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1.
Asian Pac J Allergy Immunol ; 40(4): 401-406, 2022 Dec.
Article in English | MEDLINE | ID: mdl-32416665

ABSTRACT

BACKGROUND: Skin prick test (SPT) is useful in identifying rat and mouse sensitization. OBJECTIVE: To determine the prevalence of rat and mouse sensitization by using local and commercial allergen extracts. METHODS: Patients with allergic rhinitis or asthma were recruited. SPT of local and commercial rat and mouse allergen extracts were performed. The level of rat and mouse specific IgE (sIgE) was quantified in all patients with positive SPT and randomized patients with negative SPT. RESULTS: Two hundred and thirty patients, 108 male (47%) and median age 14 years (3.2-63.5 years), were enrolled. Rat sensitization by SPT was 11.7% and mouse sensitization was 17.8%. SPT result to local rat and commercial rat allergen extracts were moderately correlated (rs = 0.51, p < 0.001), while SPT result to local mouse and commercial mouse allergen extracts showed low correlation (rs = 0.38, p < 0.001). The concordance of SPT results between local rat and commercial rat allergen extracts was 90.4%. Concordance between the local mouse and commercial mouse allergen extracts was 85.2%. When compared with rat and mouse sIgE, the concordance of local rat, commercial rat and commercial mouse allergen extract were > 80% while that of local mouse was 54.4%. No adverse effect was observed in SPT with any allergen or extract. CONCLUSIONS: The prevalence of rat and mouse sensitization was low compared to the study in USA. SPT with local rat and mouse allergen extract was safe and showed good concordance with the SPT result of commercial allergen extracts and rat and mouse sIgE levels.


Subject(s)
Immunoglobulin E , Rhinitis, Allergic , Male , Rats , Mice , Animals , Prevalence , Allergens , Rhinitis, Allergic/diagnosis , Rhinitis, Allergic/epidemiology , Skin Tests/methods , Plant Extracts
2.
Asian Pac J Allergy Immunol ; 38(2): 102-107, 2020 Jun.
Article in English | MEDLINE | ID: mdl-30447656

ABSTRACT

BACKGROUND: The standard method for diagnosing immediate wheat allergy is oral food challenge test (OFC). However, OFC can provoke anaphylaxis during the challenge process. Skin prick test (SPT) using commercial wheat extract yielded unsatisfactory result for diagnosis of wheat allergy. As a result, an in-house, alcohol-dissolved (Coca-10% EtOH) wheat extract was developed to improve accuracy of the SPT. OBJECTIVE: To determine the accuracy of in-house, alcohol-dissolved wheat extract in children with immediate wheat allergy. METHODS: This prospective cross-sectional study included children with history of immediate reaction after wheat ingestion. SPTs with commercial and in-house Coca-10% EtOH wheat extract were performed and wheat and omega-5 (ω-5) gliadin specific IgE (sIgE) were measured. Patients with no history of recent anaphylaxis after wheat ingestion underwent OFC with 31 grams of wheat flour. RESULTS: Thirty children were recruited. Thirteen of those had history of anaphylaxis after wheat ingestion. Eleven of the remaining 17 children (64.7%) had a positive result for wheat challenge test. Wheal size of 3 mm for both in-house and commercial wheat extract yielded the best accuracy for the test. Using these cutoff parameters, in-house Coca-10% EtOH wheat extract yielded 91.7% sensitivity, 66.7% specificity, and 86.7% accuracy. Comparatively, the commercial extract yielded 70.8% sensitivity, 100% specificity, and 76.6% accuracy. CONCLUSIONS: SPT using in-house Coca-10% EtOH wheat extract yielded better accuracy than commercial extract for diagnosing immediate type wheat allergy in children.


Subject(s)
Allergens/immunology , Gliadin/immunology , Plant Extracts/immunology , Plant Proteins/immunology , Wheat Hypersensitivity/diagnosis , Adolescent , Alcohols/chemistry , Allergens/chemistry , Child , Child, Preschool , Cross-Sectional Studies , Female , Humans , Hypersensitivity, Immediate , Immunoglobulin E/metabolism , Infant , Male , Plant Extracts/chemistry , Plant Proteins/chemistry , Prospective Studies , Self-Testing , Sensitivity and Specificity , Triticum/immunology
3.
Asian Pac J Allergy Immunol ; 35(4): 191-195, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28364408

ABSTRACT

BACKGROUND: Allergen extracts may be different due to the difference in dissemination of allergen-containing species in various geographical areas. Therefore, we wish to develop our own extracts to ensure the precision and quality of diagnosis. OBJECTIVES: To compare the efficacy and safety of our locally prepared pollen allergen extracts to imported ones, using skin prick testing (SPT) and serum specific IgE (sIgE) as references. METHODS: This prospective, randomized, double-blinded, self-controlled study was performed in respiratory allergic adult volunteers who are sensitized to at least one kind of pollen. Each subject was pricked with our Bermuda grass, Johnson grass and careless weed pollen allergen extracts, and also with the imported ones. sIgE levels were measured by using ImmunoCAP?. RESULTS: In 68 volunteers, our Bermuda, Johnson and careless weed extracts showed 91.2%, 45.6% and 54.4% positive SPTs, respectively, while for the imported ones 73.5%, 45.6% and 54.4% SPTs were positive, respectively. No adverse reaction was found in all procedures. The concentration of 10,000 BAU/mL of Bermuda grass, 1 : 20 w/v or 10,000 PNU/mL of Johnson grass and 1 : 40 w/v or 10,000 PNU/mL of careless weed yielded the most positive SPT results. There was no significant difference in mean wheal diameter (MWD) yielded from using local and imported extracts. Significant correlation was found between MWDs of imported pollen extracts and serum sIgE levels (p < 0.01). CONCLUSIONS: No significant difference between SPT results of local and imported pollen allergen extracts was found. Significant correlation was found between MWDs of imported pollen extract SPT and serum sIgE levels.


Subject(s)
Allergens/immunology , Antigens, Plant/immunology , Plant Extracts/immunology , Pollen/immunology , Rhinitis, Allergic, Seasonal/diagnosis , Adolescent , Adult , Cynodon/immunology , Double-Blind Method , Female , Humans , Immunoglobulin E/blood , Male , Middle Aged , Prospective Studies , Skin Tests , Sorghum/immunology , Young Adult
4.
Asian Pac J Allergy Immunol ; 28(2-3): 200-5, 2010.
Article in English | MEDLINE | ID: mdl-21038791

ABSTRACT

Pulmonary alveolar proteinosis (PAP) is characterized by intra-alveolar accumulation of lipoproteinaceous material. The severe chronic pulmonary disease and susceptibility to pulmonary infection is a prominent feature of the disease. We reported a case of postnatal-onset PAP and chronic interstitial pneumonitis in a girl with chronic respiratory distress since she was 5 months of age. A lung biopsy confirmed the diagnosis. The therapeutic bronchoalveolar lavages, a short trial of granulocyte colony-stimulation factor (G-CSF) and a combination of low dose methylprednisolone and hydroxychloroquine were used at different times without noting satisfactory improvement. Intravenous immunoglobulin (IVIG) and pulse methylprednisolone were given monthly with gradual recovery. She did not require oxygen supplement after 21 months of this combination. Our report suggested that IVIG and pulse methylprednisolone might have a potential role in the treatment of PAP with chronic interstitial pneumonitis.


Subject(s)
Lung Diseases, Interstitial/diagnosis , Lung/metabolism , Pneumocystis carinii/immunology , Pulmonary Alveolar Proteinosis/diagnosis , Chronic Disease , Cyanosis , Dyspnea , Fatal Outcome , Female , Humans , Hyperbaric Oxygenation , Immunoglobulins, Intravenous/administration & dosage , Infant , Infant, Newborn , Lung/immunology , Lung/microbiology , Lung/pathology , Lung Diseases, Interstitial/complications , Lung Diseases, Interstitial/physiopathology , Lung Diseases, Interstitial/therapy , Methylprednisolone/administration & dosage , Pneumocystis carinii/pathogenicity , Pulmonary Alveolar Proteinosis/complications , Pulmonary Alveolar Proteinosis/physiopathology , Pulmonary Alveolar Proteinosis/therapy , Respiratory Insufficiency
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