Cross reactive anti-tetanus and anti-melittin Fab fragments by phage display after tetanus toxoid immunisation.

Human antibodies and hybridomas Pub Date : 1996-01-01
M Vogel, L Lai, M P Rudolf, V Curcio-Vonlanthen, S Miescher, B M Stadler
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Abstract

Amino acid sequence homology between tetanus toxoid, a common vaccine and melittin, a bee venom allergen provided us with two antigen models for studying the production of cross reactive antibodies after immunisation. Analysis of the serum of an atopic patient recently boosted with tetanus toxoid revealed the presence of anti-melittin and anti-tetanus antibodies. From this donor a phage display Fab library was constructed five days after vaccination. Screening of this library either with melittin alone or with tetanus toxoid followed by melittin allowed the isolation of Fab fragments specific to melittin but also Fab fragments which cross react with melittin and tetanus toxoid. Amino acid analysis revealed diversity in the heavy and the light Ig chains of the melittin specific and of the cross reactive clones. Interestingly we found that the light chain recognised melittin whereas the heavy chain preferentially bound to tetanus toxoid suggesting that cross reactivity may be due to the different binding specificities of the individual Ig chains.

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破伤风类毒素免疫后噬菌体展示抗破伤风与抗蜂毒蛋白Fab交叉反应片段。
常见疫苗破伤风类毒素与蜂毒过敏原蜂毒蛋白氨基酸序列的同源性为研究免疫后交叉反应抗体的产生提供了两种抗原模型。对最近注射破伤风类毒素的一位特应性病人的血清进行分析,发现存在抗蜂毒素和抗破伤风抗体。接种疫苗5天后,利用该供体构建噬菌体展示Fab库。用蜂毒素单独或破伤风类毒素后再用蜂毒素筛选该文库,可以分离出蜂毒素特异性的Fab片段,也可以分离出与蜂毒素和破伤风类毒素交叉反应的Fab片段。氨基酸分析显示,蜂毒蛋白特异性克隆和交叉反应克隆的重、轻Ig链具有多样性。有趣的是,我们发现轻链识别蜂毒蛋白,而重链优先与破伤风类毒素结合,这表明交叉反应性可能是由于单个Ig链的不同结合特异性。
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Targeting gamma interferon to tumor cells by a genetically engineered fusion protein secreted from myeloma cells. Cross reactive anti-tetanus and anti-melittin Fab fragments by phage display after tetanus toxoid immunisation. Characterization of anti-tumor immunity derived from the inoculation of myeloma cells secreting the fusion protein RM4/IFN-tau. Lung cancer-reacting human recombinant antibody AE6F4: potential usefulness in the sputum cytodiagnosis. A rapid method for purification of monoclonal human IgM from mass culture.
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