Munoz J J, Arai H, Bergman R K, Sadowski P L
Infect Immun. 1981 Sep;33(3):820-6. doi: 10.1128/iai.33.3.820-826.1981.
We studied various biological activities of crystalline pertussigen and found that in mice as little as 0.5 ng of pertussigen induced hypersensitivity to histamine, 8 to 40 ng induced leukocytosis, 2 ng increased production of insulin, 0.1 ng increased production of immunoglobulin E and immunoglobulin G1 antibodies to hen egg albumin, 9.5 ng increased susceptibility to anaphylactic shock, and 0.5 ng increased the vascular permeability of striated muscle. We also found that in Lewis rats 20 ng of pertussigen promoted the induction of hyperacute experimental allergic encephalomyelitis. Pertussigen given intraperitoneally was toxic to mice at a dose of 546 ng. Treatment of pertussigen with glutaraldehyde eliminated this toxicity. Mice immunized with 1,700 ng of detoxified pertussigen were protected against intracerebral challenge with 3 x 10(4) viable Bordetella pertussis cells. When as little as 0.5 ng of pertussigen was given intravenously to mice, the increased susceptibility of the animals to histamine could still be detected 84 days later. The biological properties of crystalline pertussigen indicate its similarity to leukocytosis-promoting factor, Islet-activating protein, late-appearing toxic factor, and mouse-protective antigen of B. pertussis.
我们研究了结晶百日咳菌素的各种生物学活性,发现对于小鼠,低至0.5纳克的百日咳菌素即可诱导对组胺的超敏反应,8至40纳克可诱导白细胞增多,2纳克可增加胰岛素的产生,0.1纳克可增加针对卵清蛋白的免疫球蛋白E和免疫球蛋白G1抗体的产生,9.5纳克可增加对过敏性休克的易感性,0.5纳克可增加横纹肌的血管通透性。我们还发现,对于刘易斯大鼠,20纳克的百日咳菌素可促进超急性实验性过敏性脑脊髓炎的诱导。腹腔注射百日咳菌素时,546纳克的剂量对小鼠有毒性。用戊二醛处理百日咳菌素可消除这种毒性。用1700纳克解毒的百日咳菌素免疫的小鼠可抵抗3×10⁴个活百日咳博德特氏菌细胞的脑内攻击。当给小鼠静脉注射低至0.5纳克的百日咳菌素时,84天后仍可检测到动物对组胺的易感性增加。结晶百日咳菌素的生物学特性表明它与百日咳博德特氏菌的白细胞增多促进因子、胰岛激活蛋白、迟发性毒性因子和小鼠保护抗原有相似性。