant serum rSBA titer ≥128 for the respective meningococcal serogroups. Conclusion The saliva test offers an alternative screening tool to monitor protective vaccine responses up to one year after meningococcal vaccination against MenC, MenW and MenY. Future (large) longitudinal vaccination studies evaluating also clinical protection against IMD or carriage acquisition are required to validate the currently proposed threshold in saliva.http://link.springer.com/article/10.1186/s12874-018-0650-3Neisseria meningitidisCorrelate of protectionSalivary surrogate of protectionThresholdConjugate meningococcal vaccine
collection DOAJ
language English
format Article
sources DOAJ
author Mariëtte B. van Ravenhorst
Fiona R. M. van der Klis
Debbie M. van Rooijen
Elisabeth A. M. Sanders
Guy A. M. Berbers
spellingShingle Mariëtte B. van Ravenhorst
Fiona R. M. van der Klis
Debbie M. van Rooijen
Elisabeth A. M. Sanders
Guy A. M. Berbers
Use of saliva to monitor meningococcal vaccine responses: proposing a threshold in saliva as surrogate of protection
BMC Medical Research Methodology
Neisseria meningitidis
Correlate of protection
Salivary surrogate of protection
Threshold
Conjugate meningococcal vaccine
author_facet Mariëtte B. van Ravenhorst
Fiona R. M. van der Klis
Debbie M. van Rooijen
Elisabeth A. M. Sanders
Guy A. M. Berbers
author_sort Mariëtte B. van Ravenhorst
title Use of saliva to monitor meningococcal vaccine responses: proposing a threshold in saliva as surrogate of protection
title_short Use of saliva to monitor meningococcal vaccine responses: proposing a threshold in saliva as surrogate of protection
title_full Use of saliva to monitor meningococcal vaccine responses: proposing a threshold in saliva as surrogate of protection
title_fullStr Use of saliva to monitor meningococcal vaccine responses: proposing a threshold in saliva as surrogate of protection
title_full_unstemmed Use of saliva to monitor meningococcal vaccine responses: proposing a threshold in saliva as surrogate of protection
title_sort use of saliva to monitor meningococcal vaccine responses: proposing a threshold in saliva as surrogate of protection
publisher BMC
series BMC Medical Research Methodology
issn 1471-2288
publishDate 2019-01-01
description Abstract Background Mucosal antibodies against capsular polysaccharides offer protection against acquisition and carriage of encapsulated bacteria like Neisseria meningitidis serogroup C. Measurements of salivary antibodies as replacement for blood testing has important (cost-effective) advantages, particular in studies that assess the impact of large-scale vaccination or in populations in which blood sampling is difficult. This study aimed to estimate a threshold for meningococcal IgG salivary antibody levels to discriminate between unprotected and protected vaccinated individuals. Methods MenA-, MenC-, MenW- and MenY-polysaccharide (PS) specific IgG levels in serum and saliva from participants in a meningococcal vaccination study were measured using the fluorescent-bead-based multiplex immunoassay. Functional antibody titers in serum against the four serogroups were measured with serum bactericidal assay using rabbit complement (rSBA). A threshold for salivary IgG was determined by analysis of ROC curves using a serum rSBA titer ≥128 as correlate of protection. The area under the curve (AUC) was calculated to quantify the accuracy of the salivary test and was considered adequate when ≥0.80. The optimal cut-off was considered adequate when salivary IgG cut-off levels provided specificity of ≥90%. True positive rate (sensitivity), positive predictive value, and negative predictive value were calculated to explore the possible use of salivary antibody levels as a surrogate of protection. Results The best ROC curve (AUC of 0.95) was obtained for MenC, with an estimated minimum threshold of MenC-PS specific salivary IgG ≥3.54 ng/mL as surrogate of protection. An adequate AUC (> 0.80) was also observed for MenW and MenY with an estimated minimal threshold of 2.00 and 1.82 ng/mL, respectively. When applying these thresholds, all (100%) samples collected 1 month and 1 year after the (booster) meningococcal vaccination, that were defined as protective in the saliva test for MenC, MenW and MenY, corresponded with concomitant serum rSBA titer ≥128 for the respective meningococcal serogroups. Conclusion The saliva test offers an alternative screening tool to monitor protective vaccine responses up to one year after meningococcal vaccination against MenC, MenW and MenY. Future (large) longitudinal vaccination studies evaluating also clinical protection against IMD or carriage acquisition are required to validate the currently proposed threshold in saliva.
topic Neisseria meningitidis
Correlate of protection
Salivary surrogate of protection
Threshold
Conjugate meningococcal vaccine
url http://link.springer.com/article/10.1186/s12874-018-0650-3
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