| Titel | A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutation |
|---|---|
| Gepubliceerd in | Journal of Clinical Investigation. ISSN 0021-9738. |
| Auteur | Burg, van der M. (Mirjam); Zdzienicka, M.Z. (Malgorzata); Gent, van D.C. (Dik); Dongen, van J.J.M. (Jacques); Veelen, van L.R.; Verkaik, N.S. (Nicole); Wiegant, W.W. (Wouter); Hartwig, N.G. (Nico); Barendregt, B.H. (Barbara); Brugmans, L.J.L. (Linda); Raams, A. (Anja); Jaspers, N.G.J. (Nicolaas) |
| Datum | 2006-01-01 |
| Trefwoord(en) | Animals, Humans, Research Support, Non-U.S. Gov't, Mice, Reference Values, Mutation, Mice, SCID, B-Lymphocytes/*immunology, T-Lymphocytes/*immunology, DNA Ligases/*genetics, Severe Combined Immunodeficiency/*genetics/*immunology, Killer Cells, Natural/*immunology |
| Taal | Engels |
| Type | artikel |
| Samenvatting | V(D)J recombination of Ig and TCR loci is a stepwise process during which site-specific DNA double-strand breaks (DSBs) are made by RAG1/RAG2, followed by DSB repair by nonhomologous end joining. Defects in V(D)J recombination result in SCID characterized by absence of mature B and T cells. A subset of T-B-NK+ SCID patients is sensitive to ionizing radiation, and the majority of these patients have mutations in Artemis. We present a patient with a new type of radiosensitive T-B-NK+ SCID with a defect in DNA ligase IV (LIG4). To date, LIG4 mutations have only been described in a radiosensitive leukemia patient and in 4 patients with a designated LIG4 syndrome, which is associated with chromosomal instability, pancytopenia, and developmental and growth delay. The patient described here shows that a LIG4 mutation can also cause T-B-NK+ SCID without developmental defects. The LIG4-deficient SCID patient had an incomplete but severe block in precursor B cell differentiation, resulting in extremely low levels of blood B cells. The residual D(H)-J(H) junctions showed extensive nucleotide deletions, apparently caused by prolonged exonuclease activity during the delayed D(H)-J(H) ligation process. In conclusion, different LIG4 mutations can result in either a developmental defect with minor immunological abnormalities or a SCID picture with normal development. |
| Publicatie | http://hdl.handle.net/1765/8414 |
| Persistent Identifier | urn:NBN:nl:ui:15-1765/8414 |
| Metadata | XML |
| Repository | Erasmus Universiteit Rotterdam |
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