Publication: Simple measurement of iga predicts immunity and mortality in ataxia-telangiectasia
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Date
2021-09-03
Authors
Kilic, Sara S.
Authors
Zielen, Stefan
Duecker, Ruth Pia
Woelke, Sandra
Donath, Helena
Bakhtiar, Sharhzad
Buecker, Aileen
Kreyenberg, Hermann
Huenecke, Sabine
Bader, Peter
Mahlaoui, Nizar
Journal Title
Journal ISSN
Volume Title
Publisher
Springer/plenum Publishers
Abstract
Patients with ataxia-telangiectasia (A-T) suffer from progressive cerebellar ataxia, immunodeficiency, respiratory failure, and cancer susceptibility. From a clinical point of view, A-T patients with IgA deficiency show more symptoms and may have a poorer prognosis. In this study, we analyzed mortality and immunity data of 659 A-T patients with regard to IgA deficiency collected from the European Society for Immunodeficiencies (ESID) registry and from 66 patients with classical A-T who attended at the Frankfurt Goethe-University between 2012 and 2018. We studied peripheral B- and T-cell subsets and T-cell repertoire of the Frankfurt cohort and survival rates of all A-T patients in the ESID registry. Patients with A-T have significant alterations in their lymphocyte phenotypes. All subsets (CD3, CD4, CD8, CD19, CD4/CD45RA, and CD8/CD45RA) were significantly diminished compared to standard values. Patients with IgA deficiency (n = 35) had significantly lower lymphocyte counts compared to A-T patients without IgA deficiency (n = 31) due to a further decrease of naive CD4 T-cells, central memory CD4 cells, and regulatory T-cells. Although both patient groups showed affected TCR-ss repertoires compared to controls, no differences could be detected between patients with and without IgA deficiency. Overall survival of patients with IgA deficiency was significantly diminished. For the first time, our data show that patients with IgA deficiency have significantly lower lymphocyte counts and subsets, which are accompanied with reduced survival, compared to A-T patients without IgA deficiency. IgA, a simple surrogate marker, is indicating the poorest prognosis for classical A-T patients. Both non-interventional clinical trials were registered at clinicaltrials.gov 2012 (Susceptibility to infections in ataxia-telangiectasia; NCT02345135) and 2017 (Susceptibility to Infections, tumor risk and liver disease in patients with ataxia-telangiectasia; NCT03357978)
Description
Keywords
T-cell subsets, Oxidative stress, Deficiency, Atm, Infections, Receptor, Immunodeficiency, Repertoire, Generation, Phenotype, Ataxia-telangiectasia, Iga deficiency, Immunoglobulins, Immunodeficiency, Lymphopenia, Mortality, Science & technology, Life sciences & biomedicine, Immunology, Immunology