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首页> 外文期刊>Infection and immunity >Identification of functional antigenic segments of toxic shock syndrome toxin 1 by differential immunoreactivity and by differential mitogenic responses of human peripheral blood mononuclear cells, using active toxin fragments.
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Identification of functional antigenic segments of toxic shock syndrome toxin 1 by differential immunoreactivity and by differential mitogenic responses of human peripheral blood mononuclear cells, using active toxin fragments.

机译:使用活性毒素片段,通过差异免疫反应性和人外周血单核细胞的差异促有丝分裂反应,鉴定毒性休克综合征毒素1的功能性抗原区段。

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When toxic shock syndrome toxin 1 was subjected to papain hydrolysis, two serologically active fragments of 16.3 kilodaltons (16K fragment) and 12.4 kilodaltons (12K fragment) were generated, whereas a third fragment of 9.7 kilodaltons (10K fragment) was inactive. The biologic activities of the fragments were evaluated in vitro by determining their ability to promote nonspecific proliferation of human peripheral blood mononuclear cells. The 12K fragment was significantly (P less than or equal to 0.013) more stimulatory than the 16K fragment. When human peripheral blood mononuclear cells were preincubated for a period of 24 h with various concentrations of the 16K fragment, followed by incubation with a constant amount (2 x 10(-2) ng/ml) of whole toxin, the level of DNA synthesis induced by the holotoxin was reduced by approximately 60% when compared with that of controls exposed to whole toxin alone. The 12K fragment did not demonstrate a similar blocking effect. Immunoblots of the toxic shock syndrome toxin 1 digest, which were exposed to monoclonal antibodies (MAbs) developed against native toxin, depicted the presence of two different antigenic regions (epitopes). One MAb, 8-5-7, which has been shown previously to inhibit the biologic activity of the holotoxin in vitro and in vivo, reacted primarily with the 12K fragment. A second MAb, 10-6-1, that did not neutralize interleukin-1 production reacted primarily with the 16K fragment. On the basis of the differential mitogenic responses and the identification of heterologous epitopes, it was concluded that the functional region of the holotoxin can be partitioned into at least two functional segments encompassed between amino acid residues 53 and 87 and between amino acid residues 88 and 194 on the polypeptide chain.
机译:当中毒性休克综合征毒素1进行木瓜蛋白酶水解时,产生了16.3道尔顿(16K片段)和12.4道尔顿(12K片段)的两个具有血清学活性的片段,而9.7道尔顿(10K片段)的第三个片段没有活性。通过测定片段促进人外周血单核细胞非特异性增殖的能力,在体外评估了片段的生物学活性。 12K片段比16K片段具有更大的刺激性(P小于或等于0.013)。当将人外周血单核细胞与各种浓度的16K片段预孵育24小时,然后与恒定量(2 x 10(-2)ng / ml)的全毒素孵育时,DN​​A合成的水平与仅暴露于全毒素的对照相比,由全毒素诱导的毒素减少了约60%。 12K片段未显示出类似的阻断作用。暴露于针对天然毒素而开发的单克隆抗体(MAb)的中毒性休克综合症毒素1消化液的免疫印迹描述了两个不同抗原区(表位)的存在。先前已显示一种在体外和体内抑制全毒素生物活性的8-5-7单抗主要与12K片段反应。没有中和白介素-1产生的第二个单克隆抗体10-6-1主要与16K片段反应。基于不同的促有丝分裂反应和异源表位的鉴定,得出的结论是,全毒素的功能区可以被划分为至少两个包含在氨基酸残基53和87之间以及氨基酸残基88和194之间的功能区段。在多肽链上。

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