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Antigen-Specific Markers in Immunoglobulin Peptides From Rat Immune Sera

机译:大鼠免疫血清免疫球蛋白肽中的抗原特异性标记

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During infections, but also in cancer and auto-immune disease, antigen-specific antibodies arise from random recombination of germline sequences and the subsequent selection of B-cells that produce antigen-specific immunoglobulins. As antibody selection starts from a limited set of germline sequences, and immunoglobulins are refined for optimal binding to a particular antigen, we expect that the complementarity determining regions (CDR; antigen binding sites) may converge to include homologous or identical sequences in different subjects. If this is the case, peptides that relate to immunoglobulin CDRs can be used as a marker for the antigen that the immune system was exposed to. Here, we tested this hypothesis in a pilot study using an animal immunization model under controlled conditions.
机译:在感染期间,还在癌症和自身免疫疾病中,从种系序列的随机重组和随后选择产生抗原特异性免疫球蛋白的B细胞时出现抗原特异性抗体。由于抗体选择从一组有限的种系序列开始,并且免疫球蛋白被精制成对特定抗原的最佳结合,我们预计互补确定区域(CDR;抗原结合位点)可以收敛以包括在不同受试者中的同源或相同的序列。如果是这种情况,则涉及免疫球蛋白CDR的肽可以用作免疫系统暴露于免疫系统的抗原的标记物。在这里,我们在受控条件下使用动物免疫模型进行了在试验研究中测试了这一假设。

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