review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Edward J Pearce | Q91529113 |
P2093 | author name string | Jie Sun | |
Lucas Carvalho | |||
Connie Krawczyk | |||
Colleen Kane | |||
Fraser Marshall | |||
P2860 | cites work | Helminth infections: the great neglected tropical diseases | Q24648324 |
Parasitic worms and inflammatory diseases | Q24669864 | ||
C-type lectin DC-SIGN modulates Toll-like receptor signaling via Raf-1 kinase-dependent acetylation of transcription factor NF-kappaB | Q28115656 | ||
The neglected tropical diseases: the ancient afflictions of stigma and poverty and the prospects for their control and elimination | Q28248682 | ||
Dendritic cell expression of OX40 ligand acts as a costimulatory, not polarizing, signal for optimal Th2 priming and memory induction in vivo | Q28512204 | ||
Notch directly regulates Gata3 expression during T helper 2 cell differentiation | Q28594834 | ||
Direct regulation of Gata3 expression determines the T helper differentiation potential of Notch | Q28594879 | ||
Mycobacteria target DC-SIGN to suppress dendritic cell function | Q28616857 | ||
Dendritic cells: specialized and regulated antigen processing machines | Q29617085 | ||
Recognition of microorganisms and activation of the immune response | Q29617903 | ||
Dendritic cell expression of the Notch ligandjagged2 is not essential for Th2 response inductionin vivo | Q56880711 | ||
Toll-like receptor (TLR)2 and TLR3 sensing is required for dendritic cell activation, but dispensable to control Schistosoma mansoni infection and pathology | Q57158211 | ||
Schistosoma mansoni soluble egg antigens are internalized by human dendritic cells through multiple C-type lectins and suppress TLR-induced dendritic cell activation | Q57261983 | ||
Double-stranded RNAs from the Helminth ParasiteSchistosomaActivate TLR3 in Dendritic Cells | Q57518104 | ||
Selective maturation of dendritic cells byNippostrongylus brasiliensis-secreted proteins drives Th2 immune responses | Q58843220 | ||
Epithelial-cell-intrinsic IKK-β expression regulates intestinal immune homeostasis | Q59053989 | ||
Essential role for TLR4 and MyD88 in the development of chronic intestinal nematode infection | Q59549092 | ||
Induction of Th2 responses and IgE is largely due to carbohydrates functioning as adjuvants on Schistosoma mansoni egg antigens | Q73242473 | ||
Single cell analysis reveals that IL-4 receptor/Stat6 signaling is not required for the in vivo or in vitro development of CD4+ lymphocytes with a Th2 cytokine profile | Q73520544 | ||
CD8- dendritic cell activation status plays an integral role in influencing Th2 response development | Q74321435 | ||
Cutting edge: Th2 response induction by dendritic cells: a role for CD40 | Q77452185 | ||
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 | ||
Toll-like receptor 4 (TLR4) is required for protective immunity to larval Strongyloides stercoralis in mice | Q79464597 | ||
TLR signaling | Q79715393 | ||
Parasite-induced Th2 polarization is associated with down-regulated dendritic cell responsiveness to Th1 stimuli and a transient delay in T lymphocyte cycling | Q80418667 | ||
Impaired T helper 2 response to aeroallergen in helminth-infected patients with asthma | Q80895989 | ||
Helminth antigens modulate TLR-initiated dendritic cell activation | Q81111451 | ||
Dendritic cell-intrinsic expression of NF-kappa B1 is required to promote optimal Th2 cell differentiation | Q81767249 | ||
Induction of enhanced immunity to intestinal nematodes using IL-9-producing dendritic cells | Q82459181 | ||
Inhibitors of gamma-secretase block in vivo and in vitro T helper type 1 polarization by preventing Notch upregulation of Tbx21 | Q95814547 | ||
DC-SIGN mediates binding of dendritic cells to authentic pseudo-LewisY glycolipids of Schistosoma mansoni cercariae, the first parasite-specific ligand of DC-SIGN. | Q33223117 | ||
Proteomic profiling reveals that Th2-inducing dendritic cells stimulated with helminth antigens have a 'limited maturation' phenotype | Q33322908 | ||
The major glycoprotein allergen from Arachis hypogaea, Ara h 1, is a ligand of dendritic cell-specific ICAM-grabbing nonintegrin and acts as a Th2 adjuvant in vitro | Q34563241 | ||
Control of adaptive immune responses by Toll-like receptors. | Q34612562 | ||
Novel effector molecules in type 2 inflammation: lessons drawn from helminth infection and allergy | Q35607506 | ||
Immune biasing by helminth glycans. | Q35608898 | ||
Fibrotic disease and the T(H)1/T(H)2 paradigm | Q35852270 | ||
Both free-living and parasitic nematodes induce a characteristic Th2 response that is dependent on the presence of intact glycans | Q36228597 | ||
Regulatory T cells induced by parasites and the modulation of allergic responses | Q36279713 | ||
Lipopolysaccharide-enhanced, toll-like receptor 4-dependent T helper cell type 2 responses to inhaled antigen | Q36376615 | ||
Notch signaling is an important regulator of type 2 immunity. | Q36403646 | ||
Suppression of allergic airway inflammation by helminth-induced regulatory T cells | Q36403704 | ||
IL-23 and IL-17 in tuberculosis | Q37064619 | ||
Specifying helper T cell fates during immunity | Q37114508 | ||
Dendritic cells and C-type lectin receptors: coupling innate to adaptive immune responses | Q37235037 | ||
The dendritic cell-specific C-type lectin DC-SIGN is a receptor for Schistosoma mansoni egg antigens and recognizes the glycan antigen Lewis x. | Q38356935 | ||
Modulation of the allergic reactivity of slum children by helminthic infection | Q39041063 | ||
Protective effect of Schistosoma mansoni infection on allergic airway inflammation depends on the intensity and chronicity of infection | Q40184958 | ||
A helminth glycan induces APC maturation via alternative NF-kappa B activation independent of I kappa B alpha degradation | Q40388500 | ||
A novel host-parasite lipid cross-talk. Schistosomal lyso-phosphatidylserine activates toll-like receptor 2 and affects immune polarization | Q40700194 | ||
Th2 differentiation is unaffected by Jagged2 expression on dendritic cells | Q41875479 | ||
Suppression of Th2 cell development by Notch ligands Delta1 and Delta4 | Q41962999 | ||
Unique gene expression profiles of human macrophages and dendritic cells to phylogenetically distinct parasites | Q42595867 | ||
Echinococcus granulosus antigen B impairs human dendritic cell differentiation and polarizes immature dendritic cell maturation towards a Th2 cell response | Q42800205 | ||
Carbohydrate components of Taenia crassiceps metacestodes display Th2-adjuvant and anti-inflammatory properties when co-injected with bystander antigen | Q43480723 | ||
Schistosome N-glycans containing core alpha 3-fucose and core beta 2-xylose epitopes are strong inducers of Th2 responses in mice | Q43525129 | ||
Lacto-N-fucopentaose III found on Schistosoma mansoni egg antigens functions as adjuvant for proteins by inducing Th2-type response | Q43648201 | ||
Impairment of dendritic cell function by excretory-secretory products: a potential mechanism for nematode-induced immunosuppression | Q44203897 | ||
Immunomodulation via novel use of TLR4 by the filarial nematode phosphorylcholine-containing secreted product, ES-62. | Q44268237 | ||
Cutting edge: carbohydrate profiling identifies new pathogens that interact with dendritic cell-specific ICAM-3-grabbing nonintegrin on dendritic cells | Q44306886 | ||
Schistosoma mansoni antigens modulate the activity of the innate immune response and prevent onset of type 1 diabetes | Q44474619 | ||
In the absence of IL-12, CD4(+) T cell responses to intracellular pathogens fail to default to a Th2 pattern and are host protective in an IL-10(-/-) setting | Q45069275 | ||
Full development of Th2 immunity requires both innate and adaptive sources of CD154. | Q45770822 | ||
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 | ||
Maturation of dendritic cell 2 phenotype by a helminth glycan uses a Toll-like receptor 4-dependent mechanism | Q47368677 | ||
Delta1-Notch3 interactions bias the functional differentiation of activated CD4+ T cells | Q47438852 | ||
Instruction of distinct CD4 T helper cell fates by different notch ligands on antigen-presenting cells | Q47619638 | ||
A Toll-like receptor 2 ligand stimulates Th2 responses in vivo, via induction of extracellular signal-regulated kinase mitogen-activated protein kinase and c-Fos in dendritic cells | Q47810460 | ||
Upregulation of costimulatory molecules induced by lipopolysaccharide and double-stranded RNA occurs by Trif-dependent and Trif-independent pathways | Q48219736 | ||
Proteins secreted by the parasitic nematode Nippostrongylus brasiliensis act as adjuvants for Th2 responses. | Q52924766 | ||
Cutting edge: different Toll-like receptor agonists instruct dendritic cells to induce distinct Th responses via differential modulation of extracellular signal-regulated kinase-mitogen-activated protein kinase and c-Fos. | Q52956682 | ||
Lack of antigen-specific Th1 response alters granuloma formation and composition in Schistosoma mansoni-infected MyD88-/- mice. | Q52994753 | ||
TLR ligands can activate dendritic cells to provide a MyD88-dependent negative signal for Th2 cell development. | Q53875132 | ||
Phosphorylcholine mimics the effects of ES-62 on macrophages and dendritic cells. | Q54559083 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | dendritic cell | Q506253 |
hygiene | Q162297 | ||
cell function | Q95674809 | ||
P304 | page(s) | 28-34 | |
P577 | publication date | 2009-01-01 | |
P1433 | published in | Immunology | Q15754984 |
P1476 | title | Review series on helminths, immune modulation and the hygiene hypothesis: mechanisms underlying helminth modulation of dendritic cell function | |
P478 | volume | 126 |
Q37517135 | A new biophysical metric for interrogating the information content in human genome sequence variation: Proof of concept |
Q37622742 | Age, but not anthelmintic treatment, is associated with urinary neopterin levels in semi-free ranging Barbary macaques |
Q43837820 | Antiparasitic antibodies occur with similar frequency in patients with clinically established multiple sclerosis with or without oligoclonal bands in the cerebrospinal fluid |
Q47599551 | Ascaris Suum Infection Downregulates Inflammatory Pathways in the Pig Intestine In Vivo and in Human Dendritic Cells In Vitro |
Q33647423 | CD209a expression on dendritic cells is critical for the development of pathogenic Th17 cell responses in murine schistosomiasis |
Q33631398 | Chronic helminth infections protect against allergic diseases by active regulatory processes |
Q39140492 | Co-operative suppression of inflammatory responses in human dendritic cells by plant proanthocyanidins and products from the parasitic nematode Trichuris suis |
Q35272104 | Comparative community-level associations of helminth infections and microparasite shedding in wild long-tailed macaques in Bali, Indonesia |
Q91636313 | Cytokines and beyond: Regulation of innate immune responses during helminth infection |
Q41285571 | Dendritic cell expression of the C-type lectin receptor CD209a: A novel innate parasite-sensing mechanism inducing Th17 cells that drive severe immunopathology in murine schistosome infection |
Q34278895 | Dendritic cell profile induced by Schistosoma mansoni antigen in cutaneous leishmaniasis patients |
Q38944438 | Dendritic cells and parasites: from recognition and activation to immune response instruction |
Q37708039 | Dendritic cells in the gut: interaction with intestinal helminths. |
Q36368300 | Dendritic cells provide a therapeutic target for synthetic small molecule analogues of the parasitic worm product, ES-62. |
Q34023491 | Enhanced pro-inflammatory cytokine responses following Toll-like-receptor ligation in Schistosoma haematobium-infected schoolchildren from rural Gabon |
Q42639995 | Epidermal Growth Factor Receptor Expression Licenses Type-2 Helper T Cells to Function in a T Cell Receptor-Independent Fashion |
Q35062308 | Expression of TNF-α and IL-1β in splenic dendritic cells and their serum levels in mouse sparganosis |
Q34653945 | Fasciola hepatica Kunitz type molecule decreases dendritic cell activation and their ability to induce inflammatory responses |
Q41467477 | Frequency of Blood-tissue Parasitic Infections in Patients with Multiple Sclerosis, as Compared to their Family Members |
Q33565632 | Functional impairment of human myeloid dendritic cells during Schistosoma haematobium infection |
Q29392240 | HELMINTHS AND TB IN POLYNESIA: THE IMPLICATIONS FOR HEALTH PRACTICE |
Q41890686 | Harnessing the helminth secretome for therapeutic immunomodulators. |
Q34169673 | Heligmosomoides polygyrus infection can inhibit colitis through direct interaction with innate immunity. |
Q33661711 | Helminth cysteine proteases inhibit TRIF-dependent activation of macrophages via degradation of TLR3. |
Q26829956 | Helminth infections and host immune regulation |
Q37708009 | Helminth-derived immunomodulators: can understanding the worm produce the pill? |
Q34030215 | Helminth-host immunological interactions: prevention and control of immune-mediated diseases |
Q37734329 | Helminths and dendritic cells: sensing and regulating via pattern recognition receptors, Th2 and Treg responses |
Q36567307 | Helminths: Immunoregulation and Inflammatory Diseases-Which Side Are Trichinella spp. and Toxocara spp. on? |
Q36260867 | Identification of three immunodominant motifs with atypical isotype profile scattered over the Onchocerca volvulus proteome. |
Q84596983 | Infection of non-encapsulated species of Trichinella ameliorates experimental autoimmune encephalomyelitis involving suppression of Th17 and Th1 response |
Q44942699 | Malaria vaccine efficacy: overcoming the helminth hurdle |
Q35613012 | Micrometer-sized titanium particles can induce potent Th2-type responses through TLR4-independent pathways |
Q37702795 | Modulation of dendritic cell responses by parasites: a common strategy to survive |
Q27021418 | Modulation of specific and allergy-related immune responses by helminths |
Q39498673 | Recombinant Sj16 from Schistosoma japonicum contains a functional N-terminal nuclear localization signal necessary for nuclear translocation in dendritic cells and interleukin-10 production |
Q57704150 | Review series on helminths, immune modulation and the hygiene hypothesis: nematode coevolution with adaptive immunity, regulatory networks and the growth of inflammatory diseases |
Q30525273 | Schistosome-derived omega-1 drives Th2 polarization by suppressing protein synthesis following internalization by the mannose receptor |
Q35833767 | Serologic evidence that ascaris and toxoplasma infections impact inflammatory responses to Helicobacter pylori in Colombians. |
Q36045658 | Soil-transmitted helminth infections and leprosy: a cross-sectional study of the association between two major neglected tropical diseases in Indonesia |
Q33581038 | Taenia crassiceps infection attenuates multiple low-dose streptozotocin-induced diabetes |
Q34072227 | The absence of MyD88 has no effect on the induction of alternatively activated macrophage during Fasciola hepatica infection |
Q40337935 | The dynamic changes of CD3e-CD11c+ dendritic cells in spleens and bone marrow of mice infected with Schistosoma japonicum |
Q84648148 | The response of monocyte derived dendritic cells following exposure to a nematode larval carbohydrate antigen |
Q99577395 | Trichinella spiralis: inflammation modulator |
Q37213084 | Type 2 immunity and wound healing: evolutionary refinement of adaptive immunity by helminths. |
Q91644380 | Urinary suPAR: a non-invasive biomarker of infection and tissue inflammation for use in studies of large free-ranging mammals |
Q83192786 | WITHDRAWN: MyD88 is required for the recruitment of eosinophils and neutrophils but dispensable for host protective immune responses during Fasciola hepatica infection |
Q39511965 | Worming our way closer to the clinic. |
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