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May 2019; 6 (3) Views & ReviewsOpen Access

Antineuroinflammatory drugs in HIV-associated neurocognitive disorders as potential therapy

Björn Ambrosius, Ralf Gold, Andrew Chan, Simon Faissner
First published April 4, 2019, DOI: https://doi.org/10.1212/NXI.0000000000000551
Björn Ambrosius
From the Department of Neurology (B.A., R.G., S.F.), St. Josef-Hospital, Ruhr-University Bochum, Gudrunstr, Bochum, Germany; and Department of Neurology (A.C.), University Hospital Bern, Bern University, Switzerland.
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Ralf Gold
From the Department of Neurology (B.A., R.G., S.F.), St. Josef-Hospital, Ruhr-University Bochum, Gudrunstr, Bochum, Germany; and Department of Neurology (A.C.), University Hospital Bern, Bern University, Switzerland.
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Andrew Chan
From the Department of Neurology (B.A., R.G., S.F.), St. Josef-Hospital, Ruhr-University Bochum, Gudrunstr, Bochum, Germany; and Department of Neurology (A.C.), University Hospital Bern, Bern University, Switzerland.
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Simon Faissner
From the Department of Neurology (B.A., R.G., S.F.), St. Josef-Hospital, Ruhr-University Bochum, Gudrunstr, Bochum, Germany; and Department of Neurology (A.C.), University Hospital Bern, Bern University, Switzerland.
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Citation
Antineuroinflammatory drugs in HIV-associated neurocognitive disorders as potential therapy
Björn Ambrosius, Ralf Gold, Andrew Chan, Simon Faissner
Neurol Neuroimmunol Neuroinflamm May 2019, 6 (3) e551; DOI: 10.1212/NXI.0000000000000551

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Abstract

Today, HIV-infected (HIV+) patients can be treated efficiently with combined antiretroviral therapy (cART), leading to long-term suppression of viral load, in turn increasing life expectancy. While cART reduced the occurrence of HIV-associated dementia, the prevalence of subtle forms of HIV-associated neurocognitive disorders (HAND) is unchanged. This is related to persistent immune activation within the CNS, which is not addressed by cART. Pathologic processes leading to HAND consist of the release of proinflammatory cytokines, chemokines, reactive oxygen metabolites and glutamate, and the release of HIV proteins. Some of those processes can be targeted using medications with immunomodulatory and neuroprotective properties such as dimethyl fumarate, teriflunomide, or minocycline. In this review, we will summarize the knowledge about key pathogenic processes involved in HAND and potential therapeutic avenues to target HAND.

Glossary

cART=
combined antiretroviral therapy;
CPE=
CNS penetration effectiveness;
DMF=
Dimethyl fumarate;
HAND=
HIV-associated neurocognitive disorders;
NF-kB=
nuclear factor ĸß;
PML=
progressive multifocal leukoencephalopathy;
RRMS=
relapsing-remitting MS;
S1P1=
sphingosin-1 phosphate receptor 1;
SIV=
simian immunodeficiency virus

Footnotes

  • Funding information and disclosures are provided at the end of the article. Full disclosure form information provided by the authors is available with the full text of this article at Neurology.org/NN.

  • The Article Processing Charge was funded by the Ruhr-Universität Bochum.

  • Received November 3, 2018.
  • Accepted in final form February 17, 2019.
  • Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND), which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.

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