Reagan W J, Scott-Moncrieff C, Christian J, Snyder P, Kelly K, Glickman L
Department of Veterinary Pathobiology, School of Veterinary Medicine, Purdue University, West Lafayette, IN 47907, USA.
Am J Vet Res. 1998 Dec;59(12):1568-74.
To evaluate interactions of human intravenous immunoglobulin (IVIG) with canine lymphocytes and monocytes.
Heparinized blood samples from 4 clinically normal Beagles.
Binding ability of IVIG to canine lymphocytes and monocytes was measured by flow cytometry and an indirect immunofluorescent assay. Dual-staining fluorescent assays were done to determine lymphocyte subsets that bind IVIG. Competitive assays were done, using intact canine IgG and Fc fragments, and inhibition of binding was compared with that of F(ab)2 fragments. Ability of IVIG to inhibit phagocytosis of antibody-coated canine RBC also was determined, using a canine mononuclear cell phagocytic assay.
IVIG concentrations (10, 1, 0.1, and 0.01 mg/ml) bound to (mean+/-SD) 99.6+/-0.4, 92.4+/-6.1, 20.4+/-24.6 and 2.0+/-5.1 % of canine lymphocytes, respectively, Dual staining analyses with IVIG and canine lymphocyte markers indicated that IVIG bound to CD4, CD8, and B lymphocytes. The aforementioned 4 IVIG concentrations bound to 98.0+/-2.1, 85.5+/-13.5, 64.7+/-32.8, and 26.5+/-17.1 % of monocytes, respectively. Inhibition of IVIG (0.01 mg/ml) binding to monocytes was significant (P< 0.05) in the presence of 1 and 10 mg of canine IgG/ml and 1 mg of canine Fc fragments/ml. In the presence of F(ab')2 fragments of canine IgG, inhibition was not significant, suggesting that binding is Fc mediated. Co-culturing of monocytes, opsonized RBC, and the 4 concentrations of IVIG and no IVIG resulted in 11.8+/-5.1, 27.7+/-12.3, 31.8+15.1, 53.8+/-6.7, and 45 + 12% of the monocytes containing RBC, respectively. Phagocytosis inhibition was significant (P < 0.05) at an IVIG concentration of 10 mg/ml.
IVIG binds to canine lymphocytes and monocytes; binding to the latter is Fc mediated. IVIG also inhibits Fc-mediated phagocytosis of antibody-coated RBC.
Owing to its ability to inhibit Fc-mediated phagocytosis of antibody-coated RBC, IVIG may be an effective short-term treatment for dogs with immune-mediated hemolytic anemia.
评估人静脉注射免疫球蛋白(IVIG)与犬淋巴细胞和单核细胞的相互作用。
来自4只临床健康比格犬的肝素化血样。
通过流式细胞术和间接免疫荧光测定法测量IVIG与犬淋巴细胞和单核细胞的结合能力。进行双染色荧光测定以确定与IVIG结合的淋巴细胞亚群。使用完整的犬IgG和Fc片段进行竞争性测定,并将结合抑制与F(ab)2片段的结合抑制进行比较。还使用犬单核细胞吞噬测定法确定IVIG抑制抗体包被的犬红细胞吞噬作用的能力。
IVIG浓度(10、1、0.1和0.01mg/ml)分别与(平均值±标准差)99.6±0.4%、92.4±6.1%、20.4±24.6%和2.0±5.1%的犬淋巴细胞结合。IVIG与犬淋巴细胞标志物的双染色分析表明,IVIG与CD4、CD8和B淋巴细胞结合。上述4种IVIG浓度分别与98.0±2.1%、85.5±13.5%、64.7±32.8%和26.5±17.1%的单核细胞结合。在存在1mg/ml和10mg/ml犬IgG以及1mg/ml犬Fc片段的情况下,IVIG(0.01mg/ml)与单核细胞的结合抑制具有显著性(P<0.05)。在存在犬IgG的F(ab')2片段的情况下,抑制作用不显著,这表明结合是由Fc介导的。单核细胞、调理的红细胞与4种浓度的IVIG以及无IVIG共同培养,结果分别有11.8±5.1%、27.7±12.3%、31.8±15.1%、53.8±6.7%和45±12%的单核细胞含有红细胞。在IVIG浓度为10mg/ml时,吞噬抑制具有显著性(P<0.05)。
IVIG与犬淋巴细胞和单核细胞结合;与后者的结合是由Fc介导的。IVIG还抑制抗体包被的红细胞的Fc介导的吞噬作用。
由于其抑制抗体包被的红细胞的Fc介导的吞噬作用的能力,IVIG可能是免疫介导的溶血性贫血犬的一种有效的短期治疗方法。