| scholarly article | Q13442814 |
| P356 | DOI | 10.1084/JEM.20052448 |
| P8608 | Fatcat ID | release_2hj65s7ka5e7bbcjk7xkbp3qpq |
| P932 | PMC publication ID | 2118302 |
| P698 | PubMed publication ID | 16702603 |
| P5875 | ResearchGate publication ID | 7078219 |
| P2093 | author name string | David Voehringer | |
| Tiffany A Reese | |||
| Richard M Locksley | |||
| Xiaozhu Huang | |||
| Kanade Shinkai | |||
| P2860 | cites work | New fluorescent dyes for lymphocyte migration studies. Analysis by flow cytometry and fluorescence microscopy | Q28254277 |
| IL-4 acts as a myoblast recruitment factor during mammalian muscle growth | Q28505736 | ||
| Peripheral CD4 T cells rapidly accumulate at the host: parasite interface during an inflammatory Th2 memory response. | Q31041185 | ||
| IL-4 production by human basophils found in the lung following segmental allergen challenge | Q31928083 | ||
| Do eosinophils have a role in the killing of helminth parasites? | Q33846464 | ||
| Trapping and immobilization of Nippostrongylus brasiliensis larvae at the site of inoculation in primary infections of interleukin-5 transgenic mice. | Q34002145 | ||
| The instructive role of innate immunity in the acquired immune response | Q34375203 | ||
| Mice lacking all conventional MHC class II genes | Q35620743 | ||
| Interleukin-4- and interleukin-13-mediated host protection against intestinal nematode parasites | Q35884218 | ||
| IL-2 and autocrine IL-4 drive the in vivo development of antigen-specific Th2 T cells elicited by nematode parasites | Q35995946 | ||
| Complement-mediated killing of schistosomula of Schistosoma mansoni by rat eosinophils in vitro | Q36339847 | ||
| Targeted deletion of a high-affinity GATA-binding site in the GATA-1 promoter leads to selective loss of the eosinophil lineage in vivo | Q36369717 | ||
| Basophils produce IL-4 and accumulate in tissues after infection with a Th2-inducing parasite | Q36399604 | ||
| Basophils initiate IL-4 production during a memory T-dependent response | Q36403845 | ||
| Requirements for allergen-induced airway hyperreactivity in T and B cell-deficient mice | Q36438370 | ||
| An interleukin 4 (IL-4)-independent pathway for CD4+ T cell IL-4 production is revealed in IL-4 receptor-deficient mice. | Q36596732 | ||
| Accumulation of Peribronchial Mast Cells in a Mouse Model of Ovalbumin Allergen Induced Chronic Airway Inflammation: Modulation by Immunostimulatory DNA Sequences | Q38348928 | ||
| The role of L3T4+ and Lyt-2+ T cells in the IgE response and immunity to Nippostrongylus brasiliensis | Q39287203 | ||
| IL-4 treatment can cure established gastrointestinal nematode infections in immunocompetent and immunodeficient mice. | Q39379202 | ||
| Stat6 regulation of in vivo IL-4 responses | Q39529330 | ||
| Cutting edge: IL-4 receptor expression by non-bone marrow-derived cells is required to expel gastrointestinal nematode parasites. | Q39586138 | ||
| T cells are required for host protection against Brugia malayi but need not produce or respond to interleukin-4. | Q39755218 | ||
| Expulsion of Nippostrongylus brasiliensis from mice lacking antibody production potential | Q40788631 | ||
| Requirement for IL-13 independently of IL-4 in experimental asthma | Q41881960 | ||
| Simultaneous disruption of interleukin (IL)-4 and IL-13 defines individual roles in T helper cell type 2-mediated responses | Q42944667 | ||
| Multiple pathways for the initiation of T helper 2 (Th2) responses | Q42947603 | ||
| Induction by antigen of intrathymic apoptosis of CD4+CD8+TCRlo thymocytes in vivo | Q43687301 | ||
| Th2 activities induced during virgin T cell priming in the absence of IL-4, IL-13, and B cells. | Q44129501 | ||
| Mutations in T-cell antigen receptor genes alpha and beta block thymocyte development at different stages | Q44151375 | ||
| Parasite antigen-driven basophils are a major source of IL-4 in human filarial infections | Q44757017 | ||
| Analysis of type 2 immunity in vivo with a bicistronic IL-4 reporter | Q46062240 | ||
| Activation of the integrated stress response during T helper cell differentiation | Q46290572 | ||
| Direct effects of interleukin-13 on epithelial cells cause airway hyperreactivity and mucus overproduction in asthma | Q46413344 | ||
| Type 2 immunity reflects orchestrated recruitment of cells committed to IL-4 production | Q46528021 | ||
| Interleukin-13 in asthma pathogenesis | Q47894967 | ||
| Differences between IL-4R alpha-deficient and IL-4-deficient mice reveal a role for IL-13 in the regulation of Th2 responses | Q47946081 | ||
| Mast cells, basophils, and eosinophils acquire constitutive IL-4 and IL-13 transcripts during lineage differentiation that are sufficient for rapid cytokine production. | Q50781666 | ||
| Mast-cell infiltration of airway smooth muscle in asthma. | Q51715332 | ||
| Stat6 is required for mediating responses to IL-4 and for development of Th2 cells. | Q55066450 | ||
| Interleukin-5 deficient mice exhibit impaired host defence against challenge Trichinella spiralis infections | Q58061417 | ||
| Constitutive production of IL-4 and IL-10 and stimulated production of IL-8 by normal peripheral blood eosinophils | Q71120610 | ||
| Kinetics of expulsion of the nematode, Nippostrongylus brasiliensis, in mast-cell deficient W/WV mice | Q71243604 | ||
| Enhanced helminthotoxic capacity of eosinophils from patients with eosinophilia | Q71338652 | ||
| Secretion of IL-4 from human basophils. The relationship between IL-4 mRNA and protein in resting and stimulated basophils | Q72332704 | ||
| Expression of IL-5 in thymocytes/T cells leads to the development of a massive eosinophilia, extramedullary eosinophilopoiesis, and unique histopathologies | Q73025983 | ||
| Conventional, naive CD4+ T cells provide an initial source of IL-4 during Th2 differentiation | Q73084699 | ||
| 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 | ||
| Identification of basophils by immunohistochemistry in the airways of post-mortem cases of fatal asthma | Q73708145 | ||
| Protective roles of eosinophils in Nippostrongylus brasiliensis infection | Q73863391 | ||
| Immunohistochemical detection of human basophils in postmortem cases of fatal asthma | Q74595730 | ||
| Accelerated intestinal epithelial cell turnover: a new mechanism of parasite expulsion | Q81810291 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1435-1446 | |
| P577 | publication date | 2006-05-15 | |
| P1433 | published in | Journal of Experimental Medicine | Q3186912 |
| P1476 | title | Type 2 immunity is controlled by IL-4/IL-13 expression in hematopoietic non-eosinophil cells of the innate immune system | |
| P478 | volume | 203 |
| Q34500826 | A new strategy based on SmRho protein loaded chitosan nanoparticles as a candidate oral vaccine against schistosomiasis |
| Q49884244 | A sticky end for gastrointestinal helminths; the role of the mucus barrier. |
| Q34022774 | Aberrant production of IL-13 by T cells promotes exocrinopathy in Id3 knockout mice |
| Q34680834 | Accumulation of eosinophils in intestine-draining mesenteric lymph nodes occurs after Trichuris muris infection |
| Q42576928 | Activation of group 2 innate lymphoid cells: a new role for cysteinyl leukotrienes |
| Q47923410 | Administration of naloxone in combination with recombinant Plasmodium vivax AMA-1 in BALB/c mice induces mixed Th1/Th2 immune responses |
| Q36509887 | Allergic pulmonary inflammation in mice is dependent on eosinophil-induced recruitment of effector T cells |
| Q55312036 | Allocation of Interferon Gamma mRNA Positive Cells in Caecum Hallmarks a Protective Trait Against Histomonosis. |
| Q26823579 | Alternatively activated macrophages and airway disease |
| Q35742768 | An essential role for TH2-type responses in limiting acute tissue damage during experimental helminth infection |
| Q26865224 | Are basophils important mediators for helminth-induced Th2 immune responses? A debate |
| Q37196881 | Association of IL-4-590 C>T and IL-13-1112 C>T gene polymorphisms with the susceptibility to type 2 diabetes mellitus. |
| Q47612960 | Association of interleukin 4 (-590 T/C) and interleukin 4 receptor (Q551R A/G) gene polymorphisms with acne vulgaris. |
| Q33868549 | Attenuation of chronic pulmonary inflammation in A2B adenosine receptor knockout mice |
| Q36370697 | Basophils are the major producers of IL-4 during primary helminth infection |
| Q38071153 | Basophils as Key Regulators of Allergic Inflammation and Th2-type Immunity |
| Q34949249 | Basophils beyond effector cells of allergic inflammation |
| Q24613860 | Basophils function as antigen-presenting cells for an allergen-induced T helper type 2 response |
| Q37866220 | Basophils: important emerging players in allergic and anti-parasite responses. |
| Q80733934 | Basophils: in the spotlight at last |
| Q24655812 | Chitin induces accumulation in tissue of innate immune cells associated with allergy |
| Q58703285 | Concerted IL-25R and IL-4Rα signaling drive innate type 2 effector immunity for optimal helminth expulsion |
| Q41692436 | Conditional IL-4/IL-13-deficient mice reveal a critical role of innate immune cells for protective immunity against gastrointestinal helminths. |
| Q33949038 | Control of T helper 2 responses by transcription factor IRF4-dependent dendritic cells |
| Q33839830 | Critical requirement for the Wiskott-Aldrich syndrome protein in Th2 effector function |
| Q39901791 | Cutting edge: basophils are transiently recruited into the draining lymph nodes during helminth infection via IL-3, but infection-induced Th2 immunity can develop without basophil lymph node recruitment or IL-3. |
| Q36669815 | Cytokine expression by invariant natural killer T cells is tightly regulated throughout development and settings of type-2 inflammation. |
| Q40517997 | Depletion of major pathogenic cells in asthma by targeting CRTh2. |
| Q26862916 | Development and function of group 2 innate lymphoid cells |
| Q38091898 | Development of CD4 T Cell Dependent Immunity Against N. brasiliensis Infection |
| Q38252608 | Development, differentiation, and diversity of innate lymphoid cells |
| Q35624378 | Divergent expression patterns of IL-4 and IL-13 define unique functions in allergic immunity |
| Q37879452 | Diversity and dialogue in immunity to helminths. |
| Q40693199 | Dupilumab efficacy and safety in adults with uncontrolled persistent asthma despite use of medium-to-high-dose inhaled corticosteroids plus a long-acting β2 agonist: a randomised double-blind placebo-controlled pivotal phase 2b dose-ranging trial |
| Q89497781 | Dupilumab improves lung function in patients with uncontrolled, moderate-to-severe asthma |
| Q42960522 | Dynamics of CD11c(+) dendritic cell subsets in lymph nodes draining the site of intestinal nematode infection |
| Q37673990 | Emerging functions of basophils in protective and allergic immune responses |
| Q34406828 | Eosinophil secretion of granule-derived cytokines. |
| Q38076473 | Eosinophil-derived cytokines in health and disease: unraveling novel mechanisms of selective secretion |
| Q37672261 | Eosinophils and Th2 immunity: contemporary insights |
| Q35120224 | Eosinophils are important for protection, immunoregulation and pathology during infection with nematode microfilariae |
| Q38855142 | Eosinophils in Helminth Infection: Defenders and Dupes |
| Q36921021 | Eosinophils in innate immunity: an evolving story |
| Q36059786 | Eosinophils in the pathogenesis of allergic airways disease. |
| Q34630341 | Eosinophils: multifaceted biological properties and roles in health and disease |
| Q36038191 | Epithelial cell-specific Act1 adaptor mediates interleukin-25-dependent helminth expulsion through expansion of Lin(-)c-Kit(+) innate cell population. |
| Q35731933 | Genetic analysis of basophil function in vivo. |
| Q37721062 | Genotyping of IL-4 -590 (C>T) Gene in Iraqi Asthma Patients. |
| Q38573631 | Group 2 innate lymphoid cells in disease |
| Q37152701 | Hallmarks of Tissue-Resident Lymphocytes |
| Q37262993 | Helminth infections and intestinal inflammation |
| Q24648324 | Helminth infections: the great neglected tropical diseases |
| Q42117570 | Homeostasis and effector function of lymphopenia-induced "memory-like" T cells in constitutively T cell-depleted mice |
| Q40098383 | Host immune responses to the itch mite, Sarcoptes scabiei, in humans |
| Q38229984 | Host protective roles of type 2 immunity: parasite killing and tissue repair, flip sides of the same coin. |
| Q37449444 | How are T(H)1 and T(H)2 effector cells made? |
| Q36100285 | Human Peripheral Blood Mononuclear Cell Function and Dendritic Cell Differentiation Are Affected by Bisphenol-A Exposure. |
| Q24315093 | Human basophils activated by mast cell-derived IL-3 express retinaldehyde dehydrogenase-II and produce the immunoregulatory mediator retinoic acid |
| Q37372759 | IL-3 induces basophil expansion in vivo by directing granulocyte-monocyte progenitors to differentiate into basophil lineage-restricted progenitors in the bone marrow and by increasing the number of basophil/mast cell progenitors in the spleen |
| Q36512087 | IL-33 drives biphasic IL-13 production for noncanonical Type 2 immunity against hookworms |
| Q42935119 | IL-33 markedly activates murine eosinophils by an NF-κB-dependent mechanism differentially dependent upon an IL-4-driven autoinflammatory loop. |
| Q31131991 | IL-4 attenuates Th1-associated chemokine expression and Th1 trafficking to inflamed tissues and limits pathogen clearance |
| Q35034191 | IL-4Rα-associated antigen processing by B cells promotes immunity in Nippostrongylus brasiliensis infection |
| Q37397810 | IL-9-mediated survival of type 2 innate lymphoid cells promotes damage control in helminth-induced lung inflammation |
| Q24630608 | IL25 elicits a multipotent progenitor cell population that promotes T(H)2 cytokine responses |
| Q90419317 | ILC2 Activation by Protozoan Commensal Microbes |
| Q40118341 | ILC2s regulate adaptive Th2 cell functions via PD-L1 checkpoint control. |
| Q49347747 | Immunity to gastrointestinal nematode infections |
| Q34000736 | Immunobiology of intestinal eosinophils - a dogma in the changing? |
| Q24644622 | Immunoregulatory roles of eosinophils: a new look at a familiar cell |
| Q36281139 | Impact of chronic rhinosinusitis on severe asthma patients |
| Q35091220 | Inducible deletion of CD28 prior to secondary nippostrongylus brasiliensis infection impairs worm expulsion and recall of protective memory CD4⁺ T cell responses |
| Q34161524 | Inflammatory dendritic cells--not basophils--are necessary and sufficient for induction of Th2 immunity to inhaled house dust mite allergen |
| Q36468792 | Inflammatory group 2 innate lymphoid cells |
| Q64058682 | Innate Lymphoid Cells in Helminth Infections-Obligatory or Accessory? |
| Q35928131 | Innate lymphoid cells and type 2 (th2) mediated immune responses - pathogenic or beneficial? |
| Q27012728 | Innate lymphoid cells in the airways |
| Q40063411 | Innate lymphoid cells in tissue homeostasis and diseases |
| Q38071916 | Innate lymphoid cells--how did we miss them? |
| Q36694157 | Innate lymphoid type 2 cells sustain visceral adipose tissue eosinophils and alternatively activated macrophages |
| Q29619771 | Innate production of T(H)2 cytokines by adipose tissue-associated c-Kit(+)Sca-1(+) lymphoid cells |
| Q47186385 | Interactions between Innate Lymphoid Cells and Cells of the Innate and Adaptive Immune System |
| Q49231913 | Interleukin-13 +2044 G/A and +1923C/T polymorphisms are associated with asthma susceptibility in Asians: A meta-analysis |
| Q54375943 | Interleukin-13-mediated paneth cell degranulation and antimicrobial peptide release. |
| Q36044280 | Interleukin-25 induces type 2 cytokine production in a steroid-resistant interleukin-17RB+ myeloid population that exacerbates asthmatic pathology |
| Q41149769 | Interleukin-33 and Interferon-γ Counter-Regulate Group 2 Innate Lymphoid Cell Activation during Immune Perturbation |
| Q55333225 | Interleukin-4 activated macrophages mediate immunity to filarial helminth infection by sustaining CCR3-dependent eosinophilia. |
| Q35783443 | Interleukin-4 production by follicular helper T cells requires the conserved Il4 enhancer hypersensitivity site V |
| Q51697509 | Interleukin-4- and NACHT, LRR and PYD domains-containing protein 3-independent mechanisms of alum enhanced T helper type 2 responses on basophils. |
| Q36974393 | Interleukin-4-promoted T helper 2 responses enhance Nippostrongylus brasiliensis-induced pulmonary pathology. |
| Q33590452 | Intestinal epithelial cell secretion of RELM-beta protects against gastrointestinal worm infection |
| Q37263947 | MHC class II-dependent basophil-CD4+ T cell interactions promote T(H)2 cytokine-dependent immunity. |
| Q34106637 | MHCII-mediated dialog between group 2 innate lymphoid cells and CD4(+) T cells potentiates type 2 immunity and promotes parasitic helminth expulsion |
| Q40216222 | Macrophage function in tissue repair and remodeling requires IL-4 or IL-13 with apoptotic cells. |
| Q34639723 | Macrophages as IL-25/IL-33-responsive cells play an important role in the induction of type 2 immunity |
| Q26796071 | Maintenance of Immune Homeostasis through ILC/T Cell Interactions |
| Q36586043 | Mast cells recruited to mesenteric lymph nodes during helminth infection remain hypogranular and produce IL-4 and IL-6. |
| Q35956683 | Memory T(H)2 cells induce alternatively activated macrophages to mediate protection against nematode parasites |
| Q28302789 | Mouse CCL8, a CCR8 agonist, promotes atopic dermatitis by recruiting IL-5+ T(H)2 cells |
| Q39461194 | Mucosal trapping and degradation of Nippostrongylus brasiliensis occurs in the absence of STAT6. |
| Q53323729 | Natural killer T cells regulate the development of asthma. |
| Q39084322 | Negative Regulation of Type 2 Immunity |
| Q40309082 | Neutralization of nerve growth factor (NGF) inhibits the Th2 response and protects against the respiratory syncytial virus (RSV) infection |
| Q34533347 | Nippostrongylus-induced intestinal hypercontractility requires IL-4 receptor alpha-responsiveness by T cells in mice |
| Q93183514 | Nonredundant Roles of IL-21 and IL-4 in the Phased Initiation of Germinal Center B Cells and Subsequent Self-Renewal Transitions |
| Q87842237 | Notch signaling represents an important checkpoint between follicular T-helper and canonical T-helper 2 cell fate |
| Q24630261 | Nuocytes represent a new innate effector leukocyte that mediates type-2 immunity |
| Q37895407 | Nuocytes: expanding the innate cell repertoire in type-2 immunity |
| Q36502818 | Ozone exposure in a mouse model induces airway hyperreactivity that requires the presence of natural killer T cells and IL-17 |
| Q37327241 | Pivotal advance: eosinophils mediate early alum adjuvant-elicited B cell priming and IgM production |
| Q37387939 | Priming for T helper type 2 differentiation by interleukin 2-mediated induction of interleukin 4 receptor alpha-chain expression |
| Q38096294 | Protective and pathological roles of mast cells and basophils |
| Q36481763 | Protective immune mechanisms in helminth infection |
| Q84899480 | Protective immunity against the gastrointestinal nematode Nippostrongylus brasiliensis requires a broad T-cell receptor repertoire |
| Q36502869 | Pulmonary arterial remodeling induced by a Th2 immune response |
| Q26828515 | Re-defining the unique roles for eosinophils in allergic respiratory inflammation |
| Q38040602 | Recent developments in basophil research: do basophils initiate and perpetuate type 2 T-helper cell responses?. |
| Q42910800 | Regulation of the Il4 gene is independently controlled by proximal and distal 3' enhancers in mast cells and basophils |
| Q92824342 | Regulatory roles of IL-10-producing human follicular T cells |
| Q33432703 | Retnla (relmalpha/fizz1) suppresses helminth-induced Th2-type immunity |
| Q38818110 | Role of basophils in protective immunity to parasitic infections. |
| Q37690006 | Role of basophils in the initiation of Th2 responses |
| Q42150907 | Role of innate lymphocytes in infection and inflammation |
| Q92984674 | Role of viruses in asthma |
| Q35849182 | Schistosoma mansoni infection in eosinophil lineage-ablated mice |
| Q93184507 | Selective expression of constitutively activated STAT6 in intestinal epithelial cells promotes differentiation of secretory cells and protection against helminths |
| Q50095337 | Shaping Innate Lymphoid Cell Diversity. |
| Q30515732 | Spatiotemporally separated antigen uptake by alveolar dendritic cells and airway presentation to T cells in the lung |
| Q38311813 | Specification of type 2 innate lymphocytes by the transcriptional determinant Gfi1. |
| Q36699742 | Strain-specific requirement for eosinophils in the recruitment of T cells to the lung during the development of allergic asthma |
| Q35148851 | Systemic impact of intestinal helminth infections |
| Q37392523 | T cell homing to epithelial barriers in allergic disease |
| Q41088544 | T cells are the critical source of IL-4/IL-13 in a mouse model of allergic asthma |
| Q35940715 | T helper 2 (Th2) cell differentiation, type 2 innate lymphoid cell (ILC2) development and regulation of interleukin-4 (IL-4) and IL-13 production |
| Q38107790 | TH2, allergy and group 2 innate lymphoid cells |
| Q41665142 | TLR4 antagonist suppresses airway remodeling in asthma by inhibiting the T-helper 2 response |
| Q35369187 | TSLP conditions the lung immune environment for the generation of pathogenic innate and antigen-specific adaptive immune responses |
| Q82609458 | Targeting SIRP‐α protects from type 2‐driven allergic airway inflammation |
| Q36985624 | Th2 and eosinophil responses suppress inflammatory arthritis |
| Q92390564 | Th2 cell-derived IL-4/IL-13 promote ILC2 accumulation in the lung by ILC2-intrinsic STAT6 signaling in mice |
| Q37376021 | The different faces of Notch in T-helper-cell differentiation |
| Q28083968 | The differential expression of IL-4 and IL-13 and its impact on type-2 immunity |
| Q38348057 | The future of biologics: applications for food allergy |
| Q37349722 | The intestinal epithelium: sensors to effectors in nematode infection |
| Q38271331 | The messenger between worlds: the regulation of innate and adaptive type-2 immunity by innate lymphoid cells |
| Q39215742 | The role of ILC2 in hookworm infection. |
| Q48146269 | The role of innate lymphoid cells in health and disease |
| Q40184625 | The role of rare innate immune cells in Type 2 immune activation against parasitic helminths. |
| Q35826002 | Trefoil factor 2 rapidly induces interleukin 33 to promote type 2 immunity during allergic asthma and hookworm infection. |
| Q84142600 | Trichosanthin functions as Th2-type adjuvant in induction of allergic airway inflammation |
| Q36794704 | Tuft-cell-derived IL-25 regulates an intestinal ILC2-epithelial response circuit |
| Q100525847 | Type 2 and interferon inflammation regulate SARS-CoV-2 entry factor expression in the airway epithelium |
| Q35322784 | Type 2 inflammation in asthma--present in most, absent in many |
| Q37842599 | Type 2 innate immune responses and the natural helper cell. |
| Q41958092 | Type 2 innate immunity in helminth infection is induced redundantly and acts autonomously following CD11c(+) cell depletion |
| Q38239232 | Type-2 innate lymphoid cells in human allergic disease |
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