Sökning: (WFRF:(Rassenti Laura Z.))
> (2005-2009) >
Immunoglobulin gene...
Immunoglobulin gene segment usage, location and immunogenicity in mutated and unmutated chronic lymphocytic leukaemia
-
- Mauerer, Katja (författare)
- Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA
-
- Zahrieh, David (författare)
- Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA
-
- Gorgun, Gullu (författare)
- Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA
-
visa fler...
-
- Li, Aihong (författare)
- Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA
-
- Zhou, Jianbiao (författare)
- Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA
-
- Ansén, Sascha (författare)
- Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA
-
- Rassenti, Laura Z (författare)
- CLL Research Consortium, University of California San Diego, CA, USA
-
- Gribben, John G (författare)
- Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA
-
visa färre...
-
(creator_code:org_t)
- Blackwell Publishing, 2005
- 2005
- Engelska.
-
Ingår i: British Journal of Haematology. - : Blackwell Publishing. - 0007-1048 .- 1365-2141. ; 129:4, s. 499-510
- Relaterad länk:
-
https://urn.kb.se/re...
-
visa fler...
-
https://doi.org/10.1...
-
visa färre...
Abstract
Ämnesord
Stäng
- The mutational status of the variable region of the immunoglobulin heavy chain gene (IgV(H)) is an important prognostic marker in B-cell chronic lymphocytic leukaemia (B-CLL), with mutated patients having improved outcome. To examine the impact of mutational status on V(H), D(H), and J(H) gene segment location and immunogenicity, we analysed 375 IgH sequences from 356 patients with B-CLL. Although V(H) and D(H) gene usage was different in mutated compared to unmutated patients, there was no impact of gene location on frequency of use or clinical outcome. Surprisingly, somatic mutations did not increase the immunogenicity of the Ig, as assessed by predicted binding affinity of Ig-derived peptides to major histocompatibility Class I and Class II molecules. Even excluding patients using V(H)1-69, cases using the V(H)1 gene family had a poor outcome. Both mutated and unmutated CLL patients demonstrated evidence of antigen selection. The worst outcome was seen in the subset of 14 unmutated patients with similar HCDR3 amino acid sequence using V(H)1-69, D(H)3-3 and J(H)6, suggesting an antigen-driven process modulating the clinical course.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Hematologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Hematology (hsv//eng)
Nyckelord
- chronic lymphocytic leukaemia
- V(H)D(H)J(H) gene usage
- HCDR3
- antigen selection
- MHC binding affinity
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
Hitta via bibliotek
Till lärosätets databas