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疟疾疫苗RTS,S诱导产生的保护性免疫与产生γ干扰素的恶性疟原虫环子孢子蛋白特异性CD4+和CD8+ T细胞有关。

Protective immunity induced with malaria vaccine, RTS,S, is linked to Plasmodium falciparum circumsporozoite protein-specific CD4+ and CD8+ T cells producing IFN-gamma.

作者信息

Sun Peifang, Schwenk Robert, White Katherine, Stoute Jose A, Cohen Joe, Ballou W Ripley, Voss Gerald, Kester Kent E, Heppner D Gray, Krzych Urszula

机构信息

Department of Immunology, Walter Reed Army Institute of Research, Silver Spring, MD 20910, USA.

出版信息

J Immunol. 2003 Dec 15;171(12):6961-7. doi: 10.4049/jimmunol.171.12.6961.


DOI:10.4049/jimmunol.171.12.6961
PMID:14662904
Abstract

The Plasmodium falciparum circumsporozoite (CS) protein-based pre-erythrocytic stage vaccine, RTS,S, induces a high level of protection against experimental sporozoite challenge. The immune mechanisms that constitute protection are only partially understood, but are presumed to rely on Abs and T cell responses. In the present study we compared CS protein peptide-recalled IFN-gamma reactivity of pre- and RTS,S-immune lymphocytes from 20 subjects vaccinated with RTS,S. We observed elevated IFN-gamma in subjects protected by RTS,S; moreover, both CD4(+) and CD8(+) T cells produced IFN-gamma in response to CS protein peptides. Significantly, protracted protection, albeit observed only in two of seven subjects, was associated with sustained IFN-gamma response. This is the first study demonstrating correlation in a controlled Plasmodia sporozoite challenge study between protection induced by a recombinant malaria vaccine and Ag-specific T cell responses. Field-based malaria vaccine studies are in progress to validate the establishment of this cellular response as a possible in vitro correlate of protective immunity to exo-erythrocytic stage malaria vaccines.

摘要

基于恶性疟原虫环子孢子(CS)蛋白的红细胞前期疫苗RTS,S,可诱导针对实验性子孢子攻击的高水平保护。构成保护作用的免疫机制仅得到部分理解,但推测依赖于抗体和T细胞反应。在本研究中,我们比较了20名接种RTS,S的受试者的未免疫淋巴细胞和RTS,S免疫淋巴细胞对CS蛋白肽的回忆性γ干扰素反应性。我们观察到受RTS,S保护的受试者中γ干扰素水平升高;此外,CD4(+)和CD8(+) T细胞均对CS蛋白肽产生γ干扰素反应。值得注意的是,尽管仅在7名受试者中的2名中观察到,但长期保护与持续的γ干扰素反应相关。这是第一项在受控的疟原虫子孢子攻击研究中证明重组疟疾疫苗诱导的保护与抗原特异性T细胞反应之间存在相关性的研究。基于现场的疟疾疫苗研究正在进行中,以验证将这种细胞反应确立为对红细胞外期疟疾疫苗保护性免疫的可能体外相关性。

相似文献

[1]
Protective immunity induced with malaria vaccine, RTS,S, is linked to Plasmodium falciparum circumsporozoite protein-specific CD4+ and CD8+ T cells producing IFN-gamma.

J Immunol. 2003-12-15

[2]
Induction in humans of CD8+ and CD4+ T cell and antibody responses by sequential immunization with malaria DNA and recombinant protein.

J Immunol. 2004-5-1

[3]
Potent induction of focused Th1-type cellular and humoral immune responses by RTS,S/SBAS2, a recombinant Plasmodium falciparum malaria vaccine.

J Infect Dis. 1999-11

[4]
Immunization with the RTS,S/AS malaria vaccine induces IFN-γ(+)CD4 T cells that recognize only discrete regions of the circumsporozoite protein and these specificities are maintained following booster immunizations and challenge.

Vaccine. 2011-10-5

[5]
Protective antibody and CD8+ T-cell responses to the Plasmodium falciparum circumsporozoite protein induced by a nanoparticle vaccine.

PLoS One. 2012

[6]
Detection of CD4+CD45RO+ T lymphocytes producing IL-4 in response to antigens on Plasmodium falciparum erythrocytes: an in vitro correlate of protective immunity induced with attenuated Plasmodium falciparum sporozoites.

Cell Immunol. 1997-9-15

[7]
Plasmodium falciparum-specific cellular immune responses after immunization with the RTS,S/AS02D candidate malaria vaccine in infants living in an area of high endemicity in Mozambique.

Infect Immun. 2009-10

[8]
Recombinant Liver Stage Antigen-1 (LSA-1) formulated with AS01 or AS02 is safe, elicits high titer antibody and induces IFN-gamma/IL-2 CD4+ T cells but does not protect against experimental Plasmodium falciparum infection.

Vaccine. 2009-9-6

[9]
Priming with an adenovirus 35-circumsporozoite protein (CS) vaccine followed by RTS,S/AS01B boosting significantly improves immunogenicity to Plasmodium falciparum CS compared to that with either malaria vaccine alone.

Infect Immun. 2007-5

[10]
Identification of Plasmodium falciparum circumsporozoite protein-specific CD8+ T cell epitopes in a malaria exposed population.

PLoS One. 2020-2-10

引用本文的文献

[1]
The anti-circumsporozoite antibody response to repeated, seasonal booster doses of the malaria vaccine RTS,S/AS01.

NPJ Vaccines. 2025-2-6

[2]
Effect of RTS,S/AS01 vaccine booster dose on cellular immune responses in African infants and children.

NPJ Vaccines. 2024-10-25

[3]
Design and Evaluation of Chimeric Circumsporozoite Protein-Based Malaria Vaccines.

Vaccines (Basel). 2024-3-25

[4]
Multifunctional IgG/IgM antibodies and cellular cytotoxicity are elicited by the full-length MSP1 SumayaVac-1 malaria vaccine.

NPJ Vaccines. 2023-8-9

[5]
A multivalent circumsporozoite protein-based nanoparticle malaria vaccine elicits a robust and durable antibody response against the junctional epitope and the major repeats.

Bioeng Transl Med. 2023-3-28

[6]
Controlled Human Infection Models To Accelerate Vaccine Development.

Clin Microbiol Rev. 2022-9-21

[7]
Germinal center activity and B cell maturation are associated with protective antibody responses against Plasmodium pre-erythrocytic infection.

PLoS Pathog. 2022-7

[8]
Cellular and antibody response in GMZ2-vaccinated Gabonese volunteers in a controlled human malaria infection trial.

Malar J. 2022-6-17

[9]
A comprehensive study of epitopes and immune reactivity among Plasmodium species.

BMC Microbiol. 2022-3-11

[10]
The RTS,S vaccine-a chance to regain the upper hand against malaria?

Cell. 2022-3-3

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