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http://www.jimmunol.org/cgi/content/abstract/170/3/1504
The Journal of Immunology, 2003, 170: 1504-1509.
Copyright © 2003 by The
American Association of Immunologists
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* Laboratory of Immunology, Hôpital Erasme,
Université Libre de Bruxelles, Brussels, Belgium;
Department of Pediatrics and Laboratory of Microbiology, Academisch Ziekenhuis
Vrije Universiteit Brussels, Brussels, Belgium;
Department of Pediatrics, Saint-Pierre Hospital, Brussels, Belgium;
Chiron Biocine, Sienna, Italy; and ¶ Institut National de la Santé et
de la Recherche Médicale Unité 447, Institut Pasteur, Lille, France
Neonatal immaturity of the immune system is currently believed
to generally limit the induction of immune responses to vaccine
Ags and to skew them toward type 2 responses. We demonstrated here
that Bordetella pertussis infection in very young infants
(median, 2 mo old) as well as the first administration of whole-cell
pertussis vaccine induces B. pertussis Ag-specific IFN-
secretion by the PBMC of these infants. IFN-
was secreted by both CD4+ and CD8+ T lymphocytes, and the
levels of Ag-induced IFN-
secretion did not correlate with the age of the infants. Appearance
of the specific Th-1 cell-mediated immunity was accompanied by
a general shift of the cytokine secretion profile of these infants
toward a stronger Th1 profile, as evidenced by the response to
a polyclonal stimulation. We conclude that the immune system of
2-mo-old infants is developmentally mature enough to develop Th1
responses in vivo upon infection by B. pertussis or vaccination
with whole-cell pertussis vaccines.
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MATERIAL CONTAINED, PRESENTED, OR PROVIDED HERE IS FOR GENERAL INFORMATION
PURPOSES ONLY AND IS NOT TO BE CONSTRUED AS REFLECTING THE KNOWLEDGE OR OPINIONS
OF THE PUBLISHER, AND IS NOT TO BE CONSTRUED OR INTENDED AS PROVIDING MEDICAL OR
LEGAL ADVICE. THE DECISION WHETHER OR NOT TO VACCINATE IS AN IMPORTANT AND
COMPLEX ISSUE AND SHOULD BE MADE BY YOU, AND YOU ALONE, IN CONSULTATION WITH
YOUR HEALTH CARE PROVIDER.