Literature DB >> 2430422

Anti-myelin-associated glycoprotein antibody in sera from patients with demyelinating diseases.

S Sato, H Baba, T Inuzuka, T Miyatake.   

Abstract

An enzyme-linked immunosorbent assay (ELISA) was developed for quantitating anti-myelin-associated glycoprotein (MAG) IgM antibody in human sera. Absorbance values of anti-MAG antibody were higher than 0.2 at 1:80 of serum dilution in sera from some patients with demyelinating diseases of the central or peripheral nervous systems including multiple sclerosis, subacute sclerosing panencephalitis, Guillain-Barré syndrome, chronic relapsing polyradiculoneuritis and carcinomatous polyneuropathy and also some patients with autoimmune diseases such as collagen diseases and myasthenia gravis. However, absorbance values of anti-MAG antibody in sera from control individuals and patients with some other neurological diseases were less than 0.2 and considered as negative. Because of the reported existence of a cross antigenicity between MAG and lymphocyte, and especially natural killer cells, the possibility of the functional importance of anti-MAG antibody on cellular immunity is discussed with particular reference to the demyelinating diseases.

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Year:  1986        PMID: 2430422     DOI: 10.1111/j.1600-0404.1986.tb04636.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  3 in total

1.  Ataxic polyneuropathy and anti-Pr2 IgM kappa M proteinemia.

Authors:  M Arai; H Yoshino; Y Kusano; Y Yazaki; Y Ohnishi; T Miyatake
Journal:  J Neurol       Date:  1992-03       Impact factor: 4.849

2.  Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene.

Authors:  V Delague; C Bareil; S Tuffery; P Bouvagnet; E Chouery; S Koussa; T Maisonobe; J Loiselet; A Mégarbané; M Claustres
Journal:  Am J Hum Genet       Date:  2000-06-02       Impact factor: 11.025

Review 3.  Coherent somatic mutation in autoimmune disease.

Authors:  Kenneth Andrew Ross
Journal:  PLoS One       Date:  2014-07-02       Impact factor: 3.240

  3 in total

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