Ah-Ra Lee, Woo-Jin Kim, Haeyoun Choi, Sang-Hyun Kim, Su-Yeon Hong, Sang-Mu Shim, Hee Il Lee, Jae Min Song, Seong-Jun Kim, Tomohiro Ishikawa, Ji-Man Kang, Hyeon-Seok Eom, Sang-Uk Seo
{"title":"基于基因型 III 的日本脑炎疫苗对再次流行的基因型 V 的中和反应减弱。","authors":"Ah-Ra Lee, Woo-Jin Kim, Haeyoun Choi, Sang-Hyun Kim, Su-Yeon Hong, Sang-Mu Shim, Hee Il Lee, Jae Min Song, Seong-Jun Kim, Tomohiro Ishikawa, Ji-Man Kang, Hyeon-Seok Eom, Sang-Uk Seo","doi":"10.1093/infdis/jiae589","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Japanese encephalitis (JE) has been predominantly controlled through vaccination. However, the isolation of JE virus (JEV) genotype V (GV) in China in 2009, and the subsequent alarming increase in JE cases in the Republic of Korea since 2010, present a new challenge.</p><p><strong>Methods: </strong>Serum samples from individuals vaccinated with genotype III (GIII)-based JE vaccines were analyzed for neutralizing seroresponse to GV isolates.</p><p><strong>Results: </strong>Serum from immunocompromised pediatric patients vaccinated with an inactivated JE vaccine showed higher 50% plaque reduction neutralization test geometric mean titer (GMT) against GIII Nakayama (11 358; 95% confidence interval [CI], 1790-29 658), but lower GMTs against GV isolates: GV Muar (499; 95% CI, 0-2437), GV 43279 (308; 95% CI, 159-582), and GV 43413 (231; 95% CI, 108-738). Similarly, 32 healthy volunteers receiving a live attenuated JE vaccine achieved 100% seroprotection against GIII Nakayama with GMT of 338 (95% CI, 304-651) at 1 month postvaccination. However, GMTs against GV isolates were 123 (95% CI, 102-446) for GV Muar, 81 (95% CI, 63-168) for GV 43279, and 107 (95% CI, 100-322) for GV 43413, not achieving 100% seroprotection against these isolates. At 6 months postvaccination, GMT against Nakayama increased to 696 (95% CI, 409-2353), while remaining similar for GV isolates.</p><p><strong>Conclusions: </strong>Our study underscores that current GIII-based vaccines do not provide comparable protection against GV JEVs, impacting individuals in both current and potential endemic regions, as well as travelers to these regions.</p>","PeriodicalId":50179,"journal":{"name":"Journal of Infectious Diseases","volume":" ","pages":"1281-1289"},"PeriodicalIF":5.0000,"publicationDate":"2025-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genotype III-Based Japanese Encephalitis Vaccines Exhibit Diminished Neutralizing Response to Reemerging Genotype V.\",\"authors\":\"Ah-Ra Lee, Woo-Jin Kim, Haeyoun Choi, Sang-Hyun Kim, Su-Yeon Hong, Sang-Mu Shim, Hee Il Lee, Jae Min Song, Seong-Jun Kim, Tomohiro Ishikawa, Ji-Man Kang, Hyeon-Seok Eom, Sang-Uk Seo\",\"doi\":\"10.1093/infdis/jiae589\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Japanese encephalitis (JE) has been predominantly controlled through vaccination. However, the isolation of JE virus (JEV) genotype V (GV) in China in 2009, and the subsequent alarming increase in JE cases in the Republic of Korea since 2010, present a new challenge.</p><p><strong>Methods: </strong>Serum samples from individuals vaccinated with genotype III (GIII)-based JE vaccines were analyzed for neutralizing seroresponse to GV isolates.</p><p><strong>Results: </strong>Serum from immunocompromised pediatric patients vaccinated with an inactivated JE vaccine showed higher 50% plaque reduction neutralization test geometric mean titer (GMT) against GIII Nakayama (11 358; 95% confidence interval [CI], 1790-29 658), but lower GMTs against GV isolates: GV Muar (499; 95% CI, 0-2437), GV 43279 (308; 95% CI, 159-582), and GV 43413 (231; 95% CI, 108-738). Similarly, 32 healthy volunteers receiving a live attenuated JE vaccine achieved 100% seroprotection against GIII Nakayama with GMT of 338 (95% CI, 304-651) at 1 month postvaccination. However, GMTs against GV isolates were 123 (95% CI, 102-446) for GV Muar, 81 (95% CI, 63-168) for GV 43279, and 107 (95% CI, 100-322) for GV 43413, not achieving 100% seroprotection against these isolates. At 6 months postvaccination, GMT against Nakayama increased to 696 (95% CI, 409-2353), while remaining similar for GV isolates.</p><p><strong>Conclusions: </strong>Our study underscores that current GIII-based vaccines do not provide comparable protection against GV JEVs, impacting individuals in both current and potential endemic regions, as well as travelers to these regions.</p>\",\"PeriodicalId\":50179,\"journal\":{\"name\":\"Journal of Infectious Diseases\",\"volume\":\" \",\"pages\":\"1281-1289\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-06-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Infectious Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/infdis/jiae589\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/infdis/jiae589","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景:日本脑炎(JE)主要通过疫苗接种得到控制。然而,2009 年中国分离出基因 V 型日本脑炎病毒 (JEV),以及随后自 2010 年以来大韩民国日本脑炎病例的惊人增长带来了新的挑战:方法:分析接种了基于基因型 III(GIII)的 JE 疫苗的个体血清样本对 GV 分离物的中和血清反应:结果:接种了灭活 JE 疫苗的免疫力低下的儿科患者的血清对 GIII Nakayama 的 50%斑块缩小中和试验(PRNT50)几何平均滴度(GMT)较高(11 358;95% CI = 1 790,29 658),但对 GV 分离物的几何平均滴度较低:GV Muar(499;95% CI = 0,2437)、GV 43279(308;95% CI = 159,582)和 GV 43413(231;95% CI = 108,738)。同样,32 名健康志愿者在接种 JE 减毒活疫苗后 1 个月,对 GIII Nakayama 的血清保护率达到 100%,GMT 为 338(95% CI = 304,651)。然而,针对GV分离株的GMT值分别为:GV Muar为123(95% CI = 102,446),GV 43279为81(95% CI = 63,168),GV 43413为107(95% CI = 100,322),对这些分离株的血清保护率未达到100%。接种后6个月,针对中山株的GMT增加到696(95% CI = 409, 2,353),而针对GV分离株的GMT保持相似:我们的研究强调,目前基于 GIII 的疫苗不能提供针对 GV JEV 的类似保护,这对目前和潜在流行地区的个人以及前往这些地区的旅行者都有影响。
Genotype III-Based Japanese Encephalitis Vaccines Exhibit Diminished Neutralizing Response to Reemerging Genotype V.
Background: Japanese encephalitis (JE) has been predominantly controlled through vaccination. However, the isolation of JE virus (JEV) genotype V (GV) in China in 2009, and the subsequent alarming increase in JE cases in the Republic of Korea since 2010, present a new challenge.
Methods: Serum samples from individuals vaccinated with genotype III (GIII)-based JE vaccines were analyzed for neutralizing seroresponse to GV isolates.
Results: Serum from immunocompromised pediatric patients vaccinated with an inactivated JE vaccine showed higher 50% plaque reduction neutralization test geometric mean titer (GMT) against GIII Nakayama (11 358; 95% confidence interval [CI], 1790-29 658), but lower GMTs against GV isolates: GV Muar (499; 95% CI, 0-2437), GV 43279 (308; 95% CI, 159-582), and GV 43413 (231; 95% CI, 108-738). Similarly, 32 healthy volunteers receiving a live attenuated JE vaccine achieved 100% seroprotection against GIII Nakayama with GMT of 338 (95% CI, 304-651) at 1 month postvaccination. However, GMTs against GV isolates were 123 (95% CI, 102-446) for GV Muar, 81 (95% CI, 63-168) for GV 43279, and 107 (95% CI, 100-322) for GV 43413, not achieving 100% seroprotection against these isolates. At 6 months postvaccination, GMT against Nakayama increased to 696 (95% CI, 409-2353), while remaining similar for GV isolates.
Conclusions: Our study underscores that current GIII-based vaccines do not provide comparable protection against GV JEVs, impacting individuals in both current and potential endemic regions, as well as travelers to these regions.
期刊介绍:
Published continuously since 1904, The Journal of Infectious Diseases (JID) is the premier global journal for original research on infectious diseases. The editors welcome Major Articles and Brief Reports describing research results on microbiology, immunology, epidemiology, and related disciplines, on the pathogenesis, diagnosis, and treatment of infectious diseases; on the microbes that cause them; and on disorders of host immune responses. JID is an official publication of the Infectious Diseases Society of America.