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DOI 10.1016/j.jpeds.2005.07.022

Медицинская библиотека · The Journal of pediatrics · 2005

Intrinsic abnormalities of lymphocyte counts in children with down syndrome.

de Hingh Yvette C M, van der Vossen Petrus W, Gemen Eugenie F A, Mulder André B, Hop Wim C J, Brus Frank, de Vries Esther

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Аннотация

OBJECTIVE

Down syndrome (DS) is associated with an increased frequency of infections, hematologic malignancies, and autoimmune diseases, suggesting that immunodeficiency is an integral part of DS that contributes significantly to the observed increased morbidity and mortality. We determined the absolute counts of the main lymphocyte populations in a large group of DS children to gain further insight into this immunodeficiency.

STUDY

DESIGN

In a large group of children with DS (n = 96), the absolute numbers of the main lymphocyte subpopulations were determined with 3-color immunophenotyping using the lysed whole-blood method. The results were compared with previously published data in healthy children without DS.

RESULTS

In healthy children with DS, the primary expansion of T and B lymphocytes seen in healthy children without DS in the first years of life was severely abrogated. The T- lymphocyte subpopulation counts gradually reached more normal levels with time, whereas the B- lymphocyte population remained severely decreased, with 88% of values falling below the 10th percentile and 61% below the 5th percentile of normal.

CONCLUSIONS

The diminished expansion of T and B lymphocytes strongly suggests that a disturbance in the adaptive immune system is intrinsically present in DS and is not a reflection of precocious aging. Thymic alterations have been described in DS that could explain the decreased numbers of T lymphocytes, but not the striking B lymphocytopenia, seen in these children.

Для цитирования: de Hingh Yvette C M, van der Vossen Petrus W, Gemen Eugenie F A, Mulder André B, Hop Wim C J, Brus Frank, de Vries Esther. Intrinsic abnormalities of lymphocyte counts in children with down syndrome.. The Journal of pediatrics. 2005. DOI: 10.1016/j.jpeds.2005.07.022.

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