Costimulatory signals through interaction of B7.1 and CD28 prevent “veto” death of cytotoxic T cells during tumor target cell lysis

1997 ◽  
Vol 33 ◽  
pp. S34
Author(s):  
P.T. Daniel ◽  
A. Kroidl ◽  
R. Bargou ◽  
S. Cayeux ◽  
T. Blankenstein ◽  
...  
1984 ◽  
Vol 2 (2) ◽  
pp. 89-94
Author(s):  
R. C. Friedberg ◽  
L. Bitensky ◽  
J. Chayen ◽  
I. H. Muir ◽  
B. A. Askonas ◽  
...  

2002 ◽  
Vol 169 (1) ◽  
pp. 145-150 ◽  
Author(s):  
Arno Müllbacher ◽  
Mario Lobigs ◽  
Ron Tha Hla ◽  
Thao Tran ◽  
Thomas Stehle ◽  
...  

1988 ◽  
Vol 532 (1 Cytotoxic T C) ◽  
pp. 303-313 ◽  
Author(s):  
VICTOR H. ENGELHARD ◽  
JAMES R. GNARRA ◽  
JAMES SULLIVAN ◽  
GERALD L. MANDELL ◽  
LLOYD S. GRAY

1976 ◽  
Vol 143 (3) ◽  
pp. 601-614 ◽  
Author(s):  
J W Schrader ◽  
G M Edelman

Cytotoxic T lymphocytes were generated in vitro against H-2 compatible or syngeneic tumor cells. In vitro cytotoxic activity was inhibited by specific anti-H2 sera, suggesting that H-2 antigens are involved in cell lysis. Two observations directly demonstrated the participation of the H-2 antigens on the tumor cells in their lysis by H-2-compatible T cells. First, coating of the H-2 antigens on the target tumor cell reduced the number of cells lysed on subsequent exposure to cytotoxic T cells. Second, when cytotoxic T cells were activated against an H-2 compatible tumor and assayed against an H-2-incompatible tumor, anti-H-2 serum that could bind to the target cell, but not to the cytotoxic lymphocyte, inhibited lysis. H-2 antigens were also shown to be present on the cytotoxic lymphocytes. Specific antisera reacting with these H-2 antigens, but not those of the target cell, failed to inhibit lysis when small numbers of effector cells were assayed against H-2-incompatible target cells or when effector cells of F1-hybrid origin and bearing two H-2 haplotypes were assayed against a tumor cell of one of the parental strains. These findings suggest that it is the H-2 antigens on the tumor cell and not those on the cytotoxic lymphocytes that are important in cell-mediated lysis of H-2-compatible tumor cells.


1977 ◽  
Vol 197 (1129) ◽  
pp. 417-424 ◽  

K cells share certain physical characteristics with T cells. This has made it possible to apply standard cell purification techniques to be used for the enrichment of K cells. This has in turn enabled time lapse studies to be carried out at low cell density. In addition, to the similar physical characteristics, K cells have a structure and movement similar to those of cytotoxic T cells. K cell cytotoxicity does no apparent damage to the K cell and each K cell is able to kill more than one target cell. Analysis of time lapse films of cytotoxicity of mouse P815 mastocytoma cells directly confirms three inferences on the mechanism of target cell death suggested by the kinetic data in the previous paper: contact itself does not appear to damage the target cell; target cell death usually begins within 15 min of K cell contact; cell death is an explosive event with zeiosis ‘boiling' of the cytoplasm. This phenomenon is similar to that observed with T cell cytotoxicity and quite different to changes seen during lysis by antibody and complement. Analysis of films of cytotoxicity of human MRC5 cells which are glass adherent has shown that the K cell is in close apposition to the nucleus within 1 min of the first cytoplasmic changes (shrinkage).


Cell ◽  
2016 ◽  
Vol 165 (1) ◽  
pp. 100-110 ◽  
Author(s):  
Roshni Basu ◽  
Benjamin M. Whitlock ◽  
Julien Husson ◽  
Audrey Le Floc’h ◽  
Weiyang Jin ◽  
...  

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