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一种用于研究登革热疫苗和评估发病机制的新型综合A129小鼠模型。

A Novel, Comprehensive A129 Mouse Model for Investigating Dengue Vaccines and Evaluating Pathogenesis.

作者信息

Ngwe Tun Mya Myat, Nwe Khine Mya, Balingit Jean Claude, Takamatsu Yuki, Inoue Shingo, Pandey Basu Dev, Urano Takeshi, Kohara Michinori, Tsukiyama-Kohara Kyoko, Morita Kouichi

机构信息

Department of Tropical Viral Vaccine Development, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852-8523, Japan.

Department of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852-8523, Japan.

出版信息

Vaccines (Basel). 2023 Dec 15;11(12):1857. doi: 10.3390/vaccines11121857.

DOI:10.3390/vaccines11121857
PMID:38140260
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10748371/
Abstract

In search of a mouse model for use in evaluating dengue vaccines, we assessed A129 mice that lacked IFN-α/β receptors, rendering them susceptible to dengue virus (DENV) infection. To our knowledge, no reports have evaluated dengue vaccine efficiency using A129 mice. A129 mice were given a single intraperitoneal (IP) or subcutaneous (SC) injection of the vaccine, Dengvaxia. After 14 days of immunization via the IP or SC injection of Dengvaxia, the A129 mice exhibited notably elevated levels of anti-DENV immunoglobulin G and neutralizing antibodies (NAb) targeting all four DENV serotypes, with DENV-4 displaying the highest NAb levels. After challenge with DENV-2, Dengvaxia and mock-immunized mice survived, while only the mock group exhibited signs of morbidity. Viral genome levels in the serum and tissues (excluding the brain) were considerably lower in the immunized mice compared to those in the mock group. The SC administration of Dengvaxia resulted in lower viremia levels than IP administration did. Therefore, given that A129 mice manifest dengue-related morbidity, including viremia in the serum and other tissues, these mice represent a valuable model for investigating novel dengue vaccines and antiviral drugs and for exploring dengue pathogenesis.

摘要

为了寻找一种用于评估登革热疫苗的小鼠模型,我们评估了缺乏I型干扰素(IFN-α/β)受体的A129小鼠,这使得它们易受登革热病毒(DENV)感染。据我们所知,尚无使用A129小鼠评估登革热疫苗效力的报告。给A129小鼠腹腔内(IP)或皮下(SC)单次注射登革热疫苗Dengvaxia。通过IP或SC注射Dengvaxia免疫14天后,A129小鼠针对所有四种DENV血清型的抗DENV免疫球蛋白G和中和抗体(NAb)水平显著升高,其中DENV-4的NAb水平最高。用DENV-2攻击后,接种Dengvaxia疫苗的小鼠和模拟免疫的小鼠均存活,但只有模拟组出现发病迹象。与模拟组相比,免疫小鼠血清和组织(不包括脑)中的病毒基因组水平显著降低。与IP给药相比,Dengvaxia的SC给药导致病毒血症水平更低。因此,鉴于A129小鼠表现出与登革热相关的发病症状,包括血清和其他组织中的病毒血症,这些小鼠是研究新型登革热疫苗和抗病毒药物以及探索登革热发病机制的宝贵模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1342/10748371/5c9b7f55cddb/vaccines-11-01857-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1342/10748371/f6d8f5ec1c24/vaccines-11-01857-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1342/10748371/7749790a2300/vaccines-11-01857-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1342/10748371/3c77cfd94278/vaccines-11-01857-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1342/10748371/8a05e00e8d8a/vaccines-11-01857-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1342/10748371/5c9b7f55cddb/vaccines-11-01857-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1342/10748371/f6d8f5ec1c24/vaccines-11-01857-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1342/10748371/7749790a2300/vaccines-11-01857-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1342/10748371/3c77cfd94278/vaccines-11-01857-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1342/10748371/8a05e00e8d8a/vaccines-11-01857-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1342/10748371/5c9b7f55cddb/vaccines-11-01857-g005.jpg

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NPJ Vaccines. 2022 Oct 31;7(1):132. doi: 10.1038/s41541-022-00537-2.
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Vaccine-induced antibodies to contemporary strains of dengue virus type 4 show a mechanistic correlate of protective immunity.疫苗诱导的针对登革病毒 4 型当代株的抗体显示出保护性免疫的机制相关性。
Cell Rep. 2022 Jun 7;39(10):110930. doi: 10.1016/j.celrep.2022.110930.
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Current Development and Challenges of Tetravalent Live-Attenuated Dengue Vaccines.
四价减毒活疫苗的当前发展与挑战。
Front Immunol. 2022 Feb 24;13:840104. doi: 10.3389/fimmu.2022.840104. eCollection 2022.
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Three-year Efficacy and Safety of Takeda's Dengue Vaccine Candidate (TAK-003).武田公司登革热候选疫苗(TAK-003)的 3 年疗效和安全性。
Clin Infect Dis. 2022 Aug 24;75(1):107-117. doi: 10.1093/cid/ciab864.
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Chikungunya Virus Exposure Partially Cross-Protects against Mayaro Virus Infection in Mice.基孔肯雅病毒暴露可部分交叉保护小鼠免受马亚罗病毒感染。
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