文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

利什曼原虫:一种以树突状细胞为靶点的疫苗平台,也是针对利什曼病和病毒感染的下一代疫苗研究的替代病原体。

Leishmania tarentolae: a vaccine platform to target dendritic cells and a surrogate pathogen for next generation vaccine research in leishmaniases and viral infections.

机构信息

Department of Biosciences, Pediatric CRC "Romeo ed Enrica Invernizzi"-University of Milan, Milan, Italy.

Department of Veterinary Medicine, University of Bari, Valenzano, Italy.

出版信息

Parasit Vectors. 2023 Jan 26;16(1):35. doi: 10.1186/s13071-023-05651-1.


DOI:10.1186/s13071-023-05651-1
PMID:36703216
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9879565/
Abstract

Parasites of the genus Leishmania are unusual unicellular microorganisms in that they are characterized by the capability to subvert in their favor the immune response of mammalian phagocytes, including dendritic cells. Thus, in overt leishmaniasis, dendritic cells and macrophages are converted into a niche for Leishmania spp. in which the parasite, rather than being inactivated and disassembled, survives and replicates. In addition, Leishmania parasites hitchhike onto phagocytic cells, exploiting them as a mode of transport to lymphoid tissues where other phagocytic cells are potentially amenable to parasite colonization. This propensity of Leishmania spp. to target dendritic cells has led some researchers to consider the possibility that the non-pathogenic, reptile-associated Leishmania tarentolae could be exploited as a vaccine platform and vehicle for the production of antigens from different viruses and for the delivery of the antigens to dendritic cells and lymph nodes. In addition, as L. tarentolae can also be regarded as a surrogate of pathogenic Leishmania parasites, this parasite of reptiles could possibly be developed into a vaccine against human and canine leishmaniases, exploiting its immunological cross-reactivity with other Leishmania species, or, after its engineering, for the expression of antigens from pathogenic species. In this article we review published studies on the use of L. tarentolae as a vaccine platform and vehicle, mainly in the areas of leishmaniases and viral infections. In addition, a short summary of available knowledge on the biology of L. tarentolae is presented, together with information on the use of this microorganism as a micro-factory to produce antigens suitable for the serodiagnosis of viral and parasitic infections.

摘要

利什曼原虫属的寄生虫是一种不寻常的单细胞微生物,其特点是能够颠覆哺乳动物吞噬细胞(包括树突状细胞)的免疫反应,使其有利于自身。因此,在显性利什曼病中,树突状细胞和巨噬细胞被转化为利什曼原虫属的栖息地,寄生虫在其中存活和复制,而不是被失活和分解。此外,利什曼原虫寄生虫搭乘吞噬细胞,将其用作运输到淋巴组织的模式,在那里其他吞噬细胞可能容易被寄生虫定植。利什曼原虫属将目标对准树突状细胞的这种倾向,导致一些研究人员考虑是否可以利用非致病性、与爬行动物相关的利什曼原虫 tarentolae 作为疫苗平台和载体,用于生产来自不同病毒的抗原,并将抗原递送到树突状细胞和淋巴结。此外,由于利什曼原虫 tarentolae 也可以被视为致病性利什曼原虫寄生虫的替代品,这种爬行动物寄生虫有可能被开发成针对人类和犬类利什曼病的疫苗,利用其与其他利什曼原虫物种的免疫交叉反应性,或者在对其进行工程改造后,用于表达来自致病性物种的抗原。在本文中,我们回顾了关于利什曼原虫 tarentolae 作为疫苗平台和载体的已发表研究,主要集中在利什曼病和病毒感染领域。此外,还简要总结了有关利什曼原虫 tarentolae 生物学的现有知识,并介绍了利用这种微生物作为微工厂生产适合病毒和寄生虫感染血清诊断的抗原的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1395/9881383/70c1a7096d69/13071_2023_5651_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1395/9881383/6adeaf4dade0/13071_2023_5651_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1395/9881383/f1d140398ce9/13071_2023_5651_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1395/9881383/70c1a7096d69/13071_2023_5651_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1395/9881383/6adeaf4dade0/13071_2023_5651_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1395/9881383/f1d140398ce9/13071_2023_5651_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1395/9881383/70c1a7096d69/13071_2023_5651_Fig3_HTML.jpg

相似文献

[1]
Leishmania tarentolae: a vaccine platform to target dendritic cells and a surrogate pathogen for next generation vaccine research in leishmaniases and viral infections.

Parasit Vectors. 2023-1-26

[2]
Leishmania tarentolae: A new frontier in the epidemiology and control of the leishmaniases.

Transbound Emerg Dis. 2022-9

[3]
as an Antigen Delivery Platform: Dendritic Cell Maturation after Infection with a Clone Engineered to Express the SARS-CoV-2 Spike Protein.

Vaccines (Basel). 2022-5-19

[4]
Saurian-associated Leishmania tarentolae in dogs: Infectivity and immunogenicity evaluation in the canine model.

PLoS Pathog. 2024-10

[5]
Evaluation of a new live recombinant vaccine against cutaneous leishmaniasis in BALB/c mice.

Parasit Vectors. 2020-8-12

[6]
as Potential Live Vaccine Co-Expressing Distinct Salivary Gland Proteins Against Experimental Cutaneous Leishmaniasis in BALB/c Mice Model.

Front Immunol. 2022

[7]
Detection of Leishmania tarentolae in lizards, sand flies and dogs in southern Italy, where Leishmania infantum is endemic: hindrances and opportunities.

Parasit Vectors. 2021-9-8

[8]
Enhanced protective efficacy of nonpathogenic recombinant leishmania tarentolae expressing cysteine proteinases combined with a sand fly salivary antigen.

PLoS Negl Trop Dis. 2014-3-27

[9]
[Approaches and problems in vaccine development against leishmaniasis].

Turkiye Parazitol Derg. 2010

[10]
Leishmania tarentolae secreting the sand fly salivary antigen PpSP15 confers protection against Leishmania major infection in a susceptible BALB/c mice model.

Mol Immunol. 2015-10

引用本文的文献

[1]
Leishmania (Leishmania) infantum and Leishmania (Sauroleishmania) tarentolae in outdoor cats and report of infection in feline-derived peripheral blood mononuclear cells.

Parasit Vectors. 2025-8-26

[2]
Sand Fly Fauna and Prevalence of spp. in a Newly Investigated Area of Northern Italy: Emerging Epidemiological Scenarios?

Transbound Emerg Dis. 2025-7-21

[3]
Development of a novel ddPCR assay for the simultaneous detection of the protozoan parasites Leishmania infantum and Leishmania tarentolae.

Parasit Vectors. 2025-7-1

[4]
Accelerating vaccine development: Plug-and-play platforms for emerging infectious diseases.

Virus Res. 2025-6-21

[5]
Beyond , Pharmaceutical Molecule Production in Cell-Free Systems and the Use of Noncanonical Amino Acids Therein.

Chem Rev. 2025-2-12

[6]
An update on recombinant vaccines against leishmaniasis.

Indian J Med Res. 2024

[7]
Expression of key cytokines in dog macrophages infected by Leishmania tarentolae opening new avenues for the protection against Leishmania infantum.

Sci Rep. 2024-11-11

[8]
Saurian-associated Leishmania tarentolae in dogs: Infectivity and immunogenicity evaluation in the canine model.

PLoS Pathog. 2024-10

[9]
The non-pathogenic protozoon interferes with the activation of NLRP3 inflammasome in human cells: new perspectives in the control of inflammation.

Front Immunol. 2024

[10]
A novel chemically defined medium for the biotechnological and biomedical exploitation of the cell factory Leishmania tarentolae.

Sci Rep. 2024-4-26

本文引用的文献

[1]
Efficacy of mucosal vaccination using a protozoan parasite as a vehicle for antigen delivery: IgG and neutralizing response after rectal administration of LeCoVax-2, a candidate vaccine against COVID-19.

Pharmacol Res. 2022-12

[2]
Leishmania (Sauroleishmania) tarentolae isolation and sympatric occurrence with Leishmania (Leishmania) infantum in geckoes, dogs and sand flies.

PLoS Negl Trop Dis. 2022-8

[3]
Current trends in biopharmaceuticals production in Escherichia coli.

Biotechnol Lett. 2022-8

[4]
as Potential Live Vaccine Co-Expressing Distinct Salivary Gland Proteins Against Experimental Cutaneous Leishmaniasis in BALB/c Mice Model.

Front Immunol. 2022

[5]
COVID-19 Vaccines.

Infect Dis Clin North Am. 2022-6

[6]
as an Antigen Delivery Platform: Dendritic Cell Maturation after Infection with a Clone Engineered to Express the SARS-CoV-2 Spike Protein.

Vaccines (Basel). 2022-5-19

[7]
BCG-Based Vaccines Elicit Antigen-Specific Adaptive and Trained Immunity against SARS-CoV-2 and .

Vaccines (Basel). 2022-5-4

[8]
The History of Live Attenuated Gene-Deleted Vaccine Candidates.

Pathogens. 2022-4-2

[9]
COVID-19 vaccine development based on recombinant viral and bacterial vector systems: combinatorial effect of adaptive and trained immunity.

J Microbiol. 2022-3

[10]
Development of an Oral -Based Vaccine Platform against SARS-CoV-2.

Vaccines (Basel). 2022-1-1

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索