Helper T-cell deficiency in infantile genetic agranulocytosis (M. Kostmann)

A female turkish infant with congenital infantile genetic agranulocytosis was examined for its distribution of lymphocyte subclasses. Imbalances of B cells and T-cell subpopulations were found. Compared to the normal control group a relative as well as an absolute deficiency of T helper cells and an...

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Veröffentlicht in:Monatsschrift Kinderheilkunde 1983-11, Vol.131 (11), p.793-796
Hauptverfasser: Evers, K G, Burdach, S E, Ieromnimon, W, Krüger, J
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container_title Monatsschrift Kinderheilkunde
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creator Evers, K G
Burdach, S E
Ieromnimon, W
Krüger, J
description A female turkish infant with congenital infantile genetic agranulocytosis was examined for its distribution of lymphocyte subclasses. Imbalances of B cells and T-cell subpopulations were found. Compared to the normal control group a relative as well as an absolute deficiency of T helper cells and an increase of the absolute number of T suppressor cells were the most prominent findings. The importance of immunoregulatory T-cell subsets in the pathogenesis of infantile genetic agranulocytosis, disorders of hematopoiesis and granulocyte production, as well as primary and secondary immunodeficiencies is discussed.
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source MEDLINE; SpringerNature Complete Journals
subjects Agranulocytosis - complications
Agranulocytosis - congenital
Consanguinity
Female
Humans
Infant
Lymphocytosis - complications
Lymphopenia - complications
T-Lymphocytes, Helper-Inducer
T-Lymphocytes, Regulatory
title Helper T-cell deficiency in infantile genetic agranulocytosis (M. Kostmann)
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