Proteomic analysis of plasma in healthy adults receiving recombinant vaccinia virus provides novel insights into HIV-1 neutralizing antibodies

被引:0
作者
Chen, Ran [1 ]
Fu, Yuyu [1 ]
Li, Dan [1 ]
Wang, Shuhui [1 ]
Ruan, Yuhua [1 ]
Ren, Li [1 ]
Wang, Shuo [1 ]
Shen, Xiuli [1 ]
Shi, Yutao [1 ]
Shao, Yiming [1 ,2 ]
Liu, Ying [1 ]
机构
[1] Chinese Ctr Dis Control & Prevent, Natl Ctr AIDS STD Control & Prevent, Natl Key Lab Intelligent Tracking & Forecasting In, Beijing, Peoples R China
[2] Changping Lab, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
CCL23; HIV; inflammation-related protein; neutralizing antibody; vaccines; VIRAL VECTORS; T-CELLS; VACCINATION; INDUCTION; INFECTION; RESPONSES; MACAQUES;
D O I
10.1002/jmv.29749
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human immunodeficiency virus (HIV) infection is still a global public health issue, and the development of an effective prophylactic vaccine inducing potent neutralizing antibodies remains a significant challenge. This study aims to explore the inflammation-related proteins associated with the neutralizing antibodies induced by the DNA/rTV vaccine. In this study, we employed the Olink chip to analyze the inflammation-related proteins in plasma in healthy individuals receiving HIV candidate vaccine (DNA priming and recombinant vaccinia virus rTV boosting) and compared the differences between neutralizing antibody-positive (nab + ) and -negative(nab-) groups. We identified 25 differentially expressed factors and conducted enrichment and correlation analysis on them. Our results revealed that significant expression differences in artemin (ARTN) and C-C motif chemokine ligand 23 (CCL23) between nab+ and -nab- groups. Notably, the expression of CCL23 was negatively corelated to the ID50 of neutralizing antibodies and the intensity of the CD4+ T cell responses. This study enriches our understanding of the immune picture induced by the DNA/rTV vaccine, and provides insights for future HIV vaccine development.
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页数:12
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