Antibodies for the treatment of clostridium difficile-associated infection and disease
a technology for clostridium difficile and antibodies, applied in the field of antibodies for the treatment of clostridium difficile-associated infection and disease, can solve the problems of increased mortality, more frequent relapse, and failure to treat, and achieve the effect of improving the quality of li
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Generation of Neutralizing Monoclonal Antibodies Against C. difficile Toxin A and / or Toxin B
A. Immunogen Preparation
[0229]Neutralizing monoclonal antibodies directed against toxin A and / or toxin B of C. difficile were generated by immunizing mice with C. difficile toxin A toxoid (inactive form of toxin) and with active forms of toxin A and / or toxin B. The murine mAbs (PA-38: anti-toxin A mAb, ATCC # PTA-9888; PA-39: anti-toxin A and B mAb, ATCC # PTA-9692; PA-41: anti-toxin B mAb ATCC # PTA-9693; and PA-50: anti-toxin A mAb, ATCC # PTA-9694) were generated by immunizing animals with toxoid A followed by immunizations with the active form of toxin A and / or toxin B. Toxin A toxoid, toxin A, toxin B (List Biological Laboratories Inc., Campbell, Calif.) and toxin A (Techlab Inc., Blacksburg, Va.) were stored at 4° C. until use. The toxins and toxoid were derived from strain VPI 10463, a commonly used reference strain of C. difficile. Quil A adjuvant (Accurate Chemical, Westbury, N.Y.) w...
example 2
Specificity and Affinity of Anti-C difficile Toxin A and / or Toxin B mAbs of the Invention to Toxin A and / or Toxin B
[0237]A. ELISA to Determine mAb Specificity for Toxin A and / or Toxin B
[0238]ELISA plates (BD Biosciences) were coated with 50 ng / well of toxin A (List Laboratories) or 25 ng / well of toxin B (List Laboratories) overnight at 4° C. After washing plates with PBS− (PBS without calcium or magnesium, 0.05% Tween 20), wells were blocked with 200 μl of blocking buffer (PBS without calcium or magnesium, 0.1% Tween 20, 2.5% non-fat milk) for one hour at 37° C. The wash step was repeated, and hybridoma supernatants or purified mAb were added for one hour at 37° C. The plate was washed and incubated for one hour at 37° C. with goat anti-mouse IgG-Fc, horseradish peroxidase (HRP)-conjugated (Jackson Immunoresearch, West Grove, Pa.). The plate was developed with ABTS peroxidase substrate system (KPL, Gaithersburg, Md.), with ABTS peroxidase stop solution (KPL), and read on a SpectraMa...
example 3
In Vitro Cell-Based Neutralization Assays
[0244]Cell-based cytotoxicity assays employing either CHO-K1 cells or T-84 cells were used to evaluate neutralization activities of the described anti-toxin A and anti-toxin B mAbs.
A. Neutralization of Toxin A Cytotoxic Effect on CHO-K1 Cells
[0245]CHO-K1 cells were seeded (2,000 cells in 50 μL / well) in assay plates (96 well, white opaque wall, clear flat bottom plates (Perkin Elmer)). Cells were allowed to attach for 4 hours prior to treatment. Equal volumes (35 μL) of 2 μg / mL toxin A (List Biological. Laboratories) and serially diluted mAbs were mixed in reagent dilution plates (96-well round bottom plates (Falcon)) for 1 hour at 37° C., and then 50 μl of the mixture was added to each well of the plates. After incubating for 72 hours, 20 μL / well CellTiter-Blue (Promega) was added to each well. Plates were incubated for an additional 4 hours, then read on a SpectraMax M5 Plate Reader (Molecular Devices) using an excitation wavelength of 560 n...
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