Linthicum D S, Sell S, Mandy W J
Eur J Immunol. 1977 Dec;7(12):860-4. doi: 10.1002/eji.1830071208.
Surface immunoglobulin allotypes on rabbit peripheral blood lymphocytes (PBL) and spleen lymphocytes are detected by an immunoferritin labeling technique for electron microscopy. Human red blood cells, chemically coated with purified rabbit IgG of specific allotypes, served as test cells to assess the labeling specificity and efficiency. Immunoelectron microscopic labeling reveals that groups a, b, d and e allotypic specificities are readily detectable on passively coated test cells. However, only a and b group markers are detectable on lymphocytes. On rabbit PBL both a (VH of Fd region) and b (kappa chain constant region) group allotypes are detectable (73-78% and 68-77%, respectively); on spleen cells, 46% and 52-55% are positive for a and b locus allotypes, respectively. The d and e allotypes (i. e. gamma chain-specific) are undetectable on PBL or on spleen lymphocytes using this method. We conclude that the d and e group allotypes are either not present on the lymphocyte surface or are buried in the surface membrane and unacessible to the antisera used in this immunoferritin labeling technique.
采用免疫铁蛋白标记技术进行电子显微镜检查,以检测兔外周血淋巴细胞(PBL)和脾淋巴细胞表面的免疫球蛋白同种异型。用特定同种异型的纯化兔IgG进行化学包被的人红细胞用作测试细胞,以评估标记的特异性和效率。免疫电子显微镜标记显示,在被动包被的测试细胞上很容易检测到a、b、d和e同种异型特异性。然而,在淋巴细胞上只能检测到a和b组标记。在兔PBL上,a(Fd区的VH)和b(κ链恒定区)组同种异型均可检测到(分别为73 - 78%和68 - 77%);在脾细胞上,a和b位点同种异型的阳性率分别为46%和52 - 55%。使用该方法在PBL或脾淋巴细胞上未检测到d和e同种异型(即γ链特异性)。我们得出结论,d和e组同种异型要么不存在于淋巴细胞表面,要么埋藏在表面膜中,无法被该免疫铁蛋白标记技术中使用的抗血清识别。