126 related articles for article (PubMed ID: 24307730)
1. Th1 polarization of T cells injected into the cerebrospinal fluid induces brain immunosurveillance.
Fisher Y; Strominger I; Biton S; Nemirovsky A; Baron R; Monsonego A
J Immunol; 2014 Jan; 192(1):92-102. PubMed ID: 24307730
[TBL] [Abstract][Full Text] [Related]
2. IFN-γ Production by amyloid β-specific Th1 cells promotes microglial activation and increases plaque burden in a mouse model of Alzheimer's disease.
Browne TC; McQuillan K; McManus RM; O'Reilly JA; Mills KH; Lynch MA
J Immunol; 2013 Mar; 190(5):2241-51. PubMed ID: 23365075
[TBL] [Abstract][Full Text] [Related]
3. BDNF-producing, amyloid β-specific CD4 T cells as targeted drug-delivery vehicles in Alzheimer's disease.
Eremenko E; Mittal K; Berner O; Kamenetsky N; Nemirovsky A; Elyahu Y; Monsonego A
EBioMedicine; 2019 May; 43():424-434. PubMed ID: 31085101
[TBL] [Abstract][Full Text] [Related]
4. Influence of a mutation in IFN-γ receptor 2 (IFNGR2) in human cells on the generation of Th17 cells in memory T cells.
Holzer U; Reinhardt K; Lang P; Handgretinger R; Fischer N
Hum Immunol; 2013 Jun; 74(6):693-700. PubMed ID: 23459074
[TBL] [Abstract][Full Text] [Related]
5. T cells specifically targeted to amyloid plaques enhance plaque clearance in a mouse model of Alzheimer's disease.
Fisher Y; Nemirovsky A; Baron R; Monsonego A
PLoS One; 2010 May; 5(5):e10830. PubMed ID: 20520819
[TBL] [Abstract][Full Text] [Related]
6. Microglia-mediated nitric oxide cytotoxicity of T cells following amyloid beta-peptide presentation to Th1 cells.
Monsonego A; Imitola J; Zota V; Oida T; Weiner HL
J Immunol; 2003 Sep; 171(5):2216-24. PubMed ID: 12928365
[TBL] [Abstract][Full Text] [Related]
7. The mechanism of in vitro T helper cell type 1 to T helper cell type 2 switching in highly polarized Leishmania major-specific T cell populations.
Mocci S; Coffman RL
J Immunol; 1997 Feb; 158(4):1559-64. PubMed ID: 9029090
[TBL] [Abstract][Full Text] [Related]
8. ESAT-6- and CFP-10-specific Th1, Th22 and Th17 cells in tuberculous pleurisy may contribute to the local immune response against Mycobacterium tuberculosis infection.
Qiao D; Yang BY; Li L; Ma JJ; Zhang XL; Lao SH; Wu CY
Scand J Immunol; 2011 Apr; 73(4):330-7. PubMed ID: 21223348
[TBL] [Abstract][Full Text] [Related]
9. CD4+ Th2 cells function alike effector Tr1 and Th1 cells through the deletion of a single cytokine IL-6 and IL-10 gene.
Ankathatti Munegowda M; Xu S; Freywald A; Xiang J
Mol Immunol; 2012 Jun; 51(2):143-9. PubMed ID: 22424785
[TBL] [Abstract][Full Text] [Related]
10. Role of MOG-stimulated Th1 type "light up" (GFP+) CD4+ T cells for the development of experimental autoimmune encephalomyelitis (EAE).
Yura M; Takahashi I; Serada M; Koshio T; Nakagami K; Yuki Y; Kiyono H
J Autoimmun; 2001 Aug; 17(1):17-25. PubMed ID: 11488634
[TBL] [Abstract][Full Text] [Related]
11. Soluble protein but not peptide administration diverts the immune response of a clonal CD4+ T cell population to the T helper 2 cell pathway.
Degermann S; Pria E; Adorini L
J Immunol; 1996 Oct; 157(8):3260-9. PubMed ID: 8871620
[TBL] [Abstract][Full Text] [Related]
12. Type 2 immune deviation has differential effects on alloreactive CD4+ and CD8+ T cells.
Matesic D; Valujskikh A; Pearlman E; Higgins AW; Gilliam AC; Heeger PS
J Immunol; 1998 Nov; 161(10):5236-44. PubMed ID: 9820495
[TBL] [Abstract][Full Text] [Related]
13. Polarization of IL-4- and IFN-gamma-producing CD4+ T cells following activation of naive CD4+ T cells.
Nakamura T; Kamogawa Y; Bottomly K; Flavell RA
J Immunol; 1997 Feb; 158(3):1085-94. PubMed ID: 9013946
[TBL] [Abstract][Full Text] [Related]
14. Invariant NKT cells regulate experimental autoimmune uveitis through inhibition of Th17 differentiation.
Oh K; Byoun OJ; Ham DI; Kim YS; Lee DS
Eur J Immunol; 2011 Feb; 41(2):392-402. PubMed ID: 21268009
[TBL] [Abstract][Full Text] [Related]
15. Strength of TCR signal determines the costimulatory requirements for Th1 and Th2 CD4+ T cell differentiation.
Tao X; Constant S; Jorritsma P; Bottomly K
J Immunol; 1997 Dec; 159(12):5956-63. PubMed ID: 9550393
[TBL] [Abstract][Full Text] [Related]
16. Studies using antigen-presenting cells lacking expression of both B7-1 (CD80) and B7-2 (CD86) show distinct requirements for B7 molecules during priming versus restimulation of Th2 but not Th1 cytokine production.
Schweitzer AN; Sharpe AH
J Immunol; 1998 Sep; 161(6):2762-71. PubMed ID: 9743334
[TBL] [Abstract][Full Text] [Related]
17. Abeta-induced meningoencephalitis is IFN-gamma-dependent and is associated with T cell-dependent clearance of Abeta in a mouse model of Alzheimer's disease.
Monsonego A; Imitola J; Petrovic S; Zota V; Nemirovsky A; Baron R; Fisher Y; Owens T; Weiner HL
Proc Natl Acad Sci U S A; 2006 Mar; 103(13):5048-53. PubMed ID: 16549802
[TBL] [Abstract][Full Text] [Related]
18. Rapid in vivo conversion of effector T cells into Th2 cells during helminth infection.
Panzer M; Sitte S; Wirth S; Drexler I; Sparwasser T; Voehringer D
J Immunol; 2012 Jan; 188(2):615-23. PubMed ID: 22156341
[TBL] [Abstract][Full Text] [Related]
19. Th2-induced eotaxin expression and eosinophilia coexist with Th1 responses at the effector stage of lung inflammation.
Li L; Xia Y; Nguyen A; Feng L; Lo D
J Immunol; 1998 Sep; 161(6):3128-35. PubMed ID: 9743380
[TBL] [Abstract][Full Text] [Related]
20. Naive and effector CD4 T cells differ in their requirements for T cell receptor versus costimulatory signals.
Dubey C; Croft M; Swain SL
J Immunol; 1996 Oct; 157(8):3280-9. PubMed ID: 8871622
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]