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本文引用的文献

1
Cellular and humoral immune effector mechanisms required for sterile protection against sporozoite challenge induced with the novel malaria vaccine candidate CelTOS.细胞和体液免疫效应机制是新型疟疾疫苗候选物 CelTOS 诱导的无活孢子挑战产生无菌保护所必需的。
Vaccine. 2011 Aug 11;29(35):5940-9. doi: 10.1016/j.vaccine.2011.06.053. Epub 2011 Jun 29.
2
CD8+ T effector memory cells protect against liver-stage malaria.CD8+ T 效应记忆细胞可预防肝脏期疟疾。
J Immunol. 2011 Aug 1;187(3):1347-57. doi: 10.4049/jimmunol.1100302. Epub 2011 Jun 29.
3
Identification of two new protective pre-erythrocytic malaria vaccine antigen candidates.鉴定两种新的红细胞前期保护性疟疾疫苗抗原候选物。
Malar J. 2011 Mar 16;10:65. doi: 10.1186/1475-2875-10-65.
4
Immunization with pre-erythrocytic antigen CelTOS from Plasmodium falciparum elicits cross-species protection against heterologous challenge with Plasmodium berghei.用疟原虫 falciparum 的红细胞前期抗原 CelTOS 免疫可引发针对疟原虫 berghei 异源挑战的交叉物种保护。
PLoS One. 2010 Aug 19;5(8):e12294. doi: 10.1371/journal.pone.0012294.
5
Extreme CD8 T cell requirements for anti-malarial liver-stage immunity following immunization with radiation attenuated sporozoites.经辐射减毒的疟原虫孢子免疫后,抗疟肝脏期免疫需要极端的 CD8 T 细胞。
PLoS Pathog. 2010 Jul 15;6(7):e1000998. doi: 10.1371/journal.ppat.1000998.
6
Prolonged antigen presentation is required for optimal CD8+ T cell responses against malaria liver stage parasites.延长抗原提呈时间是产生针对疟疾肝期寄生虫的最佳 CD8+ T 细胞应答所必需的。
PLoS Pathog. 2010 May 6;6(5):e1000877. doi: 10.1371/journal.ppat.1000877.
7
Prime-boost immunization with adenoviral and modified vaccinia virus Ankara vectors enhances the durability and polyfunctionality of protective malaria CD8+ T-cell responses.腺病毒和改良安卡拉痘苗病毒载体的初次-加强免疫增强了保护性疟疾 CD8+T 细胞反应的持久性和多功能性。
Infect Immun. 2010 Jan;78(1):145-53. doi: 10.1128/IAI.00740-09. Epub 2009 Oct 26.
8
Genetically engineered, attenuated whole-cell vaccine approaches for malaria.用于疟疾的基因工程减毒全细胞疫苗方法。
Hum Vaccin. 2010 Jan;6(1):107-13. doi: 10.4161/hv.6.1.9654. Epub 2010 Jan 29.
9
From the circumsporozoite protein to the RTS, S/AS candidate vaccine.从环子孢子蛋白到RTS,S/AS候选疫苗。
Hum Vaccin. 2010 Jan;6(1):90-6. doi: 10.4161/hv.6.1.9677. Epub 2010 Jan 30.
10
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.重组肝期抗原-1(LSA-1)与 AS01 或 AS02 联合使用是安全的,可引发高滴度抗体并诱导 IFN-γ/IL-2 CD4+T 细胞,但不能预防实验性疟原虫感染。
Vaccine. 2010 Jul 12;28(31):5135-44. doi: 10.1016/j.vaccine.2009.08.046. Epub 2009 Sep 6.

用辐照后的子孢子免疫小鼠鉴定具有 CD8 表位的非 CSP 抗原。

Identification of non-CSP antigens bearing CD8 epitopes in mice immunized with irradiated sporozoites.

机构信息

Michael Heidelberger Division, Department of Pathology, New York University School of Medicine, NY 10016, United States.

出版信息

Vaccine. 2011 Oct 6;29(43):7335-42. doi: 10.1016/j.vaccine.2011.07.081. Epub 2011 Jul 30.

DOI:10.1016/j.vaccine.2011.07.081
PMID:21807053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3603353/
Abstract

Immunization of BALB/c mice with irradiated sporozoites (IrSp) of Plasmodium yoelii can lead to sterile immunity. The circumsporozoite protein (CSP) plays a dominant role in protection. Nevertheless after hyper-immunization with IrSp, complete protection is obtained in CSP-transgenic BALB/c mice that are T-cell tolerant to the CSP and cannot produce antibodies [CSP-Tg/JhT(-/-)]. This protection is mediated exclusively by CD8(+) T cells [1]. To identify the non-CSP protective T cell antigens, we studied the properties of 34 P. yoelii sporozoite antigens that are predicted to be secreted and to contain strong Kd-restricted CD8(+) T cell epitopes. The synthetic peptides corresponding to the epitopes were used to screen for the presence of peptide-specific CD8(+) T cells secreting interferon-γ (IFN-γ) in splenocytes from CSP-Tg/JhT(-/-) BALB/c mice hyper immunized with IrSp. However, the numbers of IFN-γ-secreting splenocytes specific for the non-CSP antigen-derived peptides were 20-100 times lower than those specific for the CSP-specific peptide. When mice were immunized with recombinant adenoviruses expressing selected non-CSP antigens, the animals were not protected against challenge with P. yoelii sporozoites although large numbers of CD8(+) specific T cells were generated.

摘要

用辐射后的约氏疟原虫(Plasmodium yoelii)孢子(IrSp)免疫 BALB/c 小鼠可以导致无菌免疫。环子孢子蛋白(CSP)在保护中起主要作用。尽管 IrSp 超免疫后,对 CSP 耐受且不能产生抗体的 CSP 转基因 BALB/c 小鼠(CSP-Tg/JhT(-/-))中获得完全保护。这种保护仅由 CD8(+) T 细胞介导[1]。为了鉴定非 CSP 保护性 T 细胞抗原,我们研究了 34 种预测分泌并含有强 Kd 限制的 CD8(+) T 细胞表位的约氏疟原虫孢子抗原的特性。相应的合成肽用于筛选来自 IrSp 超免疫的 CSP-Tg/JhT(-/-) BALB/c 小鼠脾细胞中分泌干扰素-γ(IFN-γ)的肽特异性 CD8(+) T 细胞的存在。然而,针对非 CSP 抗原衍生肽的 IFN-γ 分泌脾细胞的数量比针对 CSP 特异性肽的数量低 20-100 倍。当用表达选定的非 CSP 抗原的重组腺病毒免疫小鼠时,尽管产生了大量的 CD8(+)特异性 T 细胞,但动物未受到约氏疟原虫孢子的挑战。