Application of a commensal gut bacterium for the controlled delivery of heterologous proteins to the lower GI tract
Application of a commensal gut bacterium for the controlled delivery of heterologous proteins to the lower GI tract
批准号:
BB/L004291/1
负责人:
Simon Carding
金额:
$105.94万
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2013
资助国家:
英国
项目状态:
已结题
起止时间:
2013 至 --
中文摘要
口服给药是将治疗性蛋白质输送到肠道的首选途径。为了有效,必须克服重大障碍,包括最大限度地减少运输过程中的活动损失和控制所提供的剂量。我们的技术旨在克服这些障碍,并使用人类共生肠道细菌卵形杆菌(Bo)在肠道内输送治疗剂,以回应以膳食植物为基础的糖-木聚糖。这一药物传递平台技术将利用一种典型的Bo菌株进一步开发,该菌株产生一种有效治疗和预防肠道炎症的有效抗炎剂。确定最佳的剂量和给药方案,以及Bo和木聚糖剂量对肠道细菌的影响,并展示大肠的功能将实现这一目标。最终的成果将是一种具有强健特征的输送技术,具有临床前的安全性和治疗蛋白输送功能的证明
英文摘要
Oral administration is the preferred route for delivering therapeutic proteins to the gut. To be effective, significant obstacles including minimising loss of activity during transit and controlling the dose delivered must be overcome. Our technology is designed to overcome these obstacles and uses the human commensal gut bacterium, Bacteroides ovatus (Bo) to deliver therapeutic agents in the gut in response to the dietary plant based sugar, xylan. This drug delivery platform technology will be further developed using a characterised model Bo strain producing a potent anti-inflammatory agent that can effectively treat and prevent gut inflammation. Determining optimal dosing and delivery regimens and the impact of Bo and xylan dosing on resident gut bacteria and demonstrating functionality in the large bowel will achieve this. The final output will be a robustly characterised delivery technology with pre-clinical proof of safety and functionality for the delivery of therapeutic proteins
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DOI:
10.3389/fmicb.2016.01080
发表时间:
2016
期刊:
Frontiers in microbiology
影响因子:
5.2
作者:
[Horn N, Carvalho AL, Overweg K, Wegmann U, Carding SR, Stentz R]
通讯作者:
Stentz R
Extracellular vesicles produced by the human commensal gut bacterium Bacteroides thetaiotaomicron affect host immune pathways in a cell-type specific manner that are altered in inflammatory bowel disease
人类肠道共生细菌拟杆菌产生的细胞外囊泡以细胞类型特异性方式影响宿主免疫途径,这种方式在炎症性肠病中发生改变
DOI:
10.1101/2021.03.20.436262
发表时间:
2021
期刊:
影响因子:
--
作者:
[Gul L]
通讯作者:
Gul L
DOI:
10.1186/s40168-020-00868-z
发表时间:
2020-06-08
期刊:
MICROBIOME
影响因子:
15.5
作者:
[Durant, Lydia, Stentz, Regis, Knight, Stella C.]
通讯作者:
Knight, Stella C.
DOI:
10.3389/fmicb.2020.575595
发表时间:
2020
期刊:
Frontiers in microbiology
影响因子:
5.2
作者:
[Modasia A, Parker A, Jones E, Stentz R, Brion A, Goldson A, Defernez M, Wileman T, Ashley Blackshaw L, Carding SR]
通讯作者:
Carding SR
DOI:
10.3390/genes12101636
发表时间:
2021-10-18
期刊:
Genes
影响因子:
3.5
作者:
[Jones E, Stentz R, Telatin A, Savva GM, Booth C, Baker D, Rudder S, Knight SC, Noble A, Carding SR]
通讯作者:
Carding SR
A multidisciplinary approach to studying crypt-villus homeostasis and regeneration in the intestinal epithelium
-
批准号:BB/K017144/1
-
项目类别:Research Grant
-
资助金额:$6.34万
-
财政年份:2014
-
负责人:Simon Carding
-
依托单位:
Taiwan-Norwich: Development of an integrated platform for the study of mechanisms underlying ageing
-
批准号:BB/L026872/1
-
项目类别:Research Grant
-
资助金额:$3.21万
-
财政年份:2014
-
负责人:Simon Carding
-
依托单位:
Modelling the spatio temporal cell dynamics in the colonic crypt
-
批准号:BB/K005391/1
-
项目类别:Research Grant
-
资助金额:$0.51万
-
财政年份:2012
-
负责人:Simon Carding
-
依托单位:
海外基金