IL-12Rβ2-deficient mice of a genetically resistant background are susceptible to Leishmania major infection and develop a parasite-specific Th2 immune response

2003 ◽  
Vol 5 (4) ◽  
pp. 241-249 ◽  
Author(s):  
Habiba Chakir ◽  
Antonio Campos-Neto ◽  
Majid Mojibian ◽  
John R. Webb
2014 ◽  
Vol 8 (9) ◽  
pp. e3194 ◽  
Author(s):  
Iris J. Gonzalez-Leal ◽  
Bianca Röger ◽  
Angela Schwarz ◽  
Tanja Schirmeister ◽  
Thomas Reinheckel ◽  
...  

Biomedicines ◽  
2020 ◽  
Vol 8 (11) ◽  
pp. 452
Author(s):  
Andrés Vacas ◽  
Celia Fernández-Rubio ◽  
Esther Larrea ◽  
José Peña-Guerrero ◽  
Paul A. Nguewa

A novel serine/threonine protein kinase, LmjF.22.0810, was recently described in Leishmania major. After generating an L. major cell line overexpressing LmjF.22.0810 (named LmJ3OE), the ability of this novel protein to modulate the Th2-type immune response was analyzed. Our results suggest that the protein kinase LmjF.22.0810 might be involved in leishmaniasis outcomes. Indeed, our study outlined the LmJ3OE parasites infectivity in vitro and in vivo. Transgenic parasites displayed lower phagocytosis rates in vitro, and their promastigote forms exhibited lower expression levels of virulence factors compared to their counterparts in control parasites. In addition, LmJ3OE parasites developed significantly smaller footpad swelling in susceptible BALB/c mice. Hematoxylin–eosin staining allowed the observation of a lower inflammatory infiltrate in the footpad from LmJ3OE-infected mice compared to animals inoculated with control parasites. Gene expression of Th2-associated cytokines and effectors revealed a dramatically lower induction in interleukin (IL)-4, IL-10, and arginase 1 (ARG1) mRNA levels at the beginning of the swelling; no expression change was found in Th1-associated cytokines except for IL-12. Accordingly, such results were validated by immunohistochemistry studies, illustrating a weaker expression of ARG1 and a similar induction for inducible NO synthase (iNOS) in footpads from LmJ3OE-infected mice compared to control L. major infected animals. Furthermore, the parasite burden was lower in footpads from LmJ3OE-infected mice. Our analysis indicated that such significant smaller footpad swellings might be due to an impairment of the Th2 immune response that subsequently benefits Th1 prevalence. Altogether, these studies depict LmjF.22.0810 as a potential modulator of host immune responses to Leishmania. Finally, this promising target might be involved in the modulation of infection outcome.


2007 ◽  
Vol 249 (1) ◽  
pp. 1-7 ◽  
Author(s):  
T.U. Maioli ◽  
C.M. Carneiro ◽  
F.A. Assis ◽  
A.M.C. Faria

2012 ◽  
Vol 6 (7) ◽  
pp. e1741 ◽  
Author(s):  
Anja Kathrin Wege ◽  
Christian Florian ◽  
Wolfgang Ernst ◽  
Nicole Zimara ◽  
Ulrike Schleicher ◽  
...  

2013 ◽  
Vol 81 (7) ◽  
pp. 2546-2553 ◽  
Author(s):  
Allen D. Smith ◽  
Lumei Cheung ◽  
Ethiopia Beshah ◽  
Terez Shea-Donohue ◽  
Joseph F. Urban

ABSTRACTHeligmosomoides bakeriis a nematode with parasitic development exclusively in the small intestine of infected mice that induces a potent STAT6-dependent Th2 immune response. We previously demonstrated that host protective expulsion of adultH. bakeriworms from a challenge infection was delayed in selenium (Se)-deficient mice. In order to explore mechanisms associated with the delayed expulsion, 3-week-old female BALB/c mice were placed on a torula yeast-based diet with or without 0.2 ppm Se, and after 5 weeks, they were inoculated withH. bakeriinfective third-stage larvae (L3s). Two weeks after inoculation, the mice were treated with an anthelmintic and then rested, reinoculated with L3s, and evaluated at various times after reinoculation. Analysis of gene expression in parasite-induced cysts and surrounding tissue isolated from the intestine of infected mice showed that the local-tissue Th2 response was decreased in Se-deficient mice compared to that in Se-adequate mice. In addition, adult worms recovered from Se-deficient mice had higher ATP levels than worms from Se-adequate mice, indicating greater metabolic activity in the face of a suboptimal Se-dependent local immune response. Notably, the process of worm expulsion was restored within 2 to 4 days after feeding a Se-adequate diet to Se-deficient mice. Expulsion was associated with an increased local expression of Th2-associated genes in the small intestine, intestinal glutathione peroxidase activity, secreted Relm-β protein, anti-H. bakeriIgG1 production, and reduced worm fecundity and ATP-dependent metabolic activity.


Science ◽  
1996 ◽  
Vol 271 (5251) ◽  
pp. 987-990 ◽  
Author(s):  
N. Noben-Trauth ◽  
P. Kropf ◽  
I. M ller

Sign in / Sign up

Export Citation Format

Share Document