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在TNFα驱动的多关节炎转基因模型中,当在常规繁殖时给予TNFα消耗疗法,可改善生育能力并提高动物福利。

TNFα depleting therapy improves fertility and animal welfare in TNFα-driven transgenic models of polyarthritis when administered in their routine breeding.

作者信息

Naylor Amy J, Desanti Guillaume, Saghir Atif N, Hardy Rowan S

机构信息

1 Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.

2 Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK.

出版信息

Lab Anim. 2018 Feb;52(1):59-68. doi: 10.1177/0023677217707985. Epub 2017 May 8.

Abstract

Transgenic tumour necrosis factor alpha (TNFα)-driven models of polyarthritis such as the TNF mouse have proven to be invaluable in delineating aspects of inflammatory disease pathophysiology in humans. Unfortunately, the onset of joint destruction and inflammation in these models represents a significant detriment to breeding management. We examined whether TNFα depleting therapy 'infliximab' might represent a significant refinement in routine breeding. Clinical scores of joint inflammation were assessed in TNF males receiving either infliximab (10 mg/kg) or saline by twice-weekly intraperitoneal injection. Joint histology and bone morphology were assessed by histological analysis and micro-computed tomography (CT), respectively. Analysis of breeding was examined retrospectively in TNF males prior to, and following, regular introduction of infliximab. Clinical scores of inflammation were significantly reduced in TNF males receiving infliximab (control 6.6 arbitrary units [AU] ± 0.88 versus infliximab 4.4 AU ± 1.4; P < 0.05), while measures of pannus invasion and bone erosion by histology and micro-CT were markedly reduced. In the breeding groups, TNF males receiving infliximab injections sired more litters over their breeding lifespan (control 1.69 ± 0.22 versus infliximab 3.00 ± 0.19; P < 0.005). Furthermore, prior to infliximab, TNF males had a 26% risk of failing to sire any litters. This was reduced to 7% after the introduction of infliximab. This study is the first to report that regular administration of infliximab is effective at suppressing disease activity and improving animal welfare in TNF animals. In addition, we have shown that infliximab is highly efficacious in improving breeding behaviour and increasing the number of litters sired by TNF males.

摘要

转基因肿瘤坏死因子α(TNFα)驱动的多关节炎模型,如TNF小鼠,已被证明在描绘人类炎症性疾病病理生理学方面具有极高价值。不幸的是,这些模型中关节破坏和炎症的发作对繁殖管理造成了重大不利影响。我们研究了TNFα消耗疗法“英夫利昔单抗”是否可能是常规繁殖中的一项重大改进。通过每周两次腹腔注射,对接受英夫利昔单抗(10毫克/千克)或生理盐水的TNF雄性小鼠的关节炎症临床评分进行评估。分别通过组织学分析和微计算机断层扫描(CT)评估关节组织学和骨形态。对TNF雄性小鼠在定期引入英夫利昔单抗之前和之后的繁殖情况进行回顾性分析。接受英夫利昔单抗的TNF雄性小鼠的炎症临床评分显著降低(对照组6.6任意单位[AU]±0.88,英夫利昔单抗组4.4 AU±1.4;P<0.05),而通过组织学和微CT测量的血管翳侵袭和骨侵蚀明显减少。在繁殖组中,接受英夫利昔单抗注射的TNF雄性小鼠在其繁殖寿命内产仔更多(对照组1.69±0.22,英夫利昔单抗组3.00±0.19;P<0.005)。此外,在使用英夫利昔单抗之前,TNF雄性小鼠有26%的概率无法产仔。引入英夫利昔单抗后,这一概率降至7%。本研究首次报告,定期给予英夫利昔单抗可有效抑制TNF动物的疾病活动并改善动物福利。此外,我们还表明,英夫利昔单抗在改善繁殖行为和增加TNF雄性小鼠产仔数量方面非常有效。

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