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Targeted alpha therapy's potential to eliminate HIV-infected cells

Date:
December 21, 2015
Source:
European Commission, Joint Research Centre (JRC)
Summary:
Targeted alpha therapy has the potential to selectively eliminate HIV infected cells from the central nervous system, according to a recent study. The study shows that a specific human antibody labelled with the alpha emitter bismuth-213 can penetrate the blood brain barrier and selectively target and destroy HIV-infected cells while sparing non-infected healthy cells. These findings may open new options for the treatment of HIV associated neurocognitive disorders.
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Targeted alpha therapy has the potential to selectively eliminate HIV infected cells from the central nervous system, according to a recent study co-authored by the JRC. The study shows that a specific human antibody labelled with the alpha emitter bismuth-213 can penetrate the blood brain barrier and selectively target and destroy HIV-infected cells while sparing non-infected healthy cells. These findings may open new options for the treatment of HIV associated neurocognitive disorders.

The in vitro study that was at the basis of the scientific article was conducted in a consortium of various research organisations, including Albert Einstein College of Medicine in New York and the JRC. It has shown that the novel alpha emitter radioactive drug can penetrate a simulated human blood brain barrier without causing damage to it and selectively bind and kill HIV-infected cells residing in the central nervous system. The approach is based on the unique physical properties of alpha radiation, in particular its high energy and short path length in human tissue, to selectively address and destroy diseased cells while sparing surrounding healthy tissue.

Combined therapy against the virus (cART) allows HIV-positive patients to live much longer. There are however reservoirs within the body where the virus persists and continues to cause damage. In particular the treatment of infections of the central nervous system poses a particular challenge as the blood brain barrier limits many cART drugs from reaching effective levels in the brain. Currently, about half of all HIV infected patients are suffering from mild to moderate neurological disorders.

The study was co-funded by Bill and Melinda Gates foundation and the National Institute of Health. Albert Einstein College of Medicine and JRC have been collaborating for a decade on the joint development of targeted alpha therapy of bacterial, fungal and viral infections, including HIV.


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Materials provided by European Commission, Joint Research Centre (JRC). Note: Content may be edited for style and length.


Journal References:

  1. Ekaterina Dadachova, Mahesh C Patel, Sima Toussi, Christos Apostolidis, Alfred Morgenstern, Martin W Brechbiel, Miroslaw K Gorny, Susan Zolla-Pazner, Arturo Casadevall, Harris Goldstein. Targeted Killing of Virally Infected Cells by Radiolabeled Antibodies to Viral Proteins. PLoS Medicine, 2006; 3 (11): e427 DOI: 10.1371/journal.pmed.0030427
  2. McFarren A1, Lopez L, Williams DW, Veenstra M, Bryan RA, Goldsmith A, Morgenstern A, Bruchertseifer F, Zolla-Pazner S, Gorny MK, Eugenin EA, Berman JW, Dadachova E. A fully human antibody to gp41 selectively eliminates HIV-infected cells that transmigrated across a model human blood brain barrier. AIDS, 2015 [abstract]

Cite This Page:

European Commission, Joint Research Centre (JRC). "Targeted alpha therapy's potential to eliminate HIV-infected cells." ScienceDaily. ScienceDaily, 21 December 2015. <www.sciencedaily.com/releases/2015/12/151221071641.htm>.
European Commission, Joint Research Centre (JRC). (2015, December 21). Targeted alpha therapy's potential to eliminate HIV-infected cells. ScienceDaily. Retrieved April 19, 2024 from www.sciencedaily.com/releases/2015/12/151221071641.htm
European Commission, Joint Research Centre (JRC). "Targeted alpha therapy's potential to eliminate HIV-infected cells." ScienceDaily. www.sciencedaily.com/releases/2015/12/151221071641.htm (accessed April 19, 2024).

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