Test kits and methods for detecting H. pylori
AssigneeQuidel Corporation
InventorsAllan David Pronovost, Jan Waclaw Pawlak, Kristy S. Condon
Life of this patent
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Abstract
A sensitive and specific antigen preparation for the detection of Helicobacter pylori in biological samples is disclosed. The preparation uses a range of antigens derived from size exclusion chromatography of detergent-solubilized H. pylori cells. Serological assays such as ELISA, latex agglutination, and rapid EIA assays utilizing the improved antigen preparation, and a kit for use in these serological assays are also disclosed.
Claims6
A method for detecting the presence of antibodies resulting from Helicobacter pylori infection in a biological sample, the method comprising:
- (a) contacting the sample with a composition comprising H. pylori-derived proteins
- wherein said composition has a urease-specific activity of less than 0.34 OD.sub.550 /A.sub.280 in a urease-catalyzed assay, and the H. pylori-derived proteins in said composition, when denatured and reduced, are characterized by SDS PAGE to consist of antigens specific to H. pylori of molecular weights 120 kD;
- 66 kD;
- 62 kD;
- 59 kD;
- 52 kD;
- and 31 kD and common antigens of molecular weights 89 kD;
- 73 kD;
- 56 kD;
- 45 kD;
- 42 kD;
- 29 kD;
- 25 kD;
- 21 kD;
- and 16 kD;
- and
- wherein the amounts of antigens of 66 kD and 56 kD are greater than the amounts of any of the remaining individual antigens set forth above;
- (b) permitting the sample and said composition to form an antigen-antibody complex with respect to any antibody contained in the sample;
- and
- (c) detecting the presence of any antigen-antibody complex denoting the presence of Helicobacter pylori infection.
A method for detecting the presence of Helicobacter pylori antibodies resulting from infection in a biological sample, the method comprising:
- (a) immobilizing and drying a composition comprising H. pylori-derived proteins
- wherein said composition has a urease-specific activity of less than 0.34 OD.sub.550 /A.sub.280 in a urease-catalyzed assay, and the H. pylori-derived proteins in said composition, when denatured and reduced, are characterized by SDS PAGE to consist of antigens specific to H. pylori of molecular weights 120 kD;
- 66 kD;
- 62 kD;
- 59 kD;
- 52 kD;
- and 31 kD and common antigens of molecular weights 89 kD;
- 73 kD;
- 56 kD;
- 45 kD;
- 42 kD;
- 29 kD;
- 25 kD;
- 21 kD;
- and 16 kD;
- and
- wherein the amounts of antigens of 66 kD and 56 kD are greater than the amounts of any of the remaining individual antigens set forth above, on a solid support to obtain a dried antigen complex;
- (b) incubating the dried antigen complex with the sample to form an antigen-antibody complex;
- (c) adding enzyme-conjugated anti-Human IgG antibodies to the antigen-antibody complex and incubating to form a labeling complex;
- (d) adding a substrate for the conjugated enzyme to the labeling complex to form a developing complex;
- and
- (e) monitoring the developing complex for a change in the substrate to determine the amount of antibodies against Helicobacter pylori present in the sample.
A kit for determining the presence of antibodies formed in response to Helicobacter pylori infection in a biological sample, the kit comprising a composition comprising H. pylori-derived proteins
- wherein said composition has a urease-specific activity of less than 0.34 OD.sub.550 /A.sub.280 in a urease-catalyzed assay, and the H. pylori-derived proteins in said composition, when denatured and reduced, are characterized by SDS PAGE to consist of antigens specific to H. pylori of molecular weights 120 kD;
- 66 kD;
- 62 kD;
- 59 kD;
- 52 kD;
- and 31 kD and common antigens of molecular weights 89 kD;
- 73 kD;
- 56 kD;
- 45 kD;
- 42 kD;
- 29 kD;
- 25 kD;
- 21 kD;
- and 16 kD;
- and
- wherein the amounts of antigens of 66 kD and 56 kD are greater than the amounts of any of the remaining individual antigens set forth above.
Dependencies are inferred from the claim text.