96 related articles for article (PubMed ID: 8690891)
1. Differential activation of phospholipase C-gamma 1 and mitogen-activated protein kinase in naive and antigen-primed CD4 T cells by the peptide/MHC ligand.
Ericsson PO; Orchansky PL; Carlow DA; Teh HS
J Immunol; 1996 Mar; 156(6):2045-53. PubMed ID: 8690891
[TBL] [Abstract][Full Text] [Related]
2. The minimal number of antigen-major histocompatibility complex class II complexes required for activation of naive and primed T cells.
Kimachi K; Croft M; Grey HM
Eur J Immunol; 1997 Dec; 27(12):3310-7. PubMed ID: 9464819
[TBL] [Abstract][Full Text] [Related]
3. MHC class I signaling in T cells leads to tyrosine kinase activity and PLC-gamma 1 phosphorylation.
Skov S; Odum N; Claesson MH
J Immunol; 1995 Feb; 154(3):1167-76. PubMed ID: 7529791
[TBL] [Abstract][Full Text] [Related]
4. CD8+ memory T cells (CD44high, Ly-6C+) are more sensitive than naive cells to (CD44low, Ly-6C-) to TCR/CD8 signaling in response to antigen.
Curtsinger JM; Lins DC; Mescher MF
J Immunol; 1998 Apr; 160(7):3236-43. PubMed ID: 9531279
[TBL] [Abstract][Full Text] [Related]
5. CD4 ligands inhibit the formation of multifunctional transduction complexes involved in T cell activation.
Jabado N; Pallier A; Le Deist F; Bernard F; Fischer A; Hivroz C
J Immunol; 1997 Jan; 158(1):94-103. PubMed ID: 8977179
[TBL] [Abstract][Full Text] [Related]
6. Primed T cells are more resistant to Fas-mediated activation-induced cell death than naive T cells.
Inaba M; Kurasawa K; Mamura M; Kumano K; Saito Y; Iwamoto I
J Immunol; 1999 Aug; 163(3):1315-20. PubMed ID: 10415029
[TBL] [Abstract][Full Text] [Related]
7. gamma(c) cytokines provide multiple homeostatic signals to naive CD4(+) T cells.
Masse GX; Corcuff E; Decaluwe H; Bommhardt U; Lantz O; Buer J; Di Santo JP
Eur J Immunol; 2007 Sep; 37(9):2606-16. PubMed ID: 17683114
[TBL] [Abstract][Full Text] [Related]
8. Modulation of naive CD4 T cell activation with altered peptide ligands: the nature of the peptide and presentation in the context of costimulation are critical for a sustained response.
Rogers PR; Grey HM; Croft M
J Immunol; 1998 Apr; 160(8):3698-704. PubMed ID: 9558070
[TBL] [Abstract][Full Text] [Related]
9. UVB-irradiated dendritic cells are impaired in their APC function and tolerize primed Th1 cells but not naive CD4+ T cells.
Denfeld RW; Hara H; Tesmann JP; Martin S; Simon JC
J Leukoc Biol; 2001 Apr; 69(4):548-54. PubMed ID: 11310840
[TBL] [Abstract][Full Text] [Related]
10. The dependence for leukocyte function-associated antigen-1/ICAM-1 interactions in T cell activation cannot be overcome by expression of high density TCR ligand.
Abraham C; Griffith J; Miller J
J Immunol; 1999 Apr; 162(8):4399-405. PubMed ID: 10201975
[TBL] [Abstract][Full Text] [Related]
11. Sustained TCR signaling is required for mitogen-activated protein kinase activation and degranulation by cytotoxic T lymphocytes.
Berg NN; Puente LG; Dawicki W; Ostergaard HL
J Immunol; 1998 Sep; 161(6):2919-24. PubMed ID: 9743353
[TBL] [Abstract][Full Text] [Related]
12. Antibody-induced CD3-CD4 coligation inhibits TCR/CD3 activation in the absence of costimulatory signals in normal mouse CD4(+) T lymphocytes.
Portolés P; de Ojeda G; Criado G; Fernández-Centeno E; Rojo JM
Cell Immunol; 1999 Aug; 195(2):96-109. PubMed ID: 10448009
[TBL] [Abstract][Full Text] [Related]
13. The Src-homology domain 2-bearing protein tyrosine phosphatase-1 inhibits antigen receptor-induced apoptosis of activated peripheral T cells.
Zhang J; Somani AK; Watt S; Mills GB; Siminovitch KA
J Immunol; 1999 Jun; 162(11):6359-67. PubMed ID: 10352248
[TBL] [Abstract][Full Text] [Related]
14. A subset of splenic macrophages process and present native antigen to naive antigen-specific CD4+ T-cells from mice transgenic for an alpha beta T-cell receptor.
Askew D; Gatewood J; Olivas E; Havenith K; Walker WS
Cell Immunol; 1995 Nov; 166(1):62-70. PubMed ID: 7585982
[TBL] [Abstract][Full Text] [Related]
15. Intestinal intraepithelial lymphocytes are activated and cytolytic but do not proliferate as well as other T cells in response to mitogenic signals.
Sydora BC; Mixter PF; Holcombe HR; Eghtesady P; Williams K; Amaral MC; Nel A; Kronenberg M
J Immunol; 1993 Mar; 150(6):2179-91. PubMed ID: 8383717
[TBL] [Abstract][Full Text] [Related]
16. Peptides related to the antigenic determinant block T cell recognition of the native protein as processed by antigen-presenting cells.
Lakey EK; Margoliash E; Flouret G; Pierce SK
Eur J Immunol; 1986 Jul; 16(7):721-7. PubMed ID: 2424770
[TBL] [Abstract][Full Text] [Related]
17. The T lymphocyte response to cytochrome c. IV. Distinguishable sites on a peptide antigen which affect antigenic strength and memory.
Hansburg D; Fairwell T; Schwartz RH; Appella E
J Immunol; 1983 Jul; 131(1):319-24. PubMed ID: 6190913
[TBL] [Abstract][Full Text] [Related]
18. Early human T cell activation events with engagement of surface MHC class II.
King RL; Nguyen QV
J Cell Biochem; 1998 Sep; 70(3):346-53. PubMed ID: 9706872
[TBL] [Abstract][Full Text] [Related]
19. Naive versus memory CD4 T cell response to antigen. Memory cells are less dependent on accessory cell costimulation and can respond to many antigen-presenting cell types including resting B cells.
Croft M; Bradley LM; Swain SL
J Immunol; 1994 Mar; 152(6):2675-85. PubMed ID: 7908301
[TBL] [Abstract][Full Text] [Related]
20. Expression of phosphatidylinositol-dependent phospholipase C sensitive Qa-2 antigen is increased on peripheral blood lymphocytes of aging mice.
Armstrong MJ; Warner CM
Growth Dev Aging; 1992; 56(4):225-36. PubMed ID: 1487361
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
