Schmechel Detlef, Green Brett J, Blachere Francoise M, Janotka Erika, Beezhold Donald H
Allergy and Clinical Immunology Branch, National Institute for Occupational Safety and Health, Morgantown, WV 26505, USA.
J Allergy Clin Immunol. 2008 Mar;121(3):763-8. doi: 10.1016/j.jaci.2007.09.046. Epub 2007 Nov 26.
Alternaria alternata is recognized as an important aeroallergen indoors and outdoors, and exposure to the fungus has been identified as a risk factor for asthma. Two recent publications concluded that 95% to 99% of American homes contained detectable amounts of Alternaria antigens when analyzed with a polyclonal antibody (pAb)-based ELISA.
We investigated the cross-reactivity of the commercially available pAbs that were used in those studies.
Reactivity to 24 fungal species commonly found in indoor environments was analyzed by inhibition ELISA by using solid-phase A alternata antigen. The pAbs were also tested by immunoblotting and halogen immunoassay for a subgroup of fungi.
Spores of 7 fungi including species of Alternaria, Ulocladium, Stemphylium, Epicoccum, Drechslera, and Exserohilum strongly inhibited the binding of the pAbs when tested by ELISA. Six other fungi reacted in the ELISA at a lower level, and 11 fungal species including several Penicillium, Aspergillus, Fusarium, and Cladosporium species failed to show inhibition. The immunoblots and the halogen immunoassay staining confirmed the cross-reactivity patterns of the ELISA.
The pAbs against A alternata were found to cross-react broadly with related and nonrelated fungi. The prevalence data previously reported for A alternata should be considered to be fungal-reactive rather than A alternata-specific.
链格孢被认为是室内外重要的气传变应原,接触该真菌已被确定为哮喘的一个危险因素。最近的两篇出版物得出结论,当用基于多克隆抗体(pAb)的酶联免疫吸附测定(ELISA)进行分析时,95%至99%的美国家庭含有可检测量的链格孢抗原。
我们研究了那些研究中使用的市售多克隆抗体的交叉反应性。
通过使用固相链格孢抗原的抑制ELISA分析对室内环境中常见的24种真菌的反应性。还通过免疫印迹法和卤素免疫测定法对一组真菌测试了这些多克隆抗体。
当通过ELISA进行测试时,包括链格孢属、格孢腔菌属、匍柄霉属、附球菌属、德氏霉属和突脐孢属在内的7种真菌的孢子强烈抑制了多克隆抗体的结合。其他6种真菌在ELISA中的反应水平较低,包括几种青霉属、曲霉属、镰刀菌属和枝孢属在内的11种真菌未显示出抑制作用。免疫印迹和卤素免疫测定染色证实了ELISA的交叉反应模式。
发现针对链格孢的多克隆抗体与相关和不相关真菌广泛交叉反应。先前报道的链格孢的流行数据应被视为真菌反应性而非链格孢特异性的。