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archaeosomes 显示出针对恰加斯病疫苗的免疫佐剂潜力。

Archaeosomes display immunoadjuvant potential for a vaccine against Chagas disease.

机构信息

Programa de Nanomedicinas; Departamento de Ciencia y Tecnología; Universidad Nacional de Quilmes; Buenos Aires, Argentina.

出版信息

Hum Vaccin Immunother. 2013 Feb;9(2):409-12. doi: 10.4161/hv.22780. Epub 2013 Jan 4.


DOI:10.4161/hv.22780
PMID:23291939
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3859765/
Abstract

Archaeosomes (ARC), vesicles made from lipids extracted from Archaea, display strong adjuvant properties. In this study, we evaluated the ability of the highly stable ARC formulated from total polar lipids of a new Halorubrum tebenquichense strain found in Argentinean Patagonia, to act as adjuvant for soluble parasite antigens in developing prophylactic vaccine against the intracellular protozoan T. cruzi, the etiologic agent of Chagas disease. We demonstrated for the first time that C3H/HeN mice subcutaneously immunized with trypanosomal antigens entrapped in these ARC (ARC-TcAg) rapidly developed higher levels of circulating T. cruzi antibodies than those measured in the sera from animals receiving the antigen alone. Enhanced humoral responses elicited by ARC-TcAg presented a dominant IgG2a antibody isotype, usually associated with Th1-type immunity and resistance against T. cruzi. More importantly, ARC-TcAg-vaccinated mice displayed reduced parasitemia during early infection and were protected against an otherwise lethal challenge with the virulent Tulahuén strain of the parasite. Our findings suggest that, as an adjuvant, H. tebenquichense-derived ARC may hold great potential to develop a safe and helpful vaccine against this relevant human pathogen.

摘要

类病毒体(ARC)是由古菌提取的脂质制成的囊泡,具有很强的佐剂特性。在这项研究中,我们评估了一种新型 Halorubrum tebenquichense 菌株总极性脂质制成的高度稳定 ARC 的能力,该菌株来自阿根廷巴塔哥尼亚,可作为针对细胞内原生动物 T. cruzi(恰加斯病的病原体)的可溶性寄生虫抗原的佐剂。我们首次证明,用这些 ARC(ARC-TcAg)包埋的锥虫抗原皮下免疫 C3H/HeN 小鼠,比单独接受抗原的动物血清中测量的水平更快地产生更高水平的循环 T. cruzi 抗体。ARC-TcAg 引起的体液免疫反应表现出主导的 IgG2a 抗体同种型,通常与 Th1 型免疫和对 T. cruzi 的抵抗力相关。更重要的是,ARC-TcAg 疫苗接种的小鼠在早期感染期间寄生虫血症减少,并免受致命性的 Tulahuén 寄生虫强毒株的攻击。我们的研究结果表明,作为佐剂,源自 H. tebenquichense 的 ARC 具有很大的潜力,可开发针对这种相关人类病原体的安全有效的疫苗。

相似文献

[1]
Archaeosomes display immunoadjuvant potential for a vaccine against Chagas disease.

Hum Vaccin Immunother. 2013-1-4

[2]
Archaeosomes made of Halorubrum tebenquichense total polar lipids: a new source of adjuvancy.

BMC Biotechnol. 2009-8-13

[3]
Testing the efficacy of a multi-component DNA-prime/DNA-boost vaccine against Trypanosoma cruzi infection in dogs.

PLoS Negl Trop Dis. 2011-5-17

[4]
Expression, purification, immunogenicity, and protective efficacy of a recombinant Tc24 antigen as a vaccine against Trypanosoma cruzi infection in mice.

Vaccine. 2015-8-26

[5]
Cruzipain and Its Physiological Inhibitor, Chagasin, as a DNA-Based Therapeutic Vaccine Against .

Front Immunol. 2020

[6]
Efficacy of a trans-sialidase-ISCOMATRIX subunit vaccine candidate to protect against experimental Chagas disease.

Vaccine. 2015-3-3

[7]
TcVac1 vaccine delivery by intradermal electroporation enhances vaccine induced immune protection against Trypanosoma cruzi infection in mice.

Vaccine. 2018-11-27

[8]
A therapeutic nanoparticle vaccine against Trypanosoma cruzi in a BALB/c mouse model of Chagas disease.

Hum Vaccin Immunother. 2016-4-2

[9]
Previously unrecognized vaccine candidates control Trypanosoma cruzi infection and immunopathology in mice.

Clin Vaccine Immunol. 2008-8

[10]
Use of a purified Trypanosoma cruzi antigen and CpG oligodeoxynucleotides for immunoprotection against a lethal challenge with trypomastigotes.

Vaccine. 2003-12-8

引用本文的文献

[1]
Immunological Activity of Vaccine Systems Containing Liposomal Nanocarriers against Protozoan-induced Diseases: A Systematic Review.

Curr Med Chem. 2025

[2]
The Anti-Inflammatory Effect of Nanoarchaeosomes on Human Endothelial Cells.

Pharmaceutics. 2022-3-29

[3]
Archaeosomes and Gas Vesicles as Tools for Vaccine Development.

Front Immunol. 2021

[4]
Development of thermostable vaccine adjuvants.

Expert Rev Vaccines. 2021-5

[5]
The Synergistic Effects of Sulfated Lactosyl Archaeol Archaeosomes When Combined with Different Adjuvants in a Murine Model.

Pharmaceutics. 2021-2-2

[6]
Simplified Admix Archaeal Glycolipid Adjuvanted Vaccine and Checkpoint Inhibitor Therapy Combination Enhances Protection from Murine Melanoma.

Biomedicines. 2019-11-23

[7]
Sulfated archaeal glycolipid archaeosomes as a safe and effective vaccine adjuvant for induction of cell-mediated immunity.

Hum Vaccin Immunother. 2017-5-24

[8]
Ultradeformable Archaeosomes for Needle Free Nanovaccination with Leishmania braziliensis Antigens.

PLoS One. 2016-3-2

[9]
Active targeted drug delivery for microbes using nano-carriers.

Curr Top Med Chem. 2015

本文引用的文献

[1]
Ultradeformable archaeosomes as new topical adjuvants.

Nanomedicine. 2012-2-24

[2]
Advances and challenges towards a vaccine against Chagas disease.

Hum Vaccin. 2011-11

[3]
Archaeosomes with encapsulated antigens for oral vaccine delivery.

Vaccine. 2011-5-24

[4]
Incorporation of a synthetic mycobacterial monomycoloyl glycerol analogue stabilizes dimethyldioctadecylammonium liposomes and potentiates their adjuvant effect in vivo.

Eur J Pharm Biopharm. 2010-10-20

[5]
Archaeosomes made of Halorubrum tebenquichense total polar lipids: a new source of adjuvancy.

BMC Biotechnol. 2009-8-13

[6]
Adjuvant potential of archaeal synthetic glycolipid mimetics critically depends on the glyco head group structure.

Glycobiology. 2008-7

[7]
Rapid clonal expansion and prolonged maintenance of memory CD8+ T cells of the effector (CD44highCD62Llow) and central (CD44highCD62Lhigh) phenotype by an archaeosome adjuvant independent of TLR2.

J Immunol. 2007-2-15

[8]
Current status and future prospects for a vaccine against American trypanosomiasis.

Expert Rev Vaccines. 2005-12

[9]
Assistance of microbial glycolipid antigen processing by CD1e.

Science. 2005-11-25

[10]
Archaeosomes varying in lipid composition differ in receptor-mediated endocytosis and differentially adjuvant immune responses to entrapped antigen.

Archaea. 2003-10

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