Literature DB >> 28162005

The clinical significance of complete class switching defect in Ataxia telangiectasia patients.

Saleh Ghiasy1, Leila Parvaneh1, Gholamreza Azizi1,2, Ghazal Sadri1, Majid Zaki Dizaji1, Hassan Abolhassani1,3, Asghar Aghamohammadi1.   

Abstract

BACKGROUND: Ataxia telangiectasia (AT) is a primary immunodeficiency associated with recurrent infections. We aimed to investigate clinical and immunological classification in AT patients who suffer from a different spectrum of humoral immune defects.
METHODS: AT patients were categorized according to the ability of class switching and patients with hyper IgM (HIgM) profile were defined as class switching defect (CSD).
RESULTS: Serum immunoglobulin profile in 66 AT patients showed normal immunoglobulin level (22.8%), IgA deficiency (37.9%) and hypogammaglobulinemia (18.1%) in the majority of patients, while 21.2% had HIgM profile revealing CSD. CSD does not affect the frequency of infections, however, the frequency of lymphoproliferation (p < 0.001), and autoimmunity (p = 0.004) were significantly higher in this group. Neurologic symptoms in CSD patients are mild or appear after recurrent infections, therefore these patients were usually misdiagnosed as HIgM syndrome.
CONCLUSIONS: Although most of AT patients have reduced IgA levels or normal immunoglobulin levels, but a fraction of these patients may show CSD ensuing HIgM-profile. CSD poses affected individuals at higher risk of non-infectious complications.

Entities:  

Keywords:  Ataxia telangiectasia; IgA deficiency; class switching defect; humoral immune defects; hyper IgM syndrome; hypogammaglobulinemia; immune deficiency; infection

Mesh:

Substances:

Year:  2017        PMID: 28162005     DOI: 10.1080/1744666X.2017.1292131

Source DB:  PubMed          Journal:  Expert Rev Clin Immunol        ISSN: 1744-666X            Impact factor:   4.473


  12 in total

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2.  Granulomatous Liver Disease in Ataxia-Telangiectasia With the Hyper-IgM Phenotype: A Case Report.

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3.  Atypical Ataxia Presentation in Variant Ataxia Telangiectasia: Iranian Case-Series and Review of the Literature.

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4.  Unusual clinical manifestations and predominant stopgain ATM gene variants in a single centre cohort of ataxia telangiectasia from North India.

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5.  Genetic Risk Variants for Class Switching Recombination Defects in Ataxia-Telangiectasia Patients.

Authors:  Parisa Amirifar; Mahya Mehrmohamadi; Mohammad Reza Ranjouri; Seyed Mohammad Akrami; Nima Rezaei; Ali Saberi; Reza Yazdani; Hassan Abolhassani; Asghar Aghamohammadi
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6.  Variable Abnormalities in T and B Cell Subsets in Ataxia Telangiectasia.

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Journal:  J Clin Immunol       Date:  2020-10-14       Impact factor: 8.317

7.  The Role of Respiratory Viruses in Children with Ataxia-Telangiectasia.

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8.  Elevated IgM levels as a marker for a unique phenotype in patients with Ataxia telangiectasia.

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9.  Dystonia in Ataxia Telangiectasia: A Case Report with Novel Mutations.

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Review 10.  Inflammation, a significant player of Ataxia-Telangiectasia pathogenesis?

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