2004
DOI: 10.1016/j.niox.2004.03.002
|View full text |Cite
|
Sign up to set email alerts
|

Echinococcus multilocularis laminated-layer components and the E14t 14-3-3 recombinant protein decrease NO production by activated rat macrophages in vitro

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
28
0

Year Published

2007
2007
2017
2017

Publication Types

Select...
9
1

Relationship

2
8

Authors

Journals

citations
Cited by 53 publications
(28 citation statements)
references
References 20 publications
0
28
0
Order By: Relevance
“…Moreover, pretreatment of mice with hydatid LL induced a concomitant decrease of IFN-γ and TNF-α levels in plasma and the attenuation of iNOS and NF-κB expression in the mucosa. Moreover, other studies have described an important immunomodulatory role for hydatid LL through the downregulation of NO production in mice in vivo and in vitro [24,25]. …”
Section: Discussionmentioning
confidence: 99%
“…Moreover, pretreatment of mice with hydatid LL induced a concomitant decrease of IFN-γ and TNF-α levels in plasma and the attenuation of iNOS and NF-κB expression in the mucosa. Moreover, other studies have described an important immunomodulatory role for hydatid LL through the downregulation of NO production in mice in vivo and in vitro [24,25]. …”
Section: Discussionmentioning
confidence: 99%
“…Helminth 14-3-3 protein interacts with the TGF-β Type-1 receptor and enhances TGF-β signalling in the reactivation of tissue-arrested  Ancylostoma caninum  L3 [35]. Recombinant 14-3-3 protein reduces toxicity for the larvae of NO production from activated macrophages  in vitro [36]. Failure to recognise the FTT-2 isoform of 14-3-3 protein in L4 of mice during colitis could contribute to nematode survival.…”
Section: Discussionmentioning
confidence: 99%
“…In fact, NO may be both cytotoxic against parasites and immuno-modulatory by inhibiting cell activation. Both were found to be operating and it was especially demonstrated that the high periparasitic Nitric Oxide (NO) production by peritoneal exudate cells contributed to periparasitic immunosuppression [96, 97]; this explains why, paradoxically, iNOS deficient mice exhibit a significantly lower susceptibility towards experimental infection [98]. …”
Section: Effector and Regulatory Cells And Mechanisms In E Multilmentioning
confidence: 99%