CXCR4-activated astrocyte glutamate release via TNFα: amplification by microglia triggers neurotoxicity

…, M Domercq, L Brambilla, R Galli, D Schols… - Nature …, 2001 - nature.com
Astrocytes actively participate in synaptic integration by releasing transmitter (glutamate) via
a calcium-regulated, exocytosis-like process. Here we show that this process follows …

[HTML][HTML] STAT2 signaling restricts viral dissemination but drives severe pneumonia in SARS-CoV-2 infected hamsters

…, W Chiu, P Leyssen, E Heylen, D Schols… - Nature …, 2020 - nature.com
Emergence of SARS-CoV-2 causing COVID-19 has resulted in hundreds of thousands of
deaths. In search for key targets of effective therapeutics, robust animal models mimicking …

Inhibition of T-tropic HIV strains by selective antagonization of the chemokine receptor CXCR4

D Schols, S Struyf, JV Damme, JA Esté… - The Journal of …, 1997 - rupress.org
Bicyclams are a novel class of antiviral compounds that are highly potent and selective
inhibitors of the replication of HIV-1 and HIV-2. Surprisingly, however, when the prototype …

Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds

…, J Balzarini, M Baba, R Snoeck, D Schols… - Journal of virological …, 1988 - Elsevier
A rapid, sensitive and automated assay procedure was developed for the in vitro evaluation
of anti-HIV agents. An HTLV-I transformed T4-cell line, MT-4, which was previously shown …

[HTML][HTML] A single-dose live-attenuated YF17D-vectored SARS-CoV-2 vaccine candidate

…, C Vandermeulen, E Heylen, V Vergote, D Schols… - Nature, 2021 - nature.com
The expanding pandemic of coronavirus disease 2019 (COVID-19) requires the development
of safe, efficacious and fast-acting vaccines. Several vaccine platforms are being …

Potent and selective inhibition of HIV-1 replication in vitro by a novel series of TIBO derivatives

R Pauwels, K Andries, J Desmyter, D Schols, MJ Kukla… - Nature, 1990 - nature.com
IN the search for compounds active against human immunodeficiency virus (HIV), we have
found that members of a novel series of tetrahydro-imidazo[4,5,1-jk][l,4]-benzodiazepin-2(1H)-…

AMD3100, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor

GA Donzella, D Schols, SW Lin, JA Esté… - Nature medicine, 1998 - nature.com
The bicyclam AMD3100 (formula weight 830) blocks HIV-1 entry and membrane fusion via
the CXCR4 co-receptor, but not via CCR5. AMD3100 prevents monoclonal antibody 12G5 …

[HTML][HTML] Chemokine receptor inhibition by AMD3100 is strictly confined to CXCR4

S Hatse, K Princen, G Bridger, E De Clercq, D Schols - FEBS letters, 2002 - Elsevier
This study was undertaken to demonstrate the unique specificity of the chemokine receptor
CXCR4 antagonist AMD3100. Calcium flux assays with selected chemokine/cell …

Safety, pharmacokinetics, and antiviral activity of AMD3100, a selective CXCR4 receptor inhibitor, in HIV-1 infection

…, AC Collier, MM Lederman, D Schols… - JAIDS Journal of …, 2004 - journals.lww.com
AMD3100 is a CXCR4 receptor inhibitor with anti–HIV-1 activity in vitro. We tested the safety,
pharmacokinetics, and antiviral effect of AMD3100 administered for 10 days by continuous …

Differential antiherpesvirus and antiretrovirus effects of the (S) and (R) enantiomers of acyclic nucleoside phosphonates: potent and selective in vitro and in vivo …

…, L Naesens, R Snoeck, D Schols… - Antimicrobial Agents …, 1993 - Am Soc Microbiol
The (S)- and (R)-enantiomers of acyclic purine nucleoside phosphonate analogs (ie, 3-hydroxy-2-phosphonomethoxypropyl
[HPMP] derivatives, 3-fluoro-2-phosphonomethoxypropyl […