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 |
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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 |
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Q36370697 | Basophils are the major producers of IL-4 during primary helminth infection |
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Q37866220 | Basophils: important emerging players in allergic and anti-parasite responses. |
Q80733934 | Basophils: in the spotlight at last |
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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. |
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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. |
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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 |
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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 |
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