314 related articles for article (PubMed ID: 20733203)
21. CD4+ T cells are required to sustain CD8+ cytotoxic T-cell responses during chronic viral infection.
Matloubian M; Concepcion RJ; Ahmed R
J Virol; 1994 Dec; 68(12):8056-63. PubMed ID: 7966595
[TBL] [Abstract][Full Text] [Related]
22. An MHC class Ib-restricted CD8+ T cell response to lymphocytic choriomeningitis virus.
Chen L; Jay DC; Fairbanks JD; He X; Jensen PE
J Immunol; 2011 Dec; 187(12):6463-72. PubMed ID: 22084437
[TBL] [Abstract][Full Text] [Related]
23. Direct visualization of cross-reactive effector and memory allo-specific CD8 T cells generated in response to viral infections.
Brehm MA; Markees TG; Daniels KA; Greiner DL; Rossini AA; Welsh RM
J Immunol; 2003 Apr; 170(8):4077-86. PubMed ID: 12682237
[TBL] [Abstract][Full Text] [Related]
24. Persistence of memory CD8 T cells in MHC class I-deficient mice.
Murali-Krishna K; Lau LL; Sambhara S; Lemonnier F; Altman J; Ahmed R
Science; 1999 Nov; 286(5443):1377-81. PubMed ID: 10558996
[TBL] [Abstract][Full Text] [Related]
25. Evolution of the T cell repertoire during primary, memory, and recall responses to viral infection.
Blattman JN; Sourdive DJ; Murali-Krishna K; Ahmed R; Altman JD
J Immunol; 2000 Dec; 165(11):6081-90. PubMed ID: 11086040
[TBL] [Abstract][Full Text] [Related]
26. Induction of telomerase activity and maintenance of telomere length in virus-specific effector and memory CD8+ T cells.
Hathcock KS; Kaech SM; Ahmed R; Hodes RJ
J Immunol; 2003 Jan; 170(1):147-52. PubMed ID: 12496394
[TBL] [Abstract][Full Text] [Related]
27. Multiple layers of CD80/86-dependent costimulatory activity regulate primary, memory, and secondary lymphocytic choriomeningitis virus-specific T cell immunity.
Eberlein J; Davenport B; Nguyen TT; Victorino F; Sparwasser T; Homann D
J Virol; 2012 Feb; 86(4):1955-70. PubMed ID: 22156513
[TBL] [Abstract][Full Text] [Related]
28. CD70 deficiency impairs effector CD8 T cell generation and viral clearance but is dispensable for the recall response to lymphocytic choriomeningitis virus.
Munitic I; Kuka M; Allam A; Scoville JP; Ashwell JD
J Immunol; 2013 Feb; 190(3):1169-79. PubMed ID: 23269247
[TBL] [Abstract][Full Text] [Related]
29. Ablation of CD8 and CD4 T cell responses by high viral loads.
Fuller MJ; Zajac AJ
J Immunol; 2003 Jan; 170(1):477-86. PubMed ID: 12496434
[TBL] [Abstract][Full Text] [Related]
30. Effect of chronic viral infection on epitope selection, cytokine production, and surface phenotype of CD8 T cells and the role of IFN-gamma receptor in immune regulation.
Tewari K; Sacha J; Gao X; Suresh M
J Immunol; 2004 Feb; 172(3):1491-500. PubMed ID: 14734726
[TBL] [Abstract][Full Text] [Related]
31. Attrition of virus-specific memory CD8+ T cells during reconstitution of lymphopenic environments.
Peacock CD; Kim SK; Welsh RM
J Immunol; 2003 Jul; 171(2):655-63. PubMed ID: 12847230
[TBL] [Abstract][Full Text] [Related]
32. CD40-CD40 ligand costimulation is required for generating antiviral CD4 T cell responses but is dispensable for CD8 T cell responses.
Whitmire JK; Flavell RA; Grewal IS; Larsen CP; Pearson TC; Ahmed R
J Immunol; 1999 Sep; 163(6):3194-201. PubMed ID: 10477587
[TBL] [Abstract][Full Text] [Related]
33. Antiviral CD4 and CD8 T-cell memory: differences in the size of the response and activation requirements.
Whitmire JK; Murali-Krishna K; Altman J; Ahmed R
Philos Trans R Soc Lond B Biol Sci; 2000 Mar; 355(1395):373-9. PubMed ID: 10794058
[TBL] [Abstract][Full Text] [Related]
34. Viral antigen and extensive division maintain virus-specific CD8 T cells during chronic infection.
Shin H; Blackburn SD; Blattman JN; Wherry EJ
J Exp Med; 2007 Apr; 204(4):941-9. PubMed ID: 17420267
[TBL] [Abstract][Full Text] [Related]
35. Vaccination against lymphocytic choriomeningitis virus infection in MHC class II-deficient mice.
Holst PJ; Christensen JP; Thomsen AR
J Immunol; 2011 Apr; 186(7):3997-4007. PubMed ID: 21357263
[TBL] [Abstract][Full Text] [Related]
36. Interleukin (IL)-15 and IL-7 jointly regulate homeostatic proliferation of memory phenotype CD8+ cells but are not required for memory phenotype CD4+ cells.
Tan JT; Ernst B; Kieper WC; LeRoy E; Sprent J; Surh CD
J Exp Med; 2002 Jun; 195(12):1523-32. PubMed ID: 12070280
[TBL] [Abstract][Full Text] [Related]
37. 4-1BB ligand induces cell division, sustains survival, and enhances effector function of CD4 and CD8 T cells with similar efficacy.
Cannons JL; Lau P; Ghumman B; DeBenedette MA; Yagita H; Okumura K; Watts TH
J Immunol; 2001 Aug; 167(3):1313-24. PubMed ID: 11466348
[TBL] [Abstract][Full Text] [Related]
38. Tec kinases Itk and Rlk are required for CD8+ T cell responses to virus infection independent of their role in CD4+ T cell help.
Atherly LO; Brehm MA; Welsh RM; Berg LJ
J Immunol; 2006 Feb; 176(3):1571-81. PubMed ID: 16424186
[TBL] [Abstract][Full Text] [Related]
39. Cell-intrinsic defects in the proliferative response of antiviral memory CD8 T cells in aged mice upon secondary infection.
Decman V; Laidlaw BJ; Dimenna LJ; Abdulla S; Mozdzanowska K; Erikson J; Ertl HC; Wherry EJ
J Immunol; 2010 May; 184(9):5151-9. PubMed ID: 20368274
[TBL] [Abstract][Full Text] [Related]
40. CD40L expression by CD4
Durlanik S; Loyal L; Stark R; Sercan Alp Ö; Hartung A; Radbruch A; von Herrath M; Matzmohr N; Frentsch M; Thiel A
Eur J Immunol; 2016 Nov; 46(11):2566-2573. PubMed ID: 27562840
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
