Shen G Q, Ojo-Amaize E A, Agopian M S, Peter J B
Specialty Laboratories, Inc., Santa Monica, California 90404-3900, USA.
Clin Diagn Lab Immunol. 1996 Mar;3(2):162-6. doi: 10.1128/cdli.3.2.162-166.1996.
Silicon, in the form of sodium silicate (Na2SiO3), adsorbed onto bovine serum albumin (BSA)-precoated plates served as the solid-phase antigen in an enzyme immunoassay to detect silicate-reactive antibodies in the plasma of 40 symptomatic women with silicone breast implants, 91 asymptomatic women with silicone breast implants, 50 healthy control women, and 52 women with rheumatic diseases and without silicone breast implants, Silicate-reactive antibodies of immunoglobulin G (IgG) or IgM isotypes were detected in the plasma of 30% (12 of 40) of the symptomatic women with silicone breast implants; 9% (8 of 91) of the asymptomatic women with silicone breast implants; 5% (1 of 20) of the women without implants who had systemic lupus erythematosus; and 0% (0 of 32) of the women without implants who had either Sjögren syndrome, scleroderma, or rheumatoid arthritis. Only 2% (1 of 50) of the sera from the healthy control women contained silicate-reactive antibodies. Preincubation of sera with silicate and eight other metal compounds (including SiO2) demonstrated that the IgG and IgM antibodies bound specifically to silicate, because preincubation with Na2SiO3 inhibited more than 90% of the activity, whereas CrO3, Li2SO4, MgSO4, NiSO4, HgCl2, ZrOCl2, BeSO4, and SiO2 failed to inhibit the IgG or IgM antibody binding to the silicate-BSA plates. Furthermore, the F(ab')2 portion and not the Fc portion of the silicate-reactive IgG was reactive with BSA-bound silicate in the enzyme immunoassay. The assay for silicate-reactive antibodies was quantified by assigning arbitrary units to a standard curve composed of serial twofold dilutions of high-positive (ten times higher than the cutoff) silicate antibody sera. This novel assay is a useful method for detecting and quantifying humoral immune response to silicate.
以硅酸钠(Na₂SiO₃)形式存在的硅,吸附在牛血清白蛋白(BSA)预包被的平板上,在酶免疫测定中用作固相抗原,以检测40名有症状的硅胶乳房植入女性、91名无症状的硅胶乳房植入女性、50名健康对照女性以及52名患有风湿性疾病且无硅胶乳房植入女性血浆中的硅酸盐反应性抗体。在有症状的硅胶乳房植入女性血浆中,30%(40名中的12名)检测到免疫球蛋白G(IgG)或IgM同种型的硅酸盐反应性抗体;无症状的硅胶乳房植入女性中9%(91名中的8名);无植入物但患有系统性红斑狼疮的女性中5%(20名中的1名);无植入物但患有干燥综合征、硬皮病或类风湿关节炎的女性中0%(32名中的0名)。健康对照女性的血清中只有2%(50名中的1名)含有硅酸盐反应性抗体。血清与硅酸盐和其他八种金属化合物(包括SiO₂)预孵育表明,IgG和IgM抗体特异性结合硅酸盐,因为与Na₂SiO₃预孵育可抑制超过90%的活性,而CrO₃、Li₂SO₄、MgSO₄、NiSO₄、HgCl₂、ZrOCl₂、BeSO₄和SiO₂未能抑制IgG或IgM抗体与硅酸盐 - BSA平板的结合。此外,在酶免疫测定中,硅酸盐反应性IgG的F(ab')₂部分而非Fc部分与BSA结合的硅酸盐反应。通过为由高阳性(比临界值高十倍)硅酸盐抗体血清的系列两倍稀释组成的标准曲线指定任意单位,对硅酸盐反应性抗体测定进行定量。这种新的测定方法是检测和定量对硅酸盐的体液免疫反应的有用方法。