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C-Type Lectin Receptor Mediated Modulation of T2 Immune Responses to Allergens

dc.contributor.authorAngelina Querencias, Alba
dc.contributor.authorMartín De La Cruz, Leticia
dc.contributor.authorRocha-Muñoz, Andrés de la
dc.contributor.authorLavín Plaza, Begoña
dc.contributor.authorPalomares Gracia, Óscar
dc.date.accessioned2024-01-25T10:47:25Z
dc.date.available2024-01-25T10:47:25Z
dc.date.issued2023
dc.description.abstractPurpose of Review: Allergic diseases represent a major health problem of increasing prevalence worldwide. In allergy, dendritic cells (DCs) contribute to both the pathophysiology and the induction of healthy immune responses to the allergens. Different studies have reported that some common allergens contain glycans in their structure. C-type lectin receptors (CLRs) expressed by DCs recognize carbohydrate structures and are crucial in allergen uptake, presentation, and polarization of T cell responses. This review summarizes the recent literature regarding the role of CLRs in the regulation of type 2 immune responses to allergens. Recent Findings: In this review, we highlight the capacity of CLRs to recognize carbohydrates in common allergens triggering different signaling pathways involved in the polarization of CD4+ T cells towards specific Th2 responses. Under certain conditions, specific CLRs could also promote tolerogenic responses to allergens, which might well be exploited to develop novel therapeutic approaches of allergen-specific immunotherapy (AIT), the single treatment with potential disease-modifying capacity for allergic disease. At this regard, polymerized allergens conjugated to non-oxidized mannan (allergoid-mannan conjugated) are next-generation vaccines targeting DCs via CLRs that promote regulatory T cells, thus favoring allergen tolerance both in preclinical models and clinical trials. Summary: A better understanding of the role of CLRs in the development of allergy and in the induction of allergen tolerance might well pave the way for the design of novel strategies for allergic diseases.
dc.description.departmentDepto. de Bioquímica y Biología Molecular
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia, Innovación y Universidades (España)
dc.description.statuspub
dc.identifier.citationAngelina, A., Martín-Cruz, L., de la Rocha-Muñoz, A. et al. C-Type Lectin Receptor Mediated Modulation of T2 Immune Responses to Allergens. Curr Allergy Asthma Rep 23, 141–151 (2023). https://doi.org/10.1007/s11882-023-01067-0
dc.identifier.doi10.1007/s11882-023-01067-0
dc.identifier.essn1534-6315
dc.identifier.issn1529-7322
dc.identifier.officialurlhttps://doi.org/10.1007/s11882-023-01067-0
dc.identifier.relatedurlhttps://pubmed.ncbi.nlm.nih.gov/36720753/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/95351
dc.issue.number3
dc.journal.titleCurrent Allergy and Asthma Reports
dc.language.isoeng
dc.page.final151
dc.page.initial141
dc.publisherSpringer Nature
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-114396RB-I00/ES/CANNABINOIDES Y MECANISMOS MOLECULARES IMPLICADOS EN LA REGULACION DE CELULAS DENDRITICAS Y EPITELIALES HUMANAS: NUEVAS ESTRATEGIAS BASADAS EN CANNABINOIDES PARA ALERGIA/
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu577.1
dc.subject.keywordC-type lectin receptors (CLRs)
dc.subject.keywordType-2 immune responses Allergy
dc.subject.keywordAllergens
dc.subject.keywordAllergen-specific immunotherapy (AIT)
dc.subject.keywordMannan
dc.subject.ucmInmunología
dc.subject.ucmBioquímica (Química)
dc.subject.ucmBiología molecular (Química)
dc.subject.unesco2412 Inmunología
dc.subject.unesco2302 Bioquímica
dc.subject.unesco2403 Bioquímica
dc.subject.unesco3207.01 Alergias
dc.titleC-Type Lectin Receptor Mediated Modulation of T2 Immune Responses to Allergens
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number23
dspace.entity.typePublication
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relation.isAuthorOfPublication8ed2b79b-36d7-4380-aaf1-5da770ff691d
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relation.isAuthorOfPublication.latestForDiscovery67a57ba8-97f2-4aa6-99d3-62cfa97da7c7

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