Krop Esmeralda J M, Matsui Elizabeth C, Sharrow Scott D, Stone Martin J, Gerber Peter, van der Zee Jaring S, Chapman Martin D, Aalberse Rob C
Department of Pulmonology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Int Arch Allergy Immunol. 2007;144(4):296-304. doi: 10.1159/000106318. Epub 2007 Jul 23.
Recombinant allergens are preferred over natural allergen extracts in measuring antibodies. We tested the use of recombinant variants of the major mouse allergen Mus m 1 in detection of mouse-specific antibodies in sera of laboratory animal workers and children.
Six recombinant major urinary proteins (MUPs) were produced and antibody-binding capacity was compared to natural Mus m 1 and to mouse urine extract. In a specific subset, cross-reactivity of MUP with Mus m 1 and between the different recombinant MUPs was determined.
For IgE antibodies, MUP8 showed high cross-reactivity with Mus m 1. MUP8-specific IgE was found in 55% of the mouse urine IgE-positive sera. Specific IgG and IgG4 antibodies against natural Mus m 1 correlated strongly with antibodies against recombinant MUP8 and were cross-reactive. IgG4 levels against MUP8 and mouse urine extract correlated, but detection of mouse urine-specific IgG4 in the absence of MUP-specific IgG4 was not uncommon. Cross-reactivity of IgG antibodies between MUP8 and Mus m 1 as well as between the different MUPs was high and inhibition varied between 54 and 99%.
The mouse allergen Mus m 1 can be replaced in antibody testing by recombinant MUP8. Other MUPs, except MUP4, are interchangeable with MUP8. However, mouse urine extract showed better detection of both mouse-specific IgE and IgG4 levels. Other components in the mouse urine, like mouse albumin and other yet unidentified components, also induce IgE and IgG4 antibodies.
在检测抗体时,重组变应原比天然变应原提取物更受青睐。我们测试了主要小鼠变应原Mus m 1的重组变体在检测实验动物工作者和儿童血清中小鼠特异性抗体方面的应用。
制备了六种重组主要尿蛋白(MUP),并将其抗体结合能力与天然Mus m 1和小鼠尿提取物进行比较。在一个特定亚组中,测定了MUP与Mus m 1之间以及不同重组MUP之间的交叉反应性。
对于IgE抗体,MUP8与Mus m 1表现出高交叉反应性。在55%的小鼠尿IgE阳性血清中发现了MUP8特异性IgE。针对天然Mus m 1的特异性IgG和IgG4抗体与针对重组MUP8的抗体高度相关且具有交叉反应性。针对MUP8和小鼠尿提取物的IgG4水平相关,但在没有MUP特异性IgG4的情况下检测到小鼠尿特异性IgG4并不罕见。MUP8与Mus m 1之间以及不同MUP之间的IgG抗体交叉反应性很高,抑制率在54%至99%之间变化。
在抗体检测中,小鼠变应原Mus m 1可用重组MUP8替代。除MUP4外,其他MUP可与MUP8互换。然而,小鼠尿提取物在检测小鼠特异性IgE和IgG4水平方面表现更好。小鼠尿中的其他成分,如小鼠白蛋白和其他尚未鉴定的成分,也可诱导IgE和IgG4抗体。