Survival Mechanisms Used by Some Leishmania Species to Escape Neutrophil Killing
Details
Download: fimmu-08-01558.pdf (1434.92 [Ko])
State: Public
Version: Final published version
State: Public
Version: Final published version
Serval ID
serval:BIB_AF9E161610CB
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
Survival Mechanisms Used by Some Leishmania Species to Escape Neutrophil Killing
Journal
Frontiers in Immunology
ISSN
1664-3224
Publication state
Published
Issued date
16/11/2017
Peer-reviewed
Oui
Volume
8
Pages
1558
Language
english
Abstract
Neutrophils are the most abundant leukocytes in human blood. Upon microbial infection, they are massively and rapidly recruited from the circulation to sites of infection where they efficiently kill pathogens. To this end, neutrophils possess a variety of weapons that can be mobilized and become effective within hours following infection. However, several microbes including some Leishmania spp. have evolved a variety of mechanisms to escape neutrophil killing using these cells as a basis to better invade the host. In addition, neutrophils are also present in unhealing cutaneous lesions where their role remains to be defined. Here, we will review recent progress in the field and discuss the different strategies applied by some Leishmania parasites to escape from being killed by neutrophils and as recently described for Leishmania mexicana, even replicate within these cells. Subversion of neutrophil killing functions by Leishmania is a strategy that allows parasite spreading in the host with a consequent deleterious impact, transforming the primary protective role of neutrophils into a deleterious one.
Keywords
Leishmania, neutrophils, Leishmania survival, neutrophil extracellular traps, reactive oxygen species, neutrophil granules, Leishmania replication
Web of science
Open Access
Yes
Create date
01/12/2017 9:46
Last modification date
20/08/2019 15:19