Homing phenotypes of tumor-specific CD8 T cells are predetermined at the tumor site by crosspresenting APCs.
暂无分享,去创建一个
Curzio Rüegg | C. Rüegg | P. Walker | M. Aurrand-Lions | P. Dietrich | Pierre-Yves Dietrich | Paul R Walker | E. Contassot | R. Wilmotte | T. Calzascia | Thomas Calzascia | Michel Aurrand-Lions | Frédérick Masson | Wilma Di Berardino-Besson | Emmanuel Contassot | Rick Wilmotte | F. Masson | W. Di Berardino-Besson | W. di Berardino-Besson
[1] Simon C Watkins,et al. Delivery of Interferon-α Transfected Dendritic Cells into Central Nervous System Tumors Enhances the Antitumor Efficacy of Peripheral Peptide-Based Vaccines , 2004, Cancer Research.
[2] N. Brouwenstijn,et al. Antigen Bias in T Cell Cross-Priming , 2004, Science.
[3] Y. Shimizu,et al. Integrins and T cell-mediated immunity. , 2004, Annual review of immunology.
[4] J. Simon,et al. Dendritic Cell Immunization Route Determines CD8+ T Cell Trafficking to Inflamed Skin: Role for Tissue Microenvironment and Dendritic Cells in Establishment of T Cell-Homing Subsets1 , 2004, The Journal of Immunology.
[5] V. Engelhard,et al. Route of Immunization with Peptide-pulsed Dendritic Cells Controls the Distribution of Memory and Effector T Cells in Lymphoid Tissues and Determines the Pattern of Regional Tumor Control , 2003, The Journal of experimental medicine.
[6] B. Malissen,et al. Selective Generation of Gut Tropic T Cells in Gut-associated Lymphoid Tissue (GALT) , 2003, The Journal of experimental medicine.
[7] P. Walker,et al. Cutting Edge: Cross-Presentation as a Mechanism for Efficient Recruitment of Tumor-Specific CTL to the Brain 1 , 2003, The Journal of Immunology.
[8] J. Lannes-Vieira,et al. Essential role of VLA-4/VCAM-1 pathway in the establishment of CD8+ T-cell-mediated Trypanosoma cruzi-elicited meningoencephalitis , 2003, Journal of Neuroimmunology.
[9] Joshy Jacob,et al. Genetic tagging shows increased frequency and longevity of antigen-presenting, skin-derived dendritic cells in vivo , 2003, Nature Immunology.
[10] Wolfgang Weninger,et al. Selective imprinting of gut-homing T cells by Peyer's patch dendritic cells , 2003, Nature.
[11] A. Rudensky,et al. Distinct dendritic cell populations sequentially present antigen to CD4 T cells and stimulate different aspects of cell-mediated immunity. , 2003, Immunity.
[12] C. Ardavı́n. Origin, precursors and differentiation of mouse dendritic cells , 2003, Nature Reviews Immunology.
[13] P. Walker,et al. T-cell immune responses in the brain and their relevance for cerebral malignancies , 2003, Brain Research Reviews.
[14] Youjin Lee,et al. Complementary Role of CD4+ T Cells and Secondary Lymphoid Tissues for Cross-presentation of Tumor Antigen to CD8+ T Cells , 2003, The Journal of experimental medicine.
[15] A. Mowat,et al. Anatomical basis of tolerance and immunity to intestinal antigens , 2003, Nature Reviews Immunology.
[16] B. Engelhardt,et al. Alpha4 integrins as therapeutic targets in autoimmune disease. , 2003, The New England journal of medicine.
[17] M. Nishimura,et al. Increasing tumor antigen expression overcomes "ignorance" to solid tumors via crosspresentation by bone marrow-derived stromal cells. , 2002, Immunity.
[18] M. Kamm,et al. Intestinal dendritic cells increase T cell expression of α4β7 integrin , 2002 .
[19] D. Speiser,et al. Tumor Growth Enhances Cross-Presentation Leading to Limited T Cell Activation without Tolerance , 2002, The Journal of experimental medicine.
[20] E. Butcher,et al. Rapid Acquisition of Tissue-specific Homing Phenotypes by CD4+ T Cells Activated in Cutaneous or Mucosal Lymphoid Tissues , 2002, The Journal of experimental medicine.
[21] B. Engelhardt,et al. Alpha4-integrin-VCAM-1 binding mediates G protein-independent capture of encephalitogenic T cell blasts to CNS white matter microvessels. , 2001, The Journal of clinical investigation.
[22] R. Alon. Encephalitogenic lymphoblast recruitment to resting CNS microvasculature: a natural immunosurveillance mechanism? , 2001, The Journal of clinical investigation.
[23] Rolf M. Zinkernagel,et al. Roles of tumour localization, second signals and cross priming in cytotoxic T-cell induction , 2001, Nature.
[24] W. Heath,et al. Cutting Edge: Intravenous Soluble Antigen Is Presented to CD4 T Cells by CD8− Dendritic Cells, but Cross-Presented to CD8 T Cells by CD8+ Dendritic Cells1 , 2001, The Journal of Immunology.
[25] M. Bevan,et al. Cd8+ but Not Cd8− Dendritic Cells Cross-Prime Cytotoxic T Cells in Vivo , 2000, The Journal of experimental medicine.
[26] C. Mackay,et al. T-cell function and migration. Two sides of the same coin. , 2000, The New England journal of medicine.
[27] P. Walker,et al. The Brain Parenchyma Is Permissive for Full Antitumor CTL Effector Function, Even in the Absence of CD4 T Cells1 , 2000, The Journal of Immunology.
[28] C. Janeway,et al. Differential adhesion molecule requirements for immune surveillance and inflammatory recruitment. , 2000, Brain : a journal of neurology.
[29] M. Colombo,et al. Dendritic Cells Infiltrating Tumors Cotransduced with Granulocyte/Macrophage Colony-Stimulating Factor (Gm-Csf) and Cd40 Ligand Genes Take up and Present Endogenous Tumor-Associated Antigens, and Prime Naive Mice for a Cytotoxic T Lymphocyte Response , 1999, The Journal of experimental medicine.
[30] F. Lemonnier,et al. Single H2Kb, H2Db and double H2KbDb knockout mice: peripheral CD8+ T cell repertoire and antilymphocytic choriomeningitis virus cytolytic responses , 1999, European journal of immunology.
[31] B. Engelhardt,et al. The development of experimental autoimmune encephalomyelitis in the mouse requires alpha4-integrin but not alpha4beta7-integrin. , 1998, The Journal of clinical investigation.
[32] H. Ploegh,et al. Major histocompatibility complex (MHC) class I KbDb -/- deficient mice possess functional CD8+ T cells and natural killer cells. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[33] B. Engelhardt,et al. Adhesion molecule phenotype of T lymphocytes in inflamed CNS , 1998, Journal of Neuroimmunology.
[34] J. Kieffer,et al. Cutaneous lymphocyte antigen is a specialized form of PSGL-1 expressed on skin-homing T cells , 1997, Nature.
[35] B. Engelhardt,et al. Lymphocyte Targeting of the Central Nervous System: A Review of Afferent and Efferent CNS‐Immune Pathways , 1996, Brain pathology.
[36] D. Griffin,et al. Regulation of lymphocyte homing into the brain during viral encephalitis at various stages of infection. , 1996, Journal of immunology.
[37] L. Picker,et al. Lymphocyte Homing and Homeostasis , 1996, Science.
[38] B. Engelhardt,et al. Lymphocytes infiltrating the CNS during inflammation display a distinctive phenotype and bind to VCAM-1 but not to MAdCAM-1. , 1995, International immunology.
[39] K. Horgan,et al. Regulated expression and binding of three VLA (β1) integrin receptors on T cells , 1990, Nature.
[40] H. Pircher,et al. Tolerance induction in double specific T-cell receptor transgenic mice varies with antigen , 1989, Nature.
[41] Eric J Kunkel,et al. Chemokines and the tissue-specific migration of lymphocytes. , 2002, Immunity.
[42] E. Butcher,et al. Lymphocyte trafficking and regional immunity. , 1999, Advances in immunology.
[43] H. Ploegh,et al. Major histocompatibility complex (MHC) class I K b D b 2y2 deficient mice possess functional CD81 T cells and natural killer cells , 1998 .
[44] Goust Jm. Major histocompatibility complex. , 1990, Immunology series.