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Echinococcus granulosus (E. granulosus) infection can induce mechanical compression and a resultant inflammatory reaction within the liver tissue. EgG1Y162 shows promise as an E. granulosus vaccine candidate, though its immunogenic mechanism requires further elucidation. This study delineated the transcriptional and post - translational regulation of core Th9 pathway components mediated by EgG1Y162. The results showed that when the EgG1Y162 protein interacted with mouse spleen lymphocytes, it significantly enhanced their activity and inhibited apoptosis. Our study indicates that the EgG1Y162 protein elevates the mRNA and protein expression of IL-9, IL-4, NF-κB p65, TGF-beta 1, PU.1, and Smad3. It can also specifically recognize antibodies in the serum of E. granulosus - infected patients and sheep. These findings suggest that EgG1Y162 protein plays a role in immune response by promoting Th9 differentiation. Additionally, the IL-9 induced by EgG1Y162 might enhance the host's immune defense against E. granulosus infection. This research provides valuable theoretical support for understanding the immune regulatory mechanisms of the EgG1Y162 protein and aids in the development of related vaccines.
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http://dx.doi.org/10.1016/j.ijbiomac.2025.146515 | DOI Listing |
Int J Biol Macromol
September 2025
State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, Clinical Medicine Institute, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China. Electronic address:
Echinococcus granulosus (E. granulosus) infection can induce mechanical compression and a resultant inflammatory reaction within the liver tissue. EgG1Y162 shows promise as an E.
View Article and Find Full Text PDFBraz J Med Biol Res
November 2024
Department of Immunology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi, Xinjiang, China.
Cystic echinococcosis (CE) is a zoonotic disease caused by the infection of Echinococcus granulosus (E. granulosus) larva. Currently, blocking the pathogenic cycle chain through immunoprophylaxis has become the main research direction.
View Article and Find Full Text PDFOpen Life Sci
March 2023
Department of Immunology, Basic Medical College, Xinjiang Medical University, Xinjiang 830011, Urumqi, China.
In the early stage, our research group cloned -specific antigen, EgG1Y162, from protoscolex and adult worms of . In order to enhance the immunogenicity of the vaccine, we prepared a recombinant vaccine by tandemly linking EgG1Y162, splicing the protein and linker at the gene level. This approach is expected to improve the immunogenicity of the vaccine by enhancing the molecular weight of the protein and increasing the antigenic epitopes.
View Article and Find Full Text PDFOpen Life Sci
November 2022
Department of Immunology, Basic Medical College, Xinjiang Medical University, Urumqi, China.
Cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) is an important surface molecule of activated T cells that has a strong affinity with the B7 molecule on the surface of antigen-presenting cells. Among these molecules, the CTLA-4 extracellular region (CTLA-4 IgV) may be used as a novel immune adjuvant molecule for delivering antigens and inducing strong humoral and cellular immune responses. In this study, bioinformatics analysis was performed to determine and clone the extracellular region of Xinjiang sheep CTLA-4 (NM_001009214).
View Article and Find Full Text PDFZhongguo Xue Xi Chong Bing Fang Zhi Za Zhi
August 2022
Department of Immunology, School of Basic Medicine, Xinjiang Medical University, Urumqi, Xinjiang 830054, China.
Objective: To perform prokaryotic expression and preliminary characterization of the recombinant poly-epitope vaccine EgG1Y162-2 (4) against cystic echinococcosis.
Methods: The recombinant poly-epitope vaccine EgG1Y162-2 (4) against based on the linker GSGGSG was subjected to structural three-dimensional (3D) modeling using immunoinformatics to analyze the structural changes and evaluate the antigenicity of the vaccine. The pET30a-EgG1Y162-2 (4) recombinant plasmid was generated using double digestion with R I and I, and then transformed into competent cells.