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Effects of skeletal unloading on the antibody repertoire of tetanus toxoid and/or CpG treated C57BL/6J mice

机译:骨骼负荷对破伤风类毒素和/或CpG治疗的C57BL / 6J小鼠抗体库的影响

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摘要

Spaceflight affects the immune system, but the effects on the antibody repertoire, responsible for humoral immunity, has not been well explored. In particular, the complex gene assembly and expression process; including mutations, might make this process vulnerable. Complementarity determining region 3 (CDR3), composed of parts of the V-(D-)J-gene segments, is very important for antigen binding and can be used as an important measure of variability. Skeletal unloading, and the physiological effects of it, parallel many impacts of space flight. Therefore, we explored the impact of skeletal unloading using the antiorthostatic suspension (AOS) model. Animals were experimentally challenged with tetanus toxoid (TT) and/or the adjuvant CpG. Blood was analyzed for anti-TT antibody and corticosterone concentrations. Whole spleen tissue was prepared for repertoire characterization. AOS animals showed higher levels of corticosterone levels, but AOS alone did not affect anti-TT serum antibody levels. Administration of CpG significantly increased the circulating anti-TT antibody concentrations. AOS did alter constant gene usage resulting in higher levels of IgM and lower levels of IgG. CpG also altered constant gene region usage increasing usage of IgA. Significant changes could be detected in multiple V-, D-, and J-gene segments in both the heavy and light chains in response to AOS, TT, and CpG treatments. Analysis of class-switched only transcripts revealed a different pattern of V-gene segment usage than detected in the whole repertoire and also showed significant alterations in gene segment usage after challenge. Alterations in V/J pairing were also detected in response to challenge. CDR3 amino acid sequence overlaps were similar among treatment groups, though the addition of CpG lowered overlap in the heavy chain. We isolated 3,045 whole repertoire and 98 potentially TT-specific CDR3 sequences for the heavy chain and 569 for the light chain. Our results demonstrate that AOS alters the repertoire response to challenge with TT and/or CpG.
机译:航天会影响免疫系统,但尚未充分探讨对负责体液免疫的抗体库的影响。特别是复杂的基因组装和表达过程;包括突变,可能会使此过程变得脆弱。由V-(D-)J基因片段的一部分组成的互补决定区3(CDR3)对于抗原结合非常重要,可以用作变异性的重要指标。骨骼的卸载及其生理效应与太空飞行的许多影响平行。因此,我们使用抗体位悬架(AOS)模型探索了骨骼卸载的影响。用破伤风类毒素(TT)和/或佐剂CpG对动物进行实验性攻击。分析血液中的抗TT抗体和皮质酮浓度。准备完整的脾脏组织以进行血库表征。 AOS动物的皮质酮水平较高,但仅AOS不会影响抗TT血清抗体水平。 CpG的使用显着增加了循环中的抗TT抗体浓度。 AOS确实改变了恒定的基因用法,导致更高的IgM水平和更低的IgG水平。 CpG还改变了恒定基因区域的使用率,从而增加了IgA的使用率。响应AOS,TT和CpG处理,可以在重链和轻链的多个V,D和J基因片段中检测到重大变化。仅分类切换的转录本的分析显示,与整个曲目中检测到的V基因片段使用方式不同,并且在攻击后基因片段使用中也显示出显着变化。响应挑战,还检测到V / J配对发生变化。尽管CpG的添加降低了重链中的重叠,但是治疗组之间的CDR3氨基酸序列重叠相似。我们分离出3045个完整库,重链为98个潜在的TT特异性CDR3序列,轻链为569个。我们的结果表明,AOS改变了库对TT和/或CpG攻击的反应。

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