Leishmania major attenuates host immunity by stimulating local indoleamine 2,3-dioxygenase expression.
暂无分享,去创建一个
B. Baban | D. Munn | A. Mellor | H. Lemos | P. Chandler | A. El-Awady | L. Makala | Deyan Hou | Ahmed R. El-Awady
[1] B. Baban,et al. B-lymphoid cells with attributes of dendritic cells regulate T cells via indoleamine 2,3-dioxygenase , 2010, Proceedings of the National Academy of Sciences.
[2] C. Hunter,et al. IL-27 Regulates IL-10 and IL-17 from CD4+ Cells in Nonhealing Leishmania major Infection1 , 2009, The Journal of Immunology.
[3] B. Baban,et al. IDO Activates Regulatory T Cells and Blocks Their Conversion into Th17-Like T Cells1 , 2009, The Journal of Immunology.
[4] B. Baban,et al. Targeting the immunoregulatory indoleamine 2,3 dioxygenase pathway in immunotherapy. , 2009, Immunotherapy.
[5] H. Bang,et al. Tuberculosis Is Associated with a Down-Modulatory Lung Immune Response That Impairs Th1-Type Immunity1 , 2009, The Journal of Immunology.
[6] D. Munn,et al. Indoleamine 2,3-dioxygenase controls conversion of Foxp3+ Tregs to TH17-like cells in tumor-draining lymph nodes. , 2009, Blood.
[7] Sarman Singh,et al. Immunobiology of leishmaniasis. , 2009, Indian journal of experimental biology.
[8] Y. Belkaid,et al. Regulatory T cells in the control of host-microorganism interactions (*). , 2009, Annual review of immunology.
[9] Y. Belkaid,et al. Arming Treg cells at the inflammatory site. , 2009, Immunity.
[10] Y. Iwakura,et al. IL-17 Promotes Progression of Cutaneous Leishmaniasis in Susceptible Mice1 , 2009, The Journal of Immunology.
[11] F. Tacchini-Cottier,et al. Intralesional Regulatory T-Cell Suppressive Function during Human Acute and Chronic Cutaneous Leishmaniasis Due to Leishmania guyanensis , 2009, Infection and Immunity.
[12] Y. Belkaid,et al. Regulatory T Cells in the Control of Host-Microorganism , 2009 .
[13] P. Puccetti,et al. Indoleamine 2,3-dioxygenase in infection: the paradox of an evasive strategy that benefits the host. , 2009, Microbes and infection.
[14] G. Prendergast,et al. Chronic inflammation that facilitates tumor progression creates local immune suppression by inducing indoleamine 2,3 dioxygenase , 2008, Proceedings of the National Academy of Sciences.
[15] C. Bogdan,et al. The innate immune response against Leishmania parasites. , 2008, Immunobiology.
[16] D. Munn,et al. Creating immune privilege: active local suppression that benefits friends, but protects foes , 2008, Nature Reviews Immunology.
[17] B. Baban,et al. Plasmacytoid dendritic cells from mouse tumor-draining lymph nodes directly activate mature Tregs via indoleamine 2,3-dioxygenase. , 2007, The Journal of clinical investigation.
[18] G. Prendergast,et al. Inhibition of indoleamine 2,3-dioxygenase in dendritic cells by stereoisomers of 1-methyl-tryptophan correlates with antitumor responses. , 2007, Cancer research.
[19] Trinad Chakraborty,et al. Indoleamine 2,3-dioxygenase-expressing dendritic cells form suppurative granulomas following Listeria monocytogenes infection. , 2006, The Journal of clinical investigation.
[20] Y. Belkaid,et al. CCR5-dependent homing of naturally occurring CD4+ regulatory T cells to sites of Leishmania major infection favors pathogen persistence , 2006, The Journal of experimental medicine.
[21] N. Peters,et al. Immune privilege in sites of chronic infection: Leishmania and regulatory T cells , 2006, Immunological reviews.
[22] Y. Belkaid,et al. Infected site-restricted Foxp3+ natural regulatory T cells are specific for microbial antigens , 2006, The Journal of experimental medicine.
[23] T. van der Poll,et al. Influenza-induced expression of indoleamine 2,3-dioxygenase enhances interleukin-10 production and bacterial outgrowth during secondary pneumococcal pneumonia. , 2006, The Journal of infectious diseases.
[24] B. Baban,et al. Cutting Edge: CpG Oligonucleotides Induce Splenic CD19+ Dendritic Cells to Acquire Potent Indoleamine 2,3-Dioxygenase-Dependent T Cell Regulatory Functions via IFN Type 1 Signaling1 , 2005, The Journal of Immunology.
[25] Y. Belkaid,et al. Antigen Requirements for Efficient Priming of CD8+ T Cells by Leishmania major-Infected Dendritic Cells , 2005, Infection and Immunity.
[26] B. Baban,et al. A minor population of splenic dendritic cells expressing CD19 mediates IDO-dependent T cell suppression via type I IFN signaling following B7 ligation. , 2005, International immunology.
[27] A. Rudensky,et al. Regulatory T cell lineage specification by the forkhead transcription factor foxp3. , 2005, Immunity.
[28] B. Baban,et al. Expression of indoleamine 2,3-dioxygenase by plasmacytoid dendritic cells in tumor-draining lymph nodes. , 2004, The Journal of clinical investigation.
[29] B. Baban,et al. Indoleamine 2,3-dioxygenase expression is restricted to fetal trophoblast giant cells during murine gestation and is maternal genome specific. , 2004, Journal of reproductive immunology.
[30] D. Munn,et al. IDO and tolerance to tumors. , 2004, Trends in molecular medicine.
[31] B. Baban,et al. Cutting Edge: Induced Indoleamine 2,3 Dioxygenase Expression in Dendritic Cell Subsets Suppresses T Cell Clonal Expansion1 , 2003, The Journal of Immunology.
[32] Y. Belkaid,et al. CD4+CD25+ regulatory T cells control Leishmania major persistence and immunity , 2002, Nature.
[33] Y. Belkaid,et al. CD8+ T Cells Are Required for Primary Immunity in C57BL/6 Mice Following Low-Dose, Intradermal Challenge with Leishmania major , 2002, The Journal of Immunology.
[34] Y. Belkaid,et al. A Natural Model of Leishmania major Infection Reveals a Prolonged “Silent” Phase of Parasite Amplification in the Skin Before the Onset of Lesion Formation and Immunity , 2000, The Journal of Immunology.
[35] D. Munn,et al. Tryptophan catabolism and T-cell tolerance: immunosuppression by starvation? , 1999, Immunology today.
[36] Y. Belkaid,et al. Development of a Natural Model of Cutaneous Leishmaniasis: Powerful Effects of Vector Saliva and Saliva Preexposure on the Long-Term Outcome of Leishmania major Infection in the Mouse Ear Dermis , 1998, The Journal of experimental medicine.
[37] R. Locksley,et al. The regulation of immunity to Leishmania major. , 1995, Annual review of immunology.
[38] P. Scott. IFN-gamma modulates the early development of Th1 and Th2 responses in a murine model of cutaneous leishmaniasis. , 1991, Journal of immunology.
[39] R. Locksley,et al. Reconstitution of Leishmania immunity in severe combined immunodeficient mice using Th1- and Th2-like cell lines. , 1991, Journal of immunology.
[40] R. Locksley,et al. Induction of Th1 and Th2 CD4+ subsets during murine Leishmania major infection. , 1991, Research in immunology.
[41] H. Moll,et al. Resistance to murine cutaneous leishmaniasis is mediated by TH1 cells, but disease‐promoting CD4+ cells are different from TH2 cells , 1990, European journal of immunology.
[42] M. Lohoff,et al. Coexistence of antigen-specific TH1 and TH2 cells in genetically susceptible BALB/c mice infected with Leishmania major. , 1989, Immunobiology.
[43] R. Coffman,et al. Immunoregulation of cutaneous leishmaniasis. T cell lines that transfer protective immunity or exacerbation belong to different T helper subsets and respond to distinct parasite antigens , 1988, The Journal of experimental medicine.