304 related articles for article (PubMed ID: 10201909)
1. Selection of CD8+ T cells with highly focused specificity during viral persistence in the central nervous system.
Marten NW; Stohlman SA; Smith-Begolka W; Miller SD; Dimacali E; Yao Q; Stohl S; Goverman J; Bergmann CC
J Immunol; 1999 Apr; 162(7):3905-14. PubMed ID: 10201909
[TBL] [Abstract][Full Text] [Related]
2. Inverted immunodominance and impaired cytolytic function of CD8+ T cells during viral persistence in the central nervous system.
Bergmann CC; Altman JD; Hinton D; Stohlman SA
J Immunol; 1999 Sep; 163(6):3379-87. PubMed ID: 10477608
[TBL] [Abstract][Full Text] [Related]
3. Selection of CTL escape mutants in mice infected with a neurotropic coronavirus: quantitative estimate of TCR diversity in the infected central nervous system.
Pewe L; Heard SB; Bergmann C; Dailey MO; Perlman S
J Immunol; 1999 Dec; 163(11):6106-13. PubMed ID: 10570300
[TBL] [Abstract][Full Text] [Related]
4. Immune response to the immunodominant epitope of mouse hepatitis virus is polyclonal, but functionally monospecific in C57Bl/6 mice.
Pewe L; Perlman S
Virology; 1999 Mar; 255(1):106-16. PubMed ID: 10049826
[TBL] [Abstract][Full Text] [Related]
5. IFN-gamma is required for viral clearance from central nervous system oligodendroglia.
Parra B; Hinton DR; Marten NW; Bergmann CC; Lin MT; Yang CS; Stohlman SA
J Immunol; 1999 Feb; 162(3):1641-7. PubMed ID: 9973424
[TBL] [Abstract][Full Text] [Related]
6. Variability of persisting MHV RNA sequences constituting immune and replication-relevant domains.
Bergmann C; Dimacali E; Stohl S; Wei W; Lai MM; Tahara S; Marten N
Virology; 1998 May; 244(2):563-72. PubMed ID: 9601524
[TBL] [Abstract][Full Text] [Related]
7. Flow-microfluorometric monitoring of oligoclonal CD8+ T cell responses to an immunodominant Moloney leukemia virus-encoded epitope in vivo.
Brawand P; Biasi G; Horvath C; Cerottini JC; MacDonald HR
J Immunol; 1998 Feb; 160(4):1659-65. PubMed ID: 9469422
[TBL] [Abstract][Full Text] [Related]
8. The art of survival during viral persistence.
Stohlman SA; Ramakrishna C; Tschen SI; Hinton DR; Bergmann CC
J Neurovirol; 2002 Dec; 8 Suppl 2():53-8. PubMed ID: 12491152
[TBL] [Abstract][Full Text] [Related]
9. Theiler's virus infection of genetically susceptible mice induces central nervous system-infiltrating CTLs with no apparent viral or major myelin antigenic specificity.
Lin X; Pease LR; Murray PD; Rodriguez M
J Immunol; 1998 Jun; 160(11):5661-8. PubMed ID: 9605173
[TBL] [Abstract][Full Text] [Related]
10. Predominance of MHC class II-restricted CD4+ cytotoxic T cells against mouse hepatitis virus A59.
Heemskerk MH; Schoemaker HM; Spaan WJ; Boog CJ
Immunology; 1995 Apr; 84(4):521-7. PubMed ID: 7790024
[TBL] [Abstract][Full Text] [Related]
11. Polyclonality and multispecificity of the CTL response to a single viral epitope.
Ishikawa T; Kono D; Chung J; Fowler P; Theofilopoulos A; Kakumu S; Chisari FV
J Immunol; 1998 Dec; 161(11):5842-50. PubMed ID: 9834062
[TBL] [Abstract][Full Text] [Related]
12. CTL effector function within the central nervous system requires CD4+ T cells.
Stohlman SA; Bergmann CC; Lin MT; Cua DJ; Hinton DR
J Immunol; 1998 Mar; 160(6):2896-904. PubMed ID: 9510193
[TBL] [Abstract][Full Text] [Related]
13. Persistence, immune specificity, and functional ability of murine mutant ras epitope-specific CD4(+) and CD8(+) T lymphocytes following in vivo adoptive transfer.
Bristol JA; Schlom J; Abrams SI
Cell Immunol; 1999 May; 194(1):78-89. PubMed ID: 10357883
[TBL] [Abstract][Full Text] [Related]
14. Role of virus-specific CD4+ cytotoxic T cells in recovery from mouse hepatitis virus infection.
Wijburg OL; Heemskerk MH; Sanders A; Boog CJ; Van Rooijen N
Immunology; 1996 Jan; 87(1):34-41. PubMed ID: 8666433
[TBL] [Abstract][Full Text] [Related]
15. Virus-specific T cells in the central nervous system following infection with an avirulent neurotropic mouse hepatitis virus.
Williamson JS
Reg Immunol; 1992; 4(3):145-52. PubMed ID: 1338891
[TBL] [Abstract][Full Text] [Related]
16. Identification of a ras oncogene peptide that contains both CD4(+) and CD8(+) T cell epitopes in a nested configuration and elicits both T cell subset responses by peptide or DNA immunization.
Bristol JA; Orsini C; Lindinger P; Thalhamer J; Abrams SI
Cell Immunol; 2000 Nov; 205(2):73-83. PubMed ID: 11104579
[TBL] [Abstract][Full Text] [Related]
17. Positive selection of cytotoxic T lymphocyte escape variants during acute hepatitis C virus infection.
Guglietta S; Garbuglia AR; Pacciani V; Scottà C; Perrone MP; Laurenti L; Spada E; Mele A; Capobianchi MR; Taliani G; Folgori A; Vitelli A; Ruggeri L; Nicosia A; Piccolella E; Del Porto P
Eur J Immunol; 2005 Sep; 35(9):2627-37. PubMed ID: 16114108
[TBL] [Abstract][Full Text] [Related]
18. Generation of IL-2-dependent cytolytic T lymphocytes (CTLs) with altered TCR responses derived from antigen-dependent CTL clones.
Gullo CA; Esser MT; Fuller CL; Lam Braciale V
J Immunol; 1999 Jun; 162(11):6466-72. PubMed ID: 10352261
[TBL] [Abstract][Full Text] [Related]
19. Differential regulation of primary and secondary CD8+ T cells in the central nervous system.
Ramakrishna C; Stohlman SA; Atkinson RA; Hinton DR; Bergmann CC
J Immunol; 2004 Nov; 173(10):6265-73. PubMed ID: 15528365
[TBL] [Abstract][Full Text] [Related]
20. Visualization of polyoma virus-specific CD8+ T cells in vivo during infection and tumor rejection.
Lukacher AE; Moser JM; Hadley A; Altman JD
J Immunol; 1999 Sep; 163(6):3369-78. PubMed ID: 10477607
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]