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Capsular Serotyping of Streptococcus pneumoniae by Latex Agglutination
Published on: September 25, 2014
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Immunodetection of latex antigens
1Department of Allergy and Immunology, Children's National Medical Center, Washington, D.C. 20010.
The Journal of Allergy and Clinical Immunology
|May 1, 1994
Summary
A new biotinylated enzyme-linked immunosorbent assay (BiC ELISA) using a mouse monoclonal antibody (CRI-C) effectively detects latex antigens. This method offers a reproducible in vitro assay for latex allergy diagnostics.
Area of Science:
- Immunology
- Biochemistry
- Materials Science
Background:
- Latex protein antigens can trigger Type I hypersensitivity reactions.
- Traditional methods for latex antigen detection include protein assays, HPLC, RAST inhibition, and skin tests.
- Development of specific assays is crucial for managing latex allergies.
Purpose of the Study:
- To evaluate a mouse monoclonal antibody (CRI-C) for detecting latex antigens.
- To compare the efficacy of a novel biotinylated ELISA (BiC ELISA) with existing methods.
Main Methods:
- A mouse monoclonal antibody (CRI-C) was generated against ammoniated latex.
- Medical gloves were extracted and analyzed using standard protein assays, RAST inhibition, and a BiC ELISA.
- Assays were validated using reference proteins and sera from allergic individuals.
Main Results:
- The Bradford and bicinchoninic acid assays showed the best correlation among protein assays.
- The BiC ELISA and RAST inhibition assays correlated with protein assays but demonstrated higher specificity.
- Protein was detected in vinyl gloves by OD280, BCA, and Bradford methods.
Conclusions:
- The BiC ELISA provides an easy, reproducible in vitro method for quantifying relevant latex antigens.
- Further clinical validation is necessary to confirm the utility of the BiC ELISA in diagnosing latex allergy.
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