Involvement of carbohydrate on phospholipase A2, a bee‐venom allergen, in in vivo antigen‐specific IgE synthesis in mice

Background: Carbohydrates on allergens are known to be important for allergenicity. However, most findings have been made with epitope analysis. In this study, we investigated the involvement of N‐glycan on phospholipase A2 (PLA2), the major allergen of honeybee venom, in in vivo synthesis of specif...

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Veröffentlicht in:Allergy (Copenhagen) 1999-08, Vol.54 (8), p.811-818
Hauptverfasser: Okano, M, Satoskar, Ar, Harn, Da, Nishizaki, K, Masuda, Y, Yoshino, T
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container_issue 8
container_start_page 811
container_title Allergy (Copenhagen)
container_volume 54
creator Okano, M
Satoskar, Ar
Harn, Da
Nishizaki, K
Okano, M
Masuda, Y
Yoshino, T
description Background: Carbohydrates on allergens are known to be important for allergenicity. However, most findings have been made with epitope analysis. In this study, we investigated the involvement of N‐glycan on phospholipase A2 (PLA2), the major allergen of honeybee venom, in in vivo synthesis of specific IgE in mice. Methods: CBA/J and C57BL/6 mice were sensitized intranasally with either native or deglycosylated PLA2 in the absence of adjuvant. After repeated sensitization, serum Ab titers against PLA2 were determined. PLA2 was deglycosylated chemically with anhydrous trifluoromethanesulfonic acid (TFMS). Results: CBA/J mice showed PLA2‐specific IgE production after repeated sensitization with native PLA2. They also produced PLA2‐specific IgG1 predominantly, suggesting that Th2‐type Ab production was induced. When we used deglycosylated PLA2 as a competitor in ELISA for detecting PLA2‐specific IgE, deglycosylated PLA2 completely inhibited the binding between native PLA2 and IgE. Deglycosylated PLA2 had the same potential for inducing specific IgE synthesis as native PLA2, since sensitization with deglycosylated PLA2 also elicited IgE production in CBA/J mice. Conclusions: These results suggest that carbohydrate on PLA2 is less important than previously thought not only as a dominant IgE epitope but also in synthesis of PLA2‐specific IgE in vivo.
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However, most findings have been made with epitope analysis. In this study, we investigated the involvement of N‐glycan on phospholipase A2 (PLA2), the major allergen of honeybee venom, in in vivo synthesis of specific IgE in mice. Methods: CBA/J and C57BL/6 mice were sensitized intranasally with either native or deglycosylated PLA2 in the absence of adjuvant. After repeated sensitization, serum Ab titers against PLA2 were determined. PLA2 was deglycosylated chemically with anhydrous trifluoromethanesulfonic acid (TFMS). Results: CBA/J mice showed PLA2‐specific IgE production after repeated sensitization with native PLA2. They also produced PLA2‐specific IgG1 predominantly, suggesting that Th2‐type Ab production was induced. When we used deglycosylated PLA2 as a competitor in ELISA for detecting PLA2‐specific IgE, deglycosylated PLA2 completely inhibited the binding between native PLA2 and IgE. Deglycosylated PLA2 had the same potential for inducing specific IgE synthesis as native PLA2, since sensitization with deglycosylated PLA2 also elicited IgE production in CBA/J mice. Conclusions: These results suggest that carbohydrate on PLA2 is less important than previously thought not only as a dominant IgE epitope but also in synthesis of PLA2‐specific IgE in vivo.</description><identifier>ISSN: 0105-4538</identifier><identifier>EISSN: 1398-9995</identifier><identifier>DOI: 10.1034/j.1398-9995.1999.00096.x</identifier><identifier>PMID: 10485384</identifier><language>eng</language><publisher>Copenhagen: Blackwell Publishing Ltd</publisher><subject>Allergens - chemistry ; Allergens - immunology ; Animals ; Bee Venoms - chemistry ; Bee Venoms - immunology ; carbohydrate ; Enzyme-Linked Immunosorbent Assay ; Epitopes - immunology ; Female ; Glycosylation ; IgE ; Immunization ; Immunoglobulin E - biosynthesis ; Immunoglobulin G - blood ; intranasal sensitization ; Mesylates ; Mice ; Mice, Inbred C57BL ; Mice, Inbred CBA ; phospholipase A2 ; Phospholipases A - chemistry ; Phospholipases A - immunology ; Phospholipases A2 ; Polysaccharides - analysis ; Polysaccharides - immunology</subject><ispartof>Allergy (Copenhagen), 1999-08, Vol.54 (8), p.811-818</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1034%2Fj.1398-9995.1999.00096.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27903,27904,45554,46812</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10485384$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Okano, M</creatorcontrib><creatorcontrib>Satoskar, Ar</creatorcontrib><creatorcontrib>Harn, Da</creatorcontrib><creatorcontrib>Nishizaki, K</creatorcontrib><creatorcontrib>Okano, M</creatorcontrib><creatorcontrib>Masuda, Y</creatorcontrib><creatorcontrib>Yoshino, T</creatorcontrib><title>Involvement of carbohydrate on phospholipase A2, a bee‐venom allergen, in in vivo antigen‐specific IgE synthesis in mice</title><title>Allergy (Copenhagen)</title><addtitle>Allergy</addtitle><description>Background: Carbohydrates on allergens are known to be important for allergenicity. However, most findings have been made with epitope analysis. In this study, we investigated the involvement of N‐glycan on phospholipase A2 (PLA2), the major allergen of honeybee venom, in in vivo synthesis of specific IgE in mice. Methods: CBA/J and C57BL/6 mice were sensitized intranasally with either native or deglycosylated PLA2 in the absence of adjuvant. After repeated sensitization, serum Ab titers against PLA2 were determined. PLA2 was deglycosylated chemically with anhydrous trifluoromethanesulfonic acid (TFMS). Results: CBA/J mice showed PLA2‐specific IgE production after repeated sensitization with native PLA2. They also produced PLA2‐specific IgG1 predominantly, suggesting that Th2‐type Ab production was induced. When we used deglycosylated PLA2 as a competitor in ELISA for detecting PLA2‐specific IgE, deglycosylated PLA2 completely inhibited the binding between native PLA2 and IgE. Deglycosylated PLA2 had the same potential for inducing specific IgE synthesis as native PLA2, since sensitization with deglycosylated PLA2 also elicited IgE production in CBA/J mice. 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subjects Allergens - chemistry
Allergens - immunology
Animals
Bee Venoms - chemistry
Bee Venoms - immunology
carbohydrate
Enzyme-Linked Immunosorbent Assay
Epitopes - immunology
Female
Glycosylation
IgE
Immunization
Immunoglobulin E - biosynthesis
Immunoglobulin G - blood
intranasal sensitization
Mesylates
Mice
Mice, Inbred C57BL
Mice, Inbred CBA
phospholipase A2
Phospholipases A - chemistry
Phospholipases A - immunology
Phospholipases A2
Polysaccharides - analysis
Polysaccharides - immunology
title Involvement of carbohydrate on phospholipase A2, a bee‐venom allergen, in in vivo antigen‐specific IgE synthesis in mice
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