A interação entre a imunidade inata e adaptativa acontece durante diversas fases da resposta imune. Os Toll-like receptors (TLRs) tem importante papel na ativação de macrófagos e portanto, no conjunto de moléculas secretadas por estas células. Pouco se sabe sobre o papel destas substâncias no processo de contração da população de células T ativadas (Activation-induced cell death - AICD). Portanto, o objetivo do presente trabalho foi avaliar se macrófagos estimulados com diferentes agonistas de TLRs poderiam produzir fatores solúveis com capacidade modulatória da morte por AICD. Primeiramente, demonstramos que tanto a linhagem macrofágica J774, quanto os macrófagos derivados de medula óssea (BMDMs) expressam todos os TLRs, com excessão do TLR11. Comprovamos que estas proteínas são funcionais, uma vez que o estímulo com agonistas de TLRs leva à ativação de NF-<font face=\"Symbol\">&#954B nestes macrófagos. Finalmente, mostramos que os sobrenadantes gerados pelos macrófagos são capazes de proteger as células DO11.10 da AICD, via a regulação negativa de FasL, parcialmente mediada por PGE2. / The interaction between innate and adaptative immunity occurs in several phases of the immune response. The Toll-like receptors (TLRs) have an important role in the activation of macrophages directly acting on the molecules secreted by these cells. Little is known about the role of these secreted molecules on the survival control of activated T lymphocytes (Activation-induced cell death - AICD). Therefore, the objective of the present work was to evaluate the effects of soluble factors produced by macrophages activated with several TLRs agonists, on the survival of T lymphocytes. First we sought the expression of TRLs on both bone marrow-derived and J774 macrophage cell line and we could see that both cells express all TLRs, except for TLR 11. The stimulation of both cells with TLRs agonists leads to the expression of NF-<font face=\"Symbol\">&#954B and the production of soluble factors that are able to protect DO11.10 T lymphocyte cell line from AICD, via down regulation of FasL partially mediated by PGE2.

Submitted by Automa??o e Estat?stica (sst@bczm.ufrn.br) on 2017-10-05T19:38:54Z No. of bitstreams: 1 MeireKarlaMiguelCruz_DISSERT.pdf: 2036779 bytes, checksum: 473b18d2efcf87356709325b06611782 (MD5) / Approved for entry into archive by Arlan Eloi Leite Silva (eloihistoriador@yahoo.com.br) on 2017-10-17T22:53:55Z (GMT) No. of bitstreams: 1 MeireKarlaMiguelCruz_DISSERT.pdf: 2036779 bytes, checksum: 473b18d2efcf87356709325b06611782 (MD5) / Made available in DSpace on 2017-10-17T22:53:55Z (GMT). No. of bitstreams: 1 MeireKarlaMiguelCruz_DISSERT.pdf: 2036779 bytes, checksum: 473b18d2efcf87356709325b06611782 (MD5) Previous issue date: 2017-02-23 / C?es s?o os reservat?rios prim?rios dos parasitos do g?nero Leishmania. Receptores da imunidade inata fazem a detec??o precoce do parasito e conduzem a imunidade adaptativa espec?fica na tentativa de controlar a infec??o. Entretanto, poucos estudos tem investigado a correla??o entre a express?o de receptores da imunidade inata e a resist?ncia ou susceptibilidade em c?es infectados por Leishmania infantum. O objetivo deste estudo foi correlacionar os achados cl?nicos em c?es naturalmente infectados por L. infantum ? express?o de receptores da imunidade inata (Toll Like Receptors-TLRs e Nod Like Receptors-NLRs). Inicialmente, o soro de 76 c?es foi coletado no Centro de Controle de Zoonoses de Natal, Rio Grande do Norte, Brasil. A positividade dos c?es para L. infantum foi confirmada pela reatividade nos testes de ELISA e DPP?. Os c?es foram clinicamente avaliados e classificados como sintom?ticos (n=19), oligossintom?ticos (n=19), assintom?ticos (n=19) e n?o infectados (n=19). Os c?es naturalmente infectados por L. infantum e controles n?o infectados foram eutanasiados e fragmentos de f?gado foram coletados para quantifica??o da express?o de RNAm de TLRs (TLR1-9), NLRs (NOD1, NOD2, NLRP1 e NLRP3) citocinas (IL1?, IL-6, IL-12, IL-10, TNF?, IFN-?) e iNOS com auxilio da t?cnica de PCR em tempo real. Os resultados demonstram o aumento na express?o da maioria dos receptores do tipo Toll e do tipo Nod nos c?es naturalmente infectados por L. infantum, comparado a animais n?o infectados. Entretanto, c?es sintom?ticos apresentaram maior express?o de TLR1, TLR2, TLR3, TLR4, TLR5, TLR7, TLR8, NLRP1, NLRP3, NOD1 e IL-1? quando comparado a animais assintom?ticos, mostrando significante aumento na transcri??o destas mol?culas com a progress?o da doen?a. Por outro lado, c?es assintom?ticos apresentaram maior express?o de RNAm de citocinas (IFN-?, IL-12) e iNOS quando comparado a animais oligossintom?ticos e sintom?ticos. Este estudo gerou novos conhecimentos envolvendo receptores da imunidade inata (TLRs, NLRs) na leishmaniose visceral canina (LVC), podendo servir de base para o melhor entendimento dos mecanismos de resist?ncia ou susceptibilidade ? infec??o por L. infantum em c?es, bem como dar subs?dio a estrat?gias profil?ticas para o controle da LVC. / Dogs are the primary reservoirs of parasites of the Leishmania genus. Innate immune receptors perform early detection of the parasite and lead to specific adaptive immune response in attempt to infection control. However, few studies have investigated a correlation between the expression of innate immunity receptors and the resistance or susceptibility pattern in dogs naturally infected with Leishmania infantum. The aim of this study was to correlate the clinical status of dogs naturally infected with L. infantum with the mRNA expression levels of innate imune receptors (Toll like receptors-TLRs and Nod Like Receptors-NLRs). Initially, serum of 76 dogs was collected at the Zoonoses Control Center in Natal, Rio Grande do Norte, Brazil. The L. infantum infection in dogs was confirmed by ELISA and DPP? tests. Subsequently, animals were clinially evaluated and classified as asymptomatic (n=19), oligosymptomatic (n=19), symptomatic (n=19) and uninfected (n=19). Dogs naturally infected by L. infantum and uninfected controls were euthanasied and liver samples were collected to quantify mRNA expression of TLRs (TLR1-9), Nod Like receptors-NLRs (NOD1, NOD2, NLRP1, NLRP3), cytokines (IL1?, IL-6, IL-12, IL-10, TNF?, IFN-?) and iNOS using real-time PCR. The results demonstrate the increased expression of almost all TLRs and NLRs in dogs naturally infected by L. infantum compared with uninfected animals. However, symptomatic dogs showed higher expression of TLR1, TLR2, TLR3, TLR4, TLR5, TLR7, TLR8 NLRP1, NLRP3, NOD1 and IL-1? than asymptomatic animals, revealing significant up regulation of transcription with disease progression. On the other hand, asymptomatic dogs presented greater cytokine mRNA expression (IFN-?, IL-12) and iNOS when compared to oligosymptomatic and asymptomatic animals. This study unveil new knowledge involving innate immunity receptors (TLRs, NLRs) and cytokines in canine visceral leishmaniasis and may be used as a basis for better understanding of resistance or susceptibility mechanisms in dogs infected with L. infantum, as well as prophylactic strategies to control canine visceral leishmaniasis.

A interação entre a imunidade inata e adaptativa acontece durante diversas fases da resposta imune. Os Toll-like receptors (TLRs) tem importante papel na ativação de macrófagos e portanto, no conjunto de moléculas secretadas por estas células. Pouco se sabe sobre o papel destas substâncias no processo de contração da população de células T ativadas (Activation-induced cell death - AICD). Portanto, o objetivo do presente trabalho foi avaliar se macrófagos estimulados com diferentes agonistas de TLRs poderiam produzir fatores solúveis com capacidade modulatória da morte por AICD. Primeiramente, demonstramos que tanto a linhagem macrofágica J774, quanto os macrófagos derivados de medula óssea (BMDMs) expressam todos os TLRs, com excessão do TLR11. Comprovamos que estas proteínas são funcionais, uma vez que o estímulo com agonistas de TLRs leva à ativação de NF-<font face=\"Symbol\">&#954B nestes macrófagos. Finalmente, mostramos que os sobrenadantes gerados pelos macrófagos são capazes de proteger as células DO11.10 da AICD, via a regulação negativa de FasL, parcialmente mediada por PGE2. / The interaction between innate and adaptative immunity occurs in several phases of the immune response. The Toll-like receptors (TLRs) have an important role in the activation of macrophages directly acting on the molecules secreted by these cells. Little is known about the role of these secreted molecules on the survival control of activated T lymphocytes (Activation-induced cell death - AICD). Therefore, the objective of the present work was to evaluate the effects of soluble factors produced by macrophages activated with several TLRs agonists, on the survival of T lymphocytes. First we sought the expression of TRLs on both bone marrow-derived and J774 macrophage cell line and we could see that both cells express all TLRs, except for TLR 11. The stimulation of both cells with TLRs agonists leads to the expression of NF-<font face=\"Symbol\">&#954B and the production of soluble factors that are able to protect DO11.10 T lymphocyte cell line from AICD, via down regulation of FasL partially mediated by PGE2.