Wenxiu Wang

Dr. Wenxiu Wang


Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2016 in Virus Research
Verified
Journal Article
Closed access
WWWenxiu Wang
Wenxiu Wang
ASAbdo Said
Abdo Said
YWYan Wang
Yan Wang
QFQiang Fu
Qiang Fu
YXYueqiang Xiao
Yueqiang Xiao
SZShen Zhiqiang
Shen Zhiqiang

1 March 2018 in PLOS ONE
Verified
Journal Article
Open access
PDF file
WWWenxiu Wang
Wenxiu Wang
ASAbdelrahman Said
Abdelrahman Said
BWBaoqin Wang
Baoqin Wang
GQGuanggang Qu
Guanggang Qu
QXQingqing Xu
Qingqing Xu
SZShen Zhiqiang
Shen Zhiqiang
In this study, we report the establishment and characterization of a new epithelial cell line, goose embryonated epithelial cell line (GEE), derived from embryonic goose tissue. The purified GEE cell line can efficiently grow over 65 passages in the M199 medium supplemented with 10% fetal bovine serum at 37°C. Immunofluorescence assay was used to identify purified GEE cells as epithelial cell line by detecting expression of the Keratin-18 and -19. Further characterizations demonstrated that the GEE cell line can be continuously subcultured with (i) a high capacity to replicate for over 65 passages, (ii) a spontaneous epithelial-like morphology, (iii) constant chromosomal features and (iv) without an evidence of converting to tumorigenic cells either in vitro or in vivo study. Moreover, the GEE cell line can be effectively transfected with plasmids expressing reporter genes of different avian viruses, such as VP3, VP1 and F of goose parvo virus (GPV), duck hepatitis virus (DHV), and Newcastle disease virus (NDV), respectively. Finally, the established GEE cell line was evaluated for avian viruses infection susceptibility. Our results showed that the tested GPV, DHAV and NDV were capable to replicate in the new cell line with titers a comparatively higher to the ones detected in the traditional culture system. Accordingly, our established GEE cell line is apparently a suitable in vitro model for transgenic, and infection manipulation studies.

1 January 2023 in Journal of Animal Science
Verified
Journal Article
Closed access
PDF file
YZYan Zhang
Yan Zhang
BLBo Liu
Bo Liu
ASAbdo Said
Abdo Said
JXJinwen Xie
Jinwen Xie
FTFengrong Tian
Fengrong Tian
WWWenxiu Wang
Wenxiu Wang
Mycoplasma (M) hyopneumoniae causes enzootic pneumonia, a highly contagious respiratory disease in swine that causes significant economic losses worldwide. It is unknown whether the NLR family pyrin domain containing 3 (NLRP3) inflammasome regulates the immune response in swine during M. hyopneumoniae infection. The current study utilized an in vivo swine model of M. hyopneumoniae infection to investigate the regulatory functional role of the NLRP3 inflammasome during M. hyopneumoniae infection. Notable histopathological alterations were observed in M. hyopneumoniae-infected swine tissues, which were associated with an inflammatory response and disease progression. Swine M. hyopneumoniae infection was associated with an increase in the expression of the NLRP3 inflammasome, which stimulated pro-inflammatory cytokines such as tumour necrosis factor-alpha (TNF- α), interleukin 18 (IL-18), and interleukin 1 beta (IL-1 β). The impact of the NLRP3 inhibitor, MCC950 on NLRP3 and pro-inflammatory cytokines in M. hyopneumoniae-infected swine was examined to investigate the relationship between the NLRP3 inflammasome and M. hyopneumoniae infection. Taken together, our findings provide strong evidence that the NLRP3 inflammasome plays a critical regulatory functional role in M. hyopneumoniae infection in swine.

31 March 2025 in Vaccines
Verified
Journal Article
Open access
PDF file
YJYimin Jia
Yimin Jia
HZHui Zhu
Hui Zhu
XCXinyu Cai
Xinyu Cai
CSCun Sun
Cun Sun
YYYan Ye
Yan Ye
WWWenxiu Wang
Wenxiu Wang
Cancer is a major cause of death worldwide, and vaccine administration is an effective way to stimulate immune responses in patients and to achieve preventive and therapeutic effects. Few vaccines have been used in clinical settings because they have poor immunogenicity, and it is difficult to induce a robust immune response in patients. An adjuvant is an important component of a vaccine that can enhance the intensity, speed, and duration of immune responses. The achievements of adjuvants in the production of stable, safe, and immunogenic tumor vaccines have aroused the enthusiasm of researchers. Recent results have suggested that plant-derived adjuvants have unique advantages, such as greatly improving immune responses to cancer vaccines and promoting humoral and cellular immunity with good biocompatibility and biodegradability. When these adjuvants are used in combination with vaccines, they can not only activate the immune response in vivo but can also promote cytokine secretion and accelerate dendritic cell maturation. This review focused on the application progress of plant adjuvants, including saponins, polysaccharides, flavonoids, and plant virus-like particles, and their combination with nano-delivery systems in cancer vaccines. At the same time, we have also discussed the immunomodulatory mechanisms of these adjuvants and their prospects for improving vaccine efficacy in the treatment of cancer in the future. These promising plant adjuvants may provide prospects and a research basis for the development of tumor vaccines.

25 April 2026 in Virology Journal
Verified
Journal Article
Open access
PDF file
BLBo Liu
Bo Liu
YBYanli Bi
Yanli Bi
JXJinwen Xie
Jinwen Xie
HSHaige Su
Haige Su
LALisanework E Ayalew
Lisanework E Ayalew
WWWenxiu Wang
Wenxiu Wang
Infectious bursal disease virus (IBDV) remains a major threat to the global poultry industry, causing significant economic losses. Recent surveillance data