Physiologic and immunologic consequences of exposure to ETEC enterotoxins
接触 ETEC 肠毒素的生理和免疫后果
基本信息
- 批准号:8621432
- 负责人:
- 金额:$ 22.58万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2014
- 资助国家:美国
- 起止时间:2014-08-01 至 2016-07-31
- 项目状态:已结题
- 来源:
- 关键词:Age-YearsAnimalsAntibodiesAreaCellsCessation of lifeChildClinicalCyclic AMPCyclic GMPCyclic NucleotidesDataDeveloping CountriesDevelopmentDiarrheaDiseaseEnterotoxinsEpithelial CellsExposure toGoalsHeatingHumanHuman VolunteersImmune responseImmunityImmunoglobulin GImmunologicsInfectionInflammatoryIntestinesLifeLiquid substanceMorbidity - disease rateMovementMusNatural ImmunityOrganismPathogenesisPhysiologicalPrevalenceProductionProteinsRecurrenceRiskRoleSerumSmall IntestinesToxinVaccinationWater MovementsWorkWorld Health Organizationbasecytokineenterotoxigenic Escherichia coliimmunogenicinsightmortalitynonhuman primatepreventpublic health relevanceresponsetherapeutic vaccine
项目摘要
DESCRIPTION (provided by applicant): Enterotoxigenic E. coli (ETEC) are a significant cause of morbidity and mortality world-wide, especially in children in developing countries. The World Health Organization estimates that the annual diarrhea burden due to ETEC in children less than five years of age in the developing world is approximately 210 million cases and 380,000 deaths. ETEC cause disease by colonizing the small intestine by means of colonization factors (CFs) and by production of either a heat-labile (LT) or heat-stable (ST) enterotoxin. The majority of clinical isolates produce both enterotoxins and the physiologic or immunologic consequences of simultaneous exposure to these two potent enterotoxins are unknown. Our preliminary data indicate that when LT and ST are both present, they work additively, increasing movement of water into the intestine over and above levels observed with either toxin alone. Our preliminary data also demonstrate that the levels of inflammatory cytokines produced by intestinal epithelial cells (IECs) in response to LT are significantly reduced in animals exposed to both enterotoxins. Based on our preliminary findings, our hypotheses for the proposed studies are 1) LT combined with ST increases fluid movement (diarrhea) when compared to either toxin alone by increasing cGMP, 2) the production of ST by LT/ST ETEC can significantly reduce the ability of the host to mount an effective innate immune response and 3) the production of ST by LT/ST ETEC can significantly reduce the ability of the host to mount an effective adaptive immune response (e.g., serum and mucosal antibody) against the infecting organisms (colonizing factors or LPS) or its heat-labile toxins. The specific aims are 1) Determine the role of LT/ST on accumulation of cyclic nucleotides in T84 cells; 2) Determine the role of LT/ST on innate immune responses in the murine intestine; and 3) Determine the role of LT/ST on adaptive immune responses to enterotoxigenic E. coli. At the conclusion of these studies, we will have a better understanding of the physiologic and immunologic consequences of simultaneous exposure to the two potent enterotoxins made by these organisms (LT and ST) and will have the information necessary to transition into non-human primate studies or human trials.
性状(由申请方提供):产肠球菌E.大肠杆菌(ETEC)是世界范围内发病和死亡的重要原因,特别是在发展中国家的儿童中。据世界卫生组织估计,发展中国家5岁以下儿童每年因ETEC造成的腹泻负担约为2.1亿例,38万例死亡。ETEC通过定植因子(CF)定植小肠并产生热不稳定(LT)或热稳定(ST)肠毒素而致病。大多数临床分离株产生两种肠毒素,同时暴露于这两种强效肠毒素的生理或免疫后果尚不清楚。我们的初步数据表明,当LT和ST同时存在时,它们会产生相加作用,增加水进入肠道的运动,超过单独使用任何一种毒素时观察到的水平。我们的初步数据还表明,肠上皮细胞(IEC)在LT反应产生的炎症细胞因子的水平显着降低暴露于两种肠毒素的动物。根据我们的初步研究结果,我们的假设是:1)LT联合ST增加了液体运动(腹泻)当与单独的任一种毒素相比时,通过增加cGMP,2)LT/ST ETEC产生的ST可显著降低宿主产生有效先天免疫应答的能力,3)LT/ST ETEC产生的ST可显著降低宿主产生有效先天免疫应答的能力。ST ETEC可显著降低宿主产生有效适应性免疫应答的能力(例如,血清和粘膜抗体)对抗感染性生物体(定植因子或LPS)或其热不稳定毒素。具体目的是1)确定LT/ST对T84细胞中环核苷酸积累的作用; 2)确定LT/ST对小鼠肠中先天性免疫应答的作用;和3)确定LT/ST对肠毒素E的适应性免疫应答的作用。杆菌在这些研究结束时,我们将更好地了解同时暴露于这些生物体(LT和ST)产生的两种强效肠毒素的生理学和免疫学后果,并将获得过渡到非人灵长类动物研究或人体试验所需的信息。
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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{{ truncateString('JOHN D CLEMENTS', 18)}}的其他基金
Tulane_University_Interdisciplinary_Bioscience_Initiative
杜兰大学跨学科生物科学倡议
- 批准号:
7875910 - 财政年份:2010
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$ 22.58万 - 项目类别:
Nanocarriers for transcutaneous delivery of vaccines
用于疫苗经皮递送的纳米载体
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7208002 - 财政年份:2006
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$ 22.58万 - 项目类别:
Nanocarriers for transcutaneous delivery of vaccines
用于疫苗经皮递送的纳米载体
- 批准号:
7114798 - 财政年份:2006
- 资助金额:
$ 22.58万 - 项目类别:
Nanocarriers for transcutaneous delivery of vaccines
用于疫苗经皮递送的纳米载体
- 批准号:
7568914 - 财政年份:2006
- 资助金额:
$ 22.58万 - 项目类别:
Nanocarriers for transcutaneous delivery of vaccines
用于疫苗经皮递送的纳米载体
- 批准号:
7369729 - 财政年份:2006
- 资助金额:
$ 22.58万 - 项目类别:
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