XZXuelian Zhao

Xuelian Zhao

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Xuelian Zhao has a total of 8 co-authors. Here are the top co-authors by number of shared publications:

  • Haibo Feng

    Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and Utilization, Ministry of Education, Southwest Minzu University, Chengdu 610041, China; Institute of Qinghai-Tibetan Plateau, Southwest Minzu University, Chengdu, Sichuan 610041, PR China

    1 shared publication
  • Jing Fan

    Sichuan Industrial Institute of Antibiotics, Chengdu University, Chengdu, Sichuan 610051, China

    1 shared publication
  • Lang Lin

    College of Veterinary Medicine, Southwest University, Rongchang, Chongqing 402460, China

    1 shared publication
  • Sean P. McDonough

    Department of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA

    1 shared publication
  • Shiping Yang

    Department of Veterinary Medicine, Southwest University, Rongchang, Chongqing 402460, China

    1 shared publication
  • Xiao Yi

    Department of Veterinary Medicine, Southwest University, Rongchang, Chongqing 402460, China

    1 shared publication

Latest Publications

  • Open Access

    Phosphorylated Radix Cyathulae officinalis Polysaccharides Act as Adjuvant via Promoting Dendritic Cell Maturation

    by Haibo Feng, Sean P. McDonough, Jing Fan, Shiping Yang, Xuelian Zhao, Yong Lu, Yun Gan, Xiao Yi, Yung-Fu Chang

    The aim of this study was to investigate whether phosphorylated Radix Cyathulae officinalis Kuan polysaccharides (pRCPS) used as adjuvant with foot-and-mouth disease vaccine (FMDV) can stimulate specific humoral and cellular immune responses in ICR mice. The results demonstrated that pRCPS significantly up-regulated FMDV-specific IgG, IgG1, IgG2b and IgG2a antibody levels and splenocyte proliferation. pRCPS also promoted the killing activities of cytotoxic T lymphocytes (CTL) and natural killer cells (NK). In addition, pRCPS enhanced the expression levels of IL-2, IL-4, and IFN-γ in CD4+ T cells and the level of IFN-γ in CD8+ T cells. Importantly, pRCPS enhanced the expression of MHCII, CD40+, CD86+, and CD80+ in dendritic cells (DCs). This study indicated that phosphorylation modification could increase immune-enhancing activities of RCPS, and pRCPS could promote humoral and cellular immune responses through facilitating DC maturation.