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1.
Eur J Immunol ; 45(10): 2821-33, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26138432

RESUMO

DCs are professional APCs playing a crucial role in the initiation of T-cell responses to combat infection. However, systemic bacterial infection with various pathogens leads to DC-depletion in humans and mice. The mechanisms of pathogen-induced DC-depletion remain poorly understood. Previously, we showed that mice infected with Yersinia enterocolitica (Ye) had impaired de novo DC-development, one reason for DC-depletion. Here, we extend these studies to gain insight into the molecular mechanisms of DC-depletion and the impact of different bacteria on DC-development. We show that the number of bone marrow (BM) hematopoietic progenitors committed to the DC lineage is reduced following systemic infection with different Gram-positive and Gram-negative bacteria. This is associated with a TLR4- and IFN-γ-signaling dependent increase of committed monocyte progenitors in the BM and mature monocytes in the spleen upon Ye-infection. Adoptive transfer experiments revealed that infection-induced monopoiesis occurs at the expense of DC-development. Our data provide evidence for a general response of hematopoietic progenitors upon systemic bacterial infections to enhance monocyte production, thereby increasing the availability of innate immune cells for pathogen control, whereas impaired DC-development leads to DC-depletion, possibly driving transient immunosuppression in bacterial sepsis.


Assuntos
Diferenciação Celular/imunologia , Células Dendríticas/imunologia , Imunidade Inata , Mielopoese/imunologia , Yersiniose/imunologia , Yersinia enterocolitica/imunologia , Animais , Células Dendríticas/patologia , Células-Tronco Hematopoéticas/imunologia , Células-Tronco Hematopoéticas/patologia , Interferon gama/imunologia , Camundongos , Camundongos Knockout , Transdução de Sinais/imunologia , Receptor 4 Toll-Like/imunologia , Yersiniose/patologia
2.
PLoS One ; 8(11): e81088, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24260539

RESUMO

Leishmaniasis is caused by protozoa of the genus Leishmania and transmitted by sand flies from mammalian reservoirs to humans. In recent years, a northward spread of L. infantum from highly endemic Mediterranean countries into previously non-endemic Central European areas has been suspected based on presumed sporadic cases of autochthonous leishmaniasis. Here, we investigated whether sand flies are prevalent in Bavaria in Southern Germany, a federal state in which autochthonous cases have previously been reported. Considering the present and future climatic conditions, we determined whether Bavaria is suitable for five sand fly species with assumed spreading tendencies towards Central Europe: Phlebotomus ariasi, P. neglectus, P. perfiliewi and P. perniciosus that are known vectors for Leishmania in Europe, and P. mascittii, a suspected but not proven vector. Within Bavaria we defined sampling regions based on their climatic suitability and their spatial distance to the sites of the autochthonous cases and/or to areas of reported sand fly detection in states adjacent to Bavaria. At 155 locations in 7 sampling regions, CDC light traps were placed during 38 nights in the summers of 2009 and 2010, resulting in 202 trap-nights. All traps were negative for sand flies. The results suggest that Bavaria is not yet endemic for sand flies, but do not exclude the possibility of sporadic cases of autochthonous human or zoonotic Leishmania infections. This study, which combined methodological approaches from different disciplines, serves as reference for future surveys and risk analyses of sand flies and leishmaniasis in so far non-endemic areas of Europe.


Assuntos
Monitoramento Epidemiológico , Insetos Vetores , Modelos Estatísticos , Phlebotomus , Distribuição Animal , Animais , Clima , Previsões , Alemanha , Humanos , Insetos Vetores/classificação , Insetos Vetores/fisiologia , Leishmania infantum/fisiologia , Leishmaniose Visceral/prevenção & controle , Leishmaniose Visceral/transmissão , Phlebotomus/classificação , Phlebotomus/fisiologia , Temperatura
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