Singh Bharat, Singh Seema, Asif Abdul R, Oellerich Michael, Sharma Gainda L
CSIR-Institute of Genomics and Integrative Biology, University Campus, Mall Road, Delhi-110007, India.
Curr Protein Pept Sci. 2014;15(5):403-23. doi: 10.2174/1389203715666140512120605.
Incidence of fungal infections has increased alarmingly in past few decades. Of the fungal pathogens, the Aspergillus fumigatus has been a major cause of allergic bronchopulmonary aspergillosis (ABPA) which has five main stages--the acute, remission, exacerbation, glucocorticoid dependent and fibrotic stage. The diagnosis of ABPA remains difficult due to its overlapping clinical and radiological features with tuberculosis and cystic fibrosis. From past few decades, the crude fractions of A. fumigatus have been used for immunodiagnosis of ABPA. Most of the detection kits based on crude fractions of A. fumigatus are quite sensitive but have low specificity. Till date 21 known and 25 predicted allergens of A. fumigatus have been identified. Of these allergens, only five recombinants (rAsp f1-f4 and f6) are commercially used for diagnosis of allergic aspergillosis. Remaining allergens of A. fumigatus have been restricted for use in specific diagnosis of ABPA, due to sharing of common antigenic epitopes with other allergens. Complete sequencing of A. fumigatus genome identified 9926 genes and the reports on the proteome of A. fumigatus have shown the presence of large number of their corresponding proteins in the pathogen. The analysis of immunoproteomes developed from crude fractions of A. fumigatus by IgG/IgE reactivity with ABPA patients and animal sera have identified the panel of new antigens. A brief description on the current status of A. fumigatus antigens is provided in this review. The implementation of advance recombinant expression and peptidomic approaches on the A. fumigatus antigens may help in the selection of appropriate molecules for the development of tools for more specific early diagnosis of ABPA, and desensitization therapies for patients of allergic disorders.
在过去几十年中,真菌感染的发病率急剧上升。在真菌病原体中,烟曲霉一直是变应性支气管肺曲霉病(ABPA)的主要病因,该病有五个主要阶段——急性、缓解、加重、糖皮质激素依赖和纤维化阶段。由于ABPA的临床和放射学特征与肺结核和囊性纤维化重叠,其诊断仍然困难。在过去几十年中,烟曲霉的粗提物已被用于ABPA的免疫诊断。大多数基于烟曲霉粗提物的检测试剂盒相当敏感,但特异性较低。迄今为止,已鉴定出21种已知和25种预测的烟曲霉过敏原。在这些过敏原中,只有五种重组体(rAsp f1-f4和f6)在商业上用于诊断变应性曲霉病。由于与其他过敏原共享共同的抗原表位,烟曲霉的其余过敏原被限制用于ABPA的特异性诊断。烟曲霉基因组的完整测序鉴定出9926个基因,关于烟曲霉蛋白质组的报告显示该病原体中存在大量相应的蛋白质。通过与ABPA患者和动物血清的IgG/IgE反应性,对从烟曲霉粗提物中开发的免疫蛋白质组进行分析,已鉴定出一组新抗原。本综述简要介绍了烟曲霉抗原的现状。对烟曲霉抗原实施先进的重组表达和肽组学方法,可能有助于选择合适的分子,以开发用于ABPA更特异性早期诊断的工具,以及用于过敏性疾病患者的脱敏疗法。