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Neutrophils Reduce the Parasite Burden in Leishmania (Leishmania) amazonensis-Infected Macrophages
Author(s) -
Érico Vinícius de Souza Carmo,
Simone Katz,
C. Barbieri
Publication year - 2010
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0013815
Subject(s) - amastigote , leishmania , biology , macrophage , microbiology and biotechnology , elastase , leishmania mexicana , parasite hosting , tumor necrosis factor alpha , neutrophil extracellular traps , phagocytosis , in vitro , leishmania major , inflammation , kinetoplastida , immunology , enzyme , protozoal disease , biochemistry , computer science , malaria , world wide web
Background Studies on the role of neutrophils in Leishmania infection were mainly performed with L. (L) major , whereas less information is available for L. (L) amazonensis . Previous results from our laboratory showed a large infiltrate of neutrophils in the site of infection in a mouse strain resistant to L. (L.) amazonensis (C3H/HePas). In contrast, the susceptible strain (BALB/c) displayed a predominance of macrophages harboring a high number of amastigotes and very few neutrophils. These findings led us to investigate the interaction of inflammatory neutrophils with L. (L.) amazonensis -infected macrophages in vitro . Methodology/Principal Findings Mouse peritoneal macrophages infected with L. (L.) amazonensis were co-cultured with inflammatory neutrophils, and after four days, the infection was quantified microscopically. Data are representative of three experiments with similar results. The main findings were 1) intracellular parasites were efficiently destroyed in the co-cultures; 2) the leishmanicidal effect was similar when cells were obtained from mouse strains resistant (C3H/HePas) or susceptible (BALB/c) to L. (L.) amazonensis ; 3) parasite destruction did not require contact between infected macrophages and neutrophils; 4) tumor necrosis factor alpha (TNF-α), neutrophil elastase and platelet activating factor (PAF) were involved with the leishmanicidal activity, and 5) destruction of the parasites did not depend on generation of oxygen or nitrogen radicals, indicating that parasite clearance did not involve the classical pathway of macrophage activation by TNF-α, as reported for other Leishmania species. Conclusions/Significance The present results provide evidence that neutrophils in concert with macrophages play a previously unrecognized leishmanicidal effect on L. (L.) amazonensis . We believe these findings may help to understand the mechanisms involved in innate immunity in cutaneous infection by this Leishmania species.

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