Literature DB >> 6328404

Short communication. Glycogenosis Ib: neutrophil microbicidal defects due to impaired hexose monophosphate shunt.

R Seger, B Steinmann, L Tiefenauer, T Matsunaga, R Gitzelmann.   

Abstract

We studied neutrophil microbicidal function and oxidative metabolic activity in a patient with glycogenosis Ib. The intracellular killing defect and the respiratory burst abnormality in gycogenosis Ib neutrophils were confirmed. The impaired oxygen-dependent microbicidal activity was shown to result from impaired hexose monophosphate shunt activity (impaired endogenous NADPH synthesis) and could be corrected by homogenization of the cells, followed by the addition of exogenous NADPH. Our data are thus consistent with a possible role for glucose-6-phosphate transport in neutrophil microbicidal function. We recommend a continuous prophylaxis with co-trimoxazole in patients with glycogen storage disease Ib.

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Year:  1984        PMID: 6328404     DOI: 10.1203/00006450-198403000-00019

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  13 in total

1.  Impaired glucose transport in polymorphonuclear leukocytes in glycogen storage disease Ib.

Authors:  N Bashan; R Potashnik; Y Hagay; S W Moses
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

2.  Normal polymorphonuclear neutrophil function in a case of glycogen storage disease type Ib.

Authors:  E Bonioli; C Bellini; A Di Stefano; A Costa; S Canini; F Patrone
Journal:  Eur J Pediatr       Date:  1990-06       Impact factor: 3.183

3.  Neutrophil metabolic dysfunction in genetically heterogeneous patients with glycogen storage disease type 1b.

Authors:  K Narisawa; S Ishizawa; H Okumura; K Tada; T Kuzuya
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

4.  Intact natural killer activity in glycogenosis type Ib.

Authors:  T Hara; E Ishii; K Ohkubo; K Ueda
Journal:  Eur J Pediatr       Date:  1986-08       Impact factor: 3.183

5.  Impaired monocyte function in glycogen storage disease type Ib.

Authors:  N Ueno; M Tomita; T Ariga; M Ohkawa; S Nagano; Y Takahashi; S Arashima; S Matsumoto
Journal:  Eur J Pediatr       Date:  1986-09       Impact factor: 3.183

6.  Defective neutrophil activity in fructose-1,6-diphosphatase deficiency.

Authors:  G Biasucci; M Gigliotti; D Luotti; B Bertagnolio; E Riva
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

7.  A study of 25 patients with chronic granulomatous disease: a new classification by correlating respiratory burst, cytochrome b, and flavoprotein.

Authors:  M C Bohler; R A Seger; R Mouy; E Vilmer; A Fischer; C Griscelli
Journal:  J Clin Immunol       Date:  1986-03       Impact factor: 8.317

8.  Impaired carbohydrate metabolism of polymorphonuclear leukocytes in glycogen storage disease Ib.

Authors:  N Bashan; Y Hagai; R Potashnik; S W Moses
Journal:  J Clin Invest       Date:  1988-05       Impact factor: 14.808

9.  Postnatal regression of glucose transport in a patient with glycogen storage disease type 1b.

Authors:  J Levy; M T Abu-Ras; T Berenstein; R Potashnik; I Meisner; S W Moses; N Bashan
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

10.  Chronic inflammatory bowel disease in glycogen storage disease type 1B.

Authors:  I R Sanderson; W M Bisset; P J Milla; J V Leonard
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

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