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Literature DB >> 7499492

HLA-class II alleles in Guillain-Barré syndrome and Miller Fisher syndrome and their association with preceding Campylobacter jejuni infection.

J H Rees¹, R W Vaughan, E Kondeatis, R A Hughes.

Abstract

HLA typing for class II alleles was performed on 97 patients with Guillain-Barré syndrome or Miller Fisher syndrome and compared with 100 controls. There was a significant association between HLA-DQB1*03 and preceding Campylobacter jejuni infection (Pc = 0.05).

Entities: Disease Species

Mesh：

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Year: 1995 PMID： 7499492 DOI： 10.1016/0165-5728(95)00102-8

Source DB: PubMed Journal: J Neuroimmunol ISSN： 0165-5728 Impact factor: 3.478

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Cited

20 in total

Review 1. Ganglioside molecular mimicry and its pathological roles in Guillain-Barré syndrome and related diseases.

Authors: Robert K Yu; Seigo Usuki; Toshio Ariga
Journal: Infect Immun Date: 2006-09-11 Impact factor: 3.441

Review 2. Autoimmune responses in peripheral nerve.

Authors: H P Hartung; H Willison; S Jung; M Pette; K V Toyka; G Giegerich
Journal: Springer Semin Immunopathol Date: 1996

3. Higher frequencies of HLA DQB1*05:01 and anti-glycosphingolipid antibodies in a cluster of severe Guillain-Barré syndrome.

Authors: L Schirmer; V Worthington; U Solloch; V Loleit; V Grummel; N Lakdawala; D Grant; R Wassmuth; A H Schmidt; F Gebhardt; T F M Andlauer; J Sauter; A Berthele; M P Lunn; Bernhard Hemmer
Journal: J Neurol Date: 2016-08-02 Impact factor: 4.849

Review 4. A review of the role of genetic factors in Guillain-Barré syndrome.

Authors: Amin Safa; Tahereh Azimi; Arezou Sayad; Mohammad Taheri; Soudeh Ghafouri-Fard
Journal: J Mol Neurosci Date: 2020-10-07 Impact factor: 3.444

Review 5. Transient immunosuppression: a bridge between infection and the atypical autoimmunity of Guillain-Barré syndrome?

Authors: I Steiner; G Rosenberg; I Wirguin
Journal: Clin Exp Immunol Date: 2010-10 Impact factor: 4.330

6. Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of Microglia.

Authors: Nynke Oosterhof; Irene J Chang; Ehsan Ghayoor Karimiani; Laura E Kuil; Dana M Jensen; Ray Daza; Erica Young; Lee Astle; Herma C van der Linde; Giridhar M Shivaram; Jeroen Demmers; Caitlin S Latimer; C Dirk Keene; Emily Loter; Reza Maroofian; Tjakko J van Ham; Robert F Hevner; James T Bennett
Journal: Am J Hum Genet Date: 2019-04-11 Impact factor: 11.025

HLA-class II alleles in Guillain-Barré syndrome and Miller Fisher syndrome and their association with preceding Campylobacter jejuni infection.

Review 1. Ganglioside molecular mimicry and its pathological roles in Guillain-Barré syndrome and related diseases.

Review 2. Autoimmune responses in peripheral nerve.

3. Higher frequencies of HLA DQB1*05:01 and anti-glycosphingolipid antibodies in a cluster of severe Guillain-Barré syndrome.

Review 4. A review of the role of genetic factors in Guillain-Barré syndrome.

Review 5. Transient immunosuppression: a bridge between infection and the atypical autoimmunity of Guillain-Barré syndrome?

6. Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of Microglia.

Review 7. Guillain-Barré syndrome, transverse myelitis and infectious diseases.

Review 8. Guillain-Barré syndrome: epidemiology, pathophysiology and management.

Review 9. Inflammatory neuropathies: pathology, molecular markers and targets for specific therapeutic intervention.

10. Campylobacter jejuni from patients with Guillain-Barré syndrome preferentially expresses a GD(1a)-like epitope.