425 related articles for article (PubMed ID: 16220537)
1. Novel phenotypes and migratory properties distinguish memory CD4 T cell subsets in lymphoid and lung tissue.
Bingaman AW; Patke DS; Mane VR; Ahmadzadeh M; Ndejembi M; Bartlett ST; Farber DL
Eur J Immunol; 2005 Nov; 35(11):3173-86. PubMed ID: 16220537
[TBL] [Abstract][Full Text] [Related]
2. The migratory behavior of murine CD4+ cells of memory phenotype.
Tietz W; Hamann A
Eur J Immunol; 1997 Sep; 27(9):2225-32. PubMed ID: 9341763
[TBL] [Abstract][Full Text] [Related]
3. Chemokine-mediated control of T cell traffic in lymphoid and peripheral tissues.
Ebert LM; Schaerli P; Moser B
Mol Immunol; 2005 May; 42(7):799-809. PubMed ID: 15829268
[TBL] [Abstract][Full Text] [Related]
4. Tissue trafficking patterns of effector memory CD4+ T cells in rheumatoid arthritis.
Zhang X; Nakajima T; Goronzy JJ; Weyand CM
Arthritis Rheum; 2005 Dec; 52(12):3839-49. PubMed ID: 16329093
[TBL] [Abstract][Full Text] [Related]
5. Effector CD4 T cells are biochemically distinct from the memory subset: evidence for long-term persistence of effectors in vivo.
Ahmadzadeh M; Hussain SF; Farber DL
J Immunol; 1999 Sep; 163(6):3053-63. PubMed ID: 10477569
[TBL] [Abstract][Full Text] [Related]
6. CC chemokine receptor 7 expression by effector/memory CD4+ T cells depends on antigen specificity and tissue localization during influenza A virus infection.
Debes GF; Bonhagen K; Wolff T; Kretschmer U; Krautwald S; Kamradt T; Hamann A
J Virol; 2004 Jul; 78(14):7528-35. PubMed ID: 15220427
[TBL] [Abstract][Full Text] [Related]
7. FTY720 preferentially depletes naive T cells from peripheral and lymphoid organs.
Hofmann M; Brinkmann V; Zerwes HG
Int Immunopharmacol; 2006 Dec; 6(13-14):1902-10. PubMed ID: 17161343
[TBL] [Abstract][Full Text] [Related]
8. Phenotypic characterization of CD4+ T cells that exhibit a transendothelial migratory capacity.
Brezinschek RI; Lipsky PE; Galea P; Vita R; Oppenheimer-Marks N
J Immunol; 1995 Apr; 154(7):3062-77. PubMed ID: 7534786
[TBL] [Abstract][Full Text] [Related]
9. The strength of T cell stimulation determines IL-7 responsiveness, secondary expansion, and lineage commitment of primed human CD4+IL-7Rhi T cells.
Lozza L; Rivino L; Guarda G; Jarrossay D; Rinaldi A; Bertoni F; Sallusto F; Lanzavecchia A; Geginat J
Eur J Immunol; 2008 Jan; 38(1):30-9. PubMed ID: 18081042
[TBL] [Abstract][Full Text] [Related]
10. Heterogeneity in P-glycoprotein (multidrug resistance) activity among murine peripheral T cells: correlation with surface phenotype and effector function.
Bommhardt U; Cerottini JC; MacDonald HR
Eur J Immunol; 1994 Dec; 24(12):2974-81. PubMed ID: 7805724
[TBL] [Abstract][Full Text] [Related]
11. Naive and memory T cell subsets are differentially mobilized during physical stress.
Gannon GA; Rhind S; Shek PN; Shephard RJ
Int J Sports Med; 2002 Apr; 23(3):223-9. PubMed ID: 11914988
[TBL] [Abstract][Full Text] [Related]
12. Complex memory T-cell phenotypes revealed by coexpression of CD62L and CCR7.
Unsoeld H; Pircher H
J Virol; 2005 Apr; 79(7):4510-3. PubMed ID: 15767451
[TBL] [Abstract][Full Text] [Related]
13. The expression of CD45RB on antigen-responsive CD4+ lymphocytes: mouse strain polymorphism and different responses to distinct antigens.
Gahring LC; Ernst DN; Romball CG; Thoman ML; Torbett BE; Hobbs M; Weigle WO
Cell Immunol; 1993 May; 148(2):269-82. PubMed ID: 7684327
[TBL] [Abstract][Full Text] [Related]
14. Phenotypic and functional characterisation of CCR7+ and CCR7- CD4+ memory T cells homing to the joints in juvenile idiopathic arthritis.
Gattorno M; Prigione I; Morandi F; Gregorio A; Chiesa S; Ferlito F; Favre A; Uccelli A; Gambini C; Martini A; Pistoia V
Arthritis Res Ther; 2005; 7(2):R256-67. PubMed ID: 15743472
[TBL] [Abstract][Full Text] [Related]
15. Selective generation of gut tropic T cells in gut-associated lymphoid tissue (GALT): requirement for GALT dendritic cells and adjuvant.
Johansson-Lindbom B; Svensson M; Wurbel MA; Malissen B; Márquez G; Agace W
J Exp Med; 2003 Sep; 198(6):963-9. PubMed ID: 12963696
[TBL] [Abstract][Full Text] [Related]
16. CD62L defines a subset of pathogen-specific bovine CD4 with central memory cell characteristics.
Totté P; Duperray C; Dedieu L
Dev Comp Immunol; 2010 Feb; 34(2):177-82. PubMed ID: 19766669
[TBL] [Abstract][Full Text] [Related]
17. Distinctive role of CCR7 in migration and functional activity of naive- and effector/memory-like Treg subsets.
Menning A; Höpken UE; Siegmund K; Lipp M; Hamann A; Huehn J
Eur J Immunol; 2007 Jun; 37(6):1575-83. PubMed ID: 17474155
[TBL] [Abstract][Full Text] [Related]
18. CD4+ T cells of both the naive and the memory phenotype enter rat lymph nodes and Peyer's patches via high endothelial venules: within the tissue their migratory behavior differs.
Westermann J; Geismar U; Sponholz A; Bode U; Sparshott SM; Bell EB
Eur J Immunol; 1997 Dec; 27(12):3174-81. PubMed ID: 9464803
[TBL] [Abstract][Full Text] [Related]
19. Anti-CD3 priming generates heterogeneous antigen-specific memory CD4 T cells.
Patke DS; Ahmadzadeh M; Bingaman AW; Farber DL
Clin Immunol; 2005 Nov; 117(2):125-32. PubMed ID: 16143567
[TBL] [Abstract][Full Text] [Related]
20. Evidence that a significant number of naive T cells enter non-lymphoid organs as part of a normal migratory pathway.
Cose S; Brammer C; Khanna KM; Masopust D; Lefrançois L
Eur J Immunol; 2006 Jun; 36(6):1423-33. PubMed ID: 16708400
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
