lipoteichoic-acid and Disease-Resistance

lipoteichoic-acid has been researched along with Disease-Resistance* in 1 studies

Other Studies

1 other study(ies) available for lipoteichoic-acid and Disease-Resistance

Article	Year
The trichloroethylene metabolite S-(1,2-dichlorovinyl)-l-cysteine but not trichloroacetate inhibits pathogen-stimulated TNF-α in human extraplacental membranes in vitro. Reproductive toxicology (Elmsford, N.Y.), 2015, Volume: 52 Extraplacental membranes define the gestational compartment and provide a barrier to infectious microorganisms ascending the gravid female reproductive tract. We tested the hypothesis that bioactive metabolites of trichloroethylene (TCE) decrease pathogen-stimulated innate immune response of extraplacental membranes. Extraplacental membranes were cultured for 4, 8, and 24h with the TCE metabolites trichloroacetate (TCA) or S-(1,2-dichlorovinyl)-l-cysteine (DCVC) in the absence or presence of lipoteichoic acid (LTA) or lipopolysaccharide (LPS) to simulate infection. In addition, membranes were cocultured with DCVC and Group B Streptococcus (GBS). DCVC (5-50μM) significantly inhibited LTA-, LPS-, and GBS-stimulated cytokine release from tissue cultures as early as 4h (P≤0.05). In contrast, TCA (up to 500μM) did not inhibit LTA-stimulated cytokine release from tissue punches. Because cytokines are important mediators for host response to infectious microorganisms these findings suggest that TCE exposure could potentially modify susceptibility to infection during pregnancy. Topics: Chorion; Cysteine; Decidua; Disease Resistance; Extraembryonic Membranes; Female; Humans; Immunity; Lipopolysaccharides; Pregnancy; Streptococcal Infections; Streptococcus agalactiae; Teichoic Acids; Tissue Culture Techniques; Trichloroacetic Acid; Trichloroethylene; Tumor Necrosis Factor-alpha	2015

Article

Year

The trichloroethylene metabolite S-(1,2-dichlorovinyl)-l-cysteine but not trichloroacetate inhibits pathogen-stimulated TNF-α in human extraplacental membranes in vitro.

Reproductive toxicology (Elmsford, N.Y.), 2015, Volume: 52

Extraplacental membranes define the gestational compartment and provide a barrier to infectious microorganisms ascending the gravid female reproductive tract. We tested the hypothesis that bioactive metabolites of trichloroethylene (TCE) decrease pathogen-stimulated innate immune response of extraplacental membranes. Extraplacental membranes were cultured for 4, 8, and 24h with the TCE metabolites trichloroacetate (TCA) or S-(1,2-dichlorovinyl)-l-cysteine (DCVC) in the absence or presence of lipoteichoic acid (LTA) or lipopolysaccharide (LPS) to simulate infection. In addition, membranes were cocultured with DCVC and Group B Streptococcus (GBS). DCVC (5-50μM) significantly inhibited LTA-, LPS-, and GBS-stimulated cytokine release from tissue cultures as early as 4h (P≤0.05). In contrast, TCA (up to 500μM) did not inhibit LTA-stimulated cytokine release from tissue punches. Because cytokines are important mediators for host response to infectious microorganisms these findings suggest that TCE exposure could potentially modify susceptibility to infection during pregnancy.

Topics: Chorion; Cysteine; Decidua; Disease Resistance; Extraembryonic Membranes; Female; Humans; Immunity; Lipopolysaccharides; Pregnancy; Streptococcal Infections; Streptococcus agalactiae; Teichoic Acids; Tissue Culture Techniques; Trichloroacetic Acid; Trichloroethylene; Tumor Necrosis Factor-alpha

2015