Lopatin D E, Van Poperin N, MacCallum D K, Meyer R F, Lillie J H
Department of Oral Biology, School of Dentistry, University of Michigan, Ann Arbor 48109-0402.
Invest Ophthalmol Vis Sci. 1989 Jan;30(1):122-31.
The feline model of induced rejection of corneal allografts was employed to define the changes in the concentrations of immunoglobulins and albumin in the anterior chamber prior to, and concomitant with the rejection of the transplanted cornea. Fourteen animals received unilateral exchange corneal allografts. Aqueous humor obtained by anterior chamber paracentesis at regular intervals prior to and following the performance of the penetrating keratoplasties was analyzed for IgG, IgM and albumin concentrations using the micro enzyme-linked immunosorbant assay (ELISA). Two patterns of anterior chamber protein modulation were observed. Eight of the animals demonstrated a biphasic pattern in which both immunoglobulin and albumin concentrations were elevated two- to five-fold above presurgical values 14 days postkeratoplasty, returning to preoperative values by day 42. Three to 5 weeks after corneal rejection was induced increases in protein concentrations were observed that correlated with the appearance of clinical signs of rejection. A second, monophasic pattern of anterior chamber protein modulation following keratoplasty was observed in four of the animals. It was distinguishable from the biphasic pattern in that levels did not return to baseline values after the initial rise following keratoplasty until the rejection process was completed. The monophasic response was found to be characteristic of more rapid and vigorous corneal rejection. Examination of albumin to immunoglobulin ratios suggested that all changes in protein levels following keratoplasty were a result of increased influx of serum proteins into the anterior chamber, rather than due to local immunoglobulin synthesis.
采用猫角膜同种异体移植诱导排斥模型,以确定在移植角膜排斥反应之前及同时前房内免疫球蛋白和白蛋白浓度的变化。14只动物接受了单侧交换角膜同种异体移植。在穿透性角膜移植术前及术后定期通过前房穿刺获取房水,使用微量酶联免疫吸附测定(ELISA)分析其中IgG、IgM和白蛋白的浓度。观察到两种前房蛋白调节模式。8只动物呈现双相模式,角膜移植术后14天免疫球蛋白和白蛋白浓度均比手术前值升高2至5倍,到第42天恢复到术前值。诱导角膜排斥反应后3至5周,观察到蛋白浓度升高,且与排斥反应临床体征的出现相关。在4只动物中观察到角膜移植术后前房蛋白调节的第二种单相模式。它与双相模式的区别在于,角膜移植术后最初升高后,直到排斥反应过程结束,水平才恢复到基线值。发现单相反应是更快、更强有力的角膜排斥反应的特征。白蛋白与免疫球蛋白比率的检查表明,角膜移植术后蛋白水平的所有变化都是血清蛋白进入前房增加的结果,而非局部免疫球蛋白合成所致。