Zobrazeno 1 - 10
of 56
pro vyhledávání: '"V. K. Kuchroo"'
Autor:
N. Jacquelot, M. P. Roberti, D. P. Enot, S. Rusakiewicz, N. Ternès, S. Jegou, D. M. Woods, A. L. Sodré, M. Hansen, Y. Meirow, M. Sade-Feldman, A. Burra, S. S. Kwek, C. Flament, M. Messaoudene, C. P. M. Duong, L. Chen, B. S. Kwon, A. C. Anderson, V. K. Kuchroo, B. Weide, F. Aubin, C. Borg, S. Dalle, O. Beatrix, M. Ayyoub, B. Balme, G. Tomasic, A. M. Di Giacomo, M. Maio, D. Schadendorf, I. Melero, B. Dréno, A. Khammari, R. Dummer, M. Levesque, Y. Koguchi, L. Fong, M. Lotem, M. Baniyash, H. Schmidt, I. M. Svane, G. Kroemer, A. Marabelle, S. Michiels, A. Cavalcanti, M. J. Smyth, J. S. Weber, A. M. Eggermont, L. Zitvogel
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-13 (2017)
The clinical management of metastatic melanoma requires predictors of the response to checkpoint blockade. Here, the authors use immunological assays to identify potential prognostic/predictive biomarkers in circulating blood cells and in tumor-infil
Externí odkaz:
https://doaj.org/article/807762e56e0f4dbf9806c82c666da282
Publikováno v:
The Journal of Immunology. 159:4799-4805
CD80 (B7-1) and CD86 (B7-2) on APC provide a major costimulatory signal through interactions with CD28 on T cells. Absent from resting human T cells, CD86 is up-regulated early upon T cell activation, whereas CD80 expression appears later. Whereas T
Publikováno v:
The Journal of Immunology. 159:3100-3103
Experimental autoimmune encephalomyelitis (EAE) is an organ-specific autoimmune disease inducible in susceptible animals by myelin Ag-specific CD4+ Th1 cells. The mechanisms by which these cells induce inflammation and demyelination in the central ne
Autor:
E A Greenfield, E Howard, T Paradis, K Nguyen, F Benazzo, P McLean, P Höllsberg, G Davis, D A Hafler, A H Sharpe, G J Freeman, V K Kuchroo
Publikováno v:
The Journal of Immunology. 158:2025-2034
The B7 family of costimulatory molecules provides the second signal necessary for activation of T cells. In the absence of the second signal, responding T cells become anergic. Although predominantly expressed on professional APCs, recent evidence sh
Autor:
J A Encinas, M B Lees, R A Sobel, C Symonowicz, J M Greer, C L Shovlin, H L Weiner, C E Seidman, J G Seidman, V K Kuchroo
Publikováno v:
The Journal of Immunology. 157:2186-2192
Experimental autoimmune encephalomyelitis (EAE), a model for human multiple sclerosis, is a T cell-mediated autoimmune disease that can be induced in experimental animals by immunization with myelin Ags. Inbred strains of mice show varying degrees of
Publikováno v:
The Journal of Immunology. 156:371-379
To understand and develop strategies to intervene in autoimmune responses to myelin proteolipid protein (PLP), encephalitogenic epitopes must be identified. To expedite the identification of potentially immunogenic and encephalitogenic epitopes of PL
Autor:
S Markovic-Plese, H Fukaura, J Zhang, A al-Sabbagh, S Southwood, A Sette, V K Kuchroo, D A Hafler
Publikováno v:
The Journal of Immunology. 155:982-992
We investigated the immune response to proteolipid protein (PLP), the most abundant central nervous system myelin protein in humans. A total of 8207 short-term T cell lines were generated from 49 individuals, 39 patients with multiple sclerosis and 1
Publikováno v:
The Journal of Immunology. 154:5030-5038
Conditioned medium from Ag-specific suppressor T cell hybridomas contains soluble factors (TsF) that modulate immune responses in an Ag-specific manner. We previously generated a series of TCR-alpha- and TCR-beta- expression variants from a 4-hydroxy
Autor:
R M O'Hara, M C Byrne, V K Kuchroo, A Nagelin, M J Whitters, S Jayaraman, S L Henderson, M E Dorf, M Collins
Publikováno v:
The Journal of Immunology. 154:2075-2081
Previous studies utilizing NP (4-hydroxy, 3-nitrophenyl acetyl hapten)-specific, T suppressor hybridomas have indicated that expression of TCR-alpha, but not TCR-beta, mRNA is required for expression of Ag-specific suppressor factor bioactivity. Supp
Publikováno v:
The Journal of Immunology. 153:3326-3336
Previously, six T cell clones, which are specific for an encephalitogenic determinant of myelin proteolipid protein (PLP) peptide residues 139 to 151 (HSLGKWLGHPDKF), were derived from SJL mice and shown to use diverse TCR genes. To design TCR antago