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1
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Infect Immun. 1980 Jan;27(1):181-6. doi: 10.1128/iai.27.1.181-186.1980.
2
Recombinant chimeric yellow fever-dengue type 2 virus is immunogenic and protective in nonhuman primates.重组嵌合黄热-登革2型病毒在非人灵长类动物中具有免疫原性和保护性。
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Trans R Soc Trop Med Hyg. 1984;78(4):445-8. doi: 10.1016/0035-9203(84)90055-5.
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6
Virulence and immunogenicity of a temperature-sensitive dengue-2 virus in lower primates.温度敏感型登革2型病毒在低等灵长类动物中的毒力和免疫原性
Infect Immun. 1977 Oct;18(1):151-6. doi: 10.1128/iai.18.1.151-156.1977.
7
Construction, safety, and immunogenicity in nonhuman primates of a chimeric yellow fever-dengue virus tetravalent vaccine.一种嵌合黄热病 - 登革热病毒四价疫苗在非人灵长类动物中的构建、安全性及免疫原性
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Infect Immun. 1981 Aug;33(2):389-94. doi: 10.1128/iai.33.2.389-394.1981.
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Use of a Recombinant Gamma-2 Herpesvirus Vaccine Vector against Dengue Virus in Rhesus Monkeys.重组γ-2疱疹病毒疫苗载体在恒河猴中抗登革病毒的应用。
J Virol. 2017 Jul 27;91(16). doi: 10.1128/JVI.00525-17. Print 2017 Aug 15.
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Preparation of an attenuated dengue 4 (341750 Carib) virus vaccine. I. Pre-clinical studies.
Am J Trop Med Hyg. 1990 Aug;43(2):212-8. doi: 10.4269/ajtmh.1990.43.212.

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Dengue Virus Infection of Aedes aegypti Requires a Putative Cysteine Rich Venom Protein.埃及伊蚊感染登革病毒需要一种假定的富含半胱氨酸的毒液蛋白。
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Philos Trans R Soc Lond B Biol Sci. 2015 Aug 19;370(1675). doi: 10.1098/rstb.2014.0299.
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4
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Antiviral Res. 2014 Sep;109:160-70. doi: 10.1016/j.antiviral.2014.07.005. Epub 2014 Jul 12.
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Can non-human primates serve as models for investigating dengue disease pathogenesis?非人灵长类动物能否作为研究登革热疾病发病机制的模型?
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6
Fever versus fever: the role of host and vector susceptibility and interspecific competition in shaping the current and future distributions of the sylvatic cycles of dengue virus and yellow fever virus.发热与发热:宿主和媒介易感性以及种间竞争在塑造登革热病毒和黄热病病毒自然循环的当前和未来分布中的作用。
Infect Genet Evol. 2013 Oct;19:292-311. doi: 10.1016/j.meegid.2013.03.008. Epub 2013 Mar 20.
7
Derivation and characterization of a dengue type 1 host range-restricted mutant virus that is attenuated and highly immunogenic in monkeys.1型登革热宿主范围受限突变病毒的衍生与特性研究,该病毒在猴子体内减毒且具有高度免疫原性。
J Virol. 2002 Apr;76(7):3318-28. doi: 10.1128/jvi.76.7.3318-3328.2002.
8
Tick-borne Langat/mosquito-borne dengue flavivirus chimera, a candidate live attenuated vaccine for protection against disease caused by members of the tick-borne encephalitis virus complex: evaluation in rhesus monkeys and in mosquitoes.蜱传兰加特病毒/蚊传登革热黄病毒嵌合体,一种用于预防蜱传脑炎病毒复合体成员所致疾病的减毒活疫苗候选物:在恒河猴和蚊子中的评估
J Virol. 2001 Sep;75(17):8259-67. doi: 10.1128/jvi.75.17.8259-8267.2001.
9
Monkeys immunized with intertypic chimeric dengue viruses are protected against wild-type virus challenge.用不同血清型嵌合登革病毒免疫的猴子可抵御野生型病毒攻击。
J Virol. 1996 Jun;70(6):4162-6. doi: 10.1128/JVI.70.6.4162-4166.1996.
10
Dengue-2 vaccine: virological, immunological, and clinical responses of six yellow fever-immune recipients.登革2型疫苗:6名对黄热病免疫的接种者的病毒学、免疫学及临床反应
Infect Immun. 1981 Feb;31(2):698-703. doi: 10.1128/iai.31.2.698-703.1981.

本文引用的文献

1
Research on dengue during World War II.第二次世界大战期间关于登革热的研究。
Am J Trop Med Hyg. 1952 Jan;1(1):30-50. doi: 10.4269/ajtmh.1952.1.30.
2
Application of a microtechnique to viral serological investigations.一种微技术在病毒血清学研究中的应用。
J Immunol. 1962 Mar;88:320-9.
3
Techniques for hemagglutination and hemagglutination-inhibition with arthropod-borne viruses.节肢动物传播病毒的血凝及血凝抑制技术。
Am J Trop Med Hyg. 1958 Sep;7(5):561-73. doi: 10.4269/ajtmh.1958.7.561.
4
Dengue-2 vaccine: preparation from a small-plaque virus clone.登革热2型疫苗:由小噬斑病毒克隆株制备。
Infect Immun. 1980 Jan;27(1):175-80. doi: 10.1128/iai.27.1.175-180.1980.
5
A plaque reduction test for dengue virus neutralizing antibodies.登革病毒中和抗体的蚀斑减少试验。
J Immunol. 1967 Aug;99(2):285-90.
6
The kinetics of antibody formation.抗体形成的动力学
Prog Allergy. 1967;10:37-83.
7
Dengue-virus recovery by direct and delayed plaques in LLC-MK2 cells.登革病毒在LLC-MK2细胞中通过直接空斑和延迟空斑进行复苏。
Am J Trop Med Hyg. 1968 May;17(3):441-8. doi: 10.4269/ajtmh.1968.17.441.
8
Studies on the pathogenesis of dengue infection in monkeys. II. Clinical laboratory responses to heterologous infection.猴子登革热感染发病机制的研究。II. 对异源感染的临床实验室反应。
J Infect Dis. 1973 Jul;128(1):15-22. doi: 10.1093/infdis/128.1.15.
9
Isolation of a temperature-sensitive dengue-2 virus under conditions suitable for vaccine development.在适合疫苗研发的条件下分离出一种温度敏感的登革2型病毒。
Infect Immun. 1976 Nov;14(5):1221-7. doi: 10.1128/iai.14.5.1221-1227.1976.
10
Virulence and immunogenicity of a temperature-sensitive dengue-2 virus in lower primates.温度敏感型登革2型病毒在低等灵长类动物中的毒力和免疫原性
Infect Immun. 1977 Oct;18(1):151-6. doi: 10.1128/iai.18.1.151-156.1977.

登革2型疫苗:恒河猴的病毒血症和免疫反应

Dengue-2 vaccine: viremia and immune responses in rhesus monkeys.

作者信息

Scott R M, Nisalak A, Eckels K H, Tingpalapong M, Harrison V R, Gould D J, Chapple F E, Russell P K

出版信息

Infect Immun. 1980 Jan;27(1):181-6. doi: 10.1128/iai.27.1.181-186.1980.

DOI:10.1128/iai.27.1.181-186.1980
PMID:6766903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC550741/
Abstract

Studies were undertaken in Indian rhesus monkeys (Macaca mulatta) to determine the safety, potency, immunogenicity, and mosquito infectivity of a small-plaque, temperature-sensitive variant of dengue type 2 (DEN-2) virus, a vaccine candidate. Fifteen monkeys were inoculated subcutaneously with the vaccine virus, ten receiving 10(3.1) plaque-forming units (PFU) and five receiving 10(4.5) PFU. After primary immunization, viremia was detected in only one monkey, a recipient of the higher dose of vaccine. The recovered virus had the same growth characteristics as the vaccine strain. Aedes aegypti mosquitoes did not become infected when they were allowed to feed on monkeys that received the lower dose of vaccine. As expected, the immunization produced no evidence of illness in any of the animals. A dose response to vaccine was detected; all five of the high-dose recipients developed neutralizing antibodies, whereas only five of ten low-dose recipients did so. In both groups, neutralizing antibody was often transient. Its presence at 30 days did not always correlate with protection from viremia in those animals challenged 4 to 6 months after vaccination with wild-type DEN-2 virus. However, immunized animals developed anamnestic antibody responses after challenge, and none demonstrated adverse effects to infection. Reimmunization of monkeys 4 months after primary immunization led to the production of low-titered but persistent neutralizing antibody which protected the animals from a wild-type virus challenge.

摘要

对印度恒河猴(猕猴)进行了研究,以确定登革2型(DEN-2)病毒的一种小蚀斑、温度敏感变异株(一种候选疫苗)的安全性、效力、免疫原性和对蚊子的感染性。15只猴子皮下接种了疫苗病毒,10只接受10(3.1)蚀斑形成单位(PFU),5只接受10(4.5) PFU。初次免疫后,仅在一只接受较高剂量疫苗的猴子中检测到病毒血症。回收的病毒具有与疫苗株相同的生长特性。当埃及伊蚊吸食接受较低剂量疫苗的猴子时,它们未被感染。正如预期的那样,免疫在任何动物中均未产生疾病迹象。检测到对疫苗的剂量反应;所有5只高剂量接受者均产生了中和抗体,而10只低剂量接受者中只有5只产生了中和抗体。在两组中,中和抗体通常是短暂的。在接种野生型DEN-2病毒后4至6个月接受攻击的动物中,30天时中和抗体的存在并不总是与免受病毒血症的保护相关。然而,免疫动物在受到攻击后产生了回忆性抗体反应,且无一表现出对感染的不良反应。初次免疫4个月后对猴子进行再次免疫导致产生低滴度但持续的中和抗体,从而保护动物免受野生型病毒攻击。