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事实还是假说:多头绦虫(Taenia crassiceps)作为猪带绦虫(Taenia solium)模型,以及 S3Pvac 疫苗。

Fact or hypothesis: Taenia crassiceps as a model for Taenia solium, and the S3Pvac vaccine.

机构信息

Faculty of Veterinary Science, The University of Melbourne, Werribee, Vic., Australia.

出版信息

Parasite Immunol. 2010 Nov-Dec;32(11-12):701-9. doi: 10.1111/j.1365-3024.2010.01231.x.

DOI:10.1111/j.1365-3024.2010.01231.x
PMID:21039610
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3033518/
Abstract

Research undertaken over the past 40 years has established many of the general principals concerning immunity to taeniid cestodes. Although much is well understood about the host-protective mechanisms against taeniids and this knowledge has been exploited in studies on vaccine development, many aspects require further investigation or confirmation. Some phenomena have come to be regarded as being well established, while careful analysis of the published data would suggest that they may be better regarded as hypotheses rather than established facts. This review considers one selected issue pertaining to immunity to cestode infections and examines carefully the nature of the evidence that is available to support conclusions that have been made in this area. The issue examined is the use of Taenia crassiceps as a model for cysticercosis in pigs caused by Taenia solium, together with the S3Pvac vaccine, which has been developed based on this model. Strong evidence is found to support the conclusion that defined T. crassiceps antigens can limit intraperitoneal proliferation of the ORF strain of T. crassiceps in mice; however, the potential for these antigens to affect T. solium infection in pigs requires further confirmation.

摘要

在过去的 40 年中,已经进行了许多关于绦虫免疫的研究,确立了许多一般原则。尽管人们对宿主针对绦虫的保护机制有了很多了解,并且这方面的知识已经被应用于疫苗开发的研究中,但许多方面仍需要进一步研究或证实。有些现象已经被认为是既定事实,但仔细分析已发表的数据表明,它们可能更好地被视为假设,而不是既定事实。本综述考虑了与囊虫病免疫相关的一个选定问题,并仔细研究了支持该领域得出的结论的现有证据的性质。所检查的问题是将多头绦虫(Taenia crassiceps)用作由猪带绦虫(Taenia solium)引起的猪囊尾蚴病的模型,以及基于该模型开发的 S3Pvac 疫苗。有强有力的证据支持这样的结论,即已确定的多头绦虫抗原可以限制 ORF 株多头绦虫在小鼠中的腹腔内增殖;然而,这些抗原对猪带绦虫感染的潜在影响需要进一步证实。

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本文引用的文献

1
Fact or hypothesis: concomitant immunity in taeniid cestode infections.事实还是假说:并殖吸虫感染中的伴随免疫。
Parasite Immunol. 2010 Aug;32(8):582-9. doi: 10.1111/j.1365-3024.2010.01227.x.
2
Eradication of Taenia solium cysticercosis: a role for vaccination of pigs.消除猪囊尾蚴病:疫苗接种在其中的作用。
Int J Parasitol. 2010 Aug 15;40(10):1183-92. doi: 10.1016/j.ijpara.2010.05.001. Epub 2010 May 12.
3
Inexpensive anti-cysticercosis vaccine: S3Pvac expressed in heat inactivated M13 filamentous phage proves effective against naturally acquired Taenia solium porcine cysticercosis.廉价抗囊尾蚴病疫苗:在热灭活M13丝状噬菌体中表达的S3Pvac被证明对自然获得的猪带绦虫猪囊尾蚴病有效。
Vaccine. 2008 Jun 2;26(23):2899-905. doi: 10.1016/j.vaccine.2008.03.042. Epub 2008 Apr 10.
4
Vaccines against cysticercosis.抗囊尾蚴病疫苗
Curr Top Med Chem. 2008;8(5):415-23. doi: 10.2174/156802608783790839.
5
A new highly effective anticysticercosis vaccine expressed in transgenic papaya.一种在转基因木瓜中表达的新型高效抗囊尾蚴病疫苗。
Vaccine. 2007 May 22;25(21):4252-60. doi: 10.1016/j.vaccine.2007.02.080. Epub 2007 Mar 16.
6
Cestode vaccines: origins, current status and future prospects.绦虫疫苗:起源、现状与未来前景
Parasitology. 2006;133 Suppl:S27-42. doi: 10.1017/S003118200600179X.
7
Improvement of the synthetic tri-peptide vaccine (S3Pvac) against porcine Taenia solium cysticercosis in search of a more effective, inexpensive and manageable vaccine.针对猪带绦虫囊尾蚴病的合成三肽疫苗(S3Pvac)的改进,以寻求一种更有效、廉价且易于管理的疫苗。
Vaccine. 2007 Feb 9;25(8):1368-78. doi: 10.1016/j.vaccine.2006.10.018. Epub 2006 Oct 23.
8
Further evaluation of the synthetic peptide vaccine S3Pvac against Taenia solium cysticercosis in pigs in an endemic town of Mexico.在墨西哥一个地方性流行城镇对猪用合成肽疫苗S3Pvac抗猪带绦虫囊尾蚴病进行的进一步评估。
Parasitology. 2007 Jan;134(Pt 1):129-33. doi: 10.1017/S0031182006001132. Epub 2006 Sep 4.
9
Intrahepatic DNA vaccination: unexpected increased resistance against murine cysticercosis induced by non-specific enhanced immunity.肝内DNA疫苗接种:非特异性增强免疫诱导的对小鼠囊尾蚴病的意外增强抵抗力。
J Parasitol. 2006 Jun;92(3):655-7. doi: 10.1645/GE-665R1.1.
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Brucella spp. lumazine synthase: a novel adjuvant and antigen delivery system to effectively induce oral immunity.布鲁氏菌属的鲁马嗪合酶:一种有效诱导口服免疫的新型佐剂和抗原递送系统。
Microbes Infect. 2006 Apr;8(5):1277-86. doi: 10.1016/j.micinf.2005.12.006. Epub 2006 Feb 7.