Determination of excessive immune reactivity to real time implant debris generate
Determination of excessive immune reactivity to real time implant debris generate
批准号:
9455400
负责人:
Nadim James Hallab
金额:
$23.55万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-30 至 2019-07-31
关键词:
AlloysBiocompatible MaterialsBiologicalBioreactorsCellsChemicalsChromiumClinicalCobaltCommunitiesComplexCorrosionDevelopmentDevice DesignsDevicesEnvironmentEquilibriumFrictionFutureGenesGoalsGrantGranulomaImmuneImmune responseImmunological ModelsImplantIn SituIndustryInflammasomeInvestigationIonsKnowledgeLubricantsLymphocyteMediatingMetalsMethodsMotionNecrosisOrthopedicsOsteoclastsParticulatePartner in relationshipPhasePreclinical TestingPredictive ValuePrincipal InvestigatorProsthesis DesignProteinsReactionReactive Oxygen SpeciesSaltsSignal TransductionStimulusSurfaceT-LymphocyteTestingTimeTissuesTitaniumbasebonebone prosthesiscell typechromium hexavalent ionclinically relevantcombatdesignimmunoreactionimmunoreactivityimprovedin vitro Modelin vitro testingin vivomacrophagemetal complexnext generationnovelparticlepre-clinicalprecursor cellprogramsresponsestemtooltumor
中文摘要
项目总结
与金属微粒碎片和/或离子相关的不良局部组织反应
从模块连接和其他金属接口(例如假体/骨)释放出来的结果是
表现为肉芽肿、坏死组织、假瘤等的免疫反应。
尽管磨损和腐蚀(摩擦腐蚀)一直被认为是问题所在
危及骨科植入物的长期存活,许多人仍然不知道
宿主组织与降解产物的相互作用。我们假设金属的退化
摩擦腐蚀产生的产物是动态生物活性的(即依赖于时间),其中
植入物碎片最初具有高度的生物活性,然后随着时间的推移逐渐减少
电化学性质稳定。一旦在这项研究中得到证实,我们开发的“摩擦腐蚀”
生物反应器“将允许在降解产物和细胞之间进行直接的机械研究,
并将实现亚稳定摩擦腐蚀产品的临床前测试,这些产品是在
SITE。在这里,我们将评估实时金属摩擦腐蚀产品是否过度活性
激发天然(巨噬细胞)和获得性(淋巴细胞)免疫反应性的无菌刺激
因此,不同于由相同碎片形成的更多时间稳定的复合体。
证明植入物碎片反应性随时间变化的现象对于
了解新生产的金属种植体磨屑对临床的影响
腐蚀。它将为下一代体外测试提供一个重要的飞跃
整形外科材料。
英文摘要
PROJECT SUMMARY
Adverse local tissue reactions (ALTRs) associated with metal particulate debris and/or ions
released from modular junctions and other metal interfaces (e.g. prosthesis/bone) are the result
of immune responses which have presented as granulomas, necrotic tissue, pseudotumors, etc.
Although wear and corrosion (‘tribocorrosion’) have long been recognized as the problems
endangering the long term survival of orthopedic implants, much remains unknown about the
interaction of host tissue with degradation products. We hypothesize that metal degradation
products resulting from tribocorrosion are dynamically bioreactive (i.e. time-dependent), where
implant debris is initially highly bioreactive and then decreases over time as it becomes more
electrochemically stable. Once validated in this study, our development of a “Tribocorrosion
Bioreactor” will allow direct mechanistic investigations between degradation products and cells,
and will enable preclinical testing of meta-stable tribocorrosion products that are generated in
situ. Here, we will evaluate if real time metal tribocorrosion products are excessively reactive
aseptic stimuli eliciting both innate (macrophage) and adaptive (lymphocyte) immuno-reactivity
and, thus, differ from more time-stabilized complexes formed from the same debris.
Demonstrating the phenomenon of time-dependent implant debris reactivity is critical to
understanding the clinical impact of freshly produced metal implant debris from both wear and
corrosion. It will provide a significant leap forward into the next generation of in vitro testing of
orthopedic materials.
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依托单位:
海外基金