Results 1 to 10 of about 32,947 (176)

Physiological Corticosterone Attenuates gp120-Mediated Microglial Activation and Is Associated with Reduced Anxiety-Like Behavior in gp120-Expressing Mice

open access: yesViruses, 2023
Despite the benefits of combinatorial antiretroviral therapies (cART), virotoxic HIV proteins are still detectable within the central nervous system. Approximately half of all cART-treated patients contend with neurological impairments.
Emaya M. Moss   +3 more
doaj   +2 more sources

HIV-1 gp120 mannoses induce immunosuppressive responses from dendritic cells.

open access: yesPLoS Pathogens, 2007
The human immunodeficiency virus type 1 (HIV-1) envelope glycoprotein gp120 is a vaccine immunogen that can signal via several cell surface receptors.
Meimei Shan   +10 more
doaj   +2 more sources

Development of an Ultrasensitive ELISA Assay for Evaluating HIV-1 Envelope Glycoprotein as a Marker for Targeted Activator of Cell Kill. [PDF]

open access: yesViruses
The HIV-1 envelope glycoprotein gp120 is prominently exposed on the surface of both HIV-1 virions and infected host cells, serving as a key marker of infection.
Wu G   +11 more
europepmc   +2 more sources

Insight derived from molecular dynamics simulations into molecular motions, thermodynamics and kinetics of HIV-1 gp120. [PDF]

open access: yesPLoS ONE, 2014
Although the crystal structures of the HIV-1 gp120 core bound and pre-bound by CD4 are known, the details of dynamics involved in conformational equilibrium and transition in relation to gp120 function have remained elusive.
Peng Sang   +4 more
doaj   +1 more source

HIV-1 gp120 induces expression of IL-6 through a nuclear factor-kappa B-dependent mechanism: suppression by gp120 specific small interfering RNA. [PDF]

open access: yesPLoS ONE, 2011
In addition to its role in virus entry, HIV-1 gp120 has also been implicated in HIV-associated neurocognitive disorders. However, the mechanism(s) responsible for gp120-mediated neuroinflammation remain undefined.
Ankit Shah   +11 more
doaj   +1 more source

The glycan shield of HIV is predominantly oligomannose independently of production system or viral clade. [PDF]

open access: yesPLoS ONE, 2011
The N-linked oligomannose glycans of HIV gp120 are a target for both microbicide and vaccine design. The extent of cross-clade conservation of HIV oligomannose glycans is therefore a critical consideration for the development of HIV prophylaxes.
Camille Bonomelli   +7 more
doaj   +1 more source

A strategy for eliciting antibodies against cryptic, conserved, conformationally dependent epitopes of HIV envelope glycoprotein. [PDF]

open access: yesPLoS ONE, 2010
Novel strategies are needed for the elicitation of broadly neutralizing antibodies to the HIV envelope glycoprotein, gp120. Experimental evidence suggests that combinations of antibodies that are broadly neutralizing in vitro may protect against ...
Hanna C Kelker   +2 more
doaj   +1 more source

Synergistic cooperation between methamphetamine and HIV-1 gsp120 through the P13K/Akt pathway induces IL-6 but not IL-8 expression in astrocytes. [PDF]

open access: yesPLoS ONE, 2012
HIV-1 envelope protein gp120 has been extensively studied for neurotoxic effects that have been attributed to the increased expression of various proinflammatory cytokines in the CNS.
Ankit Shah   +4 more
doaj   +1 more source

Blood–brain barrier abnormalities caused by exposure to HIV-1 gp120 — Protection by gene delivery of antioxidant enzymes

open access: yesNeurobiology of Disease, 2010
HIV-1 effects on the blood–brain barrier (BBB) structure and function are still poorly understood in animal models based on direct administration of recombinant HIV proteins.
Jean-Pierre Louboutin   +5 more
doaj   +1 more source

A Chimeric HIV-1 gp120 Fused with Vaccinia Virus 14K (A27) Protein as an HIV Immunogen. [PDF]

open access: yesPLoS ONE, 2015
In the HIV vaccine field, there is a need to produce highly immunogenic forms of the Env protein with the capacity to trigger broad B and T-cell responses.
Aneesh Vijayan   +8 more
doaj   +1 more source

Home - About - Disclaimer - Privacy