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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Trifari, Sara Scaramuzza, Samantha Catucci, Marco Ponzoni, Maurilio Mollica, Luca Chiesa, Robert Cattaneo, Federica Lafouresse, Fanny Calvez, Ronan Vermi, William Medicina, Daniela Castiello, Maria Carmina Marangoni, Francesco Bosticardo, Marita Doglioni, Claudio Caniglia, Maurizio Aiuti, Alessandro Villa, Anna Roncarolo, Maria-Grazia Dupré, Loïc |
| Description | Country affiliation: Italy Author Affiliation: Trifari S ( San Raffaele Telethon Institute for Gene Therapy (HSR-TIGET), Milan, Italy.) |
| Abstract | BACKGROUND: The Wiskott-Aldrich syndrome (WAS) is a rare genetic disease characterized by thrombocytopenia, immunodeficiency, autoimmunity, and hematologic malignancies. Secondary mutations leading to re-expression of WAS protein (WASP) are relatively frequent in patients with WAS. OBJECTIVE: The tissue distribution and function of revertant cells were investigated in a novel case of WAS gene secondary mutation. METHODS: A vast combination of approaches was used to characterize the second-site mutation, to investigate revertant cell function, and to track their distribution over a 18-year clinical follow-up. RESULTS: The WAS gene secondary mutation was a 4-nucleotide insertion, 4 nucleotides downstream of the original deletion. This somatic mutation allowed the T-cell-restricted expression of a stable, full-length WASP with a 3-amino acid change compared with the wild-type protein. WASP(+) T cells appeared early in the spleen (age 10 years) and were highly enriched in a mesenteric lymph node at a later time (age 23 years). Revertant T cells had a diversified T-cell-receptor repertoire and displayed in vitro and in vivo selective advantage. They proliferated and produced cytokines normally on T-cell-receptor stimulation. Consistently, the revertant WASP correctly localized to the immunologic synapse and to the leading edge of migrating T cells. CONCLUSION: Despite the high proportion of functional revertant T cells, the patient still has severe infections and autoimmune disorders, suggesting that re-expression of WASP in T cells is not sufficient to normalize immune functions fully in patients with WAS. |
| File Format | HTM / HTML |
| ISSN | 00916749 |
| e-ISSN | 10976825 |
| Journal | Journal of Allergy and Clinical Immunology |
| Issue Number | 2 |
| Volume Number | 125 |
| Language | English |
| Publisher | Elsevier |
| Publisher Date | 2010-02-01 |
| Publisher Place | United States |
| Access Restriction | Open |
| Subject Keyword | Discipline Immunology Lymphoid Tissue Immunology T-lymphocytes Wiskott-aldrich Syndrome Protein Genetics Wiskott-aldrich Syndrome Amino Acid Sequence Blotting, Western Cell Separation Dna Mutational Analysis Flow Cytometry Cytology Microscopy, Confocal Molecular Sequence Data Mosaicism Mutation Polymerase Chain Reaction Research Support, Non-u.s. Gov't |
| Content Type | Text |
| Resource Type | Article Case study |
| Subject | Immunology and Allergy Immunology |
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