| scholarly article | Q13442814 |
| P50 | author | Lauren M Webb | Q56875600 |
| Georgia Perona-Wright | Q78470415 | ||
| Andrew S MacDonald | Q80897528 | ||
| P2093 | author name string | Richard K Grencis | |
| Rachel J Lundie | |||
| Stephen J Jenkins | |||
| P2860 | cites work | Novel p19 protein engages IL-12p40 to form a cytokine, IL-23, with biological activities similar as well as distinct from IL-12 | Q24290619 |
| Interleukin-10 and the interleukin-10 receptor | Q24290912 | ||
| Nuocytes represent a new innate effector leukocyte that mediates type-2 immunity | Q24630261 | ||
| IL25 elicits a multipotent progenitor cell population that promotes T(H)2 cytokine responses | Q24630608 | ||
| Helminth infections: the great neglected tropical diseases | Q24648324 | ||
| Specific microbiota direct the differentiation of IL-17-producing T-helper cells in the mucosa of the small intestine | Q24648636 | ||
| Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells | Q27860460 | ||
| Induction of intestinal Th17 cells by segmented filamentous bacteria | Q28131638 | ||
| Transforming growth factor-beta induces development of the T(H)17 lineage | Q28237370 | ||
| TGFbeta in the context of an inflammatory cytokine milieu supports de novo differentiation of IL-17-producing T cells | Q28296956 | ||
| Dendritic cell expression of OX40 ligand acts as a costimulatory, not polarizing, signal for optimal Th2 priming and memory induction in vivo | Q28512204 | ||
| CD25+CD4+ cells contribute to Th2 polarization during helminth infection by suppressing Th1 response development | Q28594824 | ||
| A distinct lineage of CD4 T cells regulates tissue inflammation by producing interleukin 17 | Q29547855 | ||
| Interleukin 17-producing CD4+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages | Q29547871 | ||
| Interleukin-23 rather than interleukin-12 is the critical cytokine for autoimmune inflammation of the brain | Q29614225 | ||
| IL-6 programs T(H)-17 cell differentiation by promoting sequential engagement of the IL-21 and IL-23 pathways | Q29614839 | ||
| An advanced culture method for generating large quantities of highly pure dendritic cells from mouse bone marrow | Q29615498 | ||
| Essential autocrine regulation by IL-21 in the generation of inflammatory T cells | Q29616147 | ||
| IL-21 initiates an alternative pathway to induce proinflammatory T(H)17 cells | Q29616148 | ||
| Innate production of T(H)2 cytokines by adipose tissue-associated c-Kit(+)Sca-1(+) lymphoid cells | Q29619771 | ||
| Quantification of clinical morbidity associated with schistosome infection in sub-Saharan Africa | Q29620602 | ||
| Exploitation of the intestinal microflora by the parasitic nematode Trichuris muris | Q30524457 | ||
| Schistosoma mansoni: genetic restriction and cytokine profile of the CD4 + T helper cell response to dominant epitope peptide of major egg antigen Sm-p40. | Q32037356 | ||
| Programming dendritic cells to induce T(H)2 and tolerogenic responses | Q33349475 | ||
| An IL-13 inhibitor blocks the development of hepatic fibrosis during a T-helper type 2-dominated inflammatory response | Q33853821 | ||
| Sustained signaling by canonical helper T cell cytokines throughout the reactive lymph node. | Q33957034 | ||
| Chronic mucocutaneous candidiasis in humans with inborn errors of interleukin-17 immunity | Q34025875 | ||
| Hepatic schistosomiasis. | Q34033201 | ||
| CD11c depletion severely disrupts Th2 induction and development in vivo | Q34161501 | ||
| Mast cell-derived interleukin 10 limits skin pathology in contact dermatitis and chronic irradiation with ultraviolet B. | Q34674471 | ||
| Coactivation of Syk kinase and MyD88 adaptor protein pathways by bacteria promotes regulatory properties of neutrophils. | Q54709609 | ||
| Dendritic cell expression of the Notch ligandjagged2 is not essential for Th2 response inductionin vivo | Q56880711 | ||
| IL-10 regulates liver pathology in acute murine Schistosomiasis mansoni but is not required for immune down-modulation of chronic disease | Q57339957 | ||
| Selective maturation of dendritic cells byNippostrongylus brasiliensis-secreted proteins drives Th2 immune responses | Q58843220 | ||
| IL-10 permits transient activation of dendritic cells to tolerize T cells and protect from central nervous system autoimmune disease | Q61971077 | ||
| Kinetics of egg production and egg excretion by Schistosoma mansoni and S. japonicum in mice infected with a single pair of worms | Q72339097 | ||
| Role of IL-6 in directing the initial immune response to schistosome eggs | Q73458414 | ||
| IL-4 protects against TNF-alpha-mediated cachexia and death during acute schistosomiasis | Q73500970 | ||
| IL-10 and the dangers of immune polarization: excessive type 1 and type 2 cytokine responses induce distinct forms of lethal immunopathology in murine schistosomiasis | Q73869153 | ||
| CD8- dendritic cell activation status plays an integral role in influencing Th2 response development | Q74321435 | ||
| Cutting edge: polarized Th cell response induction by transferred antigen-pulsed dendritic cells is dependent on IL-4 or IL-12 production by recipient cells | Q77800961 | ||
| Suppression of immune induction of collagen-induced arthritis in IL-17-deficient mice | Q79317500 | ||
| IL-23 is required for the development of severe egg-induced immunopathology in schistosomiasis and for lesional expression of IL-17 | Q80633636 | ||
| Helminth antigens modulate TLR-initiated dendritic cell activation | Q81111451 | ||
| Role of gut commensal microflora in the development of experimental autoimmune encephalomyelitis | Q84749218 | ||
| TGF-beta and IL-6 drive the production of IL-17 and IL-10 by T cells and restrain T(H)-17 cell-mediated pathology | Q34712326 | ||
| The immunobiology of schistosomiasis | Q34718128 | ||
| Dendritic cells at the host-pathogen interface. | Q34765258 | ||
| Interleukin-10 signaling in regulatory T cells is required for suppression of Th17 cell-mediated inflammation | Q34936014 | ||
| Inhibition of interleukin-17 prevents the development of arthritis in vaccinated mice challenged with Borrelia burgdorferi | Q35011581 | ||
| Regulation of innate and adaptive immunity by the commensal microbiota | Q35028444 | ||
| Enhanced protection to Mycobacterium tuberculosis infection in IL-10-deficient mice is accompanied by early and enhanced Th1 responses in the lung | Q36043946 | ||
| Downregulation of Th1 cytokine production accompanies induction of Th2 responses by a parasitic helminth, Schistosoma mansoni | Q36229789 | ||
| Dendritic cell activation and function in response to Schistosoma mansoni. | Q36476868 | ||
| Protective immune mechanisms in helminth infection | Q36481763 | ||
| In vivo equilibrium of proinflammatory IL-17+ and regulatory IL-10+ Foxp3+ RORgamma t+ T cells | Q36699777 | ||
| The pathogenic Th17 cell response to major schistosome egg antigen is sequentially dependent on IL-23 and IL-1β | Q36843026 | ||
| IL-6 promotes NK cell production of IL-17 during toxoplasmosis | Q37132980 | ||
| IL-10: the master regulator of immunity to infection | Q37143028 | ||
| Dendritic cell IL-23 and IL-1 production in response to schistosome eggs induces Th17 cells in a mouse strain prone to severe immunopathology | Q37145507 | ||
| IL-23 promotes maintenance but not commitment to the Th17 lineage | Q37183888 | ||
| Critical regulation of early Th17 cell differentiation by interleukin-1 signaling | Q37250727 | ||
| IL-10 deficiency unleashes an influenza-specific Th17 response and enhances survival against high-dose challenge | Q37297787 | ||
| Gut commensal bacteria direct a protective immune response against Toxoplasma gondii. | Q37353312 | ||
| Systemic but not local infections elicit immunosuppressive IL-10 production by natural killer cells | Q37484974 | ||
| Current concepts of the intestinal microbiota and the pathogenesis of infection | Q37838789 | ||
| Up-regulation of IL-17 is associated with bioactive IL-8 expression in Helicobacter pylori-infected human gastric mucosa | Q40846579 | ||
| Immunologic basis of disease and disease regulation in schistosomiasis. | Q41431678 | ||
| Posttranscriptional regulation of II10 gene expression allows natural killer cells to express immunoregulatory function. | Q42074930 | ||
| Th17 cells express interleukin-10 receptor and are controlled by Foxp3⁻ and Foxp3+ regulatory CD4+ T cells in an interleukin-10-dependent manner | Q42107193 | ||
| A crucial role for interleukin (IL)-1 in the induction of IL-17-producing T cells that mediate autoimmune encephalomyelitis. | Q42767100 | ||
| Interleukin-1 and IL-23 induce innate IL-17 production from gammadelta T cells, amplifying Th17 responses and autoimmunity. | Q43291517 | ||
| Distinct sources and targets of IL-10 during dendritic cell-driven Th1 and Th2 responses in vivo. | Q43420803 | ||
| A pivotal role for CD40-mediated IL-6 production by dendritic cells during IL-17 induction in vivo | Q43629857 | ||
| Schistosome infection of transgenic mice defines distinct and contrasting pathogenic roles for IL-4 and IL-13: IL-13 is a profibrotic agent | Q44826352 | ||
| Variation of hepatic fibrosis and granuloma size among mouse strains infected with Schistosoma mansoni | Q44970501 | ||
| Full development of Th2 immunity requires both innate and adaptive sources of CD154. | Q45770822 | ||
| Requirement of interleukin-17A for systemic anti-Candida albicans host defense in mice | Q45876568 | ||
| Skin and peripheral lymph node invariant NKT cells are mainly retinoic acid receptor-related orphan receptor (gamma)t+ and respond preferentially under inflammatory conditions. | Q45935220 | ||
| T cells use two directionally distinct pathways for cytokine secretion. | Q45948164 | ||
| Alternative macrophage activation is essential for survival during schistosomiasis and downmodulates T helper 1 responses and immunopathology. | Q46899191 | ||
| Cutting edge: dendritic cells copulsed with microbial and helminth antigens undergo modified maturation, segregate the antigens to distinct intracellular compartments, and concurrently induce microbe-specific Th1 and helminth-specific Th2 responses | Q47218007 | ||
| Transcription of the IL10 gene reveals allele-specific regulation at the mRNA level | Q47334707 | ||
| IL-10 is crucial for the transition from acute to chronic disease state during infection of mice with Schistosoma mansoni | Q47997804 | ||
| The pathogenesis of schistosomiasis is controlled by cooperating IL-10-producing innate effector and regulatory T cells. | Q51024754 | ||
| Severe CD4 T cell-mediated immunopathology in murine schistosomiasis is dependent on IL-12p40 and correlates with high levels of IL-17. | Q51989028 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | dendritic cell | Q506253 |
| P304 | page(s) | 2350-2358 | |
| P577 | publication date | 2012-01-27 | |
| P1433 | published in | Journal of Immunology | Q3521441 |
| P1476 | title | Concurrent bacterial stimulation alters the function of helminth-activated dendritic cells, resulting in IL-17 induction | |
| P478 | volume | 188 |
| Q36755254 | A central role for hepatic conventional dendritic cells in supporting Th2 responses during helminth infection |
| Q35549617 | A dominant role for the methyl-CpG-binding protein Mbd2 in controlling Th2 induction by dendritic cells |
| Q40653441 | Ellagic acid reduces murine schistosomiasis mansoni immunopathology via up-regulation of IL-10 and down-modulation of pro-inflammatory cytokines production. |
| Q34393281 | Increased IL-17, a Pathogenic Link between Hepatosplenic Schistosomiasis and Amyotrophic Lateral Sclerosis: A Hypothesis |
| Q36949600 | Induction and regulation of pathogenic Th17 cell responses in schistosomiasis |
| Q35429782 | Not all parasites are protective |
| Q36389513 | Persistent loss of IL-27 responsiveness in CD8+ memory T cells abrogates IL-10 expression in a recall response |
| Q27005837 | Protection and pathology during parasite infection: IL-10 strikes the balance |
| Q27329934 | S. mansoni bolsters anti-viral immunity in the murine respiratory tract |
| Q61805993 | The C-type Lectin Receptor-Driven, Th17 Cell-Mediated Severe Pathology in Schistosomiasis: Not All Immune Responses to Helminth Parasites Are Th2 Dominated |
| Q38674915 | Type I interferon is required for T helper (Th) 2 induction by dendritic cells |
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