In Vitro Bactericidal Capacity of Human Polymorphonuclear Leukocytes: Diminished Activity in Chronic Granulomatous Disease of Childhood
PG Quie, JG White, B Holmes… - The Journal of clinical …, 1967 - Am Soc Clin Investig
PG Quie, JG White, B Holmes, RA Good
The Journal of clinical investigation, 1967•Am Soc Clin InvestigDiminished bactericidal capacity was found to be characteristic of polymorphonuclear
leukocytes (PMN) from five children with the clinical syndrome of granulomatous disease of
childhood. The PMN from these children demonstrated nearly normal phagocytic capacity,
and the majority of viable bacteria, after 2 hours of incubation in the phagocytosis system,
were found associated with leukocytes. The morphology of the unstimulated
polymorphonuclear leukocytes from patients with chronic granulomatous disease was …
leukocytes (PMN) from five children with the clinical syndrome of granulomatous disease of
childhood. The PMN from these children demonstrated nearly normal phagocytic capacity,
and the majority of viable bacteria, after 2 hours of incubation in the phagocytosis system,
were found associated with leukocytes. The morphology of the unstimulated
polymorphonuclear leukocytes from patients with chronic granulomatous disease was …
Diminished bactericidal capacity was found to be characteristic of polymorphonuclear leukocytes (PMN) from five children with the clinical syndrome of granulomatous disease of childhood. The PMN from these children demonstrated nearly normal phagocytic capacity, and the majority of viable bacteria, after 2 hours of incubation in the phagocytosis system, were found associated with leukocytes.
The morphology of the unstimulated polymorphonuclear leukocytes from patients with chronic granulomatous disease was similar to those from normal persons of similar ages by light and electron microscopy. In addition, the total lysozyme and phagocytin activity of leukocyte extracts from these patients was similar to those from equal numbers of leukocytes from controls.
A striking difference in the cytoplasmic response after phagocytosis characterized the PMN of the patients with granulomatous disease. Whereas degranulation, vacuole formation, and rapid bacterial digestion were the rule in the PMN from controls, little degranulation and persistence of intact bacteria in the cytoplasm characterized disease.
The deficiency of bactericidal capacity and the minimal degranulation after active phagocytosis by the PMN of these children with an inherited syndrome suggest that separate metabolic processes are involved in phagocytosis and in intracellular digestion. Continuing study of the metabolic function of leukocytes from these children should provide an opportunity for increased understanding of the metabolic basis for degranulation and intracellular digestion in phagocytic cells.
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The Journal of Clinical Investigation