Literature DB >> 106731

The Chediak-Higashi syndrome: quantitation of a deficiency in maximal bactericidal capacity.

C C Clawson, J E Repine, J G White.   

Abstract

The maximum bactericidal capacity of neutrophils from a patient with the Chediak-Higashi syndrome (CHS) was measured by a quantitative assay in which the neutrophils were challenged with increasing multiples of Staphylococcus aureus, 502A. At various bacterial challenges from 0.5 to 65 bacteria per neutrophil, the CHS cells killed normal numbers of bacteria in 60 minutes. However, at higher ratios with a mean of 118 bacteria per neutrophil, the percentage of bacteria killed in 60 minutes by CHS neutrophils (8.1 +/- 2.3%) was significantly less (P < 0.001) than that killed by normal neutrophils (44 +/- 2.3%). The CHS neutrophils lagged in their ability to kill low challenges of bacteria (0.5 or 1.2 bacteria per neutrophil) only at 20 minutes. A hydrogen-peroxide-producing strain of Streptococcus faecalis was killed normally by the CHS neutrophils at 60 minutes, with all ratios of challenge up to 114 to 1. Electron microscopic examination of 60-minute specimens from high ratios of challenge that were stained for myeloperoxidase activity revealed a failure of many bacteria-laden phagosomes to display this marker of degranulation. The results of this study indicate that the maximal bactericidal capacity of CHS neutrophils is saturated by a significantly lower challenge of bacteria than is required to saturate normal cells. This appears to be the result of sequestration of a significant portion of these cells' bactericidal resources in the giant granules that do not participate appreciably in degranulation.

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Year:  1979        PMID: 106731      PMCID: PMC2042259     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  14 in total

1.  The Chediak-Higashi syndrome: studies of host defenses.

Authors:  S M Wolff
Journal:  Ann Intern Med       Date:  1972-02       Impact factor: 25.391

2.  Ultrastructure of bone marrow granulocytes in normal mink and mink with the homolog of the Chediak-Higashi trait of humans. I. Origin of the abnormal granules present in the neutrophils of mink with the C-HS trait.

Authors:  W C Davis; S S Spicer; W B Greene; G A Padgett
Journal:  Lab Invest       Date:  1971-04       Impact factor: 5.662

3.  Neutrophilic function in animals with the Chediak-Higashi syndrome.

Authors:  G A Padgett
Journal:  Blood       Date:  1967-06       Impact factor: 22.113

4.  Defective mononuclear leukocyte chemotaxis in the Chediak-Higashi syndrome of humans, mink, and cattle.

Authors:  J I Gallin; J A Klimerman; G A Padgett; S M Wolff
Journal:  Blood       Date:  1975-06       Impact factor: 22.113

5.  Interaction of membrane systems in blood platelets.

Authors:  J G White
Journal:  Am J Pathol       Date:  1972-02       Impact factor: 4.307

6.  Phagocytosis in chronic granulomatous disease and the Chediak-Higashi syndrome.

Authors:  T P Stossel; R K Root; M Vaughan
Journal:  N Engl J Med       Date:  1972-01-20       Impact factor: 91.245

7.  Formation of anomalous lysosomes in monocytes, neutrophils, and eosinophils from bone marrow of mice with Chédiak-Higashi syndrome.

Authors:  C Oliver; E Essner
Journal:  Lab Invest       Date:  1975-01       Impact factor: 5.662

8.  Defective granulocyte chemotaxis in the Chediak-Higashi syndrome.

Authors:  R A Clark; H R Kimball
Journal:  J Clin Invest       Date:  1971-12       Impact factor: 14.808

9.  Quantitative measurement of the bactericidal capability of neutrophils from patients and carriers of chronic granulomatous disease.

Authors:  J E Repine; C C Clawson
Journal:  J Lab Clin Med       Date:  1977-09

10.  Abnormal pattern of bactericidal activity of neutrophils deficient in granules, myeloperoxidase, and alkaline phosphatase.

Authors:  J E Repine; C C Clawson; R D Brunning
Journal:  J Lab Clin Med       Date:  1976-11
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  7 in total

1.  Chédiak-Higashi syndrome neutrophils are characterized by the absence of both normal azurophilic granules.

Authors:  B C West
Journal:  Am J Pathol       Date:  1986-01       Impact factor: 4.307

2.  Characterization of lysosomes and lysosomal enzymes from Chediak-Higashi-syndrome cultured fibroblasts.

Authors:  A L Miller; R Stein; M Sundsmo; R Y Yeh
Journal:  Biochem J       Date:  1986-09-01       Impact factor: 3.857

3.  Determination of maximal bactericidal activity in human granulocytes.

Authors:  H Hülsheger; W Stangel; J Schmidt; J Potel
Journal:  Blut       Date:  1985-03

4.  Increased incidence of menstruation-associated bactericidal defects in neutrophils from women who have recovered from toxic shock syndrome.

Authors:  E M Berger; J E Lockey; V H Aldrich; J E Repine
Journal:  Inflammation       Date:  1986-12       Impact factor: 4.092

5.  Microbicidal/cytotoxic proteins of neutrophils are deficient in two disorders: Chediak-Higashi syndrome and "specific" granule deficiency.

Authors:  T Ganz; J A Metcalf; J I Gallin; L A Boxer; R I Lehrer
Journal:  J Clin Invest       Date:  1988-08       Impact factor: 14.808

6.  The Chédiak-Higashi syndrome; the nature of the giant neutrophil granules and their interactions with cytoplasm and foreign particulates. I. Progressive enlargement of the massive inclusions in mature neutrophils. II. Manifestations of cytoplasmic injury and sequestration. III. Interactions between giant organelles and foreign particulates.

Authors:  J G White; C C Clawson
Journal:  Am J Pathol       Date:  1980-01       Impact factor: 4.307

7.  The Chédiak-Higashi syndrome: ring-shaped lysomomes in circulating monocytes.

Authors:  J G White; C C Clawson
Journal:  Am J Pathol       Date:  1979-09       Impact factor: 4.307

  7 in total

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