Short report:: Responses to Leishmania donovani in mice deficient in both phagocyte oxidase and inducible nitric oxide synthase

被引:30
作者
Murray, HW
Xiang, ZY
Ma, XJ
机构
[1] Cornell Univ, Dept Med, Weill Med Coll, New York, NY 10021 USA
[2] Cornell Univ, Dept Microbiol & Immunol, Weill Med Coll, New York, NY 10021 USA
关键词
D O I
10.4269/ajtmh.2006.74.1013
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Mice deficient in phagocyte oxidase (phox) and inducible nitric oxide synthase (iNOS), which are primary macrophage killing mechanisms, generated tissue granulomas but showed unrestrained Leishmania donovani visceral replication and suboptimal initial responsiveness to antimony treatment. Nevertheless, visceral infection was controlled post-treatment and did not recur. A phox/iNOS-independent macrophage mechanism, which was not triggered by L. donovani, emerges after chemotherapy.
引用
收藏
页码:1013 / 1015
页数:3
相关论文
共 12 条
[1]   Organ-specific and stage-dependent control of Leishmania major infection by inducible nitric oxide synthase and phagocyte NADPH oxidase [J].
Blos, M ;
Schleicher, U ;
Rocha, FJS ;
Meissner, U ;
Röllinghoff, M ;
Bogdan, C .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2003, 33 (05) :1224-1234
[2]   Prevention of relapse after chemotherapy in a chronic intracellular infection: Mechanisms in experimental visceral leishmaniasis [J].
Murray, HW .
JOURNAL OF IMMUNOLOGY, 2005, 174 (08) :4916-4923
[3]   Roles of endogenous gamma interferon and macrophage microbicidal mechanisms in host response to chemotherapy in experimental visceral leishmaniasis [J].
Murray, HW ;
Delph-Etienne, S .
INFECTION AND IMMUNITY, 2000, 68 (01) :288-293
[4]   KILLING OF INTRACELLULAR LEISHMANIA-DONOVANI BY HUMAN MONONUCLEAR PHAGOCYTES - EVIDENCE FOR OXYGEN-DEPENDENT AND OXYGEN-INDEPENDENT LEISHMANICIDAL ACTIVITY [J].
MURRAY, HW ;
CARTELLI, DM .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 72 (01) :32-44
[5]   Macrophage microbicidal mechanisms in vivo:: Reactive nitrogen versus oxygen intermediates in the killing of intracellular visceral Leishmania donovani [J].
Murray, HW ;
Nathan, CF .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (04) :741-746
[6]   IN-VITRO ANTILEISHMANIAL PROPERTIES OF TRIVALENT AND PENTAVALENT ANTIMONIAL PREPARATIONS [J].
ROBERTS, WL ;
BERMAN, JD ;
RAINEY, PM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (06) :1234-1239
[7]   Mice deficient in LRG-47 display enhanced snsceptibility to Trypanosoma cruzi infection associated with defective hemopoiesis and intracellular control of parasite growth [J].
Santiago, HC ;
Feng, CG ;
Bafica, A ;
Roffe, E ;
Arantes, RM ;
Cheever, A ;
Taylor, G ;
Vierira, LQ ;
Aliberti, J ;
Gazzinelli, RT ;
Sher, A .
JOURNAL OF IMMUNOLOGY, 2005, 175 (12) :8165-8172
[8]   Genome-wide analysis of molecular changes in IL-12-induced control of mammary carcinoma via IFN-γ-independent mechanisms [J].
Shi, XY ;
Cao, SJ ;
Mitsuhashi, M ;
Xiang, ZY ;
Ma, XJ .
JOURNAL OF IMMUNOLOGY, 2004, 172 (07) :4111-4122
[9]   Phenotype of mice and macrophages deficient in both phagocyte oxidase and inducible nitric oxide synthase [J].
Shiloh, MU ;
MacMicking, JD ;
Nicholson, S ;
Brause, JE ;
Potter, S ;
Marino, M ;
Fang, F ;
Dinauer, M ;
Nathan, C .
IMMUNITY, 1999, 10 (01) :29-38
[10]   Antimonial-induced increase in intracellular Ca2+ through non-selective cation channels in the host and the parasite is responsible for apoptosis of intracellular Leishmania donovani amastigotes [J].
Sudhandiran, G ;
Shaha, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (27) :25120-25132