scholarly journals Identification of type-specific linear epitopes in the glycoproteins gp46 and gp21 of human T-cell leukemia viruses type I and type II using synthetic peptides.

1991 ◽  
Vol 88 (13) ◽  
pp. 5754-5758 ◽  
Author(s):  
P. Horal ◽  
W. W. Hall ◽  
B. Svennerholm ◽  
J. Lycke ◽  
S. Jeansson ◽  
...  
Blood ◽  
1987 ◽  
Vol 70 (2) ◽  
pp. 432-436 ◽  
Author(s):  
M Aboud ◽  
DW Golde ◽  
N Bersch ◽  
JD Rosenblatt ◽  
IS Chen

Abstract We report here the development of a rapid and quantitative method for measuring in vitro T cell transformation by human T cell leukemia viruses type I (HTLV-I) and type II (HTLV-II). This method is based on our finding that cocultivation of lethally irradiated HTLV-producing cells with peripheral blood lymphocytes (PBLs) preactivated for 24 hours with phytohemagglutinin and interleukin-2 (IL-2) induces colony formation in methylcellulose-containing medium. Colonies of about 200 cells can be clearly distinguished from background aggregates within four to six days after cocultivation. These colonies gradually increase in size and reach 300 to 1,000 cells within 14 days after cocultivation. Cells of these colonies were infected, as evidenced by expression of viral p19 antigen and the presence of HTLV proviral sequences. These cells proved to be transformed in terms of IL-2- independent continuous growth in liquid medium. Colony formation was found to depend in a linear fashion upon the percentage of the infected cells present in the irradiated cell population and is sufficiently sensitive to detect as few as 1% of virus-producing cells.


Blood ◽  
1987 ◽  
Vol 70 (2) ◽  
pp. 432-436
Author(s):  
M Aboud ◽  
DW Golde ◽  
N Bersch ◽  
JD Rosenblatt ◽  
IS Chen

We report here the development of a rapid and quantitative method for measuring in vitro T cell transformation by human T cell leukemia viruses type I (HTLV-I) and type II (HTLV-II). This method is based on our finding that cocultivation of lethally irradiated HTLV-producing cells with peripheral blood lymphocytes (PBLs) preactivated for 24 hours with phytohemagglutinin and interleukin-2 (IL-2) induces colony formation in methylcellulose-containing medium. Colonies of about 200 cells can be clearly distinguished from background aggregates within four to six days after cocultivation. These colonies gradually increase in size and reach 300 to 1,000 cells within 14 days after cocultivation. Cells of these colonies were infected, as evidenced by expression of viral p19 antigen and the presence of HTLV proviral sequences. These cells proved to be transformed in terms of IL-2- independent continuous growth in liquid medium. Colony formation was found to depend in a linear fashion upon the percentage of the infected cells present in the irradiated cell population and is sufficiently sensitive to detect as few as 1% of virus-producing cells.


1999 ◽  
Vol 8 (1) ◽  
pp. 45-50 ◽  
Author(s):  
Siham Al-Mufti ◽  
Alexander Voevodin ◽  
Sabeeha Ahmed ◽  
Samia Al Hamdan ◽  
Abdul Azis Al-Basheer

Blood ◽  
1985 ◽  
Vol 66 (6) ◽  
pp. 1336-1342 ◽  
Author(s):  
TL Chorba ◽  
R Brynes ◽  
VS Kalyanaraman ◽  
M Telfer ◽  
R Ramsey ◽  
...  

Abstract Human T cell leukemia virus type II (HTLV-II) has been isolated from a patient (Mo) with features of leukemic reticuloendotheliosis (LRE) and from a patient with acquired immunodeficiency syndrome (AIDS). We have obtained another isolate of HTLV-II from a patient (CM) with severe hemophilia A, pancytopenia, and a 14-year history of staphylococcal and candidal infections but no evidence of T cell leukemia/lymphoma, AIDS, or LRE. Fresh mononuclear cells and cultured lymphocytes from CM express retroviral antigens indistinguishable by molecular criteria from HTLV-IIMo. Leukocyte cultures from CM yield hyperdiploid (48,XY, +2, +19) continuous lymphoid lines; human fetal cord blood lymphocytes (CBL) are transformed by cocultivation with these CM cell cultures but retain normal cytogenetic constitution. Electron microscopic examination of the CM cultures and transformed CBL reveals budding of extracellular viral particles, intracellular tubuloreticular structures, and viral particles contained within intracellular vesicles. CM cell cultures and the transformed CBL do not require exogenous interleukin 2, have T cell cytochemical features and mature T helper phenotypes, and exhibit minimal T helper and profound T suppressor activity on pokeweed mitogen-stimulated differentiation of normal B cells. These characteristics, which are similar to those observed with the first HTLV-II isolate, may represent properties of all HTLV-II-infected T cells.


Virology ◽  
1984 ◽  
Vol 139 (2) ◽  
pp. 340-345 ◽  
Author(s):  
S.F. Josephs ◽  
F. Wong-Staal ◽  
V. Manzari ◽  
R.C. Gallo ◽  
J.G. Sodroski ◽  
...  

2006 ◽  
Vol 8 (3) ◽  
pp. 169-176 ◽  
Author(s):  
Abraham M. Y. Nomura ◽  
Eugene T. Yanagihara ◽  
William A. Blattner ◽  
Gloria Y. F. Ho ◽  
Melvin S. Inamasu ◽  
...  

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