Title of article :
TLR agonist rHP-NAP as an Adjuvant of Dendritic Cell-Based Vaccine to Enhance Anti-Melanoma Response
Author/Authors :
Kang, Qiaozhen School of Life Sciences - Zhengzhou University , Hou, Meiling School of Life Sciences - Zhengzhou University , Wang, Xiaodong School of Life Sciences - Zhengzhou University , Lu, Jike School of Life Sciences - Zhengzhou University , Guo, Xun School of Life Sciences - Zhengzhou University , Ding, Cong School of Life Sciences - Zhengzhou University , Liang, Taotao School of Life Sciences - Zhengzhou University , Liu, Xin School of Life Sciences - Zhengzhou University , Ji, Zhenyu Henan Academy of Medical and Pharmaceutical Sciences - Zhengzhou University , Xie, Peng Zhengzhou Xinzhiyi Biotechnology Co. - Zhengzhou - PR China
Pages :
12
From page :
14
To page :
25
Abstract :
Melanoma is a common and malignant cutaneous tumor, which is responsible for a large proportion of skin cancer deaths. Dendritic cell (DC)-based vaccines have achieved positive results in the treatment of melanoma because of their ability to induce cytotoxic response to facilitate tumor elimination. Objective: To improve the efficacy of dendritic cell-based vaccines by the adjuvant activity of Helicobacter pylori neutrophil activating protein (HP-NAP), which is a virulence factor of Helicobacter pylori, has been proved as a TLR agonist with effective immunomodulatory activity. Methods: The recombinant HP-NAP (rHP-NAP) was expressed by using prokaryotic expression system. Dendritic cells (DCs) were cultured with granulocyte-macrophage colony-stimulating factor (GM-CSF) and IL-4. After treating with rHP-NAP, the maturation of DCs and dendritic cell-based vaccine were assayed by using flow cytometry and qRT-PCR. The activation and proliferation of T cells were measured by FCM, ELISA and MTT methods. The tumor specific cytotoxic response to resistant B16F10 was detected by using lactate dehydrogenase-release assay and qRT-PCR. Results: The recombinant HP-NAP (rHP-NAP), prepared from E. coli prokaryotic expression system, was able to significantly promote the maturation of dendritic cell-based vaccine loaded with tumor cell lysate (TCL) of B16F10 (DC-B16F10-TCL). Furthermore, it effectively induced the activation and proliferation of T cells and tumor specific cytotoxic response to resistant B16F10 melanoma tumor cells. Conclusion: These results suggested that rHP-NAP possesses the potential for use as an adjuvant of dendritic cell-based vaccine in anti-melanoma treatment.
Keywords :
Melanoma, rHP-NAP , Dendritic Cell-Based Vaccine , Cytotoxic Response
Journal title :
Astroparticle Physics
Serial Year :
2020
Record number :
2487416
Link To Document :
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