A Novel Method for Treating Bronchial Asthma with Newly Designed Histaglobulin Therapy

S. K., D. S.
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Abstract

Asthma, a chronic inflammatory disease of the airways is considered as an incurable disease and extensive research is going on in developing novel treatment. The objective of the study is to establish that the antihistamine antibody has low serum histamine binding capacity (SHBC) in allergic patients as compared to normal persons and that it can be raised with our novel method of Histaglobulin treatment thereby effecting a ‘cure’ in bronchial asthma. About 67 normal and 135 allergic persons, were identified based on serum level of total immunoglobulin E (IgE) estimated by ELISA. Antihistamine antibody was separated from serum by affinity chromatography. Presence of antihistamine antibody in the elute was confirmed by SDS-PAGE test. The antihistamine antibody was IgG, confirmed by MALDI-TOF analysis. The SHBC of the antihistamine antibody was estimated based on standard curve, plotted with different concentrations of serum antihistamine antibody by histamine ELISA test. Total Immunoglobulin E and SHBC were estimated in 135 allergic patients. In normal and allergic persons, the total IgE level was <100 IU/ml and 200 IU/ml respectively. The average SHBC of normal persons was 116 µg/ml, which was 39% more as compared to allergic patients whose average SHBC before treatment was 83.6 µg/ml. 135 allergic patients were first subjected to antihistamine, mast cell-membrane stabilizers, anti-inflammatory and bronchodilator drugs followed by histaglobulin injection. The SHBC level was raised in 122 (90.4%) patients to an average of 111.6 µg/ml. Overall, 132 (97.8%) allergic patients responded well to our treatment and were free from allergic manifestation throughout the follow-up period of about 5 years. Hence, this novel treatment with histaglobulin which has scientific basis, effective and well tolerated can be adopted across the world for effecting a cure from bronchial asthma and allergic rhinitis.
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新设计的组织球蛋白治疗支气管哮喘的新方法
哮喘是一种慢性气道炎症性疾病,被认为是一种无法治愈的疾病,目前正在进行广泛的研究以开发新的治疗方法。本研究的目的是确定与正常人相比,过敏患者的抗组胺抗体具有较低的血清组胺结合能力(SHBC),并且可以通过我们的新的组织球蛋白治疗方法来提高它,从而“治愈”支气管哮喘。采用ELISA法测定血清总免疫球蛋白E (IgE)水平,对67例正常人和135例变态反应者进行鉴定。用亲和层析法分离血清抗组胺抗体。SDS-PAGE检测证实洗脱液中存在抗组胺抗体。MALDI-TOF分析证实抗组胺抗体为IgG。根据标准曲线估计抗组胺抗体的SHBC,并通过组胺酶联免疫吸附试验绘制不同浓度的血清抗组胺抗体。测定135例过敏患者的总免疫球蛋白E和SHBC。正常人和过敏者总IgE水平分别<100 IU/ml和200 IU/ml。正常人的平均SHBC为116µg/ml,比过敏患者治疗前的平均SHBC为83.6µg/ml高出39%。135例过敏患者首先使用抗组胺药、肥大细胞膜稳定剂、抗炎药和支气管扩张剂,然后注射组织球蛋白。122例(90.4%)患者的SHBC水平升高至平均111.6µg/ml。总体而言,132例(97.8%)过敏患者对我们的治疗反应良好,在约5年的随访期间无过敏表现。因此,这种具有科学依据、有效且耐受性良好的组织球蛋白治疗方法可在世界范围内用于治疗支气管哮喘和变应性鼻炎。
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