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Protective immune response induced by cationic liposomes bearing soluble antigens improves the survival of BALB/c mice against RH strain.

作者信息

Mirahmadi Hadi, Mehravaran Ahmad, Kavand Mahdi, Salimi Khorashad Ali Reza, Rezaee Nasrin

机构信息

Department of Parasitology and Mycology, Faculty of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.

Clinical Immunology Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.

出版信息

Iran J Basic Med Sci. 2025;28(3):347-354. doi: 10.22038/ijbms.2024.82123.17770.


DOI:10.22038/ijbms.2024.82123.17770
PMID:39906621
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11790195/
Abstract

OBJECTIVES: An ideal strategy to control acute or chronic toxoplasmosis can be the development and production of an effective vaccine. Liposomes as immunoadjuvants may be utilized to boost immune reactions for various antigens. MATERIALS AND METHODS: In this study, we encapsulated soluble Toxoplasma antigen (SA) in 1, 2-Dioleoyl-3-trimethylammonium propane (DOTAP) liposomes to assess the elicited immunological response. BALB/C mice received three intramuscular injections of various formulations separated by two weeks. The kind of immune reaction that was created, the degree of protection, the percentage of BALB/c mice that survived the challenge, the immune reaction assessment with cytokine synthesis (IFN-γ, IL-4), and the titration of IgG isotypes were all evaluated. RESULTS: Compared to other groups, the liposome DOTAP + imiquimod + SA-immunized mice showed a significantly lower death rate (<0.01). Liposome DOTAP + Imiquimod + SA had higher IgG2a and IFN-γ secretion levels than the control group (<0.001 and <0.0001, respectively). CONCLUSION: According to the study's findings, the liposome DOTAP + imiquimod + SA formulation generates a cellular immunological response, making it resistant to the challenge.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb6/11790195/7303d8f0f627/IJBMS-28-347-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb6/11790195/52f91567e291/IJBMS-28-347-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb6/11790195/88aa5897abe7/IJBMS-28-347-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb6/11790195/8427986f02d4/IJBMS-28-347-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb6/11790195/5d2f990e50d5/IJBMS-28-347-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb6/11790195/7303d8f0f627/IJBMS-28-347-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb6/11790195/52f91567e291/IJBMS-28-347-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb6/11790195/88aa5897abe7/IJBMS-28-347-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb6/11790195/8427986f02d4/IJBMS-28-347-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb6/11790195/5d2f990e50d5/IJBMS-28-347-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb6/11790195/7303d8f0f627/IJBMS-28-347-g005.jpg

相似文献

[1]
Protective immune response induced by cationic liposomes bearing soluble antigens improves the survival of BALB/c mice against RH strain.

Iran J Basic Med Sci. 2025

[2]
Immunogenicity and protection effects of cationic liposome containing imiquimod adjuvant on leishmaniasis in BALB/c mice.

Iran J Basic Med Sci. 2019-8

[3]
Protective effect of DNA-mediated immunization with liposome-encapsulated GRA4 against infection of Toxoplasma gondii.

J Zhejiang Univ Sci B. 2009-7

[4]
Evaluation of protective immune responses induced by DNA vaccines encoding Toxoplasma gondii surface antigen 1 (SAG1) and 14-3-3 protein in BALB/c mice.

Parasit Vectors. 2012-11-26

[5]
Evaluation of Immune Response against Leishmaniasis in BALB/c Mice Immunized with Cationic DOTAP/DOPE/CHOL Liposomes Containing Soluble Antigens.

Iran J Parasitol. 2019

[6]
Protection via a ROM4 DNA vaccine and peptide against Toxoplasma gondii in BALB/c mice.

BMC Infect Dis. 2017-1-11

[7]
Protection induced by Leishmania Major antigens and the imiquimod adjuvant encapsulated on liposomes in experimental cutaneous leishmaniasis.

Infect Genet Evol. 2019-2-7

[8]
Evaluation of immunogenicity and protective effect of DNA vaccine encoding surface antigen1 (SAG1) of Toxoplasma gondii and TLR-5 ligand as a genetic adjuvant against acute toxoplasmosis in BALB/c mice.

Biologicals. 2019-11

[9]
Induction of protection against leishmaniasis in susceptible BALB/c mice using simple DOTAP cationic nanoliposomes containing soluble Leishmania antigen (SLA).

Acta Trop. 2013-8-2

[10]
Immunogenicity of an in-silico designed multi-epitope DNA vaccine encoding ROP21 and ROP29 of Toxoplasma gondii against both acute and chronic toxoplasmosis in BALB/c mice.

Microb Pathog. 2025-3

本文引用的文献

[1]
Evaluation of long-term immunity and protection against T. gondii after immunization with multivalent recombinant chimeric T. gondii proteins.

Sci Rep. 2023-8-10

[2]
The immune response against Toxoplasma gondii in BALB/c mice induced by mannose-modified nanoliposome of excreted/secreted antigens.

Parasitol Res. 2021-8

[3]
Targeting Strategies in Therapeutic Applications of Toxoplasmosis: Recent Advances in Liposomal Vaccine Delivery Systems.

Curr Drug Targets. 2020

[4]
Liposomes used as a vaccine adjuvant-delivery system: From basics to clinical immunization.

J Control Release. 2019-5-3

[5]
Nanomaterial-Based Vaccine Adjuvants.

J Mater Chem B. 2016-9-7

[6]
Advances in the Development of Anti-Toxoplasma gondii Vaccines: Challenges, Opportunities, and Perspectives.

Trends Parasitol. 2019-2-1

[7]
A systematic review on efficiency of microneme proteins to induce protective immunity against Toxoplasma gondii.

Eur J Clin Microbiol Infect Dis. 2019-1-24

[8]
A systematic review of Toxoplasma gondii antigens to find the best vaccine candidates for immunization.

Microb Pathog. 2018-11-3

[9]
Quantification of Toxoplasma gondii in the tissues of BALB/c mice after immunization with nanoliposomal excretory-secretory antigens using Real-Time PCR.

Comp Immunol Microbiol Infect Dis. 2018-8

[10]
Cationic liposomes formulated with a novel whole Leishmania lysate (WLL) as a vaccine for leishmaniasis in murine model.

Immunobiology. 2018

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