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Innate immune regulation of infection tolerance

Innate immune regulation of infection tolerance
感染耐受性的先天免疫调节
批准号:
MR/R00997X/1
负责人:
Marc Dionne
金额:
$50.01万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2018
资助国家:
英国
项目状态:
已结题
起止时间:
2018 至 --

项目摘要

项目成果

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中文摘要
翻译
所有生物都有免疫反应来保护自己免受感染。我们认为这些免疫反应以两种基本方式起作用:“抵抗”反应通过杀死入侵者来保护宿主,而“耐受”反应通过防止感染造成的损害来保护宿主。这两种类型的反应必须协同工作:在许多病原体存在的情况下,没有耐药性的耐药性无法使我们存活,而没有耐药性的耐药性将导致病原体数量和增殖的增加,导致我们的免疫系统无法防御的感染。许多耐药机制相对来说已经被很好地理解了,但我们对感染耐受性是如何起作用的知之甚少。例如,尽管耐受性被认为是一种潜在的治疗干预手段,但我们仍然不知道耐受性是否通常是由免疫反应激活的(“诱导”耐受性),还是耐受性是一种预先存在的状态。我们也不知道耐受性和耐药性是如何共同控制感染和保持宿主健康的。在我们的实验室里,我们研究果蝇黑腹果蝇对细菌感染的免疫反应。果蝇的免疫反应在许多方面与人类和其他哺乳动物相似,但由于果蝇体积小,价格便宜,而且繁殖时间短,我们可以研究整个动物对感染的免疫反应,而这在哺乳动物身上是不可能的。我们最近发现,具有“抗性”基因突变的果蝇在感染耐受方面也存在严重缺陷:当这些突变体感染致病菌时,它们的死亡时间明显早于非突变体果蝇,但在抗性方面没有差异(突变体和非突变体含有相同数量的细菌)。因此,这些果蝇的免疫反应表明耐受性可能是一种可诱导的性状。这是非常令人兴奋的,因为它使我们能够确定由这种基因激活的耐受性机制。我们提出的实验将侧重于这种容忍效应的三个方面。首先,我们将测量突变和非突变蝇在感染期间的代谢和行为差异。这很重要,因为代谢控制和行为被认为是耐受性的关键决定因素,但我们真的不知道这两件事在耐受性和非耐受性宿主之间有什么不同。其次,我们将测试相关基因在影响耐受性中的作用,并确定这些基因在哪些组织中起作用以促进感染耐受性。这很重要,因为它将使我们深入了解耐受性诱导的机制,并使我们能够确定耐受性在多大程度上由宿主遗传决定。最后,我们将利用这些信息以及感染所激活的基因信息,来确定耐受性诱导的遗传机制。这很重要,因为它将使我们了解能够促进宿主耐受性的具体机制,而不是对耐药性的影响。这项工作可能最终导致有能力促进感染者的耐受性。促进耐受性的疗法将有助于让免疫系统或抗生素有时间发挥作用。因此,我们希望我们对果蝇感染生物学的分析将为我们提供最终对人类疾病治疗有用的信息。
英文摘要
All living organisms have immune responses to protect them from infections. We regard these immune responses as working in two basic ways: "resistance" responses protect the host by killing invaders, while "tolerance" responses protect the host by preventing damage caused by infection. These two types of response must work together: resistance without tolerance cannot keep us alive in the presence of many pathogens, while tolerance without resistance will result in an increase in both the abundance and proliferation of pathogens, leading to infections against which our immune systems will be defenseless . Many resistance mechanisms are relatively well-understood, but we know very little about how infection tolerance works. For example, even though tolerance has been cited as a potential therapeutic intervention, we still don't know whether tolerance is generally activated by immune responses ("inducible" tolerance), or if tolerance is a pre-existing state. We also don't understand how tolerance and resistance work together in controlling infections and keeping the host healthy.In our lab, we study the immune response of the fruit-fly Drosophila melanogaster to bacterial infection. The fruit-fly's immune response is similar in many ways to those of humans and other mammals, but because flies are small, inexpensive, and have a short generation time, we can study immune responses to infection in the whole animal in ways that are impossible in mammals. We have recently discovered that flies with a genetic mutation in a "resistance" gene also have a serious defect in infection tolerance: when these mutants are infected with pathogenic bacteria, they die significantly sooner than non-mutant flies, but show no difference in terms of resistance (mutants and non-mutants contain the same number of bacteria). Thus, the immune response of these flies suggests that tolerance may be an inducible trait. This is very exciting because it allows us to identify the mechanisms of tolerance that are being activated by this gene.The experiments we propose will focus on three aspects of this tolerance effect. First, we will measure metabolic and behavioural differences between mutant and non-mutant flies during infection. This is important because metabolic control and behaviour have been suggested to be critical determinants of tolerance, but we don't really have any grasp on how these two things would be different between tolerant and non-tolerant hosts. Second, we will test the roles of related genes in affecting tolerance, and determine which tissues these genes are functioning in to promote infection tolerance. This is important because it will give us insight into the mechanisms of tolerance induction, as well as allow us to determine to what extent tolerance is determined by host genetics. Finally, we will use this information and information on genes turned on by infection, to identify the genetic mechanisms of tolerance induction. This is important because it will let us know the specific mechanisms that can promote tolerance in the host, separate from effects on resistance.This work may ultimately lead to the ability to promote tolerance in people with infections. Therapies that promote tolerance would be useful to allow the immune system or antibiotics time to work. Thus, we hope that our analyses of infection biology in fruit flies will give us information that will ultimately be useful in the treatment of human disease.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1101/2021.09.15.460306
发表时间: 2021
期刊:
影响因子: --
作者: [Rose S]
通讯作者: Rose S
A humoral stress response protects Drosophila tissues from antimicrobial peptides
体液应激反应保护果蝇组织免受抗菌肽的侵害
DOI: 10.1101/2023.07.24.550293
发表时间: 2023
期刊:
影响因子: --
作者: [Rommelaere S]
通讯作者: Rommelaere S
EslB is required for cell wall biosynthesis and modification in Listeria monocytogenes
单核细胞增生李斯特菌的细胞壁生物合成和修饰需要 EslB
DOI: 10.1101/2020.02.03.932061
发表时间: 2020
期刊:
影响因子: --
作者: [Rismondo J]
通讯作者: Rismondo J
A serine-folate metabolic unit controls resistance and tolerance of infection
丝氨酸-叶酸代谢单位控制感染的抵抗力和耐受性
DOI: 10.1101/2022.11.25.517956
发表时间: 2022
期刊:
影响因子: --
作者: [Grimes K]
通讯作者: Grimes K
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