165 related articles for article (PubMed ID: 8097227)
21. Splenic NK1.1-negative, TCR alpha beta intermediate CD4+ T cells exist in naive NK1.1 allelic positive and negative mice, with the capacity to rapidly secrete large amounts of IL-4 and IFN-gamma upon primary TCR stimulation.
Moodycliffe AM; Maiti S; Ullrich SE
J Immunol; 1999 May; 162(9):5156-63. PubMed ID: 10227987
[TBL] [Abstract][Full Text] [Related]
22. Administration of recombinant human IL-1 by Staphylococcus enterotoxin B prevents tolerance induction in vivo.
Nakata Y; Matsuda K; Uzawa A; Nomura M; Akashi M; Suzuki G
J Immunol; 1995 Nov; 155(9):4231-5. PubMed ID: 7594579
[TBL] [Abstract][Full Text] [Related]
23. Origin, differentiation, and repertoire selection of CD3+CD4-CD8- thymocytes bearing either alpha beta or gamma delta T cell receptors.
Suda T; Zlotnik A
J Immunol; 1993 Jan; 150(2):447-55. PubMed ID: 8419477
[TBL] [Abstract][Full Text] [Related]
24. The CD8 T cell response to staphylococcal enterotoxins.
Herrmann T; MacDonald HR
Semin Immunol; 1993 Feb; 5(1):33-9. PubMed ID: 8467093
[TBL] [Abstract][Full Text] [Related]
25. Nonantigen specific CD8+ T suppressor lymphocytes originate from CD8+CD28- T cells and inhibit both T-cell proliferation and CTL function.
Filaci G; Fravega M; Negrini S; Procopio F; Fenoglio D; Rizzi M; Brenci S; Contini P; Olive D; Ghio M; Setti M; Accolla RS; Puppo F; Indiveri F
Hum Immunol; 2004 Feb; 65(2):142-56. PubMed ID: 14969769
[TBL] [Abstract][Full Text] [Related]
26. The viral superantigen Mls-1a induces interferon-gamma secretion by specifically primed CD8+ cells but fails to trigger cytotoxicity.
Herrmann T; Waanders GA; Chvatchko Y; MacDonald HR
Eur J Immunol; 1992 Nov; 22(11):2789-93. PubMed ID: 1330577
[TBL] [Abstract][Full Text] [Related]
27. Functional similarity and differences between selection-independent CD4-CD8- alphabeta T cells and positively selected CD8 T cells expressing the same TCR and the induction of anergy in CD4-CD8- alphabeta T cells in antigen-expressing mice.
Caveno J; Zhang Y; Motyka B; Teh SJ; Teh HS
J Immunol; 1999 Aug; 163(3):1222-9. PubMed ID: 10415017
[TBL] [Abstract][Full Text] [Related]
28. The capacity of the natural ligands for CD28 to drive IL-4 expression in naïve and antigen-primed CD4+ and CD8+ T cells.
Bian Y; Hiraoka S; Tomura M; Zhou XY; Yashiro-Ohtani Y; Mori Y; Shimizu J; Ono S; Dunussi-Joannopoulos K; Wolf S; Fujiwara H
Int Immunol; 2005 Jan; 17(1):73-83. PubMed ID: 15569772
[TBL] [Abstract][Full Text] [Related]
29. Requirement for CD4+ T cells in V beta 4+CD8+ T cell activation associated with latent murine gammaherpesvirus infection.
Flaño E; Woodland DL; Blackman MA
J Immunol; 1999 Sep; 163(6):3403-8. PubMed ID: 10477611
[TBL] [Abstract][Full Text] [Related]
30. Establishment of T-cell lines from infiltrated NOD islets by stimulation of specific T-cell receptor V beta segments.
Maugendre D; Legrand B; Olivi M; Bedossa P; Bach JF; Carnaud C
J Autoimmun; 1993 Aug; 6(4):423-36. PubMed ID: 8105789
[TBL] [Abstract][Full Text] [Related]
31. Manipulation of the superantigen-induced lymphokine response. Selective induction of interleukin-10 or interferon-gamma synthesis in small resting CD4+ T cells.
Cardell S; Höidén I; Möller G
Eur J Immunol; 1993 Feb; 23(2):523-9. PubMed ID: 7679648
[TBL] [Abstract][Full Text] [Related]
32. Differential activation of CD8+ T cells by transforming growth factor-beta 1.
Lee HM; Rich S
J Immunol; 1993 Jul; 151(2):668-77. PubMed ID: 8335902
[TBL] [Abstract][Full Text] [Related]
33. Two separate mechanisms of T cell clonal anergy to Mls-1.
Yui K; Ishida Y; Katsumata M; Komori S; Chused TM; Abe R
J Immunol; 1993 Dec; 151(11):6062-75. PubMed ID: 8245451
[TBL] [Abstract][Full Text] [Related]
34. Class I- and class II-reactive TCRs coexpressed on CD4+ T cells both trigger CD4/CD8-shared and CD4-unique functions.
Asnagli H; Schmitt-Verhulst AM; Guimezanes A
J Immunol; 1997 May; 158(10):4533-42. PubMed ID: 9144464
[TBL] [Abstract][Full Text] [Related]
35. Comprehensive phenotypic analysis of the gut intra-epithelial lymphocyte compartment: perturbations induced by acute reovirus 1/L infection of the gastrointestinal tract.
Bharhani MS; Grewal JS; Peppler R; Enockson C; London L; London SD
Int Immunol; 2007 Apr; 19(4):567-79. PubMed ID: 17369189
[TBL] [Abstract][Full Text] [Related]
36. The immunologic function of 1B2+ double negative (CD4-CD8-) T cells in the 2C transgenic mouse.
Margenthaler JA; Flye MW
J Surg Res; 2005 Jun; 126(2):160-6. PubMed ID: 15919414
[TBL] [Abstract][Full Text] [Related]
37. Development of CD8+ effector T cells is differentially regulated by IL-18 and IL-12.
Okamoto I; Kohno K; Tanimoto T; Ikegami H; Kurimoto M
J Immunol; 1999 Mar; 162(6):3202-11. PubMed ID: 10092771
[TBL] [Abstract][Full Text] [Related]
38. IL-12 induces the production of IFN-gamma by neonatal human CD4 T cells.
Wu CY; Demeure C; Kiniwa M; Gately M; Delespesse G
J Immunol; 1993 Aug; 151(4):1938-49. PubMed ID: 8102154
[TBL] [Abstract][Full Text] [Related]
39. Differential effects of IL-12 receptor blockade with IL-12 p40 homodimer on the induction of CD4+ and CD8+ IFN-gamma-producing cells.
Piccotti JR; Chan SY; Li K; Eichwald EJ; Bishop DK
J Immunol; 1997 Jan; 158(2):643-8. PubMed ID: 8992979
[TBL] [Abstract][Full Text] [Related]
40. Immunoregulatory role of IL-10 during superantigen-induced hyporesponsiveness in vivo.
Sundstedt A; Höiden I; Rosendahl A; Kalland T; van Rooijen N; Dohlsten M
J Immunol; 1997 Jan; 158(1):180-6. PubMed ID: 8977189
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
