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1.
Asia Pacific Allergy ; (4): 55-56, 2015.
Article in English | WPRIM | ID: wpr-750008

ABSTRACT

We report a rare case of anaphylaxis due to caffeine intake. A 27-year-old woman suffered her first episode of anaphylaxis and a positive skin prick test suggested that the anaphylaxis was due to an IgE-mediated hypersensitivity reaction to caffeine. She was diagnosed with caffeine allergy and has not had an allergic reaction after avoiding foods and drinks containing caffeine. Although caffeine is known to have antiallergic effects, this case shows that caffeine can be an allergen and cause anaphylaxis.


Subject(s)
Adult , Female , Humans , Anaphylaxis , Caffeine , Food Hypersensitivity , Hypersensitivity , Hypersensitivity, Immediate , Skin
2.
Asia Pacific Allergy ; (4): 74-74, 2013.
Article in English | WPRIM | ID: wpr-749925

ABSTRACT

We would like to report the following errata in Table 4, and request that these items be revised appropriately.

3.
Asia Pacific Allergy ; (4): 75-75, 2013.
Article in English | WPRIM | ID: wpr-749924

ABSTRACT

The title of the page 256 should be corrected.

4.
Asia Pacific Allergy ; (4): 256-263, 2012.
Article in English | WPRIM | ID: wpr-749918

ABSTRACT

BACKGROUND: Asthma is characterized by a chronic inflammatory process involving high numbers of inflammatory cells and mediators which have multiple inflammatory effects on the airway. Interferon (IFN)-alpha, which is used widely for treating chronic hepatitis C, is reported to have an effect on patients with Churg-Strauss syndrome. Therefore, it may also be suitable for patients with severe asthma. OBJECTIVE: We studied the effect of IFN-alpha on airway eosinophilia in a guinea pig model of asthma and the expression of adhesion molecules on human eosinophils and vascular endothelial cells. METHODS: After antigen challenge, airway hyperresponsiveness and airway eosinophilia were measured in a guinea pig asthma model with or without airway IFN-alpha administration. Expression of adhesion molecules on eosinophils and cultured human umbilical vein endothelial cells (HUVECs) was also evaluated with or without IFN-alpha. RESULTS: IFN-alpha inhibited eosinophil recruitment into the tracheal wall and improved airway hyperresponsiveness in sensitized guinea pigs. IFN-alpha also significantly suppressed IL-1 beta-induced intercellular adhesion molecule-1 (ICAM-1) expression on HUVECs. However, IFN-alpha did not suppress platelet-activating factor-induced macrophage antigen-1 expression on human eosinophils. IFN-alpha significantly inhibited eosinophil adhesion to IL-1 beta-induced HUVECs and migration through IL-1 beta induced HUVECs. CONCLUSION: The findings suggest that the modulation of ICAM-1 in lung with pre-existing inflammation following treatment with IFN-alpha may be a novel and selective treatment for control of chronic airway inflammation and hyperresponsiveness associated with asthma.


Subject(s)
Animals , Humans , Asthma , Churg-Strauss Syndrome , Endothelial Cells , Eosinophilia , Eosinophils , Guinea Pigs , Hepatitis C, Chronic , Human Umbilical Vein Endothelial Cells , Inflammation , Intercellular Adhesion Molecule-1 , Interferon-alpha , Interferons , Interleukin-1 , Interleukin-1beta , Lung , Macrophages
5.
Asia Pacific Allergy ; (4): 195-202, 2012.
Article in English | WPRIM | ID: wpr-749908

ABSTRACT

BACKGROUND: Patients may receive negative results from a specific IgE (sIgE) test such as the ImmunoCAP (CAP) despite a documented history of systemic reaction to a Hymenoptera sting. Thus, further testing may be required using another serological method or venom skin prick tests to confirm allergy diagnosis and correct species. OBJECTIVE: To evaluate the sensitivity and the specificity of CAP and IMMULITE 3gAllergy (IMMULITE) for detecting sIgE to Paper wasp (WA) and Yellow Jacket (YJ) venoms using patient clinical history as the comparator. METHODS: Sera from 70 participants with a history of systemic reactions (SR) to WA and/or YJ stings were tested using CAP and IMMULITE. Fifty participants from this group had negative results on CAP. To assess specificity, sera from 71 participants who had never experienced either a WA or YJ sting were tested using CAP and IMMULITE. Fifty participants from this group tested positive using CAP. RESULTS: In participants with a history of systemic reaction to a Hymenoptera sting, yet who tested negative for WA and/or YJ sIgE according to CAP, the positivity rate according to IMMULITE was 20-42% using 0.10 IUA/mL as the limit of detection (LoD), per the manufacturer's specification. When the LoD for CAP (0.35 IUA/mL) was applied to the IMMULITE results, positivity according to IMMULITE was 14-26%. Overall, sensitivity, specificity, and agreement with SR were greater for IMMULITE than for CAP. For YJ: sensitivity (IMMULITE:CAP), 42.8%:28.5%; specificity, 53.5%:39.4%; agreement, 48.2%:34%. For WA, sensitivity (IMMULITE:CAP), 58.6%:28.5%; specificity, 49.3%:47.8%; agreement, 43.9%:38.3%. CONCLUSION: The IMMULITE performed well for detecting sIgE to Hymenoptera venom


Subject(s)
Humans , Bites and Stings , Diagnosis , Hymenoptera , Hypersensitivity , Immunoglobulin E , Limit of Detection , Methods , Sensitivity and Specificity , Skin , Venoms , Wasps
6.
Asia Pacific Allergy ; (4): 49-58, 2012.
Article in English | WPRIM | ID: wpr-749886

ABSTRACT

BACKGROUND: Exacerbation of asthma has a negative impact on quality of life and increases the risk of fatal asthma. One of the known risk factors for patients with a history of near-fatal asthma is reduced sensitivity to dyspnea. OBJECTIVE: We aimed to identify patients with such risk before they experienced severe exacerbation of asthma. METHODS: We analyzed asthma symptoms and peak expiratory flow rate (PEFR) values of 53 patients recorded daily in a diary over a mean period of 274 days. Patients matched their symptoms to one of eight categories ranging in severity from 'absent' to 'severe attack'. We then analyzed the relationship between PEFR and asthma symptoms by dividing the PEFR value by the values of clinical parameters, including asthma symptom level.


Subject(s)
Humans , Asthma , Dyspnea , Forced Expiratory Volume , Peak Expiratory Flow Rate , Quality of Life , Risk Factors
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