Variable presentation of primary immune deficiency: Two cases with CD3 gamma deficiency presenting with only autoimmunity. Issue 3 (16th April 2013)
- Record Type:
- Journal Article
- Title:
- Variable presentation of primary immune deficiency: Two cases with CD3 gamma deficiency presenting with only autoimmunity. Issue 3 (16th April 2013)
- Main Title:
- Variable presentation of primary immune deficiency: Two cases with CD3 gamma deficiency presenting with only autoimmunity
- Authors:
- Tokgoz, Huseyin
Caliskan, Umran
Keles, Sevgi
Reisli, İsmail
Guiu, Isabel Sánchez
Morgan, Neil V. - Abstract:
- <abstract abstract-type="main" id="pai12063-abs-0001"> <title>Abstract</title> <sec id="pai12063-sec-0001" sec-type="section"> <title>Background</title> <p>CD3 chain expression defects including CD3 gamma, epsilon, delta, and zeta chain subunits, are autosomal recessive inherited severe combined immunodeficiencies (SCID). The phenotype is usually T‐B+NK+ SCID with lymphopenia where the clinical findings may be mild (CD3γ) or severe (CD3δ, ε, ζ) owing to the underlying molecular defect. There is limited information about the disease in literature.</p> </sec> <sec id="pai12063-sec-0002" sec-type="section"> <title>Methods</title> <p>Here, we present two siblings from non‐consanguineous family with autoimmunity including Evans syndrome, autoimmune hepatitis, nephrotic syndrome, and Hashimoto's thyroiditis and with no previous history of infections. To define the molecular basis of the disease, we performed linkage analysis around the CD3 receptor cluster and found consistent linkage to this region.</p> </sec> <sec id="pai12063-sec-0003" sec-type="section"> <title>Results</title> <p>The patient one displayed low TCRαβ expression, low IgG, low IgA, low IgM, low CD3, low CD4, low CD8. The patient two also displayed low TCRαβ expression and low anti‐HBs titer. We went onto identify a homozygous splicing mutation (IVS2‐1G&gt;C) in the two affected individuals in the CD3γ gene.</p> </sec> <sec id="pai12063-sec-0004" sec-type="section"> <title>Discussion</title> <p>To date, only four<abstract abstract-type="main" id="pai12063-abs-0001"> <title>Abstract</title> <sec id="pai12063-sec-0001" sec-type="section"> <title>Background</title> <p>CD3 chain expression defects including CD3 gamma, epsilon, delta, and zeta chain subunits, are autosomal recessive inherited severe combined immunodeficiencies (SCID). The phenotype is usually T‐B+NK+ SCID with lymphopenia where the clinical findings may be mild (CD3γ) or severe (CD3δ, ε, ζ) owing to the underlying molecular defect. There is limited information about the disease in literature.</p> </sec> <sec id="pai12063-sec-0002" sec-type="section"> <title>Methods</title> <p>Here, we present two siblings from non‐consanguineous family with autoimmunity including Evans syndrome, autoimmune hepatitis, nephrotic syndrome, and Hashimoto's thyroiditis and with no previous history of infections. To define the molecular basis of the disease, we performed linkage analysis around the CD3 receptor cluster and found consistent linkage to this region.</p> </sec> <sec id="pai12063-sec-0003" sec-type="section"> <title>Results</title> <p>The patient one displayed low TCRαβ expression, low IgG, low IgA, low IgM, low CD3, low CD4, low CD8. The patient two also displayed low TCRαβ expression and low anti‐HBs titer. We went onto identify a homozygous splicing mutation (IVS2‐1G&gt;C) in the two affected individuals in the CD3γ gene.</p> </sec> <sec id="pai12063-sec-0004" sec-type="section"> <title>Discussion</title> <p>To date, only four cases have been reported with CD3γ deficiency. Occasionally, the patients present with only autoimmunity including autoimmune hemolytic anemia, vitiligo, Hashimoto's thyroiditis, and autoimmune enteropathy. However, Evans syndrome, autoimmune hepatitis, and nephrotic syndrome have not been reported in previous cases. We believe that our cases will contribute to the literature.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatric allergy and immunology. Volume 24:Issue 3(2013)
- Journal:
- Pediatric allergy and immunology
- Issue:
- Volume 24:Issue 3(2013)
- Issue Display:
- Volume 24, Issue 3 (2013)
- Year:
- 2013
- Volume:
- 24
- Issue:
- 3
- Issue Sort Value:
- 2013-0024-0003-0000
- Page Start:
- 257
- Page End:
- 262
- Publication Date:
- 2013-04-16
- Subjects:
- Allergy in children -- Periodicals
Immunologic diseases in children -- Periodicals
617 - Journal URLs:
- http://www.blackwellpublishing.com/journal.asp?ref=0905-6157&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1399-3038 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/pai.12063 ↗
- Languages:
- English
- ISSNs:
- 0905-6157
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.527000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3228.xml