J Gen Virol
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 85 (2004), 1571-1579; DOI 10.1099/vir.0.79919-0

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
Right arrow Citation Map
Services
Right arrow Email this article to a friend
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 reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Krieg, C.
Right arrow Articles by Meyerhans, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Krieg, C.
Right arrow Articles by Meyerhans, A.
Agricola
Right arrow Articles by Krieg, C.
Right arrow Articles by Meyerhans, A.
© 2004 Society for General Microbiology

Gut-homing ({alpha}4{beta}7+) Th1 memory responses after inactivated poliovirus immunization in poliovirus orally pre-immunized donors

Carsten Krieg, Reinhard Maier and Andreas Meyerhans

Institute of Medical Microbiology and Hygiene, Department of Virology, Building 47, University of the Saarland, Kirrberger Strasse, 66421 Homburg/Saar, Germany

Correspondence
Andreas Meyerhans
Andreas.Meyerhans{at}uniklinik-saarland.de

Mucosal infections are prevented by a specialized local immune system. Immune cells of this compartment can also be found in the blood and are characterized by the expression of mucosa-specific homing molecules. Here, the cellular immune responses after inactivated poliovirus immunization (IPV) in poliovirus orally pre-immunized donors were investigated. Subcutaneous IPV induced a transient increase in the proliferative response against poliovirus antigen and in the number of poliovirus-specific CD4+ T cells in the blood of the vaccinees. These cells were characterized to be of the effector memory type (CD45RA/CD45RO+/CCR7/CD27+) and expressed the homing molecule {alpha}4{beta}7, indicating their origin from the gut. Together these data show the recurrence of gut-derived poliovirus-specific cells upon IPV and evaluate the whole-blood assay as a powerful tool for monitoring the success of a vaccination.




This article has been cited by other articles:


Home page
Infect. Immun.Home page
Z. Huo, R. Sinha, E. A. McNeela, R. Borrow, R. Giemza, C. Cosgrove, P. T. Heath, K. H. G. Mills, R. Rappuoli, G. E. Griffin, et al.
Induction of Protective Serum Meningococcal Bactericidal and Diphtheria-Neutralizing Antibodies and Mucosal Immunoglobulin A in Volunteers by Nasal Insufflations of the Neisseria meningitidis Serogroup C Polysaccharide-CRM197 Conjugate Vaccine Mixed with Chitosan
Infect. Immun., December 1, 2005; 73(12): 8256 - 8265.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
R. Wahid, M. J. Cannon, and M. Chow
Virus-Specific CD4+ and CD8+ Cytotoxic T-Cell Responses and Long-Term T-Cell Memory in Individuals Vaccinated against Polio
J. Virol., May 15, 2005; 79(10): 5988 - 5995.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2004 by the Society for General Microbiology.