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P50 | author | Francisca Mutapi | Q28817248 |
Nadine Rujeni | Q28817250 | ||
P2093 | author name string | David W Taylor | |
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Schistosoma-specific helper T cell clones from subjects resistant to infection by Schistosoma mansoni are Th0/2. | Q54167174 | ||
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Proteomic identification of IPSE/alpha-1 as a major hepatotoxin secreted by Schistosoma mansoni eggs | Q28477613 | ||
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Human schistosomiasis | Q29619142 | ||
Reassessment of the cost of chronic helmintic infection: a meta-analysis of disability-related outcomes in endemic schistosomiasis | Q29619819 | ||
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T-cell activation and the balance of antibody isotypes in human lymphatic filariasis. | Q31100037 | ||
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Immunity after treatment of human schistosomiasis: association between cellular responses and resistance to reinfection | Q33615961 | ||
Rapid induction of IgE responses to a worm cysteine protease during murine pre-patent schistosome infection | Q33747036 | ||
Mast cells and basophils | Q33802344 | ||
Regulatory and activated T cells in human Schistosoma haematobium infections | Q33828497 | ||
Saturation of immunoglobulin E (IgE) binding sites by polyclonal IgE does not explain the protective effect of helminth infections against atopy | Q33883393 | ||
Schistosomes in the southwest United States and their potential for causing cercarial dermatitis or 'swimmer's itch'. | Q33941745 | ||
Measles and atopy in Guinea-Bissau | Q34062779 | ||
Allergy, parasites, and the hygiene hypothesis | Q34124658 | ||
Helminth secretions induce de novo T cell Foxp3 expression and regulatory function through the TGF-β pathway | Q34140466 | ||
Longitudinal relationship of early life immunomodulatory T cell phenotype and function to development of allergic sensitization in an urban cohort | Q34171237 | ||
A novel therapeutic approach targeting articular inflammation using the filarial nematode-derived phosphorylcholine-containing glycoprotein ES-62. | Q34220228 | ||
Changes in the reported prevalence of childhood eczema since the 1939-45 war | Q34248484 | ||
Burden of allergic disease in the UK: secondary analyses of national databases | Q34312898 | ||
Human IgE, IgG4 and resistance to reinfection with Schistosoma haematobium | Q41162010 | ||
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Negative feedback regulation of IgE synthesis by murine CD23. | Q41460286 | ||
CD21 is a ligand for CD23 and regulates IgE production | Q41609094 | ||
Schistosomiasis in Africa: an emerging tragedy in our new global health decade | Q42559175 | ||
Cost-effectiveness of omalizumab in patients with severe persistent allergic asthma | Q42612118 | ||
Expression and immune response analysis of Schistosoma japonicum VAL-1, a homologue of vespid venom allergens | Q42653662 | ||
The structure of human CD23 and its interactions with IgE and CD21. | Q42972255 | ||
Depigmented and polymerised house dust mite allergoid: allergen content, induction of IgG4 and clinical response. | Q43112818 | ||
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Strong serum inhibition of specific IgE correlated to competing IgG4, revealed by a new methodology in subjects from a S. mansoni endemic area | Q43733152 | ||
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Expansion of Foxp3+ regulatory T cells in mice infected with the filarial parasite Brugia malayi | Q44143813 | ||
Resistance to reinfection with Schistosoma mansoni in occupationally exposed adults and effect of HIV-1 co-infection on susceptibility to schistosomiasis: a longitudinal study | Q44145263 | ||
Prevalence of attention deficit/hyperactivity disorder in pediatric allergic rhinitis: a nationwide population-based study | Q44271159 | ||
Early BCG vaccination and development of atopy. | Q44438314 | ||
Schistosoma mansoni infection is associated with a reduced course of asthma | Q44438840 | ||
Contrasting cellular responses in Schistosoma haematobium infected and exposed individuals from areas of high and low transmission in Zimbabwe. | Q44503291 | ||
Long-term treatment of intestinal helminths increases mite skin-test reactivity in Gabonese schoolchildren | Q44771950 | ||
Association between allergic sensitization and attention deficit hyperactivity disorder (ADHD). | Q44976010 | ||
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Chemotherapy accelerates the development of acquired immune responses to Schistosoma haematobium infection | Q47887339 | ||
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T(H)17-associated cytokines (IL-17A and IL-17F) in severe asthma | Q48019510 | ||
Cloning of IgE from the echidna (Tachyglossus aculeatus) and a comparative analysis of epsilon chains from all three extant mammalian lineages | Q48229332 | ||
Puberty and Age-related Changes in Susceptibility to Schistosome Infection | Q48546049 | ||
Clinical significance of skin reactions to mite extracts in children with asthma | Q49190060 | ||
Schistosoma mansoni secretes a chemokine binding protein with antiinflammatory activity | Q36403130 | ||
Suppression of allergic airway inflammation by helminth-induced regulatory T cells | Q36403704 | ||
Filarial nematode secreted product ES-62 is an anti-inflammatory agent: therapeutic potential of small molecule derivatives and ES-62 peptide mimetics | Q36478837 | ||
Association of non-wheezing lower respiratory tract illnesses in early life with persistently diminished serum IgE levels. Group Health Medical Associates | Q36570217 | ||
Ascaris lumbricoides-induced interleukin-10 is not associated with atopy in schoolchildren in a rural area of the tropics | Q36606792 | ||
In utero supplementation with methyl donors enhances allergic airway disease in mice | Q36890824 | ||
Circulating CD23+ B cell subset correlates with the development of resistance to Schistosoma mansoni reinfection in occupationally exposed adults who have undergone multiple treatments | Q37085574 | ||
IgE in allergy and asthma today | Q37095248 | ||
The unacknowledged impact of chronic schistosomiasis | Q37102843 | ||
Immunoglobulin E (IgE) responses to paramyosin predict resistance to reinfection with Schistosoma japonicum and are attenuated by IgG4. | Q37191336 | ||
Human schistosomiasis mansoni: immune responses during acute and chronic phases of the infection | Q37199411 | ||
Functions of T cells in asthma: more than just T(H)2 cells. | Q37253949 | ||
T-cell regulation in helminth parasite infections: implications for inflammatory diseases | Q37273143 | ||
Omega-1, a glycoprotein secreted by Schistosoma mansoni eggs, drives Th2 responses | Q37292812 | ||
Allergies: their role in cancer prevention | Q37368161 | ||
T lymphocytes and their products in atopic allergy and asthma | Q37451378 | ||
Immune tolerance in allergy | Q37584824 | ||
The therapeutic potential of the filarial nematode-derived immunodulator, ES-62 in inflammatory disease | Q37646847 | ||
Parasitic helminths: new weapons against immunological disorders | Q37695081 | ||
IgE in the human placenta: why there? | Q37700763 | ||
Helminth-derived immunomodulators: can understanding the worm produce the pill? | Q37708009 | ||
Anti-Inflammatory Activity of Human IgG4 Antibodies by Dynamic Fab Arm Exchange | Q55178105 | ||
Reduced helminth burden increases allergen skin sensitization but not clinical allergy: a randomized, double-blind, placebo-controlled trial in Vietnam | Q56875674 | ||
Schistosoma mansoni infection alters co-stimulatory molecule expression and cell activation in asthma | Q56900213 | ||
The levels of CD4+CD25+ regulatory T cells in paediatric patients with allergic rhinitis and bronchial asthma | Q56901462 | ||
Effect of albendazole treatments on the prevalence of atopy in children living in communities endemic for geohelminth parasites: a cluster-randomised trial | Q56982710 | ||
Decreased atopy in children infected with Schistosoma haematobium: a role for parasite-induced interleukin-10 | Q56983103 | ||
β-agonist therapy and asthma mortality in Japan | Q57152848 | ||
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The phosphorycholine moiety of the filarial nematode immunomodulator ES-62 is responsible for its anti-inflammatory action in arthritis | Q57232015 | ||
Anti-Inflammatory Activity of Immunoglobulin G Resulting from Fc Sialylation | Q57253538 | ||
Human antibody responses to Schistosoma mansoni: does antigen directed, isotype restriction result in the production of blocking antibodies? | Q58312985 | ||
Th2 Cytokines Are Associated with Persistent Hepatic Fibrosis in HumanSchistosoma japonicumInfection | Q58812311 | ||
Forum: Immunology: Allergy challenged | Q59054569 | ||
Antibody-dependent cell-mediated damage to schistosomula in vitro | Q59066650 | ||
Inhibition of complement activation by IgG4 antibodies | Q61601640 | ||
The half-lives of serum immunoglobulins in adult mice. | Q61796502 | ||
Cytokine Regulation of Periportal Fibrosis in Humans Infected with Schistosoma mansoni: IFN- Is Associated with Protection Against Fibrosis and TNF- with Aggravation of Disease | Q63409796 | ||
Trends in childhood asthma: prevalence, health care utilization, and mortality | Q64127934 | ||
Clinical studies on cell-mediated immunity in patients with urinary bladder carcinoma: blastogenic response, interleukin-2 production and interferon-gamma production of lymphocytes | Q67290975 | ||
Control of allergic reactivity in human filariasis. Predominant localization of blocking antibody to the IgG4 subclass | Q68107142 | ||
Atopy in infancy predicts the severity of bronchial hyperresponsiveness in later childhood | Q68751030 | ||
Characterization of grass pollen-specific IgE, IgA, IgM classes and IgG subclasses in allergic patients | Q69679011 | ||
Undertreatment and asthma deaths | Q69868884 | ||
In-vitro antibody-dependent killing of schistosomula of Schistosoma haematobium by human eosinophils | Q69981857 | ||
Identification of gamma-E-antibodies as a carrier of reaginic activity | Q70079230 | ||
Differential expression of IgE and IgG4 specific antibody responses in asymptomatic and chronic human filariasis | Q70661025 | ||
Studies on the enhancement of human eosinophil function by mononuclear cell products in vitro | Q70706853 | ||
IgE: a molecule in search of a function | Q70862345 | ||
Schistosoma mansoni: activation of the alternative pathway of human complement by schistosomula | Q71298085 | ||
Marked amelioration of established collagen-induced arthritis by treatment with antibodies to CD23 in vivo | Q71803587 | ||
A role for parasite-induced PGE2 in IL-10-mediated host immunoregulation by skin stage schistosomula of Schistosoma mansoni | Q73086257 | ||
Inverse association between skin response to aeroallergens and Schistosoma mansoni infection | Q73145939 | ||
Schistosoma mansoni schistosomula reduce E-selectin and VCAM-1 expression in TNF-alpha-stimulated lung microvascular endothelial cells by interfering with the NF-kappaB pathway | Q73170454 | ||
Eosinophils and IgE receptors: a continuing controversy | Q73358626 | ||
Susceptibility and resistance to Schistosoma mansoni reinfection: parallel cellular and isotypic immunologic assessment | Q73668677 | ||
Expression of CD23 antigen and its ligands in children with intrinsic and extrinsic asthma | Q74119501 | ||
Immunopathology of schistosomiasis mansoni in mice and men | Q74206771 | ||
IgE versus IgG4 production can be differentially regulated by IL-10 | Q74412150 | ||
Prevalence of allergy in children in relation to prior BCG vaccination and infection with atypical mycobacteria | Q74444867 | ||
Human IgE, IgG subclass, and IgM responses to worm and egg antigens in schistosomiasis haematobium: a 12-month study of reinfection in Cameroonian children | Q74578372 | ||
Onset and persistence of childhood asthma: predictors from infancy | Q74582847 | ||
Prediction of early-onset asthma in genetically at-risk children | Q74628820 | ||
Cytokine profile associated with chronic and acute human schistosomiasis mansoni | Q79698353 | ||
Role of the low affinity IgE receptor (CD23) on the IgE response against Ascaris lumbricoides in Warao Amerindian children from Venezuela | Q80728368 | ||
Impaired T helper 2 response to aeroallergen in helminth-infected patients with asthma | Q80895989 | ||
The Schistosoma mansoni soluble proteome: a comparison across four life-cycle stages | Q80899185 | ||
Cercarial dermatitis in the UK | Q81777673 | ||
Does a 'reverse' atopic march exist? | Q82719227 | ||
This wormy world | Q83323352 | ||
Revised nomenclature for allergy for global use: Report of the Nomenclature Review Committee of the World Allergy Organization, October 2003. | Q34319335 | ||
IgG4 breaking the rules | Q34534472 | ||
Immunoglobulin G4: an odd antibody | Q34604625 | ||
T-cell subset regulation in atopy | Q34617024 | ||
CD23: an overlooked regulator of allergic disease. | Q34662928 | ||
Multiple helminth infection of the skin causes lymphocyte hypo-responsiveness mediated by Th2 conditioning of dermal myeloid cells. | Q34693180 | ||
The immunobiology of schistosomiasis | Q34718128 | ||
Induction of immunoglobulin G4 in human filariasis: an indicator of immunoregulation | Q34729333 | ||
Structural and immunologic cross-reactivity among filarial and mite tropomyosin: implications for the hygiene hypothesis | Q34787526 | ||
A soluble form of the high affinity IgE receptor, Fc-epsilon-RI, circulates in human serum | Q34841589 | ||
Differential recognition patterns of Schistosoma haematobium adult worm antigens by the human antibodies IgA, IgE, IgG1 and IgG4 | Q34891413 | ||
Evidence for an association between human resistance to Schistosoma mansoni and high anti-larval IgE levels | Q34975162 | ||
Health across the life span in the United States and England | Q35017380 | ||
Inhalant allergies in Zimbabwe: a common problem | Q35063335 | ||
Host-parasite interaction and morbidity in malaria endemic areas | Q35211697 | ||
Helminth-induced CD19+CD23hi B cells modulate experimental allergic and autoimmune inflammation | Q35230822 | ||
Eosinophil differentiation factor also has B-cell growth factor activity: proposed name interleukin 4 | Q35586725 | ||
Atopic dermatitis and the atopic march | Q35601158 | ||
Natural history of asthma in childhood--a birth cohort study | Q35626645 | ||
The anti-inflammatory potential of the filarial nematode secreted product, ES-62. | Q35668286 | ||
Early recovery from cow's milk allergy is associated with decreasing IgE and increasing IgG4 binding to cow's milk epitopes | Q35787862 | ||
How to connect an IgE-driven response with CTL activity? | Q35822890 | ||
T regulatory cells in allergy and health: a question of allergen specificity and balance. | Q35875954 | ||
Th2 response polarization during infection with the helminth parasite Schistosoma mansoni | Q35884210 | ||
Schistosome larvae stimulate macrophage cytokine production through TLR4-dependent and -independent pathways. | Q35946159 | ||
Atopy is inversely related to schistosome infection intensity: a comparative study in Zimbabwean villages with distinct levels of Schistosoma haematobium infection | Q36100646 | ||
The cercarial glycocalyx of Schistosoma mansoni. | Q36213384 | ||
Immunopathology of schistosomiasis | Q36220509 | ||
Identification of a 145,000 Mr membrane protein as the C3d receptor (CR2) of human B lymphocytes | Q36254495 | ||
Interleukin 13 induces interleukin 4-independent IgG4 and IgE synthesis and CD23 expression by human B cells. | Q36261169 | ||
Immunomodulation by filarial nematodes | Q36265018 | ||
Identification of a lymphokine that stimulates eosinophil differentiation in vitro. Its relationship to interleukin 3, and functional properties of eosinophils produced in cultures | Q36350409 | ||
How are T(H)2-type immune responses initiated and amplified? | Q36394985 | ||
P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
P6216 | copyright status | copyrighted | Q50423863 |
P304 | page(s) | 154743 | |
P577 | publication date | 2012-08-27 | |
P1433 | published in | Journal of parasitology research | Q26842368 |
P1476 | title | Human schistosome infection and allergic sensitisation | |
P478 | volume | 2012 |
Q89882526 | Antigenic cross-reactivity between Schistosoma mansoni and allergenic invertebrates putatively due to shared glycanic epitopes |
Q40331986 | Antigenic cross-reactivity between Schistosoma mansoni and peanut: a role for cross-reactive carbohydrate determinants (CCDs) and implications for the hygiene hypothesis. |
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