185 related articles for article (PubMed ID: 7853474)
1. Host response to Sendai virus in mice lacking class II major histocompatibility complex glycoproteins.
Hou S; Mo XY; Hyland L; Doherty PC
J Virol; 1995 Mar; 69(3):1429-34. PubMed ID: 7853474
[TBL] [Abstract][Full Text] [Related]
2. Delayed clearance of Sendai virus in mice lacking class I MHC-restricted CD8+ T cells.
Hou S; Doherty PC; Zijlstra M; Jaenisch R; Katz JM
J Immunol; 1992 Aug; 149(4):1319-25. PubMed ID: 1354233
[TBL] [Abstract][Full Text] [Related]
3. Clearance of Sendai virus by CD8+ T cells requires direct targeting to virus-infected epithelium.
Hou S; Doherty PC
Eur J Immunol; 1995 Jan; 25(1):111-6. PubMed ID: 7843219
[TBL] [Abstract][Full Text] [Related]
4. A role for CD4+ NK1.1+ T lymphocytes as major histocompatibility complex class II independent helper cells in the generation of CD8+ effector function against intracellular infection.
Denkers EY; Scharton-Kersten T; Barbieri S; Caspar P; Sher A
J Exp Med; 1996 Jul; 184(1):131-9. PubMed ID: 8691126
[TBL] [Abstract][Full Text] [Related]
5. Subverting lymph node trafficking by treatment with the Mel-14 monoclonal antibody to L-selectin does not prevent an effective host response to Sendai virus.
Hou S; Hyland L; Bradley LM; Watson SR; Doherty PC
J Immunol; 1995 Jul; 155(1):252-8. PubMed ID: 7541416
[TBL] [Abstract][Full Text] [Related]
6. Partitioning of responder CD8+ T cells in lymph node and lung of mice with Sendai virus pneumonia by LECAM-1 and CD45RB phenotype.
Hou S; Doherty PC
J Immunol; 1993 Jun; 150(12):5494-500. PubMed ID: 7685796
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Cooperation between cytotoxic and helper T lymphocytes in protection against lethal Sendai virus infection. Protection by T cells is MHC-restricted and MHC-regulated; a model for MHC-disease associations.
Kast WM; Bronkhorst AM; de Waal LP; Melief CJ
J Exp Med; 1986 Sep; 164(3):723-38. PubMed ID: 3018121
[TBL] [Abstract][Full Text] [Related]
9. Virus-specific CD8+ T-cell responses in mice transgenic for a T-cell receptor beta chain selected at random.
Ewing C; Allan W; Daly K; Hou S; Cole GA; Doherty PC; Blackman MA
J Virol; 1994 May; 68(5):3065-70. PubMed ID: 7908699
[TBL] [Abstract][Full Text] [Related]
10. Deficient contact hypersensitivity reaction in CD4-/- mice is because of impaired hapten-specific CD8+ T cell functions.
Saint-Mezard P; Chavagnac C; Vocanson M; Kehren J; Rozières A; Bosset S; Ionescu M; Dubois B; Kaiserlian D; Nicolas JF; Bérard F
J Invest Dermatol; 2005 Mar; 124(3):562-9. PubMed ID: 15737197
[TBL] [Abstract][Full Text] [Related]
11. Cytotoxic T lymphocyte precursor cells specific for the major histocompatibility complex class I-like antigen, Qa-2, require CD4+ T cells to become primed in vivo and to differentiate into effector cells in vitro.
Muraoka S
Eur J Immunol; 1991 Sep; 21(9):2095-103. PubMed ID: 1679712
[TBL] [Abstract][Full Text] [Related]
12. Tumour-specific CTL response requiring interactions of four different cell types and recognition of MHC class I and class II restricted tumour antigens.
Schirrmacher V; Schild HJ; Gückel B; von Hoegen P
Immunol Cell Biol; 1993 Aug; 71 ( Pt 4)():311-26. PubMed ID: 7901150
[TBL] [Abstract][Full Text] [Related]
13. Cooperation between humoral factor(s) and Lyt-2+ T cells in effective clearance of Sendai virus from infected mouse lungs.
Iwai H; Yamamoto S; Otsuka Y; Ueda K
Microbiol Immunol; 1989; 33(11):915-27. PubMed ID: 2574407
[TBL] [Abstract][Full Text] [Related]
14. Modification of the Sendai virus-specific antibody and CD8+ T-cell responses in mice homozygous for disruption of the interleukin-4 gene.
Mo XY; Sangster MY; Tripp RA; Doherty PC
J Virol; 1997 Mar; 71(3):2518-21. PubMed ID: 9032393
[TBL] [Abstract][Full Text] [Related]
15. Recruitment and proliferation of CD8+ T cells in respiratory virus infections.
Tripp RA; Hou S; McMickle A; Houston J; Doherty PC
J Immunol; 1995 Jun; 154(11):6013-21. PubMed ID: 7751644
[TBL] [Abstract][Full Text] [Related]
16. Divergence between cytotoxic effector function and tumor necrosis factor alpha production for inflammatory CD4+ T cells from mice with Sendai virus pneumonia.
Hou S; Fishman M; Murti KG; Doherty PC
J Virol; 1993 Oct; 67(10):6299-302. PubMed ID: 8396684
[TBL] [Abstract][Full Text] [Related]
17. Mice lacking CD8+ T cells develop greater numbers of IgA-producing cells in response to a respiratory virus infection.
Hyland L; Hou S; Coleclough C; Takimoto T; Doherty PC
Virology; 1994 Oct; 204(1):234-41. PubMed ID: 8091654
[TBL] [Abstract][Full Text] [Related]
18. Thymus dictates major histocompatibility complex (MHC) specificity and immune response gene phenotype of class II MHC-restricted T cells but not of class I MHC-restricted T cells.
Kast WM; de Waal LP; Melief CJ
J Exp Med; 1984 Dec; 160(6):1752-66. PubMed ID: 6096476
[TBL] [Abstract][Full Text] [Related]
19. The natural immune response to inhaled soluble protein antigens involves major histocompatibility complex (MHC) class I-restricted CD8+ T cell-mediated but MHC class II-restricted CD4+ T cell-dependent immune deviation resulting in selective suppression of immunoglobulin E production.
McMenamin C; Holt PG
J Exp Med; 1993 Sep; 178(3):889-99. PubMed ID: 8102390
[TBL] [Abstract][Full Text] [Related]
20. The cytotoxic T-lymphocyte response to Sendai virus is unimpaired in the absence of gamma interferon.
Mo XY; Tripp RA; Sangster MY; Doherty PC
J Virol; 1997 Mar; 71(3):1906-10. PubMed ID: 9032321
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
