High-throughput sequencing reveals an altered T cell repertoire in X-linked agammaglobulinemia

Copyright © 2015 Elsevier Inc. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 161(2015), 2 vom: 15. Dez., Seite 190-6
1. Verfasser: Ramesh, Manish (VerfasserIn)
Weitere Verfasser: Simchoni, Noa, Hamm, David, Cunningham-Rundles, Charlotte
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2015
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Amino acid sequence High throughput sequencing Junctional diversity T cell receptor XLA Immunoglobulin Variable Region Receptor-CD3 Complex, Antigen, T-Cell mehr... Receptors, Antigen, T-Cell DNA 9007-49-2
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245 1 0 |a High-throughput sequencing reveals an altered T cell repertoire in X-linked agammaglobulinemia 
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520 |a To examine the T cell receptor structure in the absence of B cells, the TCR β CDR3 was sequenced from DNA of 15 X-linked agammaglobulinemia (XLA) subjects and 18 male controls, using the Illumina HiSeq platform and the ImmunoSEQ analyzer. V gene usage and the V-J combinations, derived from both productive and non-productive sequences, were significantly different between XLA samples and controls. Although the CDR3 length was similar for XLA and control samples, the CDR3 region of the XLA T cell receptor contained significantly fewer deletions and insertions in V, D, and J gene segments, differences intrinsic to the V(D)J recombination process and not due to peripheral T cell selection. XLA CDR3s demonstrated fewer charged amino acid residues, more sharing of CDR3 sequences, and almost completely lacked a population of highly modified Vβ gene segments found in control DNA, suggesting both a skewed and contracted T cell repertoire in XLA 
650 4 |a Journal Article 
650 4 |a Research Support, N.I.H., Extramural 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Amino acid sequence 
650 4 |a High throughput sequencing 
650 4 |a Junctional diversity 
650 4 |a T cell receptor 
650 4 |a XLA 
650 7 |a Immunoglobulin Variable Region  |2 NLM 
650 7 |a Receptor-CD3 Complex, Antigen, T-Cell  |2 NLM 
650 7 |a Receptors, Antigen, T-Cell  |2 NLM 
650 7 |a DNA  |2 NLM 
650 7 |a 9007-49-2  |2 NLM 
700 1 |a Simchoni, Noa  |e verfasserin  |4 aut 
700 1 |a Hamm, David  |e verfasserin  |4 aut 
700 1 |a Cunningham-Rundles, Charlotte  |e verfasserin  |4 aut 
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