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High antibody and cellular responses induced to HIV-1 clade C envelope following DNA vaccines delivered by electroporation
Journal article   Open access   Peer reviewed

High antibody and cellular responses induced to HIV-1 clade C envelope following DNA vaccines delivered by electroporation

Jiangmei Yin, Anlan Dai, Jonathan LeCureux, Tatiana Arango, Michele A Kutzler, Jian Yan, Mark G Lewis, Amir Khan, Niranjan Y Sardesai, David Montefiore, …
Vaccine, v 29(39), pp 6763-6770
2011
PMID: 21195801
url
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10839813View
Accepted (AM)Open Access (License Unspecified) Open

Abstract

DNA vaccine SHIV RANTES Clade C
Clade C is the predominant HIV-1 strain infecting people in sub-Saharan Africa, India, and China and there is a critical need for a vaccine targeted to these areas. In this study we tested a DNA based vaccine that encodes the SIVgag, SIVpol and HIV-1 envelope clade C. Rhesus macaques were immunized by electroporation with the DNA plasmid encoding optimized SIVgag, SIVpol and an HIV-1 env clade C with or without the adjuvant RANTES. Animals were monitored for immune responses and challenged following the final immunization with 25 animal infectious doses (AID) of SHIV-1157ipd3N4. We found that the vaccine induced high levels of antigen specific IFN-γ producing effector cells and the capacity for CD4+ and CD8+ to proliferate upon antigen stimulation. Importantly, we found that the vaccine induced antibody titers as high as 1/4000. These antibodies were capable of neutralizing tier 1 HIV-1 viruses. Finally, when macaques were challenged with SHIV, viral loads were controlled in vaccinated groups. We conclude that immunization with a simian/human immunodeficiency virus DNA-based vaccine delivered by electroporation can induce cellular and humoral immune responses that are able to control viral replication.

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Industry collaboration
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Web of Science research areas
Immunology
Medicine, Research & Experimental
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