CVI
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Giardina, P. C.
Right arrow Articles by Hildreth, S. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Giardina, P. C.
Right arrow Articles by Hildreth, S. W.
Clinical and Diagnostic Laboratory Immunology, November 2003, p. 1136-1140, Vol. 10, No. 6
1071-412X/03/$08.00+0     DOI: 10.1128/CDLI.10.6.1136-1140.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Effect of Antigen Coating Conditions on Enzyme-Linked Immunosorbent Assay for Detection of Immunoglobulin G Antibody to Neisseria meningitidis Serogroup Y and W135 Capsular Polysaccharide Antigens in Serum

Peter C. Giardina,* Renee E. Evans, Daniel J. Sikkema, Dace Madore, and Stephen W. Hildreth{dagger}

Department of Applied Immunology and Microbiology, Wyeth Vaccines Research, Rochester, New York 14623

Received 27 May 2003/ Returned for modification 8 July 2003/ Accepted 21 July 2003

Human sera collected from 28 consenting adult volunteers were used to define assay conditions for meningococcal vaccine clinical trial serology. Immunoassay parameters were optimized with these test sera and the standard reference serum, CDC1992. Coating conditions for serogroup Y and W135 polysaccharide antigens were found to influence the predicted serum immunoglobulin G (IgG) antibody concentrations. Sera that displayed IgG antibody binding profiles most unlike that of CDC1992 were influenced the most by coating conditions. Our results suggest that presentation of specific epitopes is influenced by antigen-coating concentrations for serogroup Y and W135 polysaccharides.


* Corresponding author. Mailing address: Department of Applied Immunology and Microbiology, Wyeth Research, 77 Ridgeland Rd., Rochester, NY 14623. Phone: (585) 350-2521. Fax: (585) 350-2552. E-mail: giardip{at}wyeth.com.

{dagger} Present address: Ortho-Clinical Diagnostics, Rochester, NY 14626-5101.


Clinical and Diagnostic Laboratory Immunology, November 2003, p. 1136-1140, Vol. 10, No. 6
1071-412X/03/$08.00+0     DOI: 10.1128/CDLI.10.6.1136-1140.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Antimicrob. Agents Chemother. Clin. Microbiol. Rev. Infect. Immun.
J. Clin. Microbiol. J. Virol. ALL ASM JOURNALS

Copyright © 2003 by the American Society for Microbiology. All rights reserved.