Lower levels of CXCL-8 and IL-2 on admission as predictors of early adverse reactions to Bothrops antivenom in the Brazilian Amazon

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dc.contributorCentro Bioindustrialpt_BR
dc.contributorLab. Imunopatologiapt_BR
dc.contributorPrograma de Pós-Graduação em Ciências – Toxinologia (PPGTox)pt_BR
dc.contributor.authorSoares, Frandison G. S.pt_BR
dc.contributor.authorIbiapina, Hiochelson N.pt_BR
dc.contributor.authorSartim, Marco A.pt_BR
dc.contributor.authorFan, Hui Wenpt_BR
dc.contributor.authorMoura-da-Silva, Ana Mariapt_BR
dc.date.accessioned2022-02-16T15:18:52Z-
dc.date.available2022-02-16T15:18:52Z-
dc.date.issued2022pt_BR
dc.identifier.citationSoares FGS, Ibiapina HN., Sartim MA., Mendonça-da-Silva I, Nascimento EF, Ferreira LC.L., et al. Lower levels of CXCL-8 and IL-2 on admission as predictors of early adverse reactions to Bothrops antivenom in the Brazilian Amazon. Cytokine. 2022 Apr;152:155825. doi:10.1016/j.cyto.2022.155825.pt_BR
dc.identifier.urihttps://repositorio.butantan.gov.br/handle/butantan/4194-
dc.description.abstractSnakebite envenomings are considered a global health problem. The specific therapy for these envenomings consists of administering animal-derived antivenoms aiming to neutralize the venom toxins. Antivenoms have been used effectively to treat snakebites for more than a century; however, their administration may result in early and/or late adverse reactions. The present study presents the prevalence of early adverse reactions (EARs) towards Bothrops antivenom therapy in a health tertiary unit in the Brazilian Amazon and explores if specific plasma cytokines and chemokines from envenomed patients could be used as predictors of EARs. A cohort of patients bitten by Bothrops atrox was followed-up at the Fundação de Medicina Tropical Dr. Heitor Vieira Dourado (FMT-HVD), from 2014 to 2016. Patients were treated with the Brazilian Bothrops antivenom and CXCL-8, CCL-5, CXCL-9, CCL-2, CXCL-10, IL-6, TNF, IL-2, IL-10, IFN-y, IL-4, and IL-17A were evaluated in patients’ plasma samples before and after antivenom administration. From the total of patients (n = 186), mostly were male (82.3%), inhabiting rural areas (87.1%), with an average age of 35 years. Most of the patients (83.8%) were admitted to the hospital within 6 h after the accident, 26 (14%) reported having suffered a previous snakebite, and 97 (52.1%) received between 7 and 9 antivenom vials. The frequency of antivenom-induced EARs was 11.8% (22), resulting mostly of mild reactions. Urticaria was the major EAR manifestation (46.4%). Interestingly, CXCL-8 and IL-2 showed significantly lower levels in patients who progressed to EARs, although IL-2 levels might not represent biological relevance due the small magnitude difference between groups. This study reveals that CXCL-8 and IL-2 could play a role in the onset of EARs in pit viper envenomings.pt_BR
dc.description.sponsorship(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológicopt_BR
dc.description.sponsorship(FAPEAM) Fundação de Amparo à Pesquisa do Estado do Amazonaspt_BR
dc.description.sponsorshipThe Hamish Ogston Foundationpt_BR
dc.format.extent155825pt_BR
dc.language.isoEnglishpt_BR
dc.relation.ispartofCytokinept_BR
dc.rightsRestricted accesspt_BR
dc.titleLower levels of CXCL-8 and IL-2 on admission as predictors of early adverse reactions to Bothrops antivenom in the Brazilian Amazonpt_BR
dc.typeArticlept_BR
dc.identifier.doi10.1016/j.cyto.2022.155825pt_BR
dc.identifier.urlhttps://doi.org/10.1016/j.cyto.2022.155825pt_BR
dc.contributor.external(UEA) Universidade do Estado do Amazonaspt_BR
dc.contributor.external(FMT-HVD) Fundação de Medicina Tropical Doutor Heitor Vieira Douradopt_BR
dc.contributor.externalUniversidade Nilton Linspt_BR
dc.contributor.external(UFRR) Universidade Federal de Roraimapt_BR
dc.contributor.external(UFAM) Universidade Federal do Amazonaspt_BR
dc.contributor.external(HEMOAM) Fundação Hospitalar de Hematologia e Hemoterapia do Amazonaspt_BR
dc.contributor.external(FUAM) Fundação Alfredo da Mattapt_BR
dc.identifier.citationvolume152pt_BR
dc.subject.keywordsnakebitept_BR
dc.subject.keywordBothropspt_BR
dc.subject.keywordantivenompt_BR
dc.subject.keywordadverse reactionpt_BR
dc.subject.keywordhypersensitivitypt_BR
dc.subject.keywordcytokinept_BR
dc.subject.keywordchemokinept_BR
dc.subject.keywordCXCL-8pt_BR
dc.subject.keywordIL-2pt_BR
dc.relation.ispartofabbreviatedCytokinept_BR
dc.identifier.citationabntv. 152, 155825, abr. 2022pt_BR
dc.identifier.citationvancouver2022 Apr;152:155825pt_BR
dc.contributor.butantanFan, Hui Wen|:Pesquisador|:Centro Bioindustrialpt_BR
dc.contributor.butantanMoura-da-Silva, Ana Maria|:Pesquisador:Docente Permanente PPGTox|:Lab. Imunopatologiapt_BR
dc.sponsorship.butantan(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico¦¦307184/2020–0pt_BR
dc.sponsorship.butantan(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico¦¦303958/2018–9pt_BR
dc.sponsorship.butantan(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico¦¦309207/2020–7pt_BR
dc.sponsorship.butantan(FAPEAM) Fundação de Amparo à Pesquisa do Estado do Amazonas¦¦002/2008pt_BR
dc.sponsorship.butantan(FAPEAM) Fundação de Amparo à Pesquisa do Estado do Amazonas¦¦007/2018pt_BR
dc.sponsorship.butantan(FAPEAM) Fundação de Amparo à Pesquisa do Estado do Amazonas¦¦005/2019pt_BR
dc.sponsorship.butantan(FAPEAM) Fundação de Amparo à Pesquisa do Estado do Amazonas¦¦004/2019pt_BR
dc.sponsorship.butantan(FAPEAM) Fundação de Amparo à Pesquisa do Estado do Amazonas¦¦005/2019pt_BR
dc.sponsorship.butantan(FAPEAM) Fundação de Amparo à Pesquisa do Estado do Amazonas¦¦006/2020pt_BR
dc.sponsorship.butantanThe Hamish Ogston Foundation¦¦pt_BR
dc.identifier.bvsccBR78.1pt_BR
dc.identifier.bvsdbIBProdpt_BR
dc.description.dbindexedYespt_BR
dc.description.internalPolítica de depósito: liberado apenas preprintpt_BR
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item.openairetypeArticle-
item.languageiso639-1English-
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