Literature DB >> 423020

An inherited defect of neutrophil mobility in Shwachman syndrome.

P J Aggett, J T Harries, B A Harvey, J F Soothill.   

Abstract

Selected immunologic functions were assessed in 14 patients with the Shwachman syndrome. Nine patients were neutropenic and four had low levels of IgA or of IgM. Neutrophil mobility was significantly defective in the group of patients as a whole (in 12 it was below the lower limit of normal) and in their parents. No other consistent abnormality in immunity was found. These results suggest that the defective neutrophil mobility is a feature of Shwachman syndrome which may contribute to the vulnerability of these patients to frequent infections. The defect appears to be a primary genetic one, inherited as an autosomal recessive characteristic consistent with the assumed inheritance of Shwachman syndrome.

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Year:  1979        PMID: 423020     DOI: 10.1016/s0022-3476(79)80578-8

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  23 in total

1.  Segregation analysis in Shwachman-Diamond syndrome: evidence for recessive inheritance.

Authors:  H Ginzberg; J Shin; L Ellis; S Goobie; J Morrison; M Corey; P R Durie; J M Rommens
Journal:  Am J Hum Genet       Date:  2000-03-14       Impact factor: 11.025

2.  Lentiviral-mediated RNAi inhibition of Sbds in murine hematopoietic progenitors impairs their hematopoietic potential.

Authors:  Amy S Rawls; Alyssa D Gregory; Jill R Woloszynek; Fulu Liu; Daniel C Link
Journal:  Blood       Date:  2007-07-17       Impact factor: 22.113

3.  Neutrophil functions in patients with inherited bone marrow failure syndromes.

Authors:  Andrzej Rochowski; Chunxiang Sun; Michael Glogauer; Blanche P Alter
Journal:  Pediatr Blood Cancer       Date:  2010-11-05       Impact factor: 3.167

4.  The chemoattractant des-Arg74-C5a regulates the expression of its own receptor on a monocyte-like cell line.

Authors:  M D Barker; P J Jose; T J Williams; D R Burton
Journal:  Biochem J       Date:  1986-06-01       Impact factor: 3.857

5.  Loss of the mouse ortholog of the shwachman-diamond syndrome gene (Sbds) results in early embryonic lethality.

Authors:  Siyi Zhang; Mingjun Shi; Chi-Chung Hui; Johanna M Rommens
Journal:  Mol Cell Biol       Date:  2006-09       Impact factor: 4.272

6.  Aberrant phagocyte function in Shwachman syndrome.

Authors:  H Repo; E Savilahti; M Leirisalo-Repo
Journal:  Clin Exp Immunol       Date:  1987-07       Impact factor: 4.330

7.  Defects of serum chemoattraction and polymorphonuclear leucocyte movement in patients with primary hepatocellular carcinoma.

Authors:  A G Yousif-Kadaru; R J Wyke; I A Rajkovic; A L Eddleston; R Williams
Journal:  Clin Exp Immunol       Date:  1982-08       Impact factor: 4.330

8.  T lymphocyte mobility: defects and effects of ascorbic acid, histamine and complexed IgG.

Authors:  E M Smogorzewska; L Layward; J F Soothill
Journal:  Clin Exp Immunol       Date:  1981-01       Impact factor: 4.330

9.  Serum stimulatory activity and polymorphonuclear leucocyte movement in patients with fulminant hepatic failure.

Authors:  R J Wyke; A G Yousif-Kadaru; I A Rajkovic; A L Eddleston; R Williams
Journal:  Clin Exp Immunol       Date:  1982-11       Impact factor: 4.330

Review 10.  Clinical and molecular pathophysiology of Shwachman-Diamond syndrome: an update.

Authors:  Kasiani C Myers; Stella M Davies; Akiko Shimamura
Journal:  Hematol Oncol Clin North Am       Date:  2012-11-03       Impact factor: 3.722

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