Pyroptosis executioner gasdermin D contributes to host defense and promotes Th 1 immune response during Neospora caninum infection

2020 ◽  
Vol 286 ◽  
pp. 109254
Author(s):  
Xiaocen Wang ◽  
Xin Li ◽  
Pengtao Gong ◽  
Nan Zhang ◽  
Lu Li ◽  
...  
Parasitology ◽  
2016 ◽  
Vol 143 (5) ◽  
pp. 606-616 ◽  
Author(s):  
ADRIANA AGUADO-MARTÍNEZ ◽  
AFONSO P. BASTO ◽  
JOACHIM MÜLLER ◽  
VRENI BALMER ◽  
VERA MANSER ◽  
...  

SUMMARYImmunoprophylactic products against neosporosis during pregnancy should induce an appropriately balanced immune response. In this respect, OprI, a bacterial lipoprotein targeting toll like receptor (TLR)2, provides promising adjuvant properties. We report on the manipulation of the innate and the T-cell immune response through the fusion of OprI with the Neospora caninum chimeric protein Mic3-1-R. In contrast to Mic3-1-R, OprI-MIC3-1-R significantly activated bone-marrow dendritic cells from naïve mice. Mice immunized with OprI-Mic3-1-R induced an immune response with mixed T helper (Th)1 and Th2 properties (high levels of both immunoglobulin (Ig)G1 and IgG2a and of interleukin (IL)-10, IL-12(p70) and interferon-γ responses) whereas Mic3-1-R+saponin induced a clear Th2-biased response (low IgG2a and high IL-4 and IL-10). After mating and challenge with N. caninum, increased expression of interferon-γ was only found in placentas from OprI-Mic3-1-R immunized dams. However, no protection against vertical transmission and neonatal mortality was observed in either of the two groups. These results indicated that more exhaustive studies must be done to elucidate the immune mechanisms associated with transplacental transmission. Antigen linkage to TLR2-ligands, such as OprI, is a useful tool to investigate this enigma by reorienting the innate and adaptive immune responses against other candidate antigens in future studies.


2021 ◽  
Vol 139 ◽  
pp. 140-152
Author(s):  
Xu Zhang ◽  
Xin Li ◽  
Pengtao Gong ◽  
Xiaocen Wang ◽  
Nan Zhang ◽  
...  

2000 ◽  
Vol 90 (3) ◽  
pp. 183-191 ◽  
Author(s):  
Tetsuya Tanaka ◽  
Taketo Hamada ◽  
Noboru Inoue ◽  
Hideyuki Nagasawa ◽  
Kozo Fujisaki ◽  
...  

1995 ◽  
Vol 36 (3) ◽  
pp. 387-391
Author(s):  
A. Flagstad ◽  
Η. Ε. Jensen ◽  
Ι. Bjerkàs ◽  
Κ. Rasmussen

2017 ◽  
Vol 242 ◽  
pp. 22-23 ◽  
Author(s):  
Qing-Feng Meng ◽  
Gui-Zhe Yao ◽  
Si-Yuan Qin ◽  
Jian Wu ◽  
Xi-Chen Zhang ◽  
...  

Author(s):  
José Luis Salguero-Romero ◽  
Dora Romero-Salas ◽  
Anabel Cruz-Romero ◽  
Miguel A. Alonso-Díaz ◽  
Mariel Aguilar-Domínguez ◽  
...  

2006 ◽  
Vol 77 (3-4) ◽  
pp. 254-283 ◽  
Author(s):  
Barbara Häsler ◽  
Katharina D.C. Stärk ◽  
Heinz Sager ◽  
Bruno Gottstein ◽  
Martin Reist

2018 ◽  
Vol 18 (15) ◽  
pp. 1304-1323 ◽  
Author(s):  
Roberto Sánchez-Sánchez ◽  
Patricia Vázquez ◽  
Ignacio Ferre ◽  
Luis Miguel Ortega-Mora

Toxoplasmosis and neosporosis are closely related protozoan diseases that lead to important economic impacts in farm ruminants. Toxoplasma gondii infection mainly causes reproductive failure in small ruminants and is a widespread zoonosis, whereas Neospora caninum infection is one of the most important causes of abortion in cattle worldwide. Vaccination has been considered the most economic measure for controlling these diseases. However, despite vaccine development efforts, only a liveattenuated T. gondii vaccine has been licensed for veterinary use, and no promising vaccines against neosporosis have been developed; therefore, vaccine development remains a key goal. Additionally, drug therapy could be a valuable strategy for disease control in farm ruminants, as several drugs that limit T. gondii and N. caninum proliferation and dissemination have been evaluated. This approach may also be relevant to performing an initial drug screening for potential human therapy for zoonotic parasites. Treatments can be applied against infections in adult ruminants to minimize the outcomes of a primo-infection or the reactivation of a chronic infection during gestation or in newborn ruminants to avoid infection chronification. In this review, the current status of drug development against toxoplasmosis and neosporosis in farm ruminants is presented, and in an effort to promote additional treatment options, prospective drugs that have shown efficacy in vitro and in laboratory animal models of toxoplasmosis and neosporosis are examined.


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