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CD1d Selectively Down Regulates the Expression of the Oxidized Phospholipid-Specific E06 IgM Natural Antibody in

机译:选择性下降CD1d调节氧化磷脂特异性E06 IgM天然抗体的表达

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摘要

Natural antibodies (NAbs) are important regulators of tissue homeostasis and inflammation and are thought to have diverse protective roles in a variety of pathological states. E06 is a T15 idiotype IgM NAb exclusively produced by B-1 cells, which recognizes the phosphocholine (PC) head group in oxidized phospholipids on the surface of apoptotic cells and in oxidized LDL (OxLDL), and the PC present on the cell wall of Streptococcus pneumoniae. Here we report that titers of the E06 NAb are selectively increased several-fold in Cd1d-deficient mice, whereas total IgM and IgM antibodies recognizing other oxidation specific epitopes such as in malondialdehyde-modified LDL (MDA-LDL) and OxLDL were not increased. The high titers of E06 in Cd1d-deficient mice are not due to a global increase in IgM-secreting B-1 cells, but they are specifically due to an expansion of E06-secreting splenic B-1 cells. Thus, CD1d-mediated regulation appeared to be suppressive in nature and specific for E06 IgM-secreting cells. The CD1d-mediated regulation of the E06 NAb generation is a novel mechanism that regulates the production of this specific oxidation epitope recognizing NAb.
机译:天然抗体(NABs)是组织稳态和炎症的重要调节因子,并且被认为在各种病态状态下具有不同的保护作用。 E06是由B-1细胞专门生产的T15型IgM Nab,其识别凋亡细胞表面和氧化LDL(OxLD1)的氧化磷脂中的磷化胆碱(PC)头部,以及存在于细胞壁上的PC链球菌肺炎料。在这里,我们认为E06 Nab的滴度在CD1D缺陷小鼠中选择性地增加了几折的几折,而识别出其他氧化特异性表位的总IgM和IgM抗体不会增加。 CD1D缺陷小鼠的E06的高滴度不是由于IGM分泌B-1细胞的全局增加,但它们是由于E06分泌脾B-1细胞的膨胀。因此,CD1D介导的调节似乎在自然界中抑制,并且对E06 IgM分泌细胞特异。 CD1D介导的E06 Nab产生调节是一种新的机制,调节该特异性氧化表位的产生识别NAB。

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