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Selective depletion of plasma cells in vivo based on the specificity of their secreted antibodies

机译:浆细胞的选择性耗尽体内的基础的特异性分泌抗体

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摘要

Antibody-mediated diseases affect more than 10% of the human population. For most, no cure is available, particularly when the pathogenic antibodies are secreted by long-lived plasma cells resistant to conventional immunosuppressive therapies. Current therapeutic approaches target not only the plasma cells that secrete pathogenic antibodies, but also those providing protective antibodies. Here, in a murine model bearing long-lived plasma cells secreting anti-OVA and -chicken gamma globulin (CGG) antibodies, we describe the first-time use of an antigen-antibody (OVA/anti-CD138 antibody) conjugate for in vivo labeling and selective ablation of plasma cells that secrete antibodies specific for the antigen OVA. The selective depletion also led to a stable reduction of the corresponding serum anti-OVA antibody levels. In contrast, CGG-specific plasma cells and circulating anti-CGG antibody levels remained unchanged. The method described here should enable the development of unique causative treatment strategies for established antibody-mediated diseases sparing humoral immunity.
机译:抗体介入疾病影响的10%以上人类的人口。可用,特别是当致病性抗体分泌长寿的等离子体传统的免疫抑制细胞的抵抗力疗法。不仅是浆细胞分泌致病性抗体,但也提供保护抗体。长寿的浆细胞分泌anti-OVA和鸡丙种球蛋白(CGG)抗体,我们描述的首次使用抗原抗体(卵子/ anti-CD138抗体)共轭体内标记和选择性消融的浆细胞分泌抗体特定的抗原卵子。减少损耗也导致一个稳定的相应的血清抗体水平anti-OVA。相反,CGG-specific浆细胞循环anti-CGG抗体水平不变。使开发独特的病因治疗策略的建立抗体介入疾病保留体液免疫力。

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