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本文引用的文献

1
Mucosal and systemic T cell response in mice intragastrically infected with Neospora caninum tachyzoites.经口感染刚地弓形虫速殖子的小鼠黏膜和系统 T 细胞应答。
Vet Res. 2013 Aug 10;44(1):69. doi: 10.1186/1297-9716-44-69.
2
Antibodies and their receptors: different potential roles in mucosal defense.抗体及其受体:在黏膜防御中的不同潜在作用。
Front Immunol. 2013 Jul 16;4:200. doi: 10.3389/fimmu.2013.00200. eCollection 2013.
3
What is the global economic impact of Neospora caninum in cattle - the billion dollar question.弓形虫感染牛只对全球经济的影响——这是一个价值十亿美元的问题。
Int J Parasitol. 2013 Feb;43(2):133-42. doi: 10.1016/j.ijpara.2012.10.022. Epub 2012 Dec 12.
4
Differential effects of intranasal vaccination with recombinant NcPDI in different mouse models of Neospora caninum infection.鼻腔内接种重组 NcPDI 在不同的刚地弓形虫感染小鼠模型中的差异作用。
Parasite Immunol. 2013 Jan;35(1):11-20. doi: 10.1111/pim.12013.
5
Exploiting mucosal surfaces for the development of mucosal vaccines.开发黏膜疫苗的黏膜表面利用
Vaccine. 2011 Nov 3;29(47):8506-11. doi: 10.1016/j.vaccine.2011.09.010. Epub 2011 Sep 22.
6
Neosporosis in animals--the last five years.动物的新孢子虫病——过去五年。
Vet Parasitol. 2011 Aug 4;180(1-2):90-108. doi: 10.1016/j.vetpar.2011.05.031. Epub 2011 May 27.
7
Humoral responses and immune protection in mice immunized with irradiated T. gondii tachyzoites and challenged with three genetically distinct strains of T. gondii.经照射的弓形虫速殖子免疫小鼠的体液反应和免疫保护,并用三种遗传上不同的弓形虫分离株进行攻毒。
Immunol Lett. 2011 Aug 30;138(2):187-96. doi: 10.1016/j.imlet.2011.04.007. Epub 2011 Apr 25.
8
CpG DNA as a vaccine adjuvant.CpG DNA 作为疫苗佐剂。
Expert Rev Vaccines. 2011 Apr;10(4):499-511. doi: 10.1586/erv.10.174.
9
Immunization of female BALB/c mice with Neospora cyclophilin and/or NcSRS2 elicits specific antibody response and prevents against challenge infection by Neospora caninum.用刚地弓形虫亲环素和/或 NcSRS2 免疫雌性 BALB/c 小鼠可诱导特异性抗体反应,并防止刚地弓形虫感染。
Vaccine. 2011 Mar 16;29(13):2392-9. doi: 10.1016/j.vaccine.2011.01.041. Epub 2011 Jan 31.
10
Vaccination of mice with chitosan nanogel-associated recombinant NcPDI against challenge infection with Neospora caninum tachyzoites.用壳聚糖纳米凝胶相关的重组 NcPDI 对小鼠进行免疫接种,以抵抗刚地弓形虫速殖子的挑战感染。
Parasite Immunol. 2011 Feb;33(2):81-94. doi: 10.1111/j.1365-3024.2010.01255.x.

经鼻免疫 Neospora caninum 膜抗原对经胃肠道建立的鼠新孢子虫病的保护作用。

Protective effect of intranasal immunization with Neospora caninum membrane antigens against murine neosporosis established through the gastrointestinal tract.

机构信息

ICBAS - Instituto de Ciências Biomédicas de Abel Salazar, Universidade do Porto, Porto, Portugal; Instituto de Biologia Molecular e Celular - IBMC, Porto, Portugal.

出版信息

Immunology. 2014 Feb;141(2):256-67. doi: 10.1111/imm.12191.

DOI:10.1111/imm.12191
PMID:24128071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3904246/
Abstract

Neospora caninum is an Apicomplexa parasite that in the last two decades was acknowledged as the main pathogenic agent responsible for economic losses in the cattle industry. In the present study, the effectiveness of intranasal immunization with N. caninum membrane antigens plus CpG adjuvant was assessed in a murine model of intragastrically established neosporosis. Immunized mice presented a lower parasitic burden in the brain on infection with 5 × 10(7) tachyzoites, showing that significant protection was achieved by this immunization strategy. Intestinal IgA antibodies raised by immunization markedly agglutinated live N. caninum tachyzoites whereas previous opsonization with IgG antibodies purified from immunized mice sera reduced parasite survival within macrophage cells. Although an IgG1 : IgG2a ratio < 1 was detected in the immunized mice before and after infection, indicative of a predominant T helper type 1 immune response, no increased production of interferon-γ was detected in the spleen or mesenteric lymph nodes of the immunized mice. Altogether, these results show that mucosal immunization with N. caninum membrane proteins plus CpG adjuvant protect against intragastrically established neosporosis and indicate that parasite-specific mucosal and circulating antibodies have a protective role against this parasitic infection.

摘要

刚地弓形虫是顶复门的寄生虫,在过去二十年中被认为是导致牛养殖业经济损失的主要病原。在本研究中,通过鼻腔内免疫刚地弓形虫膜抗原加 CpG 佐剂,评估了其在经口感染建立的弓形虫病小鼠模型中的效果。用 5×10(7)速殖子感染后,免疫组小鼠脑部寄生虫负荷降低,表明这种免疫策略可显著提供保护。免疫产生的肠黏膜 IgA 抗体可明显凝集活的刚地弓形虫速殖子,而先前用从免疫鼠血清中纯化的 IgG 抗体调理可减少寄生虫在巨噬细胞内的存活。尽管在感染前后,免疫小鼠中检测到 IgG1:IgG2a 比值<1,表明存在主要的辅助性 T 细胞 1 型免疫应答,但在免疫小鼠的脾脏或肠系膜淋巴结中未检测到干扰素-γ的增加。综上所述,这些结果表明,用刚地弓形虫膜蛋白加 CpG 佐剂进行黏膜免疫可预防经口感染建立的弓形虫病,并表明寄生虫特异性黏膜和循环抗体在针对这种寄生虫感染中具有保护作用。