scholarly article | Q13442814 |
P2093 | author name string | N. Sato | |
W. A. Kuziel | |||
R. L. Reddick | |||
M. Quinones | |||
P. C. Melby | |||
S. K. Ahuja | |||
S. S. Ahuja | |||
V. Kostecki | |||
P2860 | cites work | B cell-attracting chemokine 1, a human CXC chemokine expressed in lymphoid tissues, selectively attracts B lymphocytes via BLR1/CXCR5 | Q24309316 |
Molecular cloning of a novel T cell-directed CC chemokine expressed in thymus by signal sequence trap using Epstein-Barr virus vector | Q24312084 | ||
Dendritic cells and the control of immunity | Q27860918 | ||
Defects in the generation of IFN-gamma are overcome to control infection with Leishmania donovani in CC chemokine receptor (CCR) 5-, macrophage inflammatory protein-1 alpha-, or CCR2-deficient mice | Q45040266 | ||
Differences in the onset of the inflammatory response to cutaneous leishmaniasis in resistant and susceptible mice | Q45070476 | ||
Dendritic cells in Leishmania major-immune mice harbor persistent parasites and mediate an antigen-specific T cell immune response | Q49137643 | ||
Langerhans cells transport Leishmania major from the infected skin to the draining lymph node for presentation to antigen-specific T cells | Q49155579 | ||
Host susceptibility factors to cutaneous leishmaniasis. | Q51093555 | ||
Chemokines: signal lamps for trafficking of T and B cells for development and effector function. | Q52035782 | ||
Developmental pathways of dendritic cells in vivo: distinct function, phenotype, and localization of dendritic cell subsets in FLT3 ligand-treated mice. | Q52192894 | ||
Requirement of MIP-1 alpha for an inflammatory response to viral infection. | Q52509286 | ||
Genetically resistant mice lacking interleukin-12 are susceptible to infection with Leishmania major and mount a polarized Th2 cell response. | Q52520769 | ||
Distinct patterns and kinetics of chemokine production regulate dendritic cell function. | Q54093362 | ||
Langerhans cells acquire a CD8+ dendritic cell phenotype on maturation by CD40 ligation | Q58436648 | ||
Control of TH2 polarization by the chemokine monocyte chemoattractant protein-1 | Q59089322 | ||
Dendritic cells capable of stimulating T cells in germinal centres | Q60085015 | ||
A method to recover, enumerate and identify lymphomyeloid cells present in an inflammatory dermal site: a study in laboratory mice | Q60211995 | ||
Interleukin-4 transgenic mice of resistant background are susceptible to Leishmania major infection | Q70567406 | ||
In susceptible mice, Leishmania major induce very rapid interleukin-4 production by CD4+ T cells which are NK1.1- | Q70911092 | ||
Accessory functions and mutual cooperation of murine macrophages and dendritic cells | Q71000640 | ||
Cutaneous leishmaniasis in anti-IgM-treated mice: enhanced resistance due to functional depletion of a B cell-dependent T cell involved in the suppressor pathway | Q72808043 | ||
Differential responsiveness to constitutive vs. inducible chemokines of immature and mature mouse dendritic cells | Q73017058 | ||
The role of CCR7 in TH1 and TH2 cell localization and delivery of B cell help in vivo | Q73257315 | ||
Differentiation of phagocytic monocytes into lymph node dendritic cells in vivo | Q73336913 | ||
Heterogeneity of mouse spleen dendritic cells: in vivo phagocytic activity, expression of macrophage markers, and subpopulation turnover | Q74303609 | ||
Rapid and coordinated switch in chemokine receptor expression during dendritic cell maturation | Q77353738 | ||
IL-4- and IL-4 receptor-deficient BALB/c mice reveal differences in susceptibility to Leishmania major parasite substrains | Q77404910 | ||
Contribution of dermal macrophage trafficking in the sensitization phase of contact hypersensitivity | Q77716092 | ||
CCR5 binds multiple CC-chemokines: MCP-3 acts as a natural antagonist | Q28143942 | ||
A B-cell-homing chemokine made in lymphoid follicles activates Burkitt's lymphoma receptor-1 | Q28263524 | ||
A putative chemokine receptor, BLR1, directs B cell migration to defined lymphoid organs and specific anatomic compartments of the spleen | Q28300225 | ||
Impaired monocyte migration and reduced type 1 (Th1) cytokine responses in C-C chemokine receptor 2 knockout mice | Q28585385 | ||
Severe reduction in leukocyte adhesion and monocyte extravasation in mice deficient in CC chemokine receptor 2. | Q28590391 | ||
CCR7 coordinates the primary immune response by establishing functional microenvironments in secondary lymphoid organs | Q28594485 | ||
Chemokine receptors as HIV-1 coreceptors: roles in viral entry, tropism, and disease | Q29616432 | ||
TH1 and TH2 T-cell subsets are differentially activated by macrophages and B cells in murine leishmaniasis | Q33598466 | ||
Interpretation of phenotype in genetically engineered mice | Q33637153 | ||
Lymphocyte trafficking and regional immunity. | Q33653665 | ||
Chemokines and B-cell homing to follicles. | Q33681306 | ||
The role of chemokines in regulating cell migration during humoral immune responses | Q33778602 | ||
Chemokines and cell migration in secondary lymphoid organs | Q33807114 | ||
Leukocyte migration: scent of the T zone | Q33830297 | ||
Natural and induced regulation of Th1/Th2 balance | Q33833181 | ||
Lymphotoxin alpha/beta and tumor necrosis factor are required for stromal cell expression of homing chemokines in B and T cell areas of the spleen | Q34488105 | ||
Profile of human T cell response to leishmanial antigens. Analysis by immunoblotting | Q34574468 | ||
Chemokines and the homing of dendritic cells to the T cell areas of lymphoid organs | Q34756572 | ||
Effect of C-C chemokine receptor 2 (CCR2) knockout on type-2 (schistosomal antigen-elicited) pulmonary granuloma formation: analysis of cellular recruitment and cytokine responses | Q35786914 | ||
Migration and maturation of Langerhans cells in skin transplants and explants | Q36353813 | ||
Regulation of dendritic cell numbers and maturation by lipopolysaccharide in vivo. | Q36367475 | ||
CD8alpha+ and CD8alpha- subclasses of dendritic cells direct the development of distinct T helper cells in vivo | Q36367705 | ||
In vivo detection of dendritic cell antigen presentation to CD4(+) T cells. | Q36377341 | ||
Defects in macrophage recruitment and host defense in mice lacking the CCR2 chemokine receptor | Q36380911 | ||
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 | Q36401312 | ||
Systemic migration of dendritic cells during contact sensitization. | Q38515927 | ||
Localization of antigen on lymph node dendritic cells after exposure to the contact sensitizer fluorescein isothiocyanate. Functional and morphological studies | Q38518849 | ||
Dendritic cells and the initiation of contact sensitivity to fluorescein isothiocyanate. | Q38519677 | ||
Distribution of immunogenic cells after painting with the contact sensitizers fluorescein isothiocyanate and oxazolone. Different sensitizers form immunogenic complexes with different cell populations. | Q38524932 | ||
B-cell outgrowth and ligand-specific production of IL-10 correlate with Th2 dominance in certain parasitic diseases | Q39334507 | ||
Mouse models of human genetic disease: which mouse is more like a man? | Q41283188 | ||
Regulation of immunostimulatory function and costimulatory molecule (B7-1 and B7-2) expression on murine dendritic cells. | Q41466523 | ||
Chemokine Up-regulation and activated T cell attraction by maturing dendritic cells | Q41648813 | ||
Dendritic cell development: multiple pathways to nature's adjuvants | Q41664108 | ||
Mice lacking expression of secondary lymphoid organ chemokine have defects in lymphocyte homing and dendritic cell localization | Q42064511 | ||
Mobilizing dendritic cells for tolerance, priming, and chronic inflammation | Q42576422 | ||
Dendritic cell (DC)-based anti-infective strategies: DCs engineered to secrete IL-12 are a potent vaccine in a murine model of an intracellular infection | Q42810799 | ||
Differences between IL-4- and IL-4 receptor alpha-deficient mice in chronic leishmaniasis reveal a protective role for IL-13 receptor signaling | Q43720783 | ||
The IL-4 rapidly produced in BALB/c mice after infection with Leishmania major down-regulates IL-12 receptor beta 2-chain expression on CD4+ T cells resulting in a state of unresponsiveness to IL-12. | Q44404358 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | phenotype | Q104053 |
Chemokine (C-C motif) receptor 2 | Q21495023 | ||
cell migration | Q189092 | ||
dendritic cell | Q506253 | ||
Leishmania major | Q1950715 | ||
P304 | page(s) | 205–218 | |
P577 | publication date | 2000-07-17 | |
P1433 | published in | Journal of Experimental Medicine | Q3186912 |
P1476 | title | CC chemokine receptor (CCR)2 is required for langerhans cell migration and localization of T helper cell type 1 (Th1)-inducing dendritic cells. Absence of CCR2 shifts the Leishmania major-resistant phenotype to a susceptible state dominated by Th2 c | |
P478 | volume | 192 |
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Q34634796 | Blocking junctional adhesion molecule C enhances dendritic cell migration and boosts the immune responses against Leishmania major |
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Q36346773 | CCR-2 neutralization augments murine fresh BMC activation by Staphylococcus aureus via two distinct mechanisms: at the level of ROS production and cytokine response |
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Q35848441 | CCR2 is required for CD8-induced graft-versus-host disease. |
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Q36228080 | CCR5-dependent homing of naturally occurring CD4+ regulatory T cells to sites of Leishmania major infection favors pathogen persistence |
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Q33928441 | CD8(+) but not CD8(-) dendritic cells cross-prime cytotoxic T cells in vivo. |
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Q37521995 | Chemokine gene expression in toll-like receptor-competent and -deficient mice infected with Leishmania major |
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