Identification, isolation, and characterization of a human T cell population by a monoclonal antibody

1979 ◽  
Vol 3 (3) ◽  
pp. 141-146 ◽  
Author(s):  
Richard A. Goldsby ◽  
Barbara A. Osborne ◽  
Edgar G. Engleman
1980 ◽  
pp. 121-135 ◽  
Author(s):  
Richard A. Goldsby ◽  
Barbara A. Osborne ◽  
Edgar G. Engleman

1979 ◽  
Vol 150 (6) ◽  
pp. 1472-1482 ◽  
Author(s):  
E L Reinherz ◽  
P C Kung ◽  
J M Pesando ◽  
J Ritz ◽  
G Goldstein ◽  
...  

The nature of Ia antigens which appear on human T cells after activation and the stimuli required for their expression was examined utilizing a monoclonal antibody reactive with the Ia antigen framework. T cells were purified using monoclonal antibodies directed either at the entire T-cell population (OKT3) or the T-cell inducer subset (OKT4). By indirect immunofluorescence, it was shown that the human T-cell population contains no detectable Ia+ cells in the resting state. In contrast, in excess of 60% of the T-cell population expresses Ia antigen after alloactivation in the mixed lymphocyte culture. Moreover, these Ia antigens are expressed within both the OKT4+ and OKT4- subsets. Similarly, phytohemagglutinin and concanavalin A induced approximately 20% of peripheral T cells to express Ia antigen and the expression of these antigens is not restricted to either OKT4 subset. In contrast, only the inducer T-cell population which proliferates maximally to soluble antigen expresses Ia antigens after activation by tetanus toxoid. Thus, the expression of human Ia antigens on unique T-cell subsets depends upon the activation stimuli utilized and ability of the individual subset to respond to a given stimulus. Additional studies indicated that Ia antigens appear on previously Ia- T cells after activation and do not result from clonal expansion of a small subset of Ia+ T cells.


Blood ◽  
1997 ◽  
Vol 89 (12) ◽  
pp. 4521-4530 ◽  
Author(s):  
Hervé Groux ◽  
Françoise Cottrez ◽  
Claire Montpellier ◽  
Brigitte Quatannens ◽  
Jean Coll ◽  
...  

Abstract Epstein-Barr virus (EBV) is a human lymphotropic virus whose main targets have traditionally been described as B lymphocytes and epithelial cells. Here we report the isolation and characterization of largely monoclonal transformed human T-cell lines infected by EBV. The transformed T cells expressed CD2, CD3, and either CD4 or CD8 surface molecules and more generally displayed the phenotype of naive T cells with a complete and clonal rearrangement of the T-cell receptor. None of the cell lines expressed B cells, natural killer, or myeloid antigens or had immunoglobulins genes rearrangement. They grew in the absence of growth factor; however, they all secreted interleukin-2 after mitogenic activation. Polymerase chain reaction (PCR) analysis showed the presence of EBV DNA in all these cell lines. Moreover, Southern blot analysis of one of these cell lines shows the presence of circular episomic EBV DNA, and by Northern blot or reverse transcriptase-PCR analysis, only the expression of Epstein-Barr nuclear antigen-1 (EBNA-1) and latent membrane protein-1 (LMP-1) genes was detected. Finally, the complete transformed phenotype of this T-cell line was shown by its injection into nude or recombination activating gene 2 (RAG2)-deficient mice that led to the formation of solid tumors.


1985 ◽  
Vol 4 (6) ◽  
pp. 1455-1460 ◽  
Author(s):  
V.S. Kalyanaraman ◽  
R. Narayanan ◽  
P. Feorino ◽  
R.B. Ramsey ◽  
E.L. Palmer ◽  
...  

Nature ◽  
1982 ◽  
Vol 300 (5889) ◽  
pp. 267-269 ◽  
Author(s):  
Warren J. Leonard ◽  
Joel M. Depper ◽  
Takashi Uchiyama ◽  
Kendall A. Smith ◽  
Thomas A. Waldmann ◽  
...  

1985 ◽  
Vol 98 (1) ◽  
pp. 209-217 ◽  
Author(s):  
Osamu URAYAMA ◽  
Hideaki NAGAMUNE ◽  
Makoto NAKAO ◽  
Yukichi HARA ◽  
Hiroyuki SUGIYAMA ◽  
...  

1991 ◽  
Vol 174 (4) ◽  
pp. 891-900 ◽  
Author(s):  
S M Friedman ◽  
M K Crow ◽  
J R Tumang ◽  
M Tumang ◽  
Y Q Xu ◽  
...  

While all known microbial superantigens are mitogenic for human peripheral blood lymphocytes (PBL), the functional response induced by Mycoplasma arthritidis-derived superantigen (MAM) is unique in that MAM stimulation of PBL consistently results in T cell-dependent B cell activation characterized by polyclonal IgM and IgG production. These immunostimulatory effects of MAM on the humoral arm of the human immune system warranted a more precise characterization of MAM-reactive human T cells. Using an uncloned MAM reactive human T cell line as immunogen, we have generated a monoclonal antibody (mAb) (termed C1) specific for the T cell receptor V beta gene expressed by the major fraction of MAM-reactive human T cells, V beta 17. In addition, a V beta 17- MAM-reactive T cell population exists, assessed by MAM, induced T cell proliferation and cytotoxic T cell activity. mAb C1 will be useful in characterizing the functional properties of V beta 17+ T cells and their potential role in autoimmune disease.


2006 ◽  
Vol 22 (10) ◽  
pp. 953-959 ◽  
Author(s):  
Simone Kashima ◽  
Luiz Carlos Alcantara ◽  
Osvaldo Massaiti Takayanagui ◽  
Marco Aurelio Valtas Cunha ◽  
Bernardo Galvão Castro ◽  
...  

1989 ◽  
Vol 30 (3) ◽  
pp. 162-168 ◽  
Author(s):  
Maria Lipoldova ◽  
Arthur W. Boylston ◽  
Hans Yssel ◽  
Michael J. Owen

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