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Granulocytendysfunktion

Granulocyte dysfunction. Part II. Secondary defects

II. Erworbene Störungen

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Summary

In the first part we reviewed both the molecular basis of granulocyte function and the inborn defects. The present chapter summarizes our knowledge of the secondary defects of chemotaxis, opsonisation, phagocytosis and intracellular microbicidal activity.

Zusammenfassung

Im ersten Teil dieser Übersicht haben wir einen Überblick über die molekulare Basis der Granulocytenfunktion und deren wesentlichsten angeborenen Störungen gegeben. Der vorliegende zweite Teil soll das gegenwärtige Wissen über die sekundären Störungen der Chemotaxis, Opsonierung, Phagocytose und intracellulären Keimabtötung zusammenfassen.

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  1. Department für Kinderheilkunde und Abteilung für Pathologie I der Universität Ulm, Germany

    D. Niethammer, A. Wildfeuer, E. Kleihauer & O. Haferkamp

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Niethammer, D., Wildfeuer, A., Kleihauer, E. et al. Granulocytendysfunktion. Klin Wochenschr 53, 739–746 (1975). https://doi.org/10.1007/BF01614854

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