Display Settings:

Format

Send to:

Choose Destination
See comment in PubMed Commons below
Vaccine. 2013 Jun 7;31(25):2756-61. doi: 10.1016/j.vaccine.2013.03.065. Epub 2013 Apr 11.

Evaluation of vaccine-induced antibody responses: impact of new technologies.

Author information

  • 1Health Sciences Division, RTI International, 3040 East Cornwallis Road, Research Triangle Park, NC 27709, USA. dzaccaro@rti.org

Abstract

Host response to vaccination has historically been evaluated based on a change in antibody titer that compares the post-vaccination titer to the pre-vaccination titer. A four-fold or greater increase in antigen-specific antibody has been interpreted to indicate an increase in antibody production in response to vaccination. New technologies, such as the bead-based assays, provide investigators and clinicians with precise antibody levels (reported as concentration per mL) in ranges below and above those previously available through standard assays such as ELISA. Evaluations of bead assay data to determine host response to vaccination using fold change and absolute change, with a general linear model used to calculate adjusted statistics, present very different pictures of the antibody response when pre-vaccination antibody levels are low. Absolute changes in bead assay values, although not a standard computation, appears to more accurately reflect the host response to vaccination for those individuals with extremely low pre-vaccination antibody levels. Conversely, for these same individuals, fold change may be very high while post-vaccination antibodies do not achieve seroprotective levels. Absolute change provides an alternate method to characterize host response to vaccination, especially when pre-vaccination levels are very low, and may be useful in studies designed to determine associations between host genotypes and response to vaccination.

Copyright © 2013 Elsevier Ltd. All rights reserved.

PMID:
23583812
[PubMed - indexed for MEDLINE]
PMCID:
PMC3672347
Free PMC Article

Images from this publication.See all images (4)Free text

Figure 1
Figure 2
Figure 3
Figure 4
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Elsevier Science Icon for PubMed Central
    Loading ...
    Write to the Help Desk