HIV Latency and Nanomedicine Strategies for Anti-HIV Treatment and Eradication DOI Creative Commons

Mickensone Andre,

Madhavan Nair,

Andrea Raymond

et al.

Biomedicines, Journal Year: 2023, Volume and Issue: 11(2), P. 617 - 617

Published: Feb. 18, 2023

Antiretrovirals (ARVs) reduce Human Immunodeficiency Virus (HIV) loads to undetectable levels in infected patients. However, HIV can persist throughout the body cellular reservoirs partly due inability of some ARVs cross anatomical barriers and capacity HIV-1 establish latent infection resting CD4+ T cells monocytes/macrophages. A cure for is not likely unless latency addressed delivery reservoir sites improved. Nanomedicine has been used ARV formulations improve efficacy. More specifically, researchers are exploring benefit using nanoparticles nanomedicine eradication strategies such as shock kill, block lock, others. This review will focus on mechanisms nanomedicine-based approaches treat HIV.

Language: Английский

Characterization of HIV-1 Infection in Microglia-Containing Human Cerebral Organoids DOI Creative Commons
Stephanie B. H. Gumbs, Amber Berdenis van Berlekom, Raphael Kübler

et al.

Viruses, Journal Year: 2022, Volume and Issue: 14(4), P. 829 - 829

Published: April 16, 2022

The achievement of an HIV cure is dependent on the eradication or permanent silencing HIV-latent viral reservoirs, including understudied central nervous system (CNS) reservoir. This requires a deep understanding molecular mechanisms HIV's entry into CNS, latency establishment, persistence, and reversal. Therefore, representative CNS culture models that reflect intercellular dynamics pathophysiology human brain are urgently needed in order to study reservoir HIV-induced neuropathogenesis. In this study, we characterized cerebral organoid model which microglia grow intrinsically as infection CNS. We demonstrated both organoids isolated organoid-derived (oMG), infected with replication-competent HIVbal reporter viruses, support productive via CCR5 co-receptor. Productive was only observed microglial cells. Fluorescence analysis revealed target cell. Susceptibility co-expression microglia-specific markers CD4 receptors. Altogether, will be valuable tool within research community HIV-CNS interactions, underlying HIV-associated neurological disorders (HAND), efficacy new therapeutic curative strategies

Language: Английский

Citations

45

HIV infection of non-classical cells in the brain DOI Creative Commons
Angela Wahl, Lena Al‐Harthi

Retrovirology, Journal Year: 2023, Volume and Issue: 20(1)

Published: Jan. 13, 2023

Abstract HIV-associated neurological disorders (HAND) affect up to 50% of people living with HIV (PLWH), even in the era combination antiretroviral therapy (cART). HIV-DNA can be detected cerebral spinal fluid (CSF) approximately half aviremic ART-suppressed PLWH and its presence is associated poorer neurocognitive performance. DNA + RNA cells have also been observed postmortem brain tissue individuals sustained cART suppression. In this review, we provide an overview how invades infection resident glial (astrocytes microglia). We discuss role persistent neuroinflammation HAND their potential contribution reservoir. eradication strategies that target persistently infected glia will likely needed achieve cure.

Language: Английский

Citations

35

Mechanisms underlying HIV-associated cognitive impairment and emerging therapies for its management DOI
Ronald J. Ellis, María J. Marquine, Marcus Kaul

et al.

Nature Reviews Neurology, Journal Year: 2023, Volume and Issue: 19(11), P. 668 - 687

Published: Oct. 10, 2023

Language: Английский

Citations

30

Immune Functions of Astrocytes in Viral Neuroinfections DOI Open Access
Jernej Jorgačevski, Maja Potokar

International Journal of Molecular Sciences, Journal Year: 2023, Volume and Issue: 24(4), P. 3514 - 3514

Published: Feb. 9, 2023

Neuroinfections of the central nervous system (CNS) can be triggered by various pathogens. Viruses are most widespread and have potential to induce long-term neurologic symptoms with potentially lethal outcomes. In addition directly affecting their host cells inducing immediate changes in a plethora cellular processes, viral infections CNS also trigger an intense immune response. Regulation innate response depends not only on microglia, which fundamental CNS, but astrocytes. These align blood vessels ventricle cavities, consequently, they one first cell types become infected after virus breaches CNS. Moreover, astrocytes increasingly recognized as reservoir CNS; therefore, initiated presence intracellular particles may profound effect tissue physiology morphology. should addressed terms persisting because contribute recurring sequelae. To date, different viruses originating from genetically distinct families, including Flaviviridae, Coronaviridae, Retroviridae, Togaviridae, Paramyxoviridae, Picomaviridae, Rhabdoviridae, Herpesviridae, been confirmed. Astrocytes express receptors that detect signaling cascades, leading this review, we summarize current knowledge initiate release inflammatory cytokines depict involvement functions

Language: Английский

Citations

24

Antiretroviral drug therapy does not reduce neuroinflammation in an HIV-1 infection brain organoid model DOI Creative Commons
Samuel Martínez-Meza, Thomas A. Premeaux, Stéfano M. Cirigliano

et al.

Journal of Neuroinflammation, Journal Year: 2025, Volume and Issue: 22(1)

Published: March 5, 2025

HIV-1-associated neurocognitive impairment (HIV-1-NCI) is marked by ongoing and chronic neuroinflammation with loss decline in neuronal function even when antiretroviral drug therapy (ART) successfully suppresses viral replication. Microglia, the primary reservoirs of HIV-1 central nervous system (CNS), play a significant role maintaining this neuroinflammatory state. However, understanding how generated sustained HIV-1, or impacted ART, difficult due to limited access human CNS tissue. We an vitro model admixed hematopoietic progenitor cell (HPC) derived microglia embedded into embryonic stem (ESC) Brain Organoids (BO). Microglia were infected prior co-culture. Infected co-cultured brain organoids BOs infiltrate establish for infection, "HIV-1 M-BO". M-BOs treated ART variable directions. infection was monitored p24 ELISA digital droplet PCR (ddPCR). Inflammation measured cytokine p-NF-kB levels using multiplex ELISA, flow cytometry confocal microscopy. could be create "brain" infection. Although initial source pro-inflammatory cytokines, astrocytes, neurons neural cells also had increased levels, along elevated CCL2 supernatant compared Uninfected M-BOs. suppressed virus below limit detection but did not decrease neuroinflammation. These findings indicate that are pro-inflammatory. significantly inflammation persisted ART-treated Together, these infiltrated provides robust understand impact on

Language: Английский

Citations

1

COVID-19 Lung Pathogenesis in SARS-CoV-2 Autopsy Cases DOI Creative Commons
Silvana Valdebenito,

Simon Bessis,

Djillali Annane

et al.

Frontiers in Immunology, Journal Year: 2021, Volume and Issue: 12

Published: Oct. 4, 2021

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a major public health issue. COVID-19 considered an airway/multi-systemic disease, and demise has been associated with uncontrolled immune response cytokine storm in to the virus. However, lung pathology, response, tissue damage are poorly described understood due safety concerns. Using post-mortem tissues from uninfected deadly cases as well unbiased combined analysis of histology, multi-viral host markers staining, correlative microscopy, confocal, image analysis, we identified three distinct phenotypes COVID-19-induced damage. First, hemorrhage characterized by minimal infiltration large thrombus; Second, excessive cell but no hemorrhagic events. The third phenotype correspond combination two previous ones. We observed loss alveolar wall integrity, detachment pieces, fibroblast proliferation, extensive fibrosis all phenotypes. Although studied were lethal COVID-19, strong was analyzed significant B poor T infiltrations, suggesting exhausted or compromised cellular these patients. Overall, our data show that SARS-CoV-2-induced highly heterogeneous. These individual differences need be understand long-term consequences.

Language: Английский

Citations

55

Identification, Quantification, and Characterization of HIV-1 Reservoirs in the Human Brain DOI Creative Commons
Maribel Donoso, Daniela D’Amico, Silvana Valdebenito

et al.

Cells, Journal Year: 2022, Volume and Issue: 11(15), P. 2379 - 2379

Published: Aug. 2, 2022

The major barrier to cure HIV infection is the early generation and extended survival of reservoirs in circulation tissues. Currently, techniques used detect quantify are mostly based on blood-based assays; however, it has become evident that viral remain Our study describes a novel multi-component imaging method (HIV DNA, mRNA, proteins same assay) identify, quantify, characterize tissues blood products obtained from HIV-infected individuals even when systemic replication undetectable. In human brains under ART, we identified microglia/macrophages small population astrocytes main cells with integrated DNA. Only half DNA expressed one-third proteins. Surprisingly, residual HIV-p24, gp120, nef, vpr, tat protein expression accumulation uninfected around suggesting local synthesis, secretion, bystander uptake. conclusion, our data show ART reduces size brain’s reservoirs; local/chronic secretion still occurs, indicating brain anatomical target infection.

Language: Английский

Citations

33

Near full-length HIV sequencing in multiple tissues collected postmortem reveals shared clonal expansions across distinct reservoirs during ART DOI Creative Commons
Caroline Dufour, María Julia Ruiz, Amélie Pagliuzza

et al.

Cell Reports, Journal Year: 2023, Volume and Issue: 42(9), P. 113053 - 113053

Published: Sept. 1, 2023

HIV persists in tissues during antiretroviral therapy (ART), but the relative contribution of different anatomical compartments to viral reservoir humans remains unknown. We performed an extensive characterization reservoirs two men who donated their bodies cure research and had been on suppressive ART for years. DNA is detected all tissues, with large variations across between participants. Intact genomes represent 2% 25% proviruses participants are mainly secondary lymphoid organs, spleen mediastinal lymph nodes harboring intact both individuals. Multiple copies identical found indicating that clonal expansions common sites. The majority (>85%) these expanded clones shared multiple tissues. These findings suggest infected cells expand, migrate, possibly circulate

Language: Английский

Citations

20

Ionic Liquid Coating‐Driven Nanoparticle Delivery to the Brain: Applications for NeuroHIV DOI
Christine M. Hamadani, Fakhri Mahdi,

Anya Merrell

et al.

Advanced Science, Journal Year: 2024, Volume and Issue: 11(23)

Published: April 4, 2024

Abstract Delivering cargo to the central nervous system (CNS) remains a pharmacological challenge. For infectious diseases such as HIV, CNS acts latent reservoir that is inadequately managed by systemic antiretrovirals (ARTs). ARTs thus cannot eradicate and given infection, patients experience neurological deficits collectively referred “neuroHIV”. Herein, development of bioinspired ionic liquid‐coated nanoparticles (IL‐NPs) for in situ hitchhiking on red blood cells (RBCs) reported, which enables 48% brain delivery intracarotid arterial‐ infused cargo. Moreover, IL choline trans‐2‐hexenoate (CA2HA 1:2) demonstrates preferential accumulation parenchymal microglia over endothelial post‐delivery. This study further successful loading abacavir (ABC), an ART challenging encapsulate, into IL‐NPs, verifies retention antiviral efficacy vitro. IL‐NPs are not cytotoxic primary human peripheral mononuclear (PBMCs) CA2HA 1:2 coating itself confers notable anti‐viremic capacity. In addition, vitro cell culture assays show markedly increased uptake neural compared bare PLGA nanoparticles. work debuts liquids promising nanoparticle coatings assist biodistribution has potential revolutionize cargos (i.e., drugs, viral vectors) through compartmental barriers blood‐brain‐barrier (BBB).

Language: Английский

Citations

7

Humanized Mice for Studies of HIV-1 Persistence and Elimination DOI Creative Commons
Chen Zhang,

Lubaba A. Zaman,

Larisa Y. Poluektova

et al.

Pathogens, Journal Year: 2023, Volume and Issue: 12(7), P. 879 - 879

Published: June 27, 2023

A major roadblock to achieving a cure for human immunodeficiency virus type one (HIV-1) is the persistence of latent viral infections in cells and tissue compartments an infected host. Latent HIV-1 proviral DNA persists resting memory CD4+ T mononuclear phagocytes (MPs; macrophages, microglia, dendritic cells). Tissue reservoirs both cell types reside gut, lymph nodes, bone marrow, spleen, liver, kidney, skin, adipose tissue, reproductive organs, brain. However, despite identification virus-susceptible cells, several limitations persist identifying broad persons. The include their relatively low abundance, precise latently lack biomarkers cells. While primary MP transformed lines are used interrogate mechanisms persistence, they often fail accurately reflect host environments that carry infections. Given specificity HIV-1, there few animal models replicate natural course infection with any precision. These needs underlie importance humanized mouse as valuable cost-effective tools studying latency subsequently means eliminating it. In this review, we discuss advantages mice studies eye toward using these test antiretroviral excision therapeutics. goals research use address how under which circumstances can be detected eliminated. Targeting ultimate task at hand.

Language: Английский

Citations

15