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 arrowReprints and Permissions
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 Leonard, E. G.
Right arrow Articles by Schreiber, J. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Leonard, E. G.
Right arrow Articles by Schreiber, J. R.

 Previous Article  |  Next Article 

Infection and Immunity, July 2003, p. 4186-4189, Vol. 71, No. 7
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.7.4186-4189.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Antigen Processing of the Heptavalent Pneumococcal Conjugate Vaccine Carrier Protein CRM197 Differs Depending on the Serotype of the Attached Polysaccharide

Ethan G. Leonard,1 David H. Canaday,2 Clifford V. Harding,3 and John R. Schreiber1,3*

Departments of Pediatrics,1 Medicine,2 Pathology, Case Western Reserve University, and the Division of Infectious Diseases/Allergy/Immunology/Rheumatology, Rainbow Babies and Children's Hospital, Cleveland, Ohio 441063

Received 19 February 2003/ Returned for modification 3 April 2003/ Accepted 26 April 2003

The pneumococcal (Pn) conjugate vaccine includes seven different polysaccharides (PS) conjugated to CRM197. Utilizing antigen-processing cells and a CRM197-specific mouse T-cell hybridoma, we found that the serotype of conjugated PnPS dramatically affected antigen processing of CRM197. Unconjugated CRM197 and serotype conjugates 14 and 18C were processed more efficiently.


* Corresponding author. Mailing address: Division of Infectious Diseases/Allergy/Immunology/Rheumatology, Rainbow Babies and Children's Hospital, 11100 Euclid Ave., Cleveland, OH 44106. Phone: (216) 844-3645. Fax: (216) 844-8362. E-mail: jrs3{at}po.cwru.edu.

Editor: J. D. Clements


Infection and Immunity, July 2003, p. 4186-4189, Vol. 71, No. 7
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.7.4186-4189.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Colino, J., Chattopadhyay, G., Sen, G., Chen, Q., Lees, A., Canaday, D. H., Rubtsov, A., Torres, R., Snapper, C. M. (2009). Parameters Underlying Distinct T Cell-Dependent Polysaccharide-Specific IgG Responses to an Intact Gram-Positive Bacterium versus a Soluble Conjugate Vaccine. J. Immunol. 183: 1551-1559 [Abstract] [Full Text]  
  • Chattopadhyay, G., Chen, Q., Colino, J., Lees, A., Snapper, C. M. (2009). Intact Bacteria Inhibit the Induction of Humoral Immune Responses to Bacterial-Derived and Heterologous Soluble T Cell-Dependent Antigens. J. Immunol. 182: 2011-2019 [Abstract] [Full Text]  
  • Vasilevsky, S., Colino, J., Puliaev, R., Canaday, D. H., Snapper, C. M. (2008). Macrophages Pulsed with Streptococcus pneumoniae Elicit a T Cell-Dependent Antibody Response upon Transfer into Naive Mice. J. Immunol. 181: 1787-1797 [Abstract] [Full Text]  
  • Khan, A. Q., Lees, A., Snapper, C. M. (2004). Differential Regulation of IgG Anti-Capsular Polysaccharide and Antiprotein Responses to Intact Streptococcus pneumoniae in the Presence of Cognate CD4+ T Cell Help. J. Immunol. 172: 532-539 [Abstract] [Full Text]