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KMID : 0854720030230020349
Korean Journal of Asthma, Allergy and Clinical Immunology
2003 Volume.23 No. 2 p.349 ~ p.357
Measurement of specific IgE to abalone(Haliotis discus hannai) and identification of IgE binding components
ÃÖÁ¤Èñ/Choi JH
À±¼ºÈ£/¼­À¯Áø/¼­Ã¢Èñ/³²µ¿È£/±èÀ±±Ù/¹Î°æ¾÷/¹ÚÇؽÉ/Yoon SH/Suh YJ/Suh CH/Nahm DH/Kim YK/MIn KU/Park HS
Abstract
Background£ºAbalone, which is a member of the shellfish family, can often induce severe
allergic reactions in sensitized individuals, but there have been only a few studies on its allergenic components. A recent study has identified two major allergens with molecular weights of
38 and 49 kDa in South African abalone.
Objectives£ºThe aim of this study is to evaluate skin test prevalence and IgE sensitization
to northern disk abalone (Haliotis discus hannai) which is one of the major abalones in this
country, and to identify its allergenic components.
Methods£ºSkin prick tests were performed with 62 home-made extracts of domestic foods
including abalone, turban shell, triton shell, shrimp etc. in 1,738 patients with various allergic
diseases. Serum specific IgE antibodies to abalone were determined by ELISA in 81 positive
responders on skin prick tests to abalone extract and 40 non-atopic healthy controls. ELISA
inhibition tests were performed to evaluate cross-allergenecity between abalone and other sea
foods(turban shell, triton shell, shrimp and house dust mite). Allergenic components of Haliotis
discus hannai were identified by SDS-PAGE and IgE-immunoblot analysis.
Results£ºThe positive response rate(A/H ratio¡Ã2+) to abalone on skin prick test was 4.7%
in patients with various allergic diseases. Serum spcecific IgE to abalone was detected in 23
(34.5%) of 67 patients. Serum specific IgE levels to abalone tended to increase according to
skin test reactivity without statistical significance(p>0.05). ELISA inhibition tests showed significant dose-dependent inhibitions with addition of turban shell, triton shell and shrimp extracts.
IgE immunoblot analysis showed ten allergenic components (33, 37, 40, 60, 63, 71, 76, 86, 92, 111 kDa), of which seven allergens(40, 60, 63, 71, 76, 86, 92 kd) were bound to IgE in more
than 50% of the sera tested.
Conclusion£ºThe sensitization rate to abalone was 4.7% in allergy patients. Serum specific
IgE to abalone was detected by ELISA, and 7 major allergens within abalone were identified.
Further studies will be needed to elucidate their clinical significances. (J Asthma Allergy Clin
Immunol 23: 349-57, 2003)
KEYWORD
abalone, specific IgE, IgE binding component, cross-reactivity
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