» Articles » PMID: 20595631

Impact of Short-term Combined Antiretroviral Therapy on Brain Virus Burden in Simian Immunodeficiency Virus-infected and CD8+ Lymphocyte-depleted Rhesus Macaques

Overview
Journal Am J Pathol
Publisher Elsevier
Specialty Pathology
Date 2010 Jul 3
PMID 20595631
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Antiretroviral drugs suppress virus burden in the cerebrospinal fluid of HIV-infected individuals; however, the direct effect of antiretrovirals on virus replication in brain parenchyma is poorly understood. We investigated the effect of short-term combined antiretroviral therapy (CART) on brain virus burden in rhesus monkeys using the CD8-depletion model of accelerated simian immunodeficiency virus (SIV) encephalitis. Four monkeys received CART (consisting of the nonpenetrating agents PMPA and RCV) for four weeks, beginning 28 days after SIV inoculation. Lower virus burdens were measured by real-time RT-PCR in four of four regions of brain from monkeys that received CART as compared with four SIV-infected, untreated controls; however, the difference was only significant for the frontal cortex (P < 0.05). In contrast, significantly lower virus burdens were measured in plasma and four of five lymphoid compartments from animals that received CART. Surprisingly, despite normalization of neuronal function in treated animals, the numbers of activated macrophages/microglia and the magnitude of TNF-alpha mRNA expression in brain were similar between treated animals and controls. These results suggest that short-term therapy with antiretrovirals that fail to penetrate the blood-cerebrospinal fluid barrier can reduce brain virus burden provided systemic virus burden is suppressed; however, longer treatment may be required to completely resolve encephalitic lesions and microglial activation, which may reflect the longer half-life of the principal target cells of HIV/SIV in the brain (macrophages) versus lymphoid tissues (T lymphocytes).

Citing Articles

Opioid abuse and SIV infection in non-human primates.

Deshetty U, Ray S, Singh S, Buch S, Periyasamy P J Neurovirol. 2023; 29(4):377-388.

PMID: 37418108 PMC: 10729652. DOI: 10.1007/s13365-023-01153-z.


Neuroinflammatory Profiling in SIV-Infected Chinese-Origin Rhesus Macaques on Antiretroviral Therapy.

Solis-Leal A, Siddiqui S, Wu F, Mohan M, Hu W, Doyle-Meyers L Viruses. 2022; 14(1).

PMID: 35062343 PMC: 8781366. DOI: 10.3390/v14010139.


Advances in SIV/SHIV Non-Human Primate Models of NeuroAIDS.

Moretti S, Virtuoso S, Sernicola L, Farcomeni S, Maggiorella M, Borsetti A Pathogens. 2021; 10(8).

PMID: 34451482 PMC: 8398602. DOI: 10.3390/pathogens10081018.


Myeloid and CD4 T Cells Comprise the Latent Reservoir in Antiretroviral Therapy-Suppressed SIVmac251-Infected Macaques.

Abreu C, Veenhuis R, Avalos C, Graham S, Parrilla D, Ferreira E mBio. 2019; 10(4).

PMID: 31431552 PMC: 6703426. DOI: 10.1128/mBio.01659-19.


Temporal/compartmental changes in viral RNA and neuronal injury in a primate model of NeuroAIDS.

Gonzalez R, Fell R, He J, Campbell J, Burdo T, Autissier P PLoS One. 2018; 13(5):e0196949.

PMID: 29750804 PMC: 5947913. DOI: 10.1371/journal.pone.0196949.


References
1.
Miller R, Isaacson P, Hall-Craggs M, Lucas S, Gray F, Scaravilli F . Cerebral CD8+ lymphocytosis in HIV-1 infected patients with immune restoration induced by HAART. Acta Neuropathol. 2004; 108(1):17-23. DOI: 10.1007/s00401-004-0852-0. View

2.
Fox H, Weed M, Huitron-Resendiz S, Baig J, Horn T, Dailey P . Antiviral treatment normalizes neurophysiological but not movement abnormalities in simian immunodeficiency virus-infected monkeys. J Clin Invest. 2000; 106(1):37-45. PMC: 314358. DOI: 10.1172/JCI9102. View

3.
Pierson T, McArthur J, Siliciano R . Reservoirs for HIV-1: mechanisms for viral persistence in the presence of antiviral immune responses and antiretroviral therapy. Annu Rev Immunol. 2000; 18:665-708. DOI: 10.1146/annurev.immunol.18.1.665. View

4.
Nath A, Schiess N, Venkatesan A, Rumbaugh J, Sacktor N, Mcarthur J . Evolution of HIV dementia with HIV infection. Int Rev Psychiatry. 2008; 20(1):25-31. DOI: 10.1080/09540260701861930. View

5.
Chesebro B, Wehrly K, Nishio J, Perryman S . Macrophage-tropic human immunodeficiency virus isolates from different patients exhibit unusual V3 envelope sequence homogeneity in comparison with T-cell-tropic isolates: definition of critical amino acids involved in cell tropism. J Virol. 1992; 66(11):6547-54. PMC: 240149. DOI: 10.1128/JVI.66.11.6547-6554.1992. View