1.A 24 kDa Excretory-Secretory Protein of Anisakis simplex Larvae Could Elicit Allergic Airway Inflammation in Mice.
Hye Kyung PARK ; Min Kyoung CHO ; Mi Kyung PARK ; Shin Ae KANG ; Yun Seong KIM ; Ki Uk KIM ; Min Ki LEE ; Mee Sun OCK ; Hee Jae CHA ; Hak Sun YU
The Korean Journal of Parasitology 2011;49(4):373-380
We have reported that a 24 kDa protein (22U homologous; As22U) of Anisakis simplex larvae could elicit several Th2-related chemokine gene expressions in the intestinal epithelial cell line which means that As22U may play a role as an allergen. In order to determine the contribution of As22U to allergic reactions, we treated mice with 6 times intra-nasal application of recombinant As22U (rAs22U). In the group challenged with rAs22U and ovalbumin (OVA), the number of eosinophils in the bronchial alveolar lavage fluid (BALF) was significantly increased, as compared to the group receiving only OVA. In addition, mice treated with rAs22U and OVA showed significantly increased airway hyperresponsiveness. Thus, severe inflammation around the airway and immune cell recruitment was observed in mice treated with rAs22U plus OVA. The levels of IL-4, IL-5, and IL-13 cytokines in the BALF increased significantly after treatment with rAs22U and OVA. Similarly, the levels of anti-OVA specific IgE and IgG1 increased in mice treated with rAs22U and OVA, compared to those treated only with OVA. The Gro-alpha (CXCL1) gene expression in mouse lung epithelial cells increased instantly after treatment with rAs22U, and allergy-specific chemokines eotaxin (CCL11) and thymus-and-activation-regulated-chemokine (CCL17) gene expressions significantly increased at 6 hr after treatment. In conclusion, rAs22U may induce airway allergic inflammation, as the result of enhanced Th2 and Th17 responses.
Administration, Intranasal
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Animals
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Anisakiasis/*immunology/parasitology
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Anisakis/*immunology/metabolism
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Bronchoalveolar Lavage Fluid
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Chemokines/metabolism
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Cytokines/analysis/*metabolism
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Eosinophils/metabolism
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Female
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Gene Expression Regulation/*immunology
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Helminth Proteins/*immunology
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Hypersensitivity/*immunology/parasitology
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Immunoglobulin E/immunology
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Immunoglobulin G/immunology
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Larva/immunology/metabolism
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Lung/metabolism
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Mice
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Mice, Inbred C57BL
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Recombinant Proteins/immunology
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Th17 Cells/metabolism
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Th2 Cells/metabolism
2.The Clinical Characteristics of Anisakis Allergy in Korea.
Sung Jin CHOI ; Jae Chun LEE ; Moo Jung KIM ; Gyu Young HUR ; Seung Youp SHIN ; Hae Sim PARK
The Korean Journal of Internal Medicine 2009;24(2):160-163
Anisakidae larvae can cause anisakiasis when ingested by humans. Although several groups have reported a gastrointestinal Anisakis allergy among people in Spain and Japan, our report is the first to summarize the clinical features of 10 Anisakis allergy cases in Korea. We enrolled 10 Korean patients (6 men and 4 women) who complained of aggravated allergic symptoms after ingesting raw fish or seafood. Sensitization to Anisakis was confirmed by detecting serum specific IgE to Anisakis simplex. The most common manifestation of anisakiasis was urticaria (100%), followed by abdominal pain (30%) and anaphylaxis (30%). All patients presenting with these symptoms also exhibited high serum specific IgE (0.45 to 100 kU/L) to A. simplex. Nine patients (90%) exhibited atopy and increased total serum IgE levels. The fish species suspected of carrying the Anisakis parasite were flatfish (40%), congers (40%), squid (30%), whelk (10%), and tuna (10%). Anisakis simplex should be considered as a possible causative food allergen in adult patients presenting with urticaria, angioedema, and anaphylaxis following the consumption of raw fish or seafood.
Abdominal Pain/immunology
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Adult
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Aged
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Anaphylaxis/immunology
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Angioedema/immunology
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Animals
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Anisakiasis/complications/ethnology/*immunology
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Anisakis/*immunology
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Antibodies, Helminth/*blood
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Asian Continental Ancestry Group
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Female
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Food Hypersensitivity/complications/ethnology/*immunology
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Humans
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Immunoglobulin E/*blood
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Korea/epidemiology
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Male
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Middle Aged
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Seafood/*adverse effects/parasitology
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Urticaria/immunology
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Young Adult