The genetically engineered pig heart as a bridge to allotransplantation in infants
基因工程猪心脏作为婴儿同种异体移植的桥梁
基本信息
- 批准号:10447354
- 负责人:
- 金额:$ 48.83万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-05-20 至 2022-12-31
- 项目状态:已结题
- 来源:
- 关键词:AddressAdverse eventAllograftingAntibodiesAntigensAortaB-LymphocytesBindingBiologicalBlood TransfusionCardiacCattleClinicalClinical TrialsComplexCytidine Monophosphate N-Acetylneuraminic AcidDataDatabasesDocumentationEnzymesErythrocytesFamily suidaeFocus GroupsFunctional disorderGalactoseGalactosyltransferasesGenesGenetic EngineeringHeartHeart DiseasesHeart TransplantationHeart failureHourHumanImmune responseImmune systemImmunoglobulin GImmunoglobulin MInfantInfant MortalityKnock-outKnowledgeLengthLifeLungMaintenanceMixed Function OxygenasesModelingOperative Surgical ProceduresPapioPatientsPericardial body locationPeripheral Blood Mononuclear CellPopulationPostoperative PeriodProbabilityProceduresReportingResearchT-LymphocyteTechniquesTechnologyTestingTherapeutic immunosuppressionThymectomyTimeTransplantationUnited Network for Organ SharingWaiting Listsage groupallotransplantblood groupclinical applicationcross reactivitygraft failureheart xenograftimprovedin vivomechanical circulatory supportnatural antibodiesnovelpalliationpatient populationpericardial sacpreclinical studypreventsuccesstransplant model
项目摘要
PROJECT SUMMARY/ABSTRACT
There is a critical need for novel cardiac support techniques in infants with complex cardiac disease.
A recent analysis of UNOS database from 1987 to 2016 documented only 55% of infants placed on
cardiac transplant wait list survived to transplantation. The results of mechanical circulatory support
(MCS) in infants is suboptimal. Actuarial six month survival of infants placed on MCS is reported by
PEDIMACS to be 50% and most have adverse events. These results establish a pressing need for a
new treatment paradigm in this age group. The potential of a completely implantable biologic support
for infants on the cardiac transplant list would be transformative. Our preliminary data strongly
suggest that anti-pig antibodies will not be a barrier to GEPH transplantation in infants if hearts are
taken from `triple-knockout' (TKO) pigs. These pigs lack the 3 enzymes 1,3-galactosyltransferase
(produces galactose-1,3galactose [GaL], cytidine monophosphate-N-acetylneuraminic acid
hydroxylase (produces Neu5Gc), and 1,4-acetylgalactosaminyltrnsferase (adds Sda). (Table 1).
These pigs are referred to as triple knockouts (TKO). We documented a lack of pre-formed antibodies
to red blood cells (RBCs) of TKO pigs even after complex cardiac procedures. Binding of anti-pig IgM
and IgG is greatly reduced compared with that to wild-type (i.e., unmodified [WT] pigs).
This R33 application will allow us to target enabling technology to address a major translational
clinical deficiency in the management of infants with critical cardiac disease. If successful, it
establishes a transformative platform for the management of heart failure in the infant population. To
our knowledge, we are the only research group focused on the potential application of this rapidly
developing technology in this patient population. Access to the most advanced GEPHs available
(hearts that would be suitable for transplantation in human infants) indicates the potential for data
developed in this study to provide support for clinical application within five years.
项目摘要/摘要
在患有复杂心脏疾病的婴儿中,需要新颖的心脏支持技术。
对1987年至2016年UNOS数据库的最新分析记录了55%的婴儿
CardiACC移植等待名单幸存下来透明。
(MC)婴儿是次优的六个月生存罪
Pedimacs为50%,大多数都有广告活动。
该年龄段的新处理范式。
对于心脏移植列表上的婴儿,我们的初步数据是如此。
建议如果心脏是抗铅抗体
从“三重敲除”(TKO)猪中取走。
(产生半乳糖-1,3galactos [gal],胞丁二磷酸-N-乙酰神经氨酸酸
羟化酶(产生neu5GC),1,4-乙酰乳糖酰氨基氨基植物酶(添加SDA)(表1)。
这些猪被称为三重敲除(TKO)。
即使经过复杂的心脏手术,也要对TKO猪的红细胞(RBC)。
与野生型(即未修饰的[WT]猪)相比,IgG IgG大大降低。
此R33应用程序Willow US目标是刺激技术,以解决主要的翻译
临床缺乏患有危急心脏疾病的婴儿
建立一个用于婴儿人群心力衰竭的变革平台
我们的知识,我们是搜索小组的重点是迅速的潜在应用
在该患者人群中开发技术。
(适合在人类婴儿中移植的心脏)表明数据的潜力
在这项研究中开发的旨在在五年内支持临床应用。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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David C Cleveland其他文献
A Novel Model for Xenograft Right Ventricle to Pulmonary Artery Conduit.
异种移植右心室至肺动脉导管的新模型。
- DOI:
- 发表时间:
2024 - 期刊:
- 影响因子:0
- 作者:
Chace B Mitchell;Luke M Wiggins;Winfield J. Wells;David C Cleveland;John D. Cleveland - 通讯作者:
John D. Cleveland
David C Cleveland的其他文献
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{{ truncateString('David C Cleveland', 18)}}的其他基金
The genetically engineered pig heart as a bridge to allotransplantation in infants
基因工程猪心脏作为婴儿同种异体移植的桥梁
- 批准号:
10815486 - 财政年份:2023
- 资助金额:
$ 48.83万 - 项目类别:
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