IP Library Granted Patent US 6,867,004
Granted Patent B2
US 6,867,004 · App. 10/028,181 · Granted Mar 15, 2005

Methods of using oxidized fungal antigens in antibody testing

Assignee: Focus Technologies, Inc.
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Quick Facts
Patent No.
US 6,867,004
App. No.
10/028,181
Granted
Mar 15, 2005
Kind
B2
Abstract

The present invention relates to oxidized fungal antigens and methods of making and using thereof. More particularly, the present invention provides a method for producing an oxidized fungal antigen in culture filtrate. The present invention also provides for the produced oxidized fungal antigens. Devices comprising such oxidized fungal antigens, methods for testing for fungal antibodies using the oxidized fungal antigens and methods for producing anti-fungal antibodies using oxidized fungal antigens are further provided. Antigen detection devices comprising anti-fungal antibodies raised against oxidized fungal antigens produced by the present methods are further provided.

Claims (13)

1. A method of testing an antibody to a fungus in a sample, the method comprising:

a) producing a fungal antigen suitable for testing an antibody to a fungus, comprising providing a fungal antigen as a culture filtrate, the fungal antigen having not been purified by ion exchange chromatography or isoelectric focusing from the culture filtrate, and contacting the fungal antigen with an oxidizing agent to produce an oxidized fungal antigen suitable for testing an antibody to the fungus;

b) contacting a sample suspected of containing an antibody to a fungus with the oxidized fungal antigen produced in step a) under suitable conditions to allow binding of the antibody, if present in the sample, to the oxidized fungal antigen; and

c) assessing binding between the antibody and the oxidized fungal antigen to determine the presence and/or amount of the antibody in the sample.

2. The method of claim 1 , wherein the fungus is a pathogenic fungus.

3. The method of claim 1 , wherein the sample is a clinical sample.

4. The method of claim 3 , wherein the clinical sample is a human clinical sample.

5. The method of claim 1 , wherein the fungal antigen has not been purified from the culture filtrate.

6. The method of claim 1 , wherein the oxidizing agent is periodate.

7. The method of claim 1 , further comprising a step of attaching the oxidized fungal antigen to a surface of a device suitable for testing an antibody to a fungus before contacting the antigen with the sample.

8. The method of claim 1 , wherein the binding between the antibody and the oxidized fungal antigen is assessed by a sandwich or competitive assay format.

9. The method of claim 1 , wherein the binding between the antibody and the oxidized fungal antigen is assessed by a format selected from the group consisting of an enzyme-linked immunosorbent assay (ELISA), immunoblotting, immunoprecipitation, radioimmunoassay (RIA), immunostaining, latex agglutination, indirect hemagglutination assay (IHA), complement fixation, indirect immunofluorescent assay (IFA), nephelometry, flow cytometry assay, chemiluminescence assay, lateral flow immunoassay, u-capture assay, inhibition assay and avidity assay.

10. The method of claim 1 , wherein the binding between the antibody and the oxidized fungal antigen is assessed by an ELISA format.

Assignments (2)
CHANGE OF NAME Recorded Sep 11, 2017
From: FOCUS DIAGNOSTICS, INC.
To: QUEST DIAGNOSTICS INFECTIOUS DISEASE, INC.
Reel/Frame 043811/0131 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2002
From: PRINCE, HARRY; SU, XIN; KONG, LILLY; DEVOR, KEN; ARAKELOV, SERGEI; HOGREFE, WAYNE
To: FOCUS TECHNOLOGIES, INC.
Reel/Frame 012870/0368 →
Continuity (1)
Related Publication 20030124630A1 · Jul 3, 2003