Abstract |
Lol p IV is an important allergen of ryegrass pollen. For the immunochemical identification of antigenic and/or allergenic site(s), murine monoclonal antibodies (MAbs) were prepared against Lol p IV. The hybridoma cell-culture supernatants were screened for anti-Lol p IV antibodies by a combination of ELISA and Western immunoblot analyses. The MAbs were finally purified from ascites on a Mono Q ion-exchange column. In a competitive radioimmunoassay with Lol p IV as the solid phase and 125I-labeled MAbs, it was established that MAbs 90, 91, 92, 93, and 94, although they differed in their relative affinities, recognized in common with one another an epitope designated as antigenic site A, whereas MAb 12 recognized a different epitope referred to as site B. Sites A and B were also demonstrated to constitute allergenic determinants of Lol p IV. Differences in the repertoire of specificities of the human IgE antibodies directed to Lol p IV were also demonstrated. Interestingly, it was found that sera from both allergic as well as from nonatopic individuals had IgG antibodies to sites A and/or B.
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Authors | K S Jaggi, A K Ekramoddoullah, F T Kisil, J M Dzuba-Fischer, E S Rector, A H Sehon |
Journal | The Journal of allergy and clinical immunology
(J Allergy Clin Immunol)
Vol. 83
Issue 4
Pg. 845-52
(Apr 1989)
ISSN: 0091-6749 [Print] United States |
PMID | 2708744
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Allergens
- Antibodies, Monoclonal
- Antigens, Plant
- Glycoproteins
- Immunoglobulin G
- Lol p IV protein, Lolium perenne
- Plant Proteins
- Fel d 1 protein, Felis domesticus
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Topics |
- Allergens
(analysis, metabolism)
- Animals
- Antibodies, Monoclonal
(biosynthesis)
- Antigens, Plant
- Binding Sites
- Blotting, Western
- Edible Grain
- Enzyme-Linked Immunosorbent Assay
- Glycoproteins
- Humans
- Hypersensitivity
(immunology)
- Immunoglobulin G
(analysis)
- Mice
- Plant Proteins
- Pollen
(analysis, metabolism)
- Radioimmunoassay
- Secale
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