Hypomorphic mutation of ZAP70 in human results in a late onset immunodeficiency and no autoimmunity - PubMed (original) (raw)
Case Reports
. 2009 Jul;39(7):1966-76.
doi: 10.1002/eji.200939385.
Stéphanie Dogniaux, Karine Chemin, Zofia Maciorowski, Annick Lim, Fabienne Mazerolles, Frédéric Rieux-Laucat, Marie-Claude Stolzenberg, Marianne Debre, Jean-Paul Magny, Françoise Le Deist, Alain Fischer, Claire Hivroz
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- PMID: 19548248
- DOI: 10.1002/eji.200939385
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Case Reports
Hypomorphic mutation of ZAP70 in human results in a late onset immunodeficiency and no autoimmunity
Capucine Picard et al. Eur J Immunol. 2009 Jul.
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Abstract
Complete lack of function of the tyrosine kinase ZAP70 in humans results in a severe immunodeficiency, characterized by a lack of mature CD8(+) T cells and non-functional CD4(+) T cells. We report herein an immunodeficiency with an inherited hypomorphic mutation of ZAP70 due to a single G-to-A substitution in a non-coding intron. This mutation introduces a new acceptor splice site and allows low levels of normal alternative splicing and of WT ZAP70 expression. This partial deficiency results in a compromised TCR signaling that was totally restored by increased expression of ZAP70, demonstrating that defective activation of the patient T cells was indeed caused by the low level of ZAP70 expression. This partial ZAP70 deficiency was associated with an attenuated clinical and immunological phenotype as compared with complete ZAP70 deficiency. CD4(+) helper T-cell populations including, follicular helper T cells, Th1, Th17 and Treg were detected in the blood. Finally, the patient had no manifestation of autoimmunity suggesting that the T-cell tolerogenic functions were not compromised, in contrast to what has been observed in mice carrying hypomorphic mutations of Zap70. This report extends the phenotype spectrum of ZAP70 deficiency with a residual function of ZAP70.
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