| scholarly article | Q13442814 |
| P50 | author | Rolf M. Zinkernagel | Q116064 |
| P2093 | author name string | Odermatt B | |
| Probst HC | |||
| Schwendener R | |||
| Tschannen K | |||
| Van Den Broek M | |||
| P2860 | cites work | Correlation of anti-viral B cell responses and splenic morphology with expression of B cell-specific molecules | Q74247911 |
| Marginal zone macrophages and immune responses against viruses | Q74500135 | ||
| Marginal-zone B cells | Q28201000 | ||
| In vivo depletion of CD11c+ dendritic cells abrogates priming of CD8+ T cells by exogenous cell-associated antigens | Q29615098 | ||
| Restoration of immunogenicity to passenger cell-depleted kidney allografts by the addition of donor strain dendritic cells | Q36346079 | ||
| Dendritic cells are the principal stimulators of the primary mixed leukocyte reaction in mice | Q36347446 | ||
| Protective T cell-independent antiviral antibody responses are dependent on complement | Q36375462 | ||
| Inducible transgenic mice reveal resting dendritic cells as potent inducers of CD8+ T cell tolerance. | Q40647086 | ||
| Diphtheria toxin and related proteins: effect of route of injection on toxicity and the determination of cytotoxicity for various cultured cells | Q42077155 | ||
| Priming of CTLs by lymphocytic choriomeningitis virus depends on dendritic cells | Q43845179 | ||
| Macrophages of the splenic marginal zone are essential for trapping of blood-borne particulate antigen but dispensable for induction of specific T cell responses | Q44521235 | ||
| Complement-mediated follicular localization of T-independent type-2 antigens: the role of marginal zone macrophages revisited | Q44628314 | ||
| Therapy with monoclonal antibodies by elimination of T-cell subsets in vivo | Q59082223 | ||
| Diphtheria toxin receptor–mediated conditional and targeted cell ablation in transgenic mice | Q60017797 | ||
| Marginal metallophilic cells of the mouse spleen identified by a monoclonal antibody | Q69569968 | ||
| Marginal zone macrophages in the mouse spleen identified by a monoclonal antibody. Anatomical correlation with a B cell subpopulation | Q69880909 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 398-404 | |
| P577 | publication date | 2005-09-01 | |
| P1433 | published in | Clinical and Experimental Immunology | Q15716708 |
| P1476 | title | Histological analysis of CD11c-DTR/GFP mice after in vivo depletion of dendritic cells | |
| P478 | volume | 141 |
| Q36512270 | A new view on cutaneous dendritic cell subsets in experimental leishmaniasis |
| Q53450610 | A novel CD11c.DTR transgenic mouse for depletion of dendritic cells reveals their requirement for homeostatic proliferation of natural killer cells. |
| Q37072370 | Ablation of CD11c-positive cells normalizes insulin sensitivity in obese insulin resistant animals |
| Q34501458 | Acquisition and presentation of follicular dendritic cell-bound antigen by lymph node-resident dendritic cells |
| Q36228813 | Adoptive immunotherapy induces CNS dendritic cell recruitment and antigen presentation during clearance of a persistent viral infection |
| Q44532074 | Advantages and limitations of mouse models to deplete dendritic cells |
| Q34749056 | Altered lymph node composition in diphtheria toxin receptor-based mouse models to ablate dendritic cells. |
| Q35745247 | Antibody-enhanced cross-presentation of self antigen breaks T cell tolerance |
| Q64253586 | Are Conventional Type 1 Dendritic Cells Critical for Protective Antitumor Immunity and How? |
| Q28296142 | B cell follicles and antigen encounters of the third kind |
| Q27489852 | Batf3 Deficiency Reveals a Critical Role for CD8 + Dendritic Cells in Cytotoxic T Cell Immunity |
| Q35382523 | CD11c controls herpes simplex virus 1 responses to limit virus replication during primary infection |
| Q36340018 | CD11c(hi) Dendritic Cells Regulate Ly-6C(hi) Monocyte Differentiation to Preserve Immune-privileged CNS in Lethal Neuroinflammation |
| Q55334506 | CD11c+ M1-like macrophages (MΦs) but not CD206+ M2-like MΦ are involved in folliculogenesis in mice ovary. |
| Q33556313 | CD11c+ cells are required to prevent progression from local acute lung injury to multiple organ failure and death |
| Q48424710 | CD11c-positive cells from brain, spleen, lung, and liver exhibit site-specific immune phenotypes and plastically adapt to new environments |
| Q46465306 | CD11c: not merely a murine DC marker, but also a useful vaccination target |
| Q58707686 | CD169 Macrophages Capture and Dendritic Cells Instruct: The Interplay of the Gatekeeper and the General of the Immune System |
| Q35567056 | CD169+ macrophages are sufficient for priming of CTLs with specificities left out by cross-priming dendritic cells |
| Q33760409 | CD8 T cell recall responses are regulated by the tissue tropism of the memory cell and pathogen |
| Q35209897 | CD8α(+) dendritic cells are the critical source of interleukin-12 that controls acute infection by Toxoplasma gondii tachyzoites |
| Q45160346 | CIITA-driven MHC class II expressing tumor cells can efficiently prime naive CD4+ TH cells in vivo and vaccinate the host against parental MHC-II-negative tumor cells |
| Q33246091 | CX3CR1+ interstitial dendritic cells form a contiguous network throughout the entire kidney. |
| Q36178920 | Capture of influenza by medullary dendritic cells via SIGN-R1 is essential for humoral immunity in draining lymph nodes |
| Q34089499 | Central role of conventional dendritic cells in regulation of bone marrow release and survival of neutrophils |
| Q35669056 | Chemokines control naive CD8+ T cell selection of optimal lymph node antigen presenting cells. |
| Q36033541 | Classical dendritic cells as a unique immune cell lineage. |
| Q33927128 | Conventional but not plasmacytoid dendritic cells foster the systemic virus-induced type I IFN response needed for efficient CD8 T cell priming |
| Q35901015 | Critical role of macrophages in the marginal zone in the suppression of immune responses to apoptotic cell-associated antigens |
| Q50259401 | DNGR-1(+) dendritic cells are located in meningeal membrane and choroid plexus of the noninjured brain |
| Q57178027 | DTR-mediated conditional cell ablation-Progress and challenges |
| Q40567280 | Dendritic Cells Are Dispensable for T Cell Priming and Control of Acute Lymphocytic Choriomeningitis Virus Infection. |
| Q38762699 | Dendritic Cells Cross-Present Immunogenic Lentivector-Encoded Antigen from Transduced Cells to Prime Functional T Cell Immunity |
| Q35631723 | Dendritic cell regulation of carbon tetrachloride-induced murine liver fibrosis regression |
| Q38061211 | Dendritic cell subsets in mycobacterial infection: control of bacterial growth and T cell responses |
| Q37067261 | Dendritic cells and chemokine-directed migration in transplantation: where are we headed? |
| Q37834041 | Dendritic cells in alcoholic liver injury and fibrosis |
| Q34443260 | Dendritic cells in lupus are not required for activation of T and B cells but promote their expansion, resulting in tissue damage |
| Q36157184 | Dendritic cells prime natural killer cells by trans-presenting interleukin 15 |
| Q58234954 | Dendritic cells, but not macrophages or B cells, activate major histocompatibility complex class II-restricted CD4+ T cells upon immune-complex uptake in vivo |
| Q36490200 | Depletion of CD11c⁺ cells in the CD11c.DTR model drives expansion of unique CD64⁺ Ly6C⁺ monocytes that are poised to release TNF-α |
| Q35648012 | Depletion of alveolar macrophages in CD11c diphtheria toxin receptor mice produces an inflammatory response |
| Q54982244 | Depletion of dendritic cells in perivascular adipose tissue improves arterial relaxation responses in type 2 diabetic mice. |
| Q38327168 | Determining the role of mononuclear phagocytes in prion neuroinvasion from the skin |
| Q39356533 | Direct in vivo evidence of CD4+ T cell requirement for CTL response and memory via pMHC-I targeting and CD40L signaling. |
| Q37164038 | Direct stimulation of tlr5+/+ CD11c+ cells is necessary for the adjuvant activity of flagellin |
| Q41821083 | Distinct responses of splenic dendritic cell subsets to infection with Listeria monocytogenes: maturation phenotype, level of infection, and T cell priming capacity ex vivo |
| Q37123243 | Divergent role of donor dendritic cells in rejection versus tolerance of allografts |
| Q37631418 | Dmp1 Promoter-Driven Diphtheria Toxin Receptor Transgene Expression Directs Unforeseen Effects in Multiple Tissues |
| Q44043594 | Donor antioxidant strategy prolongs cardiac allograft survival by attenuating tissue dendritic cell immunogenicity(†). |
| Q27312060 | Dynamic imaging of the effector immune response to listeria infection in vivo |
| Q33957860 | Dynamic interplay among monocyte-derived, dermal, and resident lymph node dendritic cells during the generation of vaccine immunity to fungi |
| Q36230126 | Early events regulating immunity and pathogenesis during Listeria monocytogenes infection |
| Q33591529 | Effective collaboration between marginal metallophilic macrophages and CD8+ dendritic cells in the generation of cytotoxic T cells |
| Q39506089 | Engagement of SLAMF2/CD48 prolongs the time frame of effective T cell activation by supporting mature dendritic cell survival |
| Q79760223 | Essential roles of IL-12 and dendritic cells but not IL-23 and macrophages in lupus-like diseases initiated by cell surface HSP gp96 |
| Q37437640 | Exosomal cancer immunotherapy is independent of MHC molecules on exosomes |
| Q38071421 | Experimental models to investigate the function of dendritic cell subsets: challenges and implications |
| Q37323483 | Expression of diabetes-associated genes by dendritic cells and CD4 T cells drives the loss of tolerance in nonobese diabetic mice |
| Q36021817 | Expression of the zinc finger transcription factor zDC (Zbtb46, Btbd4) defines the classical dendritic cell lineage |
| Q38497229 | Fate mapping of dendritic cells |
| Q37282246 | Form follows function: lymphoid tissue microarchitecture in antimicrobial immune defence |
| Q54341612 | Functionally relevant neutrophilia in CD11c diphtheria toxin receptor transgenic mice. |
| Q38985483 | Functions of Murine Dendritic Cells |
| Q38758325 | Generation and labeling of murine bone marrow-derived dendritic cells with Qdot nanocrystals for tracking studies |
| Q37129841 | Geography and plumbing control the T cell response to infection |
| Q47122664 | Harnessing Apoptotic Cell Clearance to Treat Autoimmune Arthritis. |
| Q53301956 | Heterogeneity in a mouse model of histiocytosis: transformation of Langerin+ dendritic cells, macrophages, and precursors. |
| Q61812341 | Human Dendritic Cells: Their Heterogeneity and Clinical Application Potential in Cancer Immunotherapy |
| Q34387183 | IL-10-producing Th1 cells and disease progression are regulated by distinct CD11c⁺ cell populations during visceral leishmaniasis |
| Q42513140 | Impairment of podocyte function by diphtheria toxin--a new reversible proteinuria model in mice |
| Q34545982 | In vivo ablation of CD11c-positive dendritic cells increases susceptibility to herpes simplex virus type 1 infection and diminishes NK and T-cell responses |
| Q27321691 | In vivo approaches reveal a key role for DCs in CD4+ T cell activation and parasite clearance during the acute phase of experimental blood-stage malaria |
| Q46521758 | In vivo dendritic cell depletion reduces breeding efficiency, affecting implantation and early placental development in mice |
| Q36458651 | Infected dendritic cells are sufficient to mediate the adjuvant activity generated by Venezuelan equine encephalitis virus replicon particles |
| Q35679555 | Inflammation switches the differentiation program of Ly6Chi monocytes from antiinflammatory macrophages to inflammatory dendritic cells in the colon. |
| Q36275683 | Inflammatory monocytes activate memory CD8(+) T and innate NK lymphocytes independent of cognate antigen during microbial pathogen invasion |
| Q37777426 | Kidney dendritic cells in acute and chronic renal disease |
| Q34549822 | LTβR signaling in dendritic cells induces a type I IFN response that is required for optimal clonal expansion of CD8+ T cells |
| Q36242772 | Long-Term Depletion of Conventional Dendritic Cells Cannot Be Maintained in an Atherosclerotic Zbtb46-DTR Mouse Model |
| Q37125748 | Lung dendritic cells induce migration of protective T cells to the gastrointestinal tract |
| Q35758610 | Lymph Node Macrophages Restrict Murine Cytomegalovirus Dissemination |
| Q38001317 | Lymph node macrophages |
| Q27348931 | MIF Promotes Classical Activation and Conversion of Inflammatory Ly6C(high) Monocytes into TipDCs during Murine Toxoplasmosis |
| Q34685137 | Macrophage depletion impairs corneal wound healing after autologous transplantation in mice |
| Q38832516 | Macrophage-epithelial interactions in pulmonary alveoli |
| Q27318440 | Macrophages Subvert Adaptive Immunity to Urinary Tract Infection |
| Q38734834 | Macrophages: sentinels and regulators of the immune system |
| Q36502893 | Microbe sampling by mucosal dendritic cells is a discrete, MyD88-independent step in DeltainvG S. Typhimurium colitis |
| Q38214042 | Monocytes and macrophages: developmental pathways and tissue homeostasis |
| Q36228955 | Monocytes give rise to mucosal, but not splenic, conventional dendritic cells |
| Q41676655 | Mouse CD8alpha+ DCs and human BDCA3+ DCs are major producers of IFN-lambda in response to poly IC. |
| Q42562940 | Multiple effects of dendritic cell depletion on murine norovirus infection |
| Q38247413 | Murine and Human Model Systems for the Study of Dendritic Cell Immunobiology |
| Q36229299 | NK cell activation in visceral leishmaniasis requires TLR9, myeloid DCs, and IL-12, but is independent of plasmacytoid DCs. |
| Q42767669 | Organ-dependent in vivo priming of naive CD4+, but not CD8+, T cells by plasmacytoid dendritic cells |
| Q33632038 | Ovarian dendritic cells act as a double-edged pro-ovulatory and anti-inflammatory sword |
| Q51066336 | Ovarian steroid hormone-regulated uterine remodeling occurs independently of macrophages in mice. |
| Q37251088 | Peripheral dendritic cells are essential for both the innate and adaptive antiviral immune responses in the central nervous system |
| Q40277761 | Plasma cell differentiation in T-independent type 2 immune responses is independent of CD11c(high) dendritic cells |
| Q37634704 | Presentation of Autoantigen in Peripheral Lymph Nodes Is Sufficient for Priming Autoreactive CD8+ T Cells. |
| Q40171970 | Priming of CD8+ T cell responses by pathogens typically depends on CD70-mediated interactions with dendritic cells |
| Q37139269 | Probing in vivo dendritic cell functions by conditional cell ablation. |
| Q35009470 | Prolonged antigen presentation following an acute virus infection requires direct and then cross-presentation |
| Q27314913 | Prolonged antigen presentation is required for optimal CD8+ T cell responses against malaria liver stage parasites |
| Q36818027 | Re(de)fining the dendritic cell lineage. |
| Q47109113 | Receptor Activator of NF-κB Orchestrates Activation of Antiviral Memory CD8 T Cells in the Spleen Marginal Zone. |
| Q36667250 | Renal dendritic cells stimulate IL-10 production and attenuate nephrotoxic nephritis |
| Q37333339 | Role of dendritic cells and alveolar macrophages in regulating early host defense against pulmonary infection with Cryptococcus neoformans |
| Q54469377 | Roles of dendritic cells in murine hepatic warm and liver transplantation-induced cold ischemia/reperfusion injury. |
| Q37316503 | SIGNR1-negative red pulp macrophages protect against acute streptococcal sepsis after Leishmania donovani-induced loss of marginal zone macrophages |
| Q42253353 | Salivary gland resident APCs are Flt3L- and CCR2-independent macrophage-like cells incapable of cross-presentation |
| Q37223456 | Selected Toll-like receptor ligands and viruses promote helper-independent cytotoxic T cell priming by upregulating CD40L on dendritic cells |
| Q36609044 | Selective delivery of beta cell antigen to dendritic cells in vivo leads to deletion and tolerance of autoreactive CD8+ T cells in NOD mice. |
| Q30278837 | Sphingosine 1-Phosphate Receptor 3-Deficient Dendritic Cells Modulate Splenic Responses to Ischemia-Reperfusion Injury |
| Q51013895 | Splenic CD8α⁺ dendritic cells undergo rapid programming by cytosolic bacteria and inflammation to induce protective CD8⁺ T-cell memory. |
| Q86635254 | Splenic extrafollicular reactions and BM plasma cells sustain IgM response associated with hypercholesterolemia |
| Q33756646 | Steady state dendritic cells present parenchymal self-antigen and contribute to, but are not essential for, tolerization of naive and Th1 effector CD4 cells |
| Q34334277 | Stimulation of CD8+ T cells following diphtheria toxin-mediated antigen delivery into dendritic cells |
| Q37949247 | Studying the mononuclear phagocyte system in the molecular age. |
| Q41485418 | Subcapsular sinus macrophages prevent CNS invasion on peripheral infection with a neurotropic virus. |
| Q82347082 | Successful Treatment of Acute Lung Injury with Pitavastatin in Septic Mice: Potential Role of Glucocorticoid Receptor Expression in Alveolar Macrophages |
| Q35090589 | THE MULTIFACETED ROLE OF T CELL-MEDIATED IMMUNITY IN PATHOGENESIS AND RESISTANCE TO MYCOPLASMA RESPIRATORY DISEASE |
| Q36835483 | Targeted delivery of lipid antigen to macrophages via the CD169/sialoadhesin endocytic pathway induces robust invariant natural killer T cell activation |
| Q35995130 | The B subunit of Escherichia coli heat-labile toxin alters the development and antigen-presenting capacity of dendritic cells |
| Q33747604 | The Female Lower Genital Tract Is a Privileged Compartment with IL-10 Producing Dendritic Cells and Poor Th1 Immunity following Chlamydia trachomatis Infection |
| Q37082455 | The cell biology of cross-presentation and the role of dendritic cell subsets |
| Q26823101 | The diverse roles of mononuclear phagocytes in prion disease pathogenesis |
| Q82755268 | The elimination of Anaplasma phagocytophilum requires CD4+ T cells, but is independent of Th1 cytokines and a wide spectrum of effector mechanisms |
| Q30514281 | The location of splenic NKT cells favours their rapid activation by blood-borne antigen |
| Q35922950 | The loss of renal dendritic cells and activation of host adaptive immunity are long-term effects of ischemia/reperfusion injury following syngeneic kidney transplantation |
| Q37008376 | The mechanism of splenic invariant NKT cell activation dictates localization in vivo |
| Q38193162 | The role of lymph node sinus macrophages in host defense |
| Q39549081 | The subcellular location of antigen expressed by adenoviral vectors modifies adaptive immunity but not dependency on cross-presenting dendritic cells |
| Q38097109 | Transcriptional and epigenetic networks in the development and maturation of dendritic cells |
| Q37475213 | Trapping of naive lymphocytes triggers rapid growth and remodeling of the fibroblast network in reactive murine lymph nodes |
| Q45324796 | Tumor Necrosis Factor-Mediated Survival of CD169+ Cells Promotes Immune Activation during Vesicular Stomatitis Virus Infection |
| Q51028084 | Two immune arms to stop one gut. |
| Q40706395 | Type I Interferon Released by Myeloid Dendritic Cells Reversibly Impairs Cytomegalovirus Replication by Inhibiting Immediate Early Gene Expression |
| Q36632113 | Use of mouse models to study the mechanisms and consequences of RBC clearance. |
| Q41086977 | Visualization of bone marrow monocyte mobilization using Cx3cr1gfp/+Flt3L-/- reporter mouse by multiphoton intravital microscopy. |
| Q36455286 | XCR1+ dendritic cells promote memory CD8+ T cell recall upon secondary infections with Listeria monocytogenes or certain viruses |
| Q28594572 | Zbtb46 expression distinguishes classical dendritic cells and their committed progenitors from other immune lineages |
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