Literature DB >> 3490729

Immunoglobulin abnormalities in patients with myotonic dystrophy.

A Suzumura, H Yamada, Y Matsuoka, I Sobue.   

Abstract

In order to further investigate immunoglobulin (Ig) abnormalities in patients with myotonic dystrophy (MyD), we examined 65 patients with MyD for their serum concentration of IgG in relation to their immunological functions as well as other clinical and laboratory findings. Turnover of IgG was also examined. We found significant and selective reduction of serum IgG in patients with MyD. The serum concentration of IgG in patients with MyD had a significant negative correlation with duration of illness, which suggested that serum IgG levels in MyD decreased constantly throughout the disease course. Peripheral blood lymphocyte subpopulations, including functional T cell subsets, in vitro lymphocyte proliferation, and in vitro IgG production were normal. The plasma cell population in bone marrow was also normal. The IgG turnover study using 125I-labelled IgG as a tracer revealed an increased extravascular IgG pool, and an increased capillary permeability of intravascular IgG into the extravascular compartment, in patients with MyD. These observations suggested that the Ig abnormalities in patients with MyD were not due to a broader immunological derangements as previously postulated by other authors. The abnormal distribution of IgG is a possible factor leading to reduced serum concentration of IgG in patients with MyD.

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Year:  1986        PMID: 3490729     DOI: 10.1111/j.1600-0404.1986.tb04639.x

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


  5 in total

Review 1.  Does (CUG)n repeat in DMPK mRNA 'paint' chromosome 19 to suppress distant genes to create the diverse phenotype of myotonic dystrophy?: A new hypothesis of long-range cis autosomal inactivation.

Authors:  R P Junghans; A Ebralidze; B Tiwari
Journal:  Neurogenetics       Date:  2001-03       Impact factor: 2.660

2.  Massive abscess with prolonged respiratory failure due to newly diagnosed myotonic dystrophy: A case report.

Authors:  Koshi Ota; Yoshitsugu Nakamura; Eriko Nakamura; Shogo Takashima; Masahiro Oka; Kanna Ota; Masahide Sakaue; Yohei Sano; Akira Takasu
Journal:  Medicine (Baltimore)       Date:  2019-04       Impact factor: 1.817

Review 3.  Enhanced serum immunoglobulin G clearance in myotonic dystrophy-associated hypogammaglobulinemia: a case series and review of the literature.

Authors:  Sarah C Sasson; Alastair Corbett; Andrew J McLachlan; R Chen; S A Adelstein; Sean Riminton; Sandhya Limaye
Journal:  J Med Case Rep       Date:  2019-11-20

Review 4.  Role of Immunoglobulins in Muscular Dystrophies and Inflammatory Myopathies.

Authors:  Andrea Farini; Chiara Villa; Luana Tripodi; Mariella Legato; Yvan Torrente
Journal:  Front Immunol       Date:  2021-07-14       Impact factor: 7.561

5.  Blood Transcriptome Profiling Links Immunity to Disease Severity in Myotonic Dystrophy Type 1 (DM1).

Authors:  Sylvia Nieuwenhuis; Joanna Widomska; Paul Blom; Peter-Bram A C 't Hoen; Baziel G M van Engelen; Jeffrey C Glennon
Journal:  Int J Mol Sci       Date:  2022-03-12       Impact factor: 5.923

  5 in total

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