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Parasite Immunol ; 31(4): 188-98, 2009 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19292770

RESUMEN

CBA/J mice are resistant to Leishmania major infection but are permissive to L. amazonensis infection. In addition, CBA/J macrophages control L. major but not L. amazonensis infection in vitro. Phagocytosis by macrophages is known to determine the outcome of Leishmania infection. Pattern recognition receptors (PRR) adorning antigen presenting cell surfaces are known to coordinate the link between innate and adaptive immunity. The macrophage receptor with collagenous structure (MARCO) is a PRR that is preferably expressed by macrophages and is capable of binding Gram-positive and Gram-negative bacteria. No research on the role of MARCO in Leishmania-macrophage interactions has been reported. Here, we demonstrate, for the first time, that MARCO expression by CBA/J macrophages is increased in response to both in vitro and in vivo L. major infections, but not to L. amazonensis infection. In addition, a specific anti-MARCO monoclonal antibody reduced L. major infection of macrophages by 30%-40% in vitro. The draining lymph nodes of anti-MARCO-treated mice displayed a reduced presence of immunolabelled parasite and parasite antigens, as well as a reduced inflammatory response. These results support the hypothesis that MARCO has a role in macrophage infection by L. major in vitro as well as in vivo.


Asunto(s)
Leishmania major/inmunología , Leishmaniasis/inmunología , Leishmaniasis/metabolismo , Macrófagos Peritoneales/inmunología , Receptores Inmunológicos/biosíntesis , Animales , Anticuerpos Antiprotozoarios/inmunología , Anticuerpos Antiprotozoarios/metabolismo , Inmunidad Innata , Leishmania major/metabolismo , Leishmania mexicana/inmunología , Leishmania mexicana/metabolismo , Leishmaniasis/parasitología , Leishmaniasis/patología , Ganglios Linfáticos/inmunología , Ganglios Linfáticos/patología , Macrófagos Peritoneales/metabolismo , Ratones , Ratones Endogámicos CBA , Receptores Inmunológicos/genética , Receptores Inmunológicos/inmunología , Receptores Depuradores/biosíntesis , Receptores Depuradores/genética , Receptores Depuradores/inmunología , Activación Transcripcional , Regulación hacia Arriba
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