Immunodeficiency in ataxia telangiectasia is correlated strongly with the presence of two null mutations in the ataxia telangiectasia mutated gene

E R Staples, E M McDermott, A Reiman, P J Byrd, S Ritchie, A M R Taylor, E G Davies

Research output: Contribution to journalArticle

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Abstract

Immunodeficiency affects over half of all patients with ataxia telangiectasia (A-T) and when present can contribute significantly to morbidity and mortality. A retrospective review of clinical history, immunological findings, ataxia telangiectasia mutated (ATM) enzyme activity and ATM mutation type was conducted on 80 consecutive patients attending the National Clinic for Ataxia Telangiectasia, Nottingham, UK between 1994 and 2006. The aim was to characterize the immunodeficiency in A-T and determine its relationship to the ATM mutations present. Sixty-one patients had mutations resulting in complete loss of ATM kinase activity (group A) and 19 patients had leaky splice or missense mutations resulting in residual kinase activity (group B). There was a significantly higher proportion of patients with recurrent sinopulmonary infections in group A compared with group B (31 of 61 versus four of 19 P = 0.03) and a greater need for prophylactic antibiotics (30 of 61 versus one of 19 P = 0.001). Comparing group A with group B patients, 25 of 46 had undetectable/low immunoglobulin A (IgA) levels compared with none of 19; T cell lymphopenia was found in 28 of 56 compared with one of 18 and B cell lymphopenia in 35 of 55 compared with four of 18 patients (P = 0.00004, 0.001 and 0.003 respectively). Low IgG2 subclass levels and low levels of antibodies to pneumococcal polysaccharide were more common in group A than group B (16 of 27 versus one of 11 P = 0.01; 34/43 versus six of 17 P = 0.002) patients. Ig replacement therapy was required in 10 (12.5%) of the whole cohort, all in group A. In conclusion, A-T patients with no ATM kinase activity had a markedly more severe immunological phenotype than those expressing low levels of ATM activity.

Original languageEnglish
Pages (from-to)214-220
Number of pages7
JournalClinical and Experimental Immunology
Volume153
Issue number2
DOIs
Publication statusPublished - Aug 2008

Fingerprint

Ataxia Telangiectasia
Mutation
Genes
Lymphopenia
Phosphotransferases
Missense Mutation
Immunoglobulin A
Polysaccharides
B-Lymphocytes
Immunoglobulin G
Anti-Bacterial Agents
Morbidity
T-Lymphocytes
Phenotype

Keywords

  • Adolescent
  • Adult
  • Antibodies, Bacterial
  • Ataxia Telangiectasia
  • Ataxia Telangiectasia Mutated Proteins
  • B-Lymphocytes
  • Cell Cycle Proteins
  • Child
  • Child, Preschool
  • DNA-Binding Proteins
  • Humans
  • Immunoglobulin A
  • Immunoglobulin G
  • Immunoglobulins, Intravenous
  • Lymphocyte Count
  • Lymphopenia
  • Middle Aged
  • Mutation, Missense
  • Protein-Serine-Threonine Kinases
  • Retrospective Studies
  • Streptococcus pneumoniae
  • T-Lymphocytes
  • Tumor Suppressor Proteins
  • Journal Article
  • Research Support, Non-U.S. Gov't

Cite this

Immunodeficiency in ataxia telangiectasia is correlated strongly with the presence of two null mutations in the ataxia telangiectasia mutated gene. / Staples, E R; McDermott, E M; Reiman, A; Byrd, P J; Ritchie, S; Taylor, A M R; Davies, E G.

In: Clinical and Experimental Immunology, Vol. 153, No. 2, 08.2008, p. 214-220.

Research output: Contribution to journalArticle

Staples, E R ; McDermott, E M ; Reiman, A ; Byrd, P J ; Ritchie, S ; Taylor, A M R ; Davies, E G. / Immunodeficiency in ataxia telangiectasia is correlated strongly with the presence of two null mutations in the ataxia telangiectasia mutated gene. In: Clinical and Experimental Immunology. 2008 ; Vol. 153, No. 2. pp. 214-220.
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AB - Immunodeficiency affects over half of all patients with ataxia telangiectasia (A-T) and when present can contribute significantly to morbidity and mortality. A retrospective review of clinical history, immunological findings, ataxia telangiectasia mutated (ATM) enzyme activity and ATM mutation type was conducted on 80 consecutive patients attending the National Clinic for Ataxia Telangiectasia, Nottingham, UK between 1994 and 2006. The aim was to characterize the immunodeficiency in A-T and determine its relationship to the ATM mutations present. Sixty-one patients had mutations resulting in complete loss of ATM kinase activity (group A) and 19 patients had leaky splice or missense mutations resulting in residual kinase activity (group B). There was a significantly higher proportion of patients with recurrent sinopulmonary infections in group A compared with group B (31 of 61 versus four of 19 P = 0.03) and a greater need for prophylactic antibiotics (30 of 61 versus one of 19 P = 0.001). Comparing group A with group B patients, 25 of 46 had undetectable/low immunoglobulin A (IgA) levels compared with none of 19; T cell lymphopenia was found in 28 of 56 compared with one of 18 and B cell lymphopenia in 35 of 55 compared with four of 18 patients (P = 0.00004, 0.001 and 0.003 respectively). Low IgG2 subclass levels and low levels of antibodies to pneumococcal polysaccharide were more common in group A than group B (16 of 27 versus one of 11 P = 0.01; 34/43 versus six of 17 P = 0.002) patients. Ig replacement therapy was required in 10 (12.5%) of the whole cohort, all in group A. In conclusion, A-T patients with no ATM kinase activity had a markedly more severe immunological phenotype than those expressing low levels of ATM activity.

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