Publications by authors named "T L Vassilev"

Previous studies have shown that polyreactive antibodies play an important role in the frontline defense against the dissemination of pathogens in the pre-immune host. Interestingly, antigen-binding polyreactivity can not only be inherent, but also acquired post-translationally. The ability of individual monoclonal IgG and IgE antibodies to acquire polyreactivity following contact with various agents that destabilize protein structure (urea, low pH) or have a pro-oxidative potential (heme, ferrous ions) has been studied in detail.

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The aim of the study was to assess the effect of different experimental conditions on registration of microcracks by means of micro-computed tomography. Twenty roots of permanent lower incisors were instrumented with SAF system, filled with a single-cone technique and retreated with the Pro Taper Universal Retreatment system. Each sample was measured in dry, water, and moist conditions.

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Article Synopsis
  • Researchers studied how different substances can change how well a specific protein in our body, called secretory immunoglobulin A (sIgA), can grab onto germs like viruses and bacteria.
  • They tested sIgA by exposing it to things like acidic solutions, free heme, and some metal ions to see how these affected its ability to bind to germs.
  • They found that acidic solutions made sIgA bind better to various germs, more than the other treatments, which means it could help our body respond to infections more effectively.
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Mild modification of intravenous immunoglobulin (IVIG) has been reported to result in enhanced polyspecificity and leveraged therapeutic effects in animal models of inflammation. Here, we observed that IVIG modification by ferrous ions, heme or low pH exposure, shifted the repertoires of specificities in different directions. Ferrous ions exposed Fe(II)-IVIG, but not heme or low pH exposed IVIG, showed increased pro-apoptotic effects on neutrophil granulocytes that relied on a FAS-dependent mechanism.

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Specific antibody reactivities are routinely used as biomarkers, but the antibody repertoire reactivity (igome) profiles are still neglected. Here, we propose rationally designed peptide arrays as efficient probes for these system level biomarkers. Most IgM antibodies are characterized by few somatic mutations, polyspecificity, and physiological autoreactivity with housekeeping function.

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