Results 11 to 20 of about 6,286 (187)

Filling the Gaps in Antagonist CCR5 Binding, a Retrospective and Perspective Analysis

open access: yesFrontiers in Immunology, 2022
The large number of pathologies that position CCR5 as a central molecular determinant substantiates the studies aimed at understanding receptor-ligand interactions, as well as the development of compounds that efficiently block this receptor.
Yerkezhan Amerzhanova, Luca Vangelista
doaj   +1 more source

The role of CCR5 in HIV-associated neurocognitive disorders

open access: yesHeliyon, 2022
While combination antiretroviral therapy (cART) has successfully increased the lifespan of individuals infected with HIV, a significant portion of this population remains affected by HIV-associated neurocognitive disorder (HAND). C-C chemokine receptor 5
Cecile Riviere-Cazaux   +3 more
doaj   +1 more source

Molecular determinants of antagonist interactions with chemokine receptors CCR2 and CCR5

open access: yesBiophysical Journal, 2023
Abstract By driving monocyte chemotaxis, the chemokine receptor CCR2 shapes inflammatory responses and the formation of tumor microenvironments. This makes it a promising target in inflammation and immuno-oncology; however, despite extensive efforts, there are no FDA-approved CCR2-targeting therapeutics.
John R.D. Dawson   +10 more
openaire   +3 more sources

Blockade of Autocrine CCL5 Responses Inhibits Zika Virus Persistence and Spread in Human Brain Microvascular Endothelial Cells

open access: yesmBio, 2021
Zika virus (ZIKV) is a neurovirulent flavivirus that uniquely causes fetal microcephaly, is sexually transmitted, and persists in patients for up to 6 months.
Megan C. Mladinich   +4 more
doaj   +1 more source

Alterations in chemokine receptor CCR5 activity influence tumor cell biology in human cholangiocarcinoma cell lines

open access: yesAnnals of Hepatology, 2021
Introduction and objectives: Intrahepatic (I-CCA) and extrahepatic (E-CCA) cholangiocarcinoma (CCA) have different growth patterns and risks for tumor metastasis. Inhibition and/or activation of the chemokine receptor CCR subclasses have been reported to
Jiaqi Yang   +3 more
doaj   +1 more source

Computational study of the structural ensemble of CC chemokine receptor type 5 (CCR5) and its interactions with different ligands.

open access: yesPLoS ONE, 2022
CC Chemokine receptor 5 (CCR5), a member of the Superfamily of G Protein-Coupled Receptors (GPCRs), is an important effector in multiple physiopathological processes such as inflammatory and infectious entities, including central nervous system ...
Guillermo Goode-Romero, Laura Dominguez
doaj   +1 more source

Targeting CCR5 as a Component of an HIV-1 Therapeutic Strategy

open access: yesFrontiers in Immunology, 2022
Globally, human immunodeficiency virus type 1 (HIV-1) infection is a major health burden for which successful therapeutic options are still being investigated.
Hager Mohamed   +6 more
doaj   +1 more source

The therapeutic potential of C-C chemokine receptor antagonists in nonalcoholic steatohepatitis

open access: yesExploration of Medicine, 2020
Pooled prevalence of nonalcoholic fatty liver disease (NAFLD) globally is about 25%. Nonalcoholic steatohepatitis (NASH) with advanced fibrosis has been linked with substantial morbidity and mortality, without having to-date any licensed treatment.
Michael Doulberis   +4 more
doaj   +1 more source

Evolution of Multiple Domains of the HIV-1 Envelope Glycoprotein during Coreceptor Switch with CCR5 Antagonist Therapy

open access: yesMicrobiology Spectrum, 2022
HIV-1 uses CD4 as a receptor and chemokine receptors CCR5 and/or CXCR4 as coreceptors. CCR5 antagonists are a class of antiretrovirals used to inhibit viral entry.
Yueqi Du   +7 more
doaj   +1 more source

CCR5/CXCR4 Dual Antagonism for the Improvement of HIV Infection Therapy

open access: yesMolecules, 2019
HIV entry in the host cell requires the interaction with the CD4 membrane receptor, and depends on the activation of one or both co-receptors CCR5 and CXCR4.
Fedora Grande   +8 more
doaj   +1 more source

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