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Ana Carolina Oliveira
Researcher at Federal University of Rio de Janeiro
Publications - 40
Citations - 1365
Ana Carolina Oliveira is an academic researcher from Federal University of Rio de Janeiro. The author has contributed to research in topics: Trypanosoma cruzi & Medicine. The author has an hindex of 17, co-authored 28 publications receiving 1094 citations.
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Journal ArticleDOI
Gut microbial metabolites limit the frequency of autoimmune T cells and protect against type 1 diabetes
Eliana Mariño,James L. Richards,Keiran H. McLeod,Dragana Stanley,Yu Anne Yap,Jacinta Knight,Craig R. M. McKenzie,Jan Kranich,Ana Carolina Oliveira,Fernando J. Rossello,Fernando J. Rossello,Fernando J. Rossello,Balasubramanian Krishnamurthy,Christian M. Nefzger,Christian M. Nefzger,Christian M. Nefzger,Laurence Macia,Laurence Macia,Alison N. Thorburn,Alan G. Baxter,Grant Morahan,Lee H. Wong,Jose M. Polo,Jose M. Polo,Jose M. Polo,Robert J. Moore,Trevor Lockett,Julie M. Clarke,David L. Topping,Leonard C. Harrison,Charles R. Mackay +30 more
TL;DR: Medicinal foods or metabolites might represent an effective and natural approach for countering the numerous immunological defects that contribute to T cell–dependent autoimmune diseases.
Journal ArticleDOI
Expression of functional TLR4 confers proinflammatory responsiveness to Trypanosoma cruzi glycoinositolphospholipids and higher resistance to infection with T. cruzi.
Ana Carolina Oliveira,Jaqueline R. Peixoto,Luciana Barros de Arruda,Marco Antônio Campos,Ricardo T. Gazzinelli,Douglas T. Golenbock,Shizuo Akira,José O. Previato,Lucia Mendonça-Previato,Alberto Nobrega,Maria Bellio +10 more
TL;DR: The results demonstrate that natural resistance to T. cruzi is TLR4 dependent, most likely due toTLR4 recognition of their GIPLs, and find that TLR 4-mutant mice were hypersusceptible to the infection, as evidenced by a higher parasitemia and earlier mortality.
Journal ArticleDOI
The Immune Response to Trypanosoma cruzi: Role of Toll-Like Receptors and Perspectives for Vaccine Development.
TL;DR: The role of TLR-activated pathways in the modulation of both innate and acquired immune responses to T. cruzi infection is focused on and the state of the art of vaccine research and development against the causative agent of Chagas disease is discussed.
Journal ArticleDOI
Impaired innate immunity in Tlr4(-/-) mice but preserved CD8+ T cell responses against Trypanosoma cruzi in Tlr4-, Tlr2-, Tlr9- or Myd88-deficient mice.
Ana Carolina Oliveira,Bruna Cunha de Alencar,Fanny Tzelepis,Weberton Klezewsky,Raquel N. da Silva,Fabieni S. Neves,Gisele S. Cavalcanti,Silvia Beatriz Boscardin,Marise P. Nunes,Marcelo F. Santiago,Alberto Nobrega,Mauricio M. Rodrigues,Maria Bellio +12 more
TL;DR: Results indicate that TLR4, as well as previously shown for TLR2, TLR9 and MyD88, contributes to the innate immune response and, consequently, resistance in the acute phase of infection, although each of these pathways is not individually essential for the generation of class I-restricted responses against T. cruzi.
Journal ArticleDOI
Miltefosine induces programmed cell death in Leishmania amazonensis promastigotes
Fernanda A. Marinho,Keyla C. S. Gonçalves,Selma Soares de Oliveira,Ana Carolina Oliveira,Maria Bellio,Claudia M. d’Avila-Levy,André L.S. Santos,Marta H. Branquinha +7 more
TL;DR: Results indicate that miltefosine causes apoptosis-like death in L. amazonensis promastigote cells using a similar process that is observed in Leishmania donovani.