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Perspect Med Virol. 1985;1:127-186. doi: 10.1016/S0168-7069(08)70012-0. Epub 2008 May 29.
2
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本文引用的文献

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THE NATURAL HISTORY OF HUMAN POLIOMYELITIS : I. DISTRIBUTION OF VIRUS IN NERVOUS AND NON-NERVOUS TISSUES.人类脊髓灰质炎的自然史:I. 病毒在神经组织和非神经组织中的分布。
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2
PROTECTIVE ACTION OF CERTAIN CHEMICALS AGAINST INFECTION OF MONKEYS WITH NASALLY INSTILLED POLIOMYELITIS VIRUS.某些化学物质预防经鼻腔接种脊髓灰质炎病毒感染猴子的保护作用。
J Exp Med. 1936 May 31;63(6):877-92. doi: 10.1084/jem.63.6.877.
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Experience With the Picric Acid-Alum Spray in the Prevention of Poliomyelitis in Alabama, 1936.1936年在阿拉巴马州使用苦味酸明矾喷雾剂预防脊髓灰质炎的经验
Am J Public Health Nations Health. 1937 Feb;27(2):103-11. doi: 10.2105/ajph.27.2.103.
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INSECTS AND EPIDEMIOLOGY OF POLIOMYELITIS.昆虫与脊髓灰质炎流行病学
Science. 1942 Mar 20;95(2464):300-1. doi: 10.1126/science.95.2464.300.
5
The survival of poliomyelitis and Coxsackie viruses following their ingestion by flies.脊髓灰质炎病毒和柯萨奇病毒被苍蝇摄取后的存活情况。
J Exp Med. 1952 Sep;96(3):255-71. doi: 10.1084/jem.96.3.255.
6
Immune responses in human volunteers upon oral administration of a rodent-adapted strain of poliomyelitis virus.人类志愿者口服适应啮齿动物的脊髓灰质炎病毒株后的免疫反应。
Am J Hyg. 1952 Jan;55(1):108-24. doi: 10.1093/oxfordjournals.aje.a119499.
7
The recovery of virus from regional lymph nodes of fatal human cases of poliomyelitis.从脊髓灰质炎致死人类病例的局部淋巴结中分离出病毒。
Am J Med Sci. 1951 Sep;222(3):292-9. doi: 10.1097/00000441-195109000-00007.
8
Second attacks of paralytic poliomyelitis in human beings in relation to immunity, virus types and virulence, with a report of two cases, and four other individuals in Baltimore, 1944, infected with virus of the Leon type.人类麻痹性脊髓灰质炎的再次发作与免疫、病毒类型及毒力的关系,附两例报告及1944年在巴尔的摩另外四名感染莱昂型病毒者的情况。
Am J Hyg. 1951 Sep;54(2):174-90. doi: 10.1093/oxfordjournals.aje.a119475.
9
Limitation of fecal and pharyngeal poliovirus excretion in Salk-vaccinated children. A family study during a type 1 poliomyelitis epidemic.接种索尔克疫苗儿童粪便和咽部脊髓灰质炎病毒排泄的局限性。1型脊髓灰质炎流行期间的一项家庭研究。
Am J Hyg. 1962 Sep;76:173-95. doi: 10.1093/oxfordjournals.aje.a120272.
10
Live, orally given poliovirus vaccine. Effects of rapid mass immunization on population under conditions of massive enteric infection with other viruses.口服脊髓灰质炎活疫苗。在其他病毒引起大规模肠道感染的情况下,快速大规模免疫对人群的影响。
JAMA. 1960 Aug 6;173:1521-6. doi: 10.1001/jama.1960.03020320001001.

第4章 小核糖核酸病毒感染

Chapter 4 Picornavirus infections.

出版信息

Perspect Med Virol. 1985;1:127-186. doi: 10.1016/S0168-7069(08)70012-0. Epub 2008 May 29.

DOI:10.1016/S0168-7069(08)70012-0
PMID:32287579
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7134062/
Abstract

The oldest member of the Picornaviruses group is polio virus, which was recognized early by clinicians because of its characteristic paralytic disease. This chapter examines the polio virus in regard to its virology, disease, and prevention by vaccines and chemoprophylaxis. Polio has been well controlled in most developed countries using live or inactivated vaccines. Research work has intensified using genetic engineering techniques to produce live attenuated viruses with defined and stable mutations so as to prevent reversion to virulence, and also to produce immunogenic oligopeptides or proteins for a new generation of inactivated polio vaccines. Chemotherapy is therefore not required for polio infections. In contrast, neither vaccines have been developed against rhinovirus infections, nor are the vaccines thought to have a use, unless broadly reacting antigenic determinants can be located. Several interesting but only weakly effective antiviral compounds have been selected against rhinoviruses and this is a major research area at present. Studies continue also with interferon, but because of toxicity problems these look less interesting at present. Sequence and biochemical data is now available for several additional enterovirus strains and this could open new possibilities both with antivirals or vaccines (for example synthetic peptides) in the near future.

摘要

小核糖核酸病毒科中最古老的成员是脊髓灰质炎病毒,由于其典型的麻痹性疾病,临床医生很早就认识到了它。本章将从病毒学、疾病以及通过疫苗和化学预防进行预防等方面来研究脊髓灰质炎病毒。在大多数发达国家,使用减毒活疫苗或灭活疫苗已很好地控制了脊髓灰质炎。利用基因工程技术加强了研究工作,以生产具有明确和稳定突变的减毒活病毒,从而防止病毒回复毒力,同时也生产用于新一代灭活脊髓灰质炎疫苗的免疫原性寡肽或蛋白质。因此,脊髓灰质炎感染不需要进行化学治疗。相比之下,针对鼻病毒感染既没有研发出疫苗,也认为疫苗没有用处,除非能找到广泛反应的抗原决定簇。已经筛选出了几种针对鼻病毒的有趣但效果较弱的抗病毒化合物,这是目前的一个主要研究领域。对干扰素的研究也在继续,但由于毒性问题,目前这些研究看起来不那么有吸引力。现在已有几种其他肠道病毒株的序列和生化数据,这可能在不久的将来为抗病毒药物或疫苗(例如合成肽)带来新的可能性。