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1.
China Journal of Chinese Materia Medica ; (24): 1588-1595, 2019.
Article in Chinese | WPRIM | ID: wpr-774518

ABSTRACT

In this paper,immune fingerprint was used to screen the allergenic components of Shuanghuanglian Injection(SHLI) by enzyme-linked immuno sorbent assay(ELISA) combined with HPLC/MS method. ELISA-embedded anti-IgE antibody could successfully adsorb allergens in SHLI and its plasma samples containing drugs through different routes of administration,suggesting that SHLI can induce type I hypersensitivity in rats. HPLC fingerprints and MS map of SHLI and drug-containing plasma samples from different routes of administration before and after anti-IgE antibody adsorption were established. According to the similarity evaluation of HPLC fingerprints and analysis results MS map,the sensitization of traditional Chinese medicine injections can be changed by different administration methods. There were 22 kinds of components that can be adsorbed by specific anti-Ig E antibodies in Shuanghuanglian Injection and its drug-containing plasma,most of them were acids and nitrogen compounds. Based on supramolecular theory,it was inferred that these compounds came from SHLI or body,and may form supramolecular hapten,which results in immunotoxicity and allergic reaction when being used as injection instead of oral liquid. Immune fingerprint is not only used to screen out single component allergen,but also more comprehensive,sensitive and easy to operate. It can provide reference for the future research methods of allergic reaction of traditional Chinese medicine injections.


Subject(s)
Animals , Rats , Allergens , Chromatography, High Pressure Liquid , Drugs, Chinese Herbal , Chemistry , Enzyme-Linked Immunosorbent Assay , Hypersensitivity , Injections , Medicine, Chinese Traditional
2.
Allergy, Asthma & Immunology Research ; : 362-365, 2014.
Article in English | WPRIM | ID: wpr-132494

ABSTRACT

Angioedema with eosinophilia (AE) is a very rare allergy disease, case reports of which have been published sporadically since 1984. Here, we retrospectively analyzed the clinical features of 10 AE patients in Korea. Nine of the 10 subjects were young females, ranging from 23 to 38 years old. Twenty percent of the subjects had episodic-type AE with high serum IgM and eosinophil counts, while 80% were non-episodic type with normal serum IgM levels but high eosinophil counts. All patients had used systemic corticosteroids to control AE. One patient with refractory episodic-type AE was treated with anti-IgE antibody. This is the first study to evaluate the clinical characteristics of AE in a Korean population.


Subject(s)
Female , Humans , Adrenal Cortex Hormones , Angioedema , Eosinophilia , Eosinophils , Hypersensitivity , Immunoglobulin M , Korea , Retrospective Studies
3.
Allergy, Asthma & Immunology Research ; : 362-365, 2014.
Article in English | WPRIM | ID: wpr-132491

ABSTRACT

Angioedema with eosinophilia (AE) is a very rare allergy disease, case reports of which have been published sporadically since 1984. Here, we retrospectively analyzed the clinical features of 10 AE patients in Korea. Nine of the 10 subjects were young females, ranging from 23 to 38 years old. Twenty percent of the subjects had episodic-type AE with high serum IgM and eosinophil counts, while 80% were non-episodic type with normal serum IgM levels but high eosinophil counts. All patients had used systemic corticosteroids to control AE. One patient with refractory episodic-type AE was treated with anti-IgE antibody. This is the first study to evaluate the clinical characteristics of AE in a Korean population.


Subject(s)
Female , Humans , Adrenal Cortex Hormones , Angioedema , Eosinophilia , Eosinophils , Hypersensitivity , Immunoglobulin M , Korea , Retrospective Studies
4.
Asia Pacific Allergy ; (4): 209-214, 2013.
Article in English | WPRIM | ID: wpr-749966

ABSTRACT

In commemorate the 9th Asia Pacific Congress of Allergy, Asthma, and Clinical Immunology (APCAACI) in Taipei, Taiwan in November this year, some of the seminar works and contributions by the researchers from Taiwan to the advance in the field of allergy and clinical immunology, such as DNA vaccine, traditional Chinese medicine, anti-IgE antibody, and personalized medicine for severe drug allergic reaction, are summarized in this special review.


Subject(s)
Allergy and Immunology , Asia , Asthma , DNA , Hypersensitivity , Medicine, Chinese Traditional , Precision Medicine , Taiwan
5.
Allergy, Asthma & Immunology Research ; : 305-308, 2012.
Article in English | WPRIM | ID: wpr-148481

ABSTRACT

Allergic bronchopulmonary aspergillosis (ABPA) is a complex disease, triggered by a hypersensitivity reaction to the allergen Aspergillus fumigatus. This disease occurs frequently in patients with cystic fibrosis and severe asthma in Western countries, with a prevalence of 2%-15%. However, there have been only a few case reports in Korea. We investigated the clinical and immunological features of patients with ABPA. Ten adult patients diagnosed with ABPA, according to Greenberger's criteria, were analyzed during the period January 2001 to December 2010 in a tertiary hospital. Skin-prick tests, pulmonary function tests, and high-resolution computed tomography (HRCT) were performed, and total serum IgE and A. fumigatus-specific IgE were measured. The patient cohort consisted of men who were middle-aged (median, 62.5; range, 19.0-79.0 years) at the diagnosis of ABPA with a long duration of asthma (median, 15.0; range, 1-48 years). Approximately 40% of the patients had a history of pulmonary tuberculosis more than 10 years prior to the study (median 23.5; range, 10.0-31.0 years) accompanied by severe obstructive lung function and radiological post-tuberculous destructive lung lesions. These patients also tended to have increased levels of immunologic parameters, such as total eosinophil count, total IgE, and A. fumigates-specific IgE, compared to those without tuberculosis sequels. Two patients with steroid-dependent asthma were treated with anti-IgE therapy and showed good responses. We report the clinical features of 10 ABPA patients, including 4 with histories of post-tuberculosis destructive lesions. Furthermore, anti-IgE antibody therapy may be an alternative strategy in cases of steroid-dependent ABPA.


Subject(s)
Adult , Humans , Male , Antibodies, Anti-Idiotypic , Aspergillosis, Allergic Bronchopulmonary , Aspergillus fumigatus , Asthma , Cohort Studies , Cystic Fibrosis , Eosinophils , Hypersensitivity , Immunoglobulin E , Korea , Lung , Prevalence , Respiratory Function Tests , Tertiary Care Centers , Tuberculosis , Tuberculosis, Pulmonary
6.
Salud(i)ciencia (Impresa) ; 14(3): 105-107, mayo 2006.
Article in Spanish | LILACS | ID: biblio-1292814

ABSTRACT

Autoimmune urticaria occurs in patients in whom there are functional autoantibodies directed against FcepsilonR1 and IgE. The antibodies concerned are of subtypes IgG1 and IgG3. It is generally more severe and treatment-resistant. The significance of diagnosing autoimmune urticaria is that patients can be offered an explanation for an otherwise unremitting and puzzling condition. It also opens up the prospect of effective treatment by immunomodulatory treatment in selected patients with autoimmune urticaria. The utologous serum skin test is used as a screening test for autoimmune urticaria. The sensitivity and specificity are about 80% respectively. The diagnosis can be confirmed by demonstrating release of histamine from target basophils or dermal mast cells. Treatment of autoimmune urticaria involves the use of low sedation H1 antihistamines in licensed dosages. Off-label dosages are used if the condition is still poorly controlled. Prednisolone can be used in acute and severe flare-ups. Immunomodulatory treatment with cyclosporin can be considered in recalcitrant cases.


La urticaria autoinmune aparece en pacientes que generan autoanticuerpos funcionales contra el FcepsilonR1 y la IgE. Los anticuerpos involucrados pertenecen al subtipo IgG1 e IgG3. Generalmente es una forma de urticaria más grave y resistente al tratamiento. La importancia de diagnosticar urticaria autoinmune radica en que al hacerlo los enfermos pueden recibir una explicación acerca de una enfermedad desconcertante y que habitualmente no remite. En casos seleccionados de urticaria autoinmune también se abre un espectro de tratamientos eficaces que incluyen terapias inmunomuduladoras. La prueba de suero autólogo se utiliza como estudio de rastreo para esta patología. La sensibilidad y especificidad son cercanas al 80%. El diagnóstico puede confirmarse mediante la demostración de liberación de histamina de basófilos o células cebadas de dermis. El tratamiento de la urticaria autoinmune consiste en la utilización de antihistamínicos H1 con escaso efecto sedante en las dosis recomendadas. Las dosis superiores a las habituales se utilizan en pacientes en quienes la enfermedad se controla escasamente. En casos agudos y durante las exacerbaciones puede administrarse prednisolona. El tratamiento inmunomodulador con ciclosporina puede considerarse en casos refractarios.


Subject(s)
Humans , Chronic Urticaria , Serum , Antibodies
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