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*
Department of Pneumology/Immunology, Childrens Hospital, Berlin, Germany; and
Institute of Laboratory Medicine and Pathobiochemistry, Charité-Campus Virchow-Klinikum of Humboldt University, 13353 Berlin, Germany
Cognate interaction between TCRs and MHC class II molecules plays
an important role in initiating the allergen-specific immune response.
Therefore, we analyzed the TCR distribution of human PBLs of 56 atopic
and nonatopic (NA) individuals, including 4 monozygotic twin pairs,
from two extended and four nuclear families. The expression of 23 Vß
and 3 V
elements was analyzed. The blood samples of symptomatic
birch pollen-sensitized individuals that were taken
6 wk after the
birch pollen season (n = 8) showed a significantly
higher frequency of Vß16.1+ and Vß20.1+ T
cells compared with the blood samples of birch pollen-sensitized
individuals that were obtained out of allergen season
(n = 10) or from NA individuals
(p < 0.0005 and p < 0.0001,
respectively). Allergen-specific lymphocyte proliferation was detected
in the allergic individuals, and the distribution of
Vß16.1+ and Vß20.1+ T cells returned to
normal levels after the pollen season. The frequency of these
Vß-expressing T cells correlated with the levels of allergen-specific
IgE Abs. In addition, cat-sensitized individuals (n
= 8) showed a significantly higher frequency of Vß17.1-expressing T
cells than did NA individuals (p < 0.005). Our
results indicate restricted TCR-Vß gene usage in
cat and birch pollen allergies; we suggest that both genetic and
environmental factors contribute to TCR-Vß gene
expression and to the development of a specific T cell
response.
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