Amplification of a gene coding for human T-cell differentiation antigen

Nature ◽  
1983 ◽  
Vol 306 (5941) ◽  
pp. 385-387 ◽  
Author(s):  
Paula Kavathas ◽  
Leonard A. Herzenberg
1991 ◽  
Vol 33 (5-6) ◽  
pp. 352-360 ◽  
Author(s):  
Kazuhiro Yoshikawa ◽  
Masao Seto ◽  
Ryuzo Ueda ◽  
Yuichi Obata ◽  
Kunihiro Notake ◽  
...  

1985 ◽  
Vol 11 (3) ◽  
pp. 217-222 ◽  
Author(s):  
Ikuya Tsuge ◽  
Kazuhiko R. Utsumi ◽  
Ryuzo Ueda ◽  
Shigeru Takamoto ◽  
Toshitada Takahashi

1985 ◽  
Vol 161 (2) ◽  
pp. 429-434 ◽  
Author(s):  
V P Sukhatme ◽  
A C Vollmer ◽  
J Erikson ◽  
M Isobe ◽  
C Croce ◽  
...  

We have mapped the gene encoding the T cell differentiation antigen Leu-2/T8 to human chromosome 2 by hybridization of a Leu-2/T8 complementary DNA clone to DNA from a panel of mouse-human cell hybrids. In situ hybridization further localizes the gene to the 2p1 region in close proximity to the Ig kappa light chain gene. The Leu-2/T8 gene translocates with C kappa to chromosome 8 in a Burkitt lymphoma line carrying a t(2;8) translocation. These data support the hypothesis that Leu-2/T8 is the human homologue of the mouse Lyt-2,3 antigen.


1980 ◽  
Vol 11-11 (1) ◽  
pp. 429-439 ◽  
Author(s):  
Paul J. Martin ◽  
John A. Hansen ◽  
Robert C. Nowinski ◽  
Melissa A. Brown

1986 ◽  
Vol 14 (19) ◽  
pp. 7817-7817 ◽  
Author(s):  
A.M. Bowcock ◽  
P. Kavathas ◽  
R. F. Margolskee ◽  
L. Herzenberg ◽  
L. L. Cavalli-Sforza

2020 ◽  
Vol 117 (24) ◽  
pp. 13740-13749 ◽  
Author(s):  
Yusuke Higuchi ◽  
Jun-ichirou Yasunaga ◽  
Yu Mitagami ◽  
Hirotake Tsukamoto ◽  
Kazutaka Nakashima ◽  
...  

Human T cell leukemia virus type 1 (HTLV-1) is the etiologic agent of a T cell neoplasm and several inflammatory diseases. A viral gene, HTLV-1 bZIP factor (HBZ), induces pathogenic Foxp3-expressing T cells and triggers systemic inflammation and T cell lymphoma in transgenic mice, indicating its significance in HTLV-1–associated diseases. Here we show that, unexpectedly, a proinflammatory cytokine, IL-6, counteracts HBZ-mediated pathogenesis. Loss of IL-6 accelerates inflammation and lymphomagenesis in HBZ transgenic mice. IL-6 innately inhibits regulatory T cell differentiation, suggesting that IL-6 functions as a suppressor against HBZ-associated complications. HBZ up-regulates expression of the immunosuppressive cytokine IL-10. IL-10 promotes T cell proliferation only in the presence of HBZ. As a mechanism of growth promotion by IL-10, HBZ interacts with STAT1 and STAT3 and modulates the IL-10/JAK/STAT signaling pathway. These findings suggest that HTLV-1 promotes the proliferation of infected T cells by hijacking the machinery of regulatory T cell differentiation. IL-10 induced by HBZ likely suppresses the host immune response and concurrently promotes the proliferation of HTLV-1 infected T cells.


Blood ◽  
1996 ◽  
Vol 88 (3) ◽  
pp. 970-976 ◽  
Author(s):  
RP Hasserjian ◽  
JC Aster ◽  
F Davi ◽  
DS Weinberg ◽  
J Sklar

Abstract The Notch gene family encodes transmembrane proteins that have been implicated in control of diverse cellular differentiation events in the fly, frog, and mouse. Mammalian Notch1 is expressed at high levels in thymus and is mutated in a subset of human T-cell acute lymphoblastic neoplasms, suggesting a role in T-cell differentiation. To investigate the patterns of expression of NOTCH1 protein in thymocytes of the developing and mature thymus, antibodies raised against NOTCH1 were used to perform immunohistochemical and flow cytometric analyses. Strong staining for NOTCH1 within the fetal murine thymus was observed as early as 13.5 days postcoitum. By 17.5 days postcoitum, preferential staining of superficial cortical thymocytes was observed, with weak staining of developing medulla. Flow cytometric analysis and immunohistochemical staining of flow-sorted cells confirmed that the highest levels of NOTCH1 expression in adult murine thymus were present in immature cortical thymocytes (CD24high, CD4-CD8-). In contrast, NOTCH1 expression was low or absent in more mature cortical thymocytes (CD24low, CD4+CD8+), whereas intermediate levels of expression were observed in CD4+CD8- and CD4-CD8+ cells. These data indicate a dynamic pattern of NOTCH1 expression during T-cell differentiation and suggest that downregulation of NOTCH1 may be required for maturation of cortical thymocytes.


Author(s):  
Jean Plum ◽  
Magda De Smedt ◽  
Georges Leclercq ◽  
Bart Vandekerckhove ◽  
Tom Taghon

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