| Literature DB >> 19586803 |
R van Gent1, C M van Tilburg, E E Nibbelke, S A Otto, J F Gaiser, P L Janssens-Korpela, E A M Sanders, J A M Borghans, N M Wulffraat, M B Bierings, A C Bloem, K Tesselaar.
Abstract
Work in the past years has led to a refined phenotypical description of functionally distinct T- and B-cell subsets. Since both lymphocyte compartments are established and undergo dramatic changes during childhood, redefined pediatric reference values of both compartments are needed. In a cohort of 145 healthy children, aged 0-18 years, the relative and absolute numbers of the various T- and B-cell subsets were determined. In addition, we found that besides thymic output, naive (CD27(+)CD45RO(-)) T-cell proliferation contributed significantly to the establishment of the naive T-cell compartment. At birth, regulatory (CD25(+)CD127(-)CD4(+)) T cells (Tregs) mainly had a naive (CD27(+)CD45RO(-)) phenotype whereas 'memory or effector-like' (CD45RO(+)) Tregs accumulated slowly during childhood. Besides the CD27(+)IgM(+)IgD(+) memory B-cell population, the recently identified CD27(-)IgG(+) and CD27(-)IgA(+) memory B-cell populations were already present at birth. These data provide reference values of the T- and B-cell compartments during childhood for studies of immunological disorders or immune reconstitution in children.Entities:
Mesh:
Year: 2009 PMID: 19586803 DOI: 10.1016/j.clim.2009.05.020
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969