Avaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniae
Ano de defesa: | 2019 |
---|---|
Autor(a) principal: | |
Orientador(a): | |
Banca de defesa: | |
Tipo de documento: | Dissertação |
Tipo de acesso: | Acesso aberto |
Idioma: | por |
Instituição de defesa: |
Universidade Católica de Brasília
|
Programa de Pós-Graduação: |
Programa Stricto Sensu em Ciências Genômicas e Biotecnologia
|
Departamento: |
Escola de Saúde e Medicina
|
País: |
Brasil
|
Palavras-chave em Português: | |
Palavras-chave em Inglês: | |
Área do conhecimento CNPq: | |
Resumo em Inglês: | Klebsiella pneumoniae is a microorganism of great relevance in clinical context because it presents resistance to several antibiotics, besides possessing the ability to evade the immune system of the host. Antimicrobial therapy has encountered several barriers mainly due to the emergence of multiresistant strains, which reinforces the need to formulate new antimicrobial and adjuvant agents. Within this scenario, immunomodulatory peptides may be an alternative for the protection of the host immune system in this type of infection. Therefore, the objective of this work was to evaluate the immunomodulatory potential of the Synoeca-MP peptide against an in vitro model of K. pneumoniae, evaluating inflammatory mediators. Knowing that K. pneumoniae strains that present capsules have greater virulence and respond differently to treatments, the presence of this capsule was initially evaluated in the strains of K. pneumoniae (Kp2177569 and ATCC 13883) used in this study. Subsequently, cell viability, nitric oxide production and inflammatory mediators, such as tumor necrosis factor alpha and interleukin 10, were evaluated in RAW 264.7 cells, incubated with heat-inactivated K. pneumoniae antigens, Synoeca-MP and levofloxacin and the combination of both. In the presence of the antigens, the viability was maintained and the production of nitric oxide increased when compared to the control. It was observed that the presence of Synoeca-MP and levofloxacin did not alter the production of nitric oxide. However, when this association was incubated with the cells stimulated in the presence of K. pneumoniae antigen ATCC 13883 it was observed that TNF-α levels were maintained, in addition to a reduction in IL-10 production. In this way, from the obtained results, the association is able to present a low modulating action of pro and anti-inflammatory mediators. |
Link de acesso: | https://bdtd.ucb.br:8443/jspui/handle/tede/2606 |
Resumo: | Klebsiella pneumoniae is a microorganism of great relevance in clinical context because it presents resistance to several antibiotics, besides possessing the ability to evade the immune system of the host. Antimicrobial therapy has encountered several barriers mainly due to the emergence of multiresistant strains, which reinforces the need to formulate new antimicrobial and adjuvant agents. Within this scenario, immunomodulatory peptides may be an alternative for the protection of the host immune system in this type of infection. Therefore, the objective of this work was to evaluate the immunomodulatory potential of the Synoeca-MP peptide against an in vitro model of K. pneumoniae, evaluating inflammatory mediators. Knowing that K. pneumoniae strains that present capsules have greater virulence and respond differently to treatments, the presence of this capsule was initially evaluated in the strains of K. pneumoniae (Kp2177569 and ATCC 13883) used in this study. Subsequently, cell viability, nitric oxide production and inflammatory mediators, such as tumor necrosis factor alpha and interleukin 10, were evaluated in RAW 264.7 cells, incubated with heat-inactivated K. pneumoniae antigens, Synoeca-MP and levofloxacin and the combination of both. In the presence of the antigens, the viability was maintained and the production of nitric oxide increased when compared to the control. It was observed that the presence of Synoeca-MP and levofloxacin did not alter the production of nitric oxide. However, when this association was incubated with the cells stimulated in the presence of K. pneumoniae antigen ATCC 13883 it was observed that TNF-α levels were maintained, in addition to a reduction in IL-10 production. In this way, from the obtained results, the association is able to present a low modulating action of pro and anti-inflammatory mediators. |
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Dias, Simoni Camposhttp://lattes.cnpq.br/1564224041415405Rezende, Taia Maria Bertohttp://lattes.cnpq.br/2108543063213963http://lattes.cnpq.br/3310611951004235Ferreira, Arthur Corrêa Resende2019-07-08T14:49:58Z2019-03-08FERREIRA, Arthur Corrêa Resende. Avaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniae. 2019. 74 f. Dissertação (Programa Stricto Sensu em Ciências Genômicas e Biotecnologia) - Universidade Católica de Brasília, Brasília, 2019.https://bdtd.ucb.br:8443/jspui/handle/tede/2606Klebsiella pneumoniae is a microorganism of great relevance in clinical context because it presents resistance to several antibiotics, besides possessing the ability to evade the immune system of the host. Antimicrobial therapy has encountered several barriers mainly due to the emergence of multiresistant strains, which reinforces the need to formulate new antimicrobial and adjuvant agents. Within this scenario, immunomodulatory peptides may be an alternative for the protection of the host immune system in this type of infection. Therefore, the objective of this work was to evaluate the immunomodulatory potential of the Synoeca-MP peptide against an in vitro model of K. pneumoniae, evaluating inflammatory mediators. Knowing that K. pneumoniae strains that present capsules have greater virulence and respond differently to treatments, the presence of this capsule was initially evaluated in the strains of K. pneumoniae (Kp2177569 and ATCC 13883) used in this study. Subsequently, cell viability, nitric oxide production and inflammatory mediators, such as tumor necrosis factor alpha and interleukin 10, were evaluated in RAW 264.7 cells, incubated with heat-inactivated K. pneumoniae antigens, Synoeca-MP and levofloxacin and the combination of both. In the presence of the antigens, the viability was maintained and the production of nitric oxide increased when compared to the control. It was observed that the presence of Synoeca-MP and levofloxacin did not alter the production of nitric oxide. However, when this association was incubated with the cells stimulated in the presence of K. pneumoniae antigen ATCC 13883 it was observed that TNF-α levels were maintained, in addition to a reduction in IL-10 production. In this way, from the obtained results, the association is able to present a low modulating action of pro and anti-inflammatory mediators.Klebsiella pneumoniae é um microrganismo de grande relevância em contexto clínico por apresentar resistência a diversos antibióticos, além de possuir a capacidade de evadir o sistema imune do hospedeiro. A terapia antimicrobiana tem encontrado diversos entraves principalmente devido ao surgimento de cepas multirresistentes o que reforça a necessidade de formulação de novo agentes antimicrobianos e coadjuvantes. Dentro deste cenário, peptídeos imunomoduladores podem ser uma alternativa para a proteção do sistema imune do hospedeiro nesse tipo de infecção. Sendo assim, o objetivo desse trabalho foi avaliar o potencial imunomodulador do peptídeo Synoeca-MP frente a um modelo in vitro de K. pneumoniae, avaliando mediadores inflamatórios. Sabendo que as cepas de K. pneumoniae que apresentam cápsula possuem maior virulência e respondem diferentemente aos tratamentos, inicialmente avaliou-se a presença desta cápsula nas cepas de K. pneumoniae (Kp2177569 e ATCC 13883) utilizadas neste estudo. Posteriormente, avaliou-se a viabilidade celular, a produção de óxido nítrico e mediadores inflamatórios, como fator de necrose tumoral alfa e interleucina 10, em células RAW 264.7, incubadas com antígenos de K. pneumoniae inativados pelo calor, Synoeca-MP e levofloxacina e a combinação de ambos. Na presença dos antígenos a viabilidade foi mantida e a produção de óxido nítrico aumentou quando comparado ao controle. Observou-se que a presença da associação Synoeca-MP e levofloxacina não alterou a produção de óxido nítrico. No entanto, quando esta associação foi incubada com as células estimuladas na presença de antígeno de K. pneumoniae ATCC 13883 observou-se que os níveis de TNF-α foram mantidos, além de uma redução na produção de IL-10. Desta maneira, a partir dos resultados obtidos, a associação é capaz de apresentar uma baixa ação moduladora de mediadores pró e anti-inflamatórios.Submitted by Sara Ribeiro (sara.ribeiro@ucb.br) on 2019-07-08T14:49:42Z No. of bitstreams: 1 ArthurCorreaResendeFerreiraDissertacao2019.pdf: 955328 bytes, checksum: aa510d848fdc0ec5abb39f3c35abba02 (MD5)Approved for entry into archive by Sara Ribeiro (sara.ribeiro@ucb.br) on 2019-07-08T14:49:58Z (GMT) No. of bitstreams: 1 ArthurCorreaResendeFerreiraDissertacao2019.pdf: 955328 bytes, checksum: aa510d848fdc0ec5abb39f3c35abba02 (MD5)Made available in DSpace on 2019-07-08T14:49:58Z (GMT). No. of bitstreams: 1 ArthurCorreaResendeFerreiraDissertacao2019.pdf: 955328 bytes, checksum: aa510d848fdc0ec5abb39f3c35abba02 (MD5) Previous issue date: 2019-03-08application/pdfhttps://bdtd.ucb.br:8443/jspui/retrieve/6527/ArthurCorreaResendeFerreiraDissertacao2019.pdf.jpgporUniversidade Católica de BrasíliaPrograma Stricto Sensu em Ciências Genômicas e BiotecnologiaUCBBrasilEscola de Saúde e MedicinaSynoeca-MPSistema imuneKlebsiella pneumoniaePeptídeo antimicrobianoMediadores inflamatóriosAntimicrobial peptideImmune systemCNPQ::CIENCIAS BIOLOGICASAvaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniaeinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UCBinstname:Universidade Católica de Brasíliainstacron:UCBTHUMBNAILArthurCorreaResendeFerreiraDissertacao2019.pdf.jpgArthurCorreaResendeFerreiraDissertacao2019.pdf.jpgimage/jpeg6245https://bdtd.ucb.br:8443/jspui/bitstream/tede/2606/4/ArthurCorreaResendeFerreiraDissertacao2019.pdf.jpg268c34e430fe5d1d1974c295743de6bdMD54TEXTArthurCorreaResendeFerreiraDissertacao2019.pdf.txtArthurCorreaResendeFerreiraDissertacao2019.pdf.txttext/plain114345https://bdtd.ucb.br:8443/jspui/bitstream/tede/2606/3/ArthurCorreaResendeFerreiraDissertacao2019.pdf.txteedbdc05419b9f5db980e8c2d916e4fbMD53ORIGINALArthurCorreaResendeFerreiraDissertacao2019.pdfArthurCorreaResendeFerreiraDissertacao2019.pdfapplication/pdf955328https://bdtd.ucb.br:8443/jspui/bitstream/tede/2606/2/ArthurCorreaResendeFerreiraDissertacao2019.pdfaa510d848fdc0ec5abb39f3c35abba02MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81831https://bdtd.ucb.br:8443/jspui/bitstream/tede/2606/1/license.txtd7d5e5ec75089f122abe937645a56120MD51tede/2606oai:bdtd.ucb.br:tede/26062019-07-09 01:05:58.824Biblioteca Digital de Dissertações da Universidade Católica de Brasília - UCBsdi@ucb.brTElDRU4/QSBERSBESVNUUklCVUk/P08gTj9PLUVYQ0xVU0lWQQoKQ29tIGEgYXByZXNlbnRhPz9vIGRlc3RhIGxpY2VuP2EsIHZvYz8gKGF1dG9yIG91IG8gdGl0dWxhciBkb3MgZGlyZWl0b3MgZGUgYXV0b3IpIGNvbmNlZGUgPyBVbml2ZXJzaWRhZGUgQ2F0P2xpY2EgZGUgQnJhcz9saWEgKFVDQikgbyBkaXJlaXRvIG4/by1leGNsdXNpdm8gZGUgcmVwcm9kdXppciwgdHJhZHV6aXIgKGNvbmZvcm1lIGRlZmluaWRvIGFiYWl4byksIGUvb3UgZGlzdHJpYnVpciBhIHN1YSB0ZXNlIG91IGRpc3NlcnRhPz9vIChpbmNsdWluZG8gbyByZXN1bW8pIHBvciB0b2RvIG8gbXVuZG8gbm8gZm9ybWF0byBpbXByZXNzbyBlIGVsZXRyP25pY28gZSBlbSBxdWFscXVlciBtZWlvLCBpbmNsdWluZG8gb3MgZm9ybWF0b3MgP3VkaW8gb3Ugdj9kZW8uCgpWb2M/IGNvbmNvcmRhIHF1ZSBhIFVDQiBwb2RlLCBzZW0gYWx0ZXJhciBvIGNvbnRlP2RvLCB0cmFuc3BvciBhIHN1YSB0ZXNlIG91IGRpc3NlcnRhPz9vIHBhcmEgcXVhbHF1ZXIgbWVpbyBvdSBmb3JtYXRvIHBhcmEgZmlucyBkZSBwcmVzZXJ2YT8/by4KClZvYz8gdGFtYj9tIGNvbmNvcmRhIHF1ZSBhIFVDQiBwb2RlIG1hbnRlciBtYWlzIGRlIHVtYSBjP3BpYSBhIHN1YSB0ZXNlIG91IGRpc3NlcnRhPz9vIHBhcmEgZmlucyBkZSBzZWd1cmFuP2EsIGJhY2stdXAgZSBwcmVzZXJ2YT8/by4KClZvYz8gZGVjbGFyYSBxdWUgYSBzdWEgdGVzZSBvdSBkaXNzZXJ0YT8/byA/IG9yaWdpbmFsIGUgcXVlIHZvYz8gdGVtIG8gcG9kZXIgZGUgY29uY2VkZXIgb3MgZGlyZWl0b3MgY29udGlkb3MgbmVzdGEgbGljZW4/YS4gVm9jPyB0YW1iP20gZGVjbGFyYSBxdWUgbyBkZXA/c2l0byBkYSBzdWEgdGVzZSBvdSBkaXNzZXJ0YT8/byBuP28gaW5mcmluZ2UgZGlyZWl0b3MgYXV0b3JhaXMgZGUgbmluZ3U/bS4KCkNhc28gYSBzdWEgdGVzZSBvdSBkaXNzZXJ0YT8/byBjb250ZW5oYSBtYXRlcmlhbCBxdWUgdm9jPyBuP28gcG9zc3VpIGEgdGl0dWxhcmlkYWRlIGRvcyBkaXJlaXRvcyBhdXRvcmFpcywgdm9jPyBkZWNsYXJhIHF1ZSBvYnRldmUgYSBwZXJtaXNzP28gaXJyZXN0cml0YSBkbyBkZXRlbnRvciBkb3MgZGlyZWl0b3MgYXV0b3JhaXMgcGFyYSBjb25jZWRlciA/IFVDQiBvcyBkaXJlaXRvcyBhcHJlc2VudGFkb3MgbmVzdGEgbGljZW4/YSwgZSBxdWUgZXNzZSBtYXRlcmlhbCBkZSBwcm9wcmllZGFkZSBkZSB0ZXJjZWlyb3MgZXN0PyBjbGFyYW1lbnRlIGlkZW50aWZpY2FkbyBlIHJlY29uaGVjaWRvIG5vIHRleHRvIG91IG5vIGNvbnRlP2RvIGRhIHRlc2Ugb3UgZGlzc2VydGE/P28gb3JhIGRlcG9zaXRhZGEuCgpDYXNvIGEgdGVzZSBvdSBkaXNzZXJ0YT8/byBkZXBvc2l0YWRhIHRlbmhhIHNpZG8gcmVzdWx0YWRvIGRlIHVtIHBhdHJvYz9uaW8gb3UgYXBvaW8gZGUgdW1hIGFnP25jaWEgZGUgZm9tZW50byBvdSBvdXRybyBvcmdhbmlzbW8gcXVlIG4/byBzZWphIGEgVUNCLCB2b2M/IGRlY2xhcmEgcXVlIHJlc3BlaXRvdSB0b2RvcyBlIHF1YWlzcXVlciBkaXJlaXRvcyBkZSByZXZpcz9vIGNvbW8gdGFtYj9tIGFzIGRlbWFpcyBvYnJpZ2E/P2VzIGV4aWdpZGFzIHBvciBjb250cmF0byBvdSBhY29yZG8uCgpBIFVDQiBzZSBjb21wcm9tZXRlIGEgaWRlbnRpZmljYXIgY2xhcmFtZW50ZSBvIHNldSBub21lIChzKSBvdSBvKHMpIG5vbWUocykgZG8ocykgZGV0ZW50b3IoZXMpIGRvcyBkaXJlaXRvcyBhdXRvcmFpcyBkYSB0ZXNlIG91IGRpc3NlcnRhPz9vLCBlIG4/byBmYXI/IHF1YWxxdWVyIGFsdGVyYT8/bywgYWw/bSBkYXF1ZWxhcyBjb25jZWRpZGFzIHBvciBlc3RhIGxpY2VuP2EuCg== |
dc.title.por.fl_str_mv |
Avaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniae |
title |
Avaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniae |
spellingShingle |
Avaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniae Ferreira, Arthur Corrêa Resende Synoeca-MP Sistema imune Klebsiella pneumoniae Peptídeo antimicrobiano Mediadores inflamatórios Antimicrobial peptide Immune system CNPQ::CIENCIAS BIOLOGICAS |
title_short |
Avaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniae |
title_full |
Avaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniae |
title_fullStr |
Avaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniae |
title_full_unstemmed |
Avaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniae |
title_sort |
Avaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniae |
author |
Ferreira, Arthur Corrêa Resende |
author_facet |
Ferreira, Arthur Corrêa Resende |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Dias, Simoni Campos |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/1564224041415405 |
dc.contributor.advisor-co1.fl_str_mv |
Rezende, Taia Maria Berto |
dc.contributor.advisor-co1Lattes.fl_str_mv |
http://lattes.cnpq.br/2108543063213963 |
dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/3310611951004235 |
dc.contributor.author.fl_str_mv |
Ferreira, Arthur Corrêa Resende |
contributor_str_mv |
Dias, Simoni Campos Rezende, Taia Maria Berto |
dc.subject.por.fl_str_mv |
Synoeca-MP Sistema imune Klebsiella pneumoniae Peptídeo antimicrobiano Mediadores inflamatórios |
topic |
Synoeca-MP Sistema imune Klebsiella pneumoniae Peptídeo antimicrobiano Mediadores inflamatórios Antimicrobial peptide Immune system CNPQ::CIENCIAS BIOLOGICAS |
dc.subject.eng.fl_str_mv |
Antimicrobial peptide Immune system |
dc.subject.cnpq.fl_str_mv |
CNPQ::CIENCIAS BIOLOGICAS |
dc.description.abstract.eng.fl_txt_mv |
Klebsiella pneumoniae is a microorganism of great relevance in clinical context because it presents resistance to several antibiotics, besides possessing the ability to evade the immune system of the host. Antimicrobial therapy has encountered several barriers mainly due to the emergence of multiresistant strains, which reinforces the need to formulate new antimicrobial and adjuvant agents. Within this scenario, immunomodulatory peptides may be an alternative for the protection of the host immune system in this type of infection. Therefore, the objective of this work was to evaluate the immunomodulatory potential of the Synoeca-MP peptide against an in vitro model of K. pneumoniae, evaluating inflammatory mediators. Knowing that K. pneumoniae strains that present capsules have greater virulence and respond differently to treatments, the presence of this capsule was initially evaluated in the strains of K. pneumoniae (Kp2177569 and ATCC 13883) used in this study. Subsequently, cell viability, nitric oxide production and inflammatory mediators, such as tumor necrosis factor alpha and interleukin 10, were evaluated in RAW 264.7 cells, incubated with heat-inactivated K. pneumoniae antigens, Synoeca-MP and levofloxacin and the combination of both. In the presence of the antigens, the viability was maintained and the production of nitric oxide increased when compared to the control. It was observed that the presence of Synoeca-MP and levofloxacin did not alter the production of nitric oxide. However, when this association was incubated with the cells stimulated in the presence of K. pneumoniae antigen ATCC 13883 it was observed that TNF-α levels were maintained, in addition to a reduction in IL-10 production. In this way, from the obtained results, the association is able to present a low modulating action of pro and anti-inflammatory mediators. |
dc.description.abstract.por.fl_txt_mv |
Klebsiella pneumoniae é um microrganismo de grande relevância em contexto clínico por apresentar resistência a diversos antibióticos, além de possuir a capacidade de evadir o sistema imune do hospedeiro. A terapia antimicrobiana tem encontrado diversos entraves principalmente devido ao surgimento de cepas multirresistentes o que reforça a necessidade de formulação de novo agentes antimicrobianos e coadjuvantes. Dentro deste cenário, peptídeos imunomoduladores podem ser uma alternativa para a proteção do sistema imune do hospedeiro nesse tipo de infecção. Sendo assim, o objetivo desse trabalho foi avaliar o potencial imunomodulador do peptídeo Synoeca-MP frente a um modelo in vitro de K. pneumoniae, avaliando mediadores inflamatórios. Sabendo que as cepas de K. pneumoniae que apresentam cápsula possuem maior virulência e respondem diferentemente aos tratamentos, inicialmente avaliou-se a presença desta cápsula nas cepas de K. pneumoniae (Kp2177569 e ATCC 13883) utilizadas neste estudo. Posteriormente, avaliou-se a viabilidade celular, a produção de óxido nítrico e mediadores inflamatórios, como fator de necrose tumoral alfa e interleucina 10, em células RAW 264.7, incubadas com antígenos de K. pneumoniae inativados pelo calor, Synoeca-MP e levofloxacina e a combinação de ambos. Na presença dos antígenos a viabilidade foi mantida e a produção de óxido nítrico aumentou quando comparado ao controle. Observou-se que a presença da associação Synoeca-MP e levofloxacina não alterou a produção de óxido nítrico. No entanto, quando esta associação foi incubada com as células estimuladas na presença de antígeno de K. pneumoniae ATCC 13883 observou-se que os níveis de TNF-α foram mantidos, além de uma redução na produção de IL-10. Desta maneira, a partir dos resultados obtidos, a associação é capaz de apresentar uma baixa ação moduladora de mediadores pró e anti-inflamatórios. |
description |
Klebsiella pneumoniae is a microorganism of great relevance in clinical context because it presents resistance to several antibiotics, besides possessing the ability to evade the immune system of the host. Antimicrobial therapy has encountered several barriers mainly due to the emergence of multiresistant strains, which reinforces the need to formulate new antimicrobial and adjuvant agents. Within this scenario, immunomodulatory peptides may be an alternative for the protection of the host immune system in this type of infection. Therefore, the objective of this work was to evaluate the immunomodulatory potential of the Synoeca-MP peptide against an in vitro model of K. pneumoniae, evaluating inflammatory mediators. Knowing that K. pneumoniae strains that present capsules have greater virulence and respond differently to treatments, the presence of this capsule was initially evaluated in the strains of K. pneumoniae (Kp2177569 and ATCC 13883) used in this study. Subsequently, cell viability, nitric oxide production and inflammatory mediators, such as tumor necrosis factor alpha and interleukin 10, were evaluated in RAW 264.7 cells, incubated with heat-inactivated K. pneumoniae antigens, Synoeca-MP and levofloxacin and the combination of both. In the presence of the antigens, the viability was maintained and the production of nitric oxide increased when compared to the control. It was observed that the presence of Synoeca-MP and levofloxacin did not alter the production of nitric oxide. However, when this association was incubated with the cells stimulated in the presence of K. pneumoniae antigen ATCC 13883 it was observed that TNF-α levels were maintained, in addition to a reduction in IL-10 production. In this way, from the obtained results, the association is able to present a low modulating action of pro and anti-inflammatory mediators. |
publishDate |
2019 |
dc.date.accessioned.fl_str_mv |
2019-07-08T14:49:58Z |
dc.date.issued.fl_str_mv |
2019-03-08 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
status_str |
publishedVersion |
format |
masterThesis |
dc.identifier.citation.fl_str_mv |
FERREIRA, Arthur Corrêa Resende. Avaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniae. 2019. 74 f. Dissertação (Programa Stricto Sensu em Ciências Genômicas e Biotecnologia) - Universidade Católica de Brasília, Brasília, 2019. |
dc.identifier.uri.fl_str_mv |
https://bdtd.ucb.br:8443/jspui/handle/tede/2606 |
identifier_str_mv |
FERREIRA, Arthur Corrêa Resende. Avaliação da produção de mediadores inflamatórios por macrófagos murinos estimulados com Synoeca-MP e levofloxacina na presença de cepas de Klebsiella pneumoniae. 2019. 74 f. Dissertação (Programa Stricto Sensu em Ciências Genômicas e Biotecnologia) - Universidade Católica de Brasília, Brasília, 2019. |
url |
https://bdtd.ucb.br:8443/jspui/handle/tede/2606 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Católica de Brasília |
dc.publisher.program.fl_str_mv |
Programa Stricto Sensu em Ciências Genômicas e Biotecnologia |
dc.publisher.initials.fl_str_mv |
UCB |
dc.publisher.country.fl_str_mv |
Brasil |
dc.publisher.department.fl_str_mv |
Escola de Saúde e Medicina |
publisher.none.fl_str_mv |
Universidade Católica de Brasília |
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Biblioteca Digital de Dissertações da Universidade Católica de Brasília - UCB |
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