We observed enhanced
tumor rejection in DGKζ - deficient mice and DKO mice relative to WT or Cbl - b — deficient mice.
The decreased tumor size and enhanced
tumor rejection in DGKζ - deficient mice indirectly suggests that enhanced Erk signaling may be superior to enhanced NF - κΒ activation in facilitating T cell activity against tumor, especially because DKO mice did not exhibit improved tumor control relative to DGKζ − / − mice.
This did induce an immune response but only led to
tumor rejection in one - quarter of the animals.»
Not exact matches
Key studies
in mice showed that NF - κB can mediate immune
rejection of
tumors.
The
rejection of the
tumor then worked
in 80 percent of the test animals.
Ectopic expression of retinoic acid early inducible - 1 gene (RAE - 1) permits natural killer cell - mediated
rejection of a MHC class I - bearing
tumor in vivo.
Lyt phenotype of T cells
in lymphoid tissues and blocking of
tumor rejection.
The symposium features presentations by Philippa Marrack and John Kappler talking on the T cell repertoire; William Paul on interleukin 4 as a prototypic immunoregulatory cytokine; Timothy Springer on lymphocyte trafficking; Pamela Bjorkman on structural studies of MHC and MHC - related proteins, and Jack Strominger on peptide presentation by class I and II MHC proteins; Thierry Boon on genes coding for
tumor rejection antigens, including the first
tumor antigen, MAGE - 1; and Philip Greenberg on the modification of T cells for adoptive therapy by retroviral - mediated gene insertion Since then, the symposia series has attracted leading immunologists
in the cancer vaccine and antibody fields, providing them with a comprehensive view of the promises and challenges
in the development of cancer immunotherapies.
Onizuka S, Tawara I, Shimizu J, Sakaguchi S, Fujita T, Nakayama E.
Tumor rejection by
in vivo administration of anti-CD25 (interleukin - 2 receptor alpha) monoclonal antibody.
In their study, DN T cells displayed allospecific cytotoxicity in vitro and mediated tumor allograft rejection in viv
In their study, DN T cells displayed allospecific cytotoxicity
in vitro and mediated tumor allograft rejection in viv
in vitro and mediated
tumor allograft
rejection in viv
in vivo.
James P. Allison and Matthew Krummel demonstrate that a monoclonal antibody directed against the CTLA - 4 molecule
in a mouse model of melanoma could result
in the
rejection of
tumors and that this
rejection also resulted
in immunity to a second exposure to
tumor cells.
Thus,
in a single experiment, the authors demonstrated that (1) CD4 + and CD8 + T - cells were the mediators of immune system
rejection of transplanted
tumor cells, and (2) d42m1 escape
tumors develop from T - cell - dependent selection favoring cells without the spectrin - B2 antigen.
IDO1 has been implicated
in immune modulation through its ability to limit T cell function and engage mechanisms of immune tolerance, and as such preventing
tumor rejection.
Moreover, knock
in animal models for syngeneic studies and allowing us to isolate transgenic armed effector cells are developed
in order to show proof of concept for the diverse applicability of our modular targeting systems including for
tumor diseases, autoimmune diseases, GvHD, transplantation /
rejection as well as viral infections.
This single - celled algae also increases the activity of Natural Killer (NK) cells, a type of white blood cell that plays a major role
in host
rejection of
tumors.