Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Serum IgD concentrations in immunodeficiency diseases.

O Sanal1, F Ersoy, I Tezcan

  • 1Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara.

The Turkish Journal of Pediatrics
|July 1, 1990
PubMed
Summary

Serum Immunoglobulin D (IgD) levels were higher in ataxia-telangiectasia patients but not significantly different in selective IgA deficiency patients compared to controls. IgD levels did not correlate with infection frequency.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Primary Immunodeficiency Disorders in children with Non-Cystic Fibrosis Bronchiectasis.

European annals of allergy and clinical immunology·2020
Same author

Characteristics of patients with C1 esterase inhibitor deficiency: a single center study.

European annals of allergy and clinical immunology·2020
Same author

Bone marrow transplantation with Favorable outcome in three patients with LPS-responsive beige-like anchor (LRBA) deficiency.

Clinical immunology (Orlando, Fla.)·2019
Same author

A Novel Homozygous Mutation With Different Clinical Presentations in 2 IRAK-4-Deficient Siblings: First Case With Recurrent Salmonellosis and Non-Hodgkin Lymphoma.

Journal of investigational allergology & clinical immunology·2018
Same author

Clinical and genetic features of the patients with X-Linked agammaglobulinemia from Turkey: Single-centre experience.

Scandinavian journal of immunology·2018
Same author

Investigation of Genetic Defects in Severe Combined Immunodeficiency Patients from Turkey by Targeted Sequencing.

Scandinavian journal of immunology·2017

Area of Science:

  • Immunology
  • Clinical Medicine
  • Genetics

Background:

  • Primary immunodeficiency diseases (PIDs) are a heterogeneous group of disorders affecting the immune system.
  • Immunoglobulin D (IgD) is a less understood antibody isotype with a role in immune regulation.
  • Specific PIDs, like ataxia-telangiectasia and selective IgA deficiency, present unique immunological challenges.

Purpose of the Study:

  • To investigate serum Immunoglobulin D (IgD) levels in patients with well-defined primary immunodeficiency diseases.
  • To compare IgD levels between patients with ataxia-telangiectasia and selective IgA deficiency and healthy controls.
  • To explore potential correlations between serum IgD levels and clinical manifestations such as infections.

Main Methods:

  • Serum samples were collected from 66 patients diagnosed with primary immunodeficiency diseases.

Related Experiment Videos

  • Patients were categorized into major groups: ataxia-telangiectasia (n=38) and selective IgA deficiency (n=11).
  • Serum IgD levels were quantified and compared against control groups; correlations with clinical data were analyzed.
  • Main Results:

    • Patients with ataxia-telangiectasia exhibited a trend towards higher serum IgD levels compared to controls.
    • No significant difference in serum IgD levels was observed in patients with selective IgA deficiency versus controls.
    • Serum IgD levels did not correlate with the frequency of infections or associated disorders in either patient group.

    Conclusions:

    • Serum IgD levels may be altered in specific primary immunodeficiency diseases like ataxia-telangiectasia.
    • Selective IgA deficiency does not appear to be associated with significant changes in serum IgD levels.
    • Further research is warranted to elucidate the role of IgD in the pathogenesis and clinical course of primary immunodeficiencies.