Munoz J J, Peacock M G
Department of Health and Human Services, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Hamilton, Montana.
Cell Immunol. 1990 May;127(2):327-36. doi: 10.1016/0008-8749(90)90136-f.
Pertussigen (pertussis toxin (PT] is one of the most effective stimulators of IgE production in mice and rats. Employing flow microfluorimetric analysis (FMF), we showed that PT increases the percentage of blood and spleen lymphocytes with IgE on their surface. The percentage of IgE-bearing cells in the spleen of normal untreated C57Bl/10SCN mice of various ages varied from 2.2 to 12.2%, with an average value of 6.1 +/- 5.4%. In mice treated with 400 ng of PT and 1 mg of chicken egg albumin (EA), the percentage of these cells increased, 14 days after immunization, to an average value of 31.1 +/- 2.2%. Immunization of mice with PT alone increase the percentage of IgE-bearing cells only slightly (13.1 +/- 2.2% of the splenic lymphocytes) while injection of 1 mg of EA alone did not have any detectable action. As little as 6 ng of PT, when given simultaneously with 1 mg of EA, increased the percentage of IgE-bearing lymphocytes. A booster dose of 10 micrograms of EA given on Day 14 induced a further increase in the percentage of these cells even when as little as 0.039 ng of PT had been given at the time of initial immunization. PT was effective when given 4 days before or 5 days after EA. EA was effective when given 4 days before or 4 days after PT, but not 8 days after. The increase in IgE-bearing cells was mainly due to cytophilic binding of IgE to receptors for the epsilon chain of IgE (Fc epsilon) on the surface of lymphocytes rather than to a greater number of IgE-producing cells. This was shown by removing the IgE from Fc epsilon receptors by acid treatment which reduced the percentage of IgE-bearing cells to nearly normal values. The antibodies of IgE class with specificity to EA were increased dramatically, while antibodies with specificity to PT were not detected.
百日咳菌素(百日咳毒素[PT])是小鼠和大鼠中最有效的IgE产生刺激剂之一。采用流式微量荧光分析(FMF),我们发现PT可增加血液和脾脏中表面带有IgE的淋巴细胞百分比。不同年龄的正常未处理C57Bl/10SCN小鼠脾脏中带有IgE的细胞百分比在2.2%至12.2%之间变化,平均值为6.1±5.4%。在用400 ng PT和1 mg鸡卵白蛋白(EA)处理的小鼠中,免疫14天后,这些细胞的百分比增加到平均值31.1±2.2%。单独用PT免疫小鼠仅轻微增加了带有IgE的细胞百分比(脾脏淋巴细胞的13.1±2.2%),而单独注射1 mg EA则没有任何可检测到的作用。与1 mg EA同时给予低至6 ng的PT,可增加带有IgE的淋巴细胞百分比。在第14天给予10μg EA的加强剂量,即使在初次免疫时仅给予低至0.039 ng的PT,也会导致这些细胞百分比进一步增加。PT在EA前4天或后5天给予时有效。EA在PT前4天或后4天给予时有效,但在PT后8天给予无效。带有IgE的细胞增加主要是由于IgE与淋巴细胞表面IgEε链受体(Fcε)的嗜细胞性结合,而不是由于产生IgE的细胞数量增加。这通过酸处理从Fcε受体上去除IgE得以证明,酸处理可将带有IgE的细胞百分比降低至接近正常值。对EA具有特异性的IgE类抗体显著增加,而未检测到对PT具有特异性的抗体。