scholarly journals Molecular Analyses of MHC Genes and T Cell Receptor V.BETA. Gene Usage in the NOD Mouse and Its Nondiabetic Sister Strains.

Author(s):  
Yukio KOIDE ◽  
Takato O. YOSHIDA
1995 ◽  
Vol 48 (1) ◽  
pp. M46-M50 ◽  
Author(s):  
P J Tighe ◽  
J V Forrester ◽  
J Liversidge ◽  
H F Sewell

2002 ◽  
Vol 119 (2) ◽  
pp. 377-383 ◽  
Author(s):  
Achim K. Moesta ◽  
Animesh A. Sinha ◽  
Mong-Shang Lin ◽  
Luis A. Diaz

1998 ◽  
Vol 85 (1) ◽  
pp. 22-32 ◽  
Author(s):  
Bruno Gran ◽  
Donella Gestri ◽  
Alessandra Sottini ◽  
Eugenia Quiròs Roldàn ◽  
Alessandra Bettinardi ◽  
...  

Blood ◽  
1989 ◽  
Vol 74 (7) ◽  
pp. 2508-2518 ◽  
Author(s):  
JP de Villartay ◽  
AB Pullman ◽  
R Andrade ◽  
E Tschachler ◽  
O Colamenici ◽  
...  

Abstract We analyzed the gene rearrangements associated with the newly described delta T-cell receptor (TCR) gene from a series of 19 consecutive precursor T-cell (lymphoblastic) neoplasms that represent discrete stages surrounding the TCR gene rearrangement process. Significantly, the delta TCR gene showed rearrangement in most (13 of 19) of these T cells, and in addition it was rearranged in two cells displaying no rearrangement for any other TCR gene. Our survey showed three types of delta gene rearrangements associated with cell-surface TCR expression that presumably represent usage of three V delta genes. This analysis demonstrates (1) a major subclass of human precursor T-cell neoplasms belonging to the gamma/delta T-cell receptor-rearranging subtype; (2) a narrow repertoire of human V delta gene usage; and (3) the utility of delta gene rearrangements as a diagnostic clonal marker in precursor T lymphoblastic neoplasms.


1998 ◽  
Vol 5 (6) ◽  
pp. 428-434
Author(s):  
Horng-yunn Dou ◽  
Jaw-Ching Wu ◽  
Wei-li Peng ◽  
Chungming Chang ◽  
Wei-Kuang Chi ◽  
...  

1994 ◽  
Vol 180 (3) ◽  
pp. 1171-1176 ◽  
Author(s):  
P Dellabona ◽  
E Padovan ◽  
G Casorati ◽  
M Brockhaus ◽  
A Lanzavecchia

The T cell receptor (TCR)-alpha/beta CD4-8- (double negative, DN) T cell subset is characterized by an oligoclonal repertoire and a restricted V gene usage. By immunizing mice with a DN T cell clone we generated two monoclonal antibodies (mAbs) against V alpha 24 and V beta 11, which have been reported to be preferentially expressed in DN T cells. Using these antibodies, we could investigate the expression and pairing of these V alpha and V beta gene products among different T cell subsets. V alpha 24 is rarely expressed among CD4+ and especially CD8+ T cells. In these cases it is rearranged to different J alpha segments, carries N nucleotides, and pairs with different V beta. Remarkably, V alpha 24 is frequently expressed among DN T cells and is always present as an invariant rearrangement with J alpha Q, without N region diversity. This invariant V alpha 24 chain is always paired to V beta 11. This unique V alpha 24-J alpha Q/V beta 11 TCR was found in expanded DN clones from all the individuals tested. These findings suggest that the frequent occurrence of cells carrying this invariant TCR is due to peripheral expansion of rare clones after recognition of a nonpolymorphic ligand.


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