Utilizing gametocyte immunity to reduce malaria transmission

利用配子体免疫减少疟疾传播

基本信息

  • 批准号:
    MR/T016272/1
  • 负责人:
  • 金额:
    $ 278.2万
  • 依托单位:
  • 依托单位国家:
    英国
  • 项目类别:
    Research Grant
  • 财政年份:
    2020
  • 资助国家:
    英国
  • 起止时间:
    2020 至 无数据
  • 项目状态:
    未结题

项目摘要

The continuing success of the current malaria elimination campaign requires novel tools to efficiently block human infection and subsequent transmission of the parasite to mosquitoes. Current transmission blocking strategies target the development of the parasite in the mosquito stage, requiring complicated mosquito feeding readouts to measure efficacy. We recently identified the bone marrow as the major site of transmission stage development during infection. Based on this finding we hypothesized that the underlying host parasite interactions could be exploited to block parasite transmission. Indeed our preliminary studies demonstrate natural immune responses against parasite surface antigens and their functionality in terms of immune clearance. Here we utilize this new understanding to systematically define the immunity targeting malaria transmission with the ultimate goal of prioritizing a set of novel transmission blocking vaccine candidates.
当前消除疟疾运动的持续成功需要新的工具来有效地阻止人类感染和随后的寄生虫传播给蚊子。目前的传播阻断策略针对的是蚊子阶段寄生虫的发育,需要复杂的蚊子摄食数据来衡量效果。我们最近发现骨髓是感染期间传播阶段发展的主要部位。基于这一发现,我们假设潜在的宿主与寄生虫的相互作用可以被利用来阻止寄生虫的传播。事实上,我们的初步研究证明了对寄生虫表面抗原的自然免疫反应及其在免疫清除方面的功能。在这里,我们利用这一新认识系统地定义针对疟疾传播的免疫,最终目标是优先考虑一套新的传播阻断疫苗候选。

项目成果

期刊论文数量(2)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
The acquisition of humoral immune responses targeting Plasmodium falciparum sexual stages in controlled human malaria infections.
  • DOI:
    10.3389/fimmu.2022.930956
  • 发表时间:
    2022
  • 期刊:
  • 影响因子:
    7.3
  • 作者:
    de Jong, Roos M.;Alkema, Manon;Oulton, Tate;Dumont, Elin;Teelen, Karina;Nakajima, Rie;de Assis, Rafael Ramiro;Press, Kathleen W. Dantzler;Ngotho, Priscilla;Tetteh, Kevin K. A.;Felgner, Phil;Marti, Matthias;Collins, Katharine A.;Drakeley, Chris;Bousema, Teun;Stone, Will J. R.
  • 通讯作者:
    Stone, Will J. R.
Plasmodium falciparum serology: A comparison of two protein production methods for analysis of antibody responses by protein microarray.
  • DOI:
    10.1371/journal.pone.0273106
  • 发表时间:
    2022
  • 期刊:
  • 影响因子:
    3.7
  • 作者:
    Oulton, Tate;Obiero, Joshua;Rodriguez, Isabel;Ssewanyana, Isaac;Dabbs, Rebecca A.;Bachman, Christine M.;Greenhouse, Bryan;Drakeley, Chris;Felgner, Phil L.;Stone, Will;Tetteh, Kevin K. A.
  • 通讯作者:
    Tetteh, Kevin K. A.
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Matthias Marti其他文献

Validation of the protein kinase PfCLK3 as a multi-stage cross species malarial drug target
验证蛋白激酶 PfCLK3 作为多阶段跨物种疟疾药物靶点
  • DOI:
    10.1101/404459
  • 发表时间:
    2018
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Mahmood M. Alam;A. Sánchez;O. Janha;E. Flannery;Amit Mahindra;Kopano Mapesa;Nicolas M. B. Brancucci;Y. Antonova;K. Crouch;Nelson V. Simwela;J. Akinwale;D. Mitcheson;L. Solyakov;Kate Dudek;Carolyn Jones;Cleofé Zapatero;C. Doerig;Davis C. Nwakanma;Maria Jesús Vázquez;Gonzalo Colmenarejo;Maria Jesús Lafuente;María L León;Andrew P. Waters;Andrew G. Jamieson;León Elena Fernandez Alvaro;Matthias Marti;E. Winzeler;F. Gamo;Andrew B. Tobin
  • 通讯作者:
    Andrew B. Tobin
A Major Step towards Defining the Elusive Stumpy Inducing Factor in <em>Trypanosoma brucei</em>
  • DOI:
    10.1016/j.pt.2018.11.009
  • 发表时间:
    2019-01-01
  • 期刊:
  • 影响因子:
  • 作者:
    Lauriane Sollelis;Matthias Marti
  • 通讯作者:
    Matthias Marti
emPlasmodium falciparum/em gametocyte production correlates with genetic markers of parasite replication but is not influenced by experimental exposure to mosquito biting
恶性疟原虫配子体的产生与寄生虫复制的遗传标记相关,但不受实验性蚊虫叮咬暴露的影响
  • DOI:
    10.1016/j.ebiom.2024.105190
  • 发表时间:
    2024-07-01
  • 期刊:
  • 影响因子:
    10.800
  • 作者:
    Sara Lynn Blanken;Aissata Barry;Kjerstin Lanke;Moussa Guelbeogo;Alphonse Ouedraogo;Issiaka Soulama;Sam Aboubacar Coulibaly;Karina Teelen;Wouter Graumans;Elin Dumont;Will Stone;Jordache Ramjith;Matthias Marti;Carolina M. Andrade;Chris Drakeley;Katharine Collins;Alfred Tiono;Teun Bousema
  • 通讯作者:
    Teun Bousema
Genome-wide gene expression profiles throughout human malaria parasite liver stage development in humanized mice
在人源化小鼠中人类疟原虫肝脏阶段发育的全基因组基因表达谱
  • DOI:
    10.1038/s41564-024-01905-5
  • 发表时间:
    2025-01-31
  • 期刊:
  • 影响因子:
    19.400
  • 作者:
    Gigliola Zanghí;Hardik Patel;Jenny L. Smith;Nelly Camargo;Yeji Bae;Eva Hesping;Justin A. Boddey;Kannan Venugopal;Matthias Marti;Erika L. Flannery;Vorada Chuenchob;Matthew E. Fishbaugher;Sebastian A. Mikolajczak;Wanlapa Roobsoong;Jetsumon Sattabongkot;Priya Gupta;Lucia Pazzagli;Nastaran Rezakhani;William Betz;Kiera Hayes;Debashree Goswami;Ashley M. Vaughan;Stefan H. I. Kappe
  • 通讯作者:
    Stefan H. I. Kappe
Plasmodium blood stage development requires the chromatin remodeller Snf2L
疟原虫血液阶段的发育需要染色质重塑因子 Snf2L
  • DOI:
    10.1038/s41586-025-08595-x
  • 发表时间:
    2025-02-19
  • 期刊:
  • 影响因子:
    48.500
  • 作者:
    Maria Theresia Watzlowik;Elisabeth Silberhorn;Sujaan Das;Ritwik Singhal;Kannan Venugopal;Simon Holzinger;Barbara Stokes;Ella Schadt;Lauriane Sollelis;Victoria A. Bonnell;Matthew Gow;Andreas Klingl;Matthias Marti;Manuel Llinás;Markus Meissner;Gernot Längst
  • 通讯作者:
    Gernot Längst

Matthias Marti的其他文献

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{{ truncateString('Matthias Marti', 18)}}的其他基金

Defining molecular determinants of Plasmodium falciparum hematopoietic infection using single cell profiling and genetics
使用单细胞分析和遗传学定义恶性疟原虫造血系统感染的分子决定因素
  • 批准号:
    EP/Y003705/1
  • 财政年份:
    2023
  • 资助金额:
    $ 278.2万
  • 项目类别:
    Fellowship
MRC FAPESP: Defining the role of the hematopoietic parasite reservoir in Plasmodium vivax infection and pathology
MRC FAPESP:定义造血寄生虫储存库在间日疟原虫感染和病理学中的作用
  • 批准号:
    MR/W018802/1
  • 财政年份:
    2022
  • 资助金额:
    $ 278.2万
  • 项目类别:
    Research Grant
Synthetic Biology - organoids and engineered tissues as in vitro research platforms in infection and immunity
合成生物学 - 类器官和工程组织作为感染和免疫的体外研究平台
  • 批准号:
    BB/X005003/1
  • 财政年份:
    2022
  • 资助金额:
    $ 278.2万
  • 项目类别:
    Research Grant

相似海外基金

Characterization of P. falciparum gametocyte-essential genes using a novel genetic screen
使用新型遗传筛选表征恶性疟原虫配子体必需基因
  • 批准号:
    10462425
  • 财政年份:
    2022
  • 资助金额:
    $ 278.2万
  • 项目类别:
Characterization of P. falciparum gametocyte-essential genes using a novel genetic screen
使用新型遗传筛选表征恶性疟原虫配子体必需基因
  • 批准号:
    10619569
  • 财政年份:
    2022
  • 资助金额:
    $ 278.2万
  • 项目类别:
Identification of Novel Efficacious Anti-Malarial Transmission Blocking Antigens Targeting the Female Gametocyte
鉴定针对雌性配子体的新型有效抗疟疾传播阻断抗原
  • 批准号:
    MR/W025701/1
  • 财政年份:
    2022
  • 资助金额:
    $ 278.2万
  • 项目类别:
    Research Grant
Can malaria transmission be prevented through catastrophic failure of gametocyte quiescence?
配子体静止的灾难性失败能否预防疟疾传播?
  • 批准号:
    MR/V010034/1
  • 财政年份:
    2021
  • 资助金额:
    $ 278.2万
  • 项目类别:
    Fellowship
Identification & Evaluation of Novel Malaria Anti-Gametocyte Transmission Blocking Vaccine Candidate Antigens
鉴别
  • 批准号:
    10665613
  • 财政年份:
    2019
  • 资助金额:
    $ 278.2万
  • 项目类别:
Identification & Evaluation of Novel Malaria Anti-Gametocyte Transmission Blocking Vaccine Candidate Antigens
鉴别
  • 批准号:
    9817022
  • 财政年份:
    2019
  • 资助金额:
    $ 278.2万
  • 项目类别:
Identification & Evaluation of Novel Malaria Anti-Gametocyte Transmission Blocking Vaccine Candidate Antigens
鉴别
  • 批准号:
    10455482
  • 财政年份:
    2019
  • 资助金额:
    $ 278.2万
  • 项目类别:
A chemical proteomics survey of Plasmodium gametocyte development
疟原虫配子细胞发育的化学蛋白质组学调查
  • 批准号:
    9537357
  • 财政年份:
    2018
  • 资助金额:
    $ 278.2万
  • 项目类别:
Plasmodium vivax 48/45 gametocyte protein: functional characterization and vaccine potential assessment in preclinical studies
间日疟原虫 48/45 配子体蛋白:临床前研究中的功能表征和疫苗潜力评估
  • 批准号:
    9007904
  • 财政年份:
    2016
  • 资助金额:
    $ 278.2万
  • 项目类别:
Plasmodium vivax 48/45 gametocyte protein: functional characterization and vaccine potential assessment in preclinical studies
间日疟原虫 48/45 配子体蛋白:临床前研究中的功能表征和疫苗潜力评估
  • 批准号:
    9305832
  • 财政年份:
    2016
  • 资助金额:
    $ 278.2万
  • 项目类别:
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