79 related articles for article (PubMed ID: 8099015)
1. Antigen processing and presentation of human rhinovirus to CD4 T cells is facilitated by binding to cellular receptors for virus.
Hastings GZ; Francis MJ; Rowlands DJ; Chain BM
Eur J Immunol; 1993 Jun; 23(6):1340-5. PubMed ID: 8099015
[TBL] [Abstract][Full Text] [Related]
2. Epitope analysis of the T cell response to a complex antigen: proliferative responses to human rhinovirus capsids.
Hastings GZ; Francis MJ; Rowlands DJ; Chain BM
Eur J Immunol; 1993 Sep; 23(9):2300-5. PubMed ID: 7690329
[TBL] [Abstract][Full Text] [Related]
3. Virus-induced eosinophil mediator release requires antigen-presenting and CD4+ T cells.
Davoine F; Cao M; Wu Y; Ajamian F; Ilarraza R; Kokaji AI; Moqbel R; Adamko DJ
J Allergy Clin Immunol; 2008 Jul; 122(1):69-77, 77.e1-2. PubMed ID: 18472150
[TBL] [Abstract][Full Text] [Related]
4. Binding of human rhinovirus and T cells to intercellular adhesion molecule-1 on human fibroblasts. Discordance between effects of IL-1 and IFN-gamma.
Piela-Smith TH; Aneiro L; Korn JH
J Immunol; 1991 Sep; 147(6):1831-6. PubMed ID: 1679837
[TBL] [Abstract][Full Text] [Related]
5. Human anti-idiotypic T lymphocyte clones are activated by autologous anti-rabies virus antibodies presented in association with HLA-DQ molecules.
UytdeHaag F; Claassen I; Bunschoten H; Loggen H; Ottenhoff T; Teeuwsen V; Osterhaus A
J Mol Cell Immunol; 1987; 3(3):145-55. PubMed ID: 2908179
[TBL] [Abstract][Full Text] [Related]
6. Proliferative responses of T cells primed against human rhinovirus to other rhinovirus serotypes.
Hastings GZ; Rowlands DJ; Francis MJ
J Gen Virol; 1991 Dec; 72 ( Pt 12)():2947-52. PubMed ID: 1722503
[TBL] [Abstract][Full Text] [Related]
7. Dendritic type, accessory cells within the mammalian thymic microenvironment. Antigen presentation in the dendritic neuro-endocrine-immune cellular network.
Bodey B; Bodey B; Kaiser HE
In Vivo; 1997; 11(4):351-70. PubMed ID: 9292303
[TBL] [Abstract][Full Text] [Related]
8. Concerted antigen presentation by dendritic cells and B cells is necessary for optimal CD4 T-cell immunity in vivo.
Kleindienst P; Brocker T
Immunology; 2005 Aug; 115(4):556-64. PubMed ID: 16011524
[TBL] [Abstract][Full Text] [Related]
9. Mechanism of enhanced antigen presentation by B cells activated with anti-mu plus interferon-gamma: role of B7-2 in the activation of naive and memory CD4+ T cells.
Morokata T; Kato T; Igarashi O; Nariuchi H
Eur J Immunol; 1995 Jul; 25(7):1992-8. PubMed ID: 7542599
[TBL] [Abstract][Full Text] [Related]
10. Production of minor lymphocyte stimulatory-1a antigen from activated CD4+ or CD8+ T cells.
Arase-Fukushi N; Arase H; Ogasawara K; Good RA; Onoé K
J Immunol; 1993 Nov; 151(9):4445-54. PubMed ID: 8104995
[TBL] [Abstract][Full Text] [Related]
11. Isolated receptor binding domains of HTLV-1 and HTLV-2 envelopes bind Glut-1 on activated CD4+ and CD8+ T cells.
Kinet S; Swainson L; Lavanya M; Mongellaz C; Montel-Hagen A; Craveiro M; Manel N; Battini JL; Sitbon M; Taylor N
Retrovirology; 2007 May; 4():31. PubMed ID: 17504522
[TBL] [Abstract][Full Text] [Related]
12. Antigen presentation by B lymphocytes to CD4+ T lymphocytes in vivo: importance for B lymphocyte and T lymphocyte activation.
Finkelman FD; Lees A; Morris SC
Semin Immunol; 1992 Aug; 4(4):247-55. PubMed ID: 1356502
[TBL] [Abstract][Full Text] [Related]
13. Binding of radiation leukemia viruses to a thymic lymphoma involves some class I molecules on the T cell as well as the T cell receptor complex.
O'Neill HC
J Mol Cell Immunol; 1989; 4(4):213-23. PubMed ID: 2558669
[TBL] [Abstract][Full Text] [Related]
14. An evolutionary conserved mechanism of T cell activation by microbial toxins. Evidence for different affinities of T cell receptor-toxin interaction.
Fleischer B; Gerardy-Schahn R; Metzroth B; Carrel S; Gerlach D; Köhler W
J Immunol; 1991 Jan; 146(1):11-7. PubMed ID: 1670601
[TBL] [Abstract][Full Text] [Related]
15. Exogenous and endogenous antigens are differentially presented by mast cells to CD4+ T lymphocytes.
Frandji P; Tkaczyk C; Oskeritzian C; David B; Desaymard C; Mécheri S
Eur J Immunol; 1996 Oct; 26(10):2517-28. PubMed ID: 8898968
[TBL] [Abstract][Full Text] [Related]
16. Eosinophils bind rhinovirus and activate virus-specific T cells.
Handzel ZT; Busse WW; Sedgwick JB; Vrtis R; Lee WM; Kelly EA; Gern JE
J Immunol; 1998 Feb; 160(3):1279-84. PubMed ID: 9570544
[TBL] [Abstract][Full Text] [Related]
17. Antigen targeting to antigen-presenting cells enhances presentation to class II-restricted T lymphocytes.
Scardino A; Paroli M; De Petrillo G; Michel ML; Barnaba V
Immunology; 1994 Jan; 81(1):167-70. PubMed ID: 7907575
[TBL] [Abstract][Full Text] [Related]
18. Dendritic cells purified from myeloma are primed with tumor-specific antigen (idiotype) and activate CD4+ T cells.
Dembic Z; Schenck K; Bogen B
Proc Natl Acad Sci U S A; 2000 Mar; 97(6):2697-702. PubMed ID: 10706628
[TBL] [Abstract][Full Text] [Related]
19. Cultured human Langerhans' cells are superior to fresh cells at presenting native HIV-1 protein antigens to specific CD4+ T-cell lines.
Girolomoni G; Valle MT; Zacchi V; Costa MG; Giannetti A; Manca F
Immunology; 1996 Feb; 87(2):310-6. PubMed ID: 8698396
[TBL] [Abstract][Full Text] [Related]
20. IL-4 synthesis by in vivo primed keyhole limpet hemocyanin-specific CD4+ T cells. I. Influence of antigen concentration and antigen-presenting cell type.
DeKruyff RH; Fang Y; Umetsu DT
J Immunol; 1992 Dec; 149(11):3468-76. PubMed ID: 1358971
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]