Inhibition of HIV virus by neutralizing Vhh attached to dual functional liposomes encapsulating dapivirine
Article
Wang, S., Michiels, J., Ariën, K., New, R., Vanham, G. and Roitt, I. 2016. Inhibition of HIV virus by neutralizing Vhh attached to dual functional liposomes encapsulating dapivirine. Nanoscale Research Letters. 11 (1), pp. 1-10. https://doi.org/10.1186/s11671-016-1558-7
Type | Article |
---|---|
Title | Inhibition of HIV virus by neutralizing Vhh attached to dual functional liposomes encapsulating dapivirine |
Authors | Wang, S., Michiels, J., Ariën, K., New, R., Vanham, G. and Roitt, I. |
Abstract | Although highly active antiretroviral therapy (HAART) has greatly improved the life expectancy of HIV/AIDS patients, the treatment is not curative. It is a global challenge which fosters an urgent need to develop an effective drug or neutralizing antibody delivery approach for the prevention and treatment of this disease. Due to the low density of envelope spikes with restricted mobility present on the surface of HIV virus, which limit the antibody potency and allow virus mutation and escape from the immune system, it is important for a neutralizing antibody to form bivalent or multivalent bonds with the virus. Liposome constructs could fulfil this need due to the flexible mobility of the membrane with its attached antibodies and the capacity for drug encapsulation. In this study, we evaluated the neutralization activity of a range of liposome formulations in different sizes coated with anti-gp120 llama antibody fragments (Vhhs) conjugated via either non-covalent metal chelation or a covalent linkage. The non-covalent construct demonstrated identical binding affinity to HIV-1 envelope glycoprotein gp120 and neutralizing ability for HIV virus as free Vhh. Although covalently linked Vhh showed significant binding affinity to gp120, it unexpectedly had a lower neutralization potency. This may be due to the comparability in size of the viral and liposome particles restricting the number which can be bound to the liposome surface so involving only a fraction of the antibodies, whereas non-covalently attached antibodies dissociate from the surface after acting with gp120 and free the remainder to bind further viruses. Covalently conjugated Vhh might also trigger the cellular uptake of a liposome-virion complex. To explore the possible ability of the antibody-coated liposomes to have a further function, we encapsulated the hydrophobic antiviral drug dapivirine into both of the non-covalently and covalently conjugated liposome formulations, both of which revealed high efficacy in reducing viral replication in vitro. Thus, dual function liposomes may lead to a novel strategy for the prophylaxis of HIV/AIDS by combining the neutralizing activity of Vhh with antiviral effects of high drug concentrations. |
Research Group | Biomarkers for Cancer group |
Publisher | Springer Open |
Journal | Nanoscale Research Letters |
ISSN | 1931-7573 |
Electronic | 1556-276X |
Publication dates | |
Online | 28 Jul 2016 |
31 Dec 2016 | |
Publication process dates | |
Deposited | 03 Nov 2016 |
Accepted | 16 Jul 2016 |
Submitted | 03 Feb 2016 |
Output status | Published |
Publisher's version | License |
Copyright Statement | © 2016 The Author(s). Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
Digital Object Identifier (DOI) | https://doi.org/10.1186/s11671-016-1558-7 |
Language | English |
https://repository.mdx.ac.uk/item/86v3x
Download files
34
total views2
total downloads3
views this month0
downloads this month