Pooja Tiwary, Krishil Oswal, Ryan Varghese, Harsh Anchan, Mitul Oswal
{"title":"多表位疫苗:绘制猴痘预防和控制的新前沿。","authors":"Pooja Tiwary, Krishil Oswal, Ryan Varghese, Harsh Anchan, Mitul Oswal","doi":"10.1007/s13577-025-01255-2","DOIUrl":null,"url":null,"abstract":"<p><p>Monkeypox is a viral zoonotic infection that has emerged as a significant public health threat recently. The world has experienced a global outbreak of the Monkeypox virus (MPXV), with 124,753 confirmed cases in 128 countries and a total of 272 fatalities as of February 13, 2025. This alarming increase in cases demands immediate attention to the underlying causes of the surge. The World Health Organization (WHO) has endorsed the use of the MVA-BN vaccine, which was previously approved for smallpox prevention. However, there are currently no antiviral treatments approved by the FDA for MPXV. In addition, the emergence of mutations in MPXV strains poses challenges for the development and effectiveness of viable vaccines. Developing conventional vaccines is typically expensive, time-consuming, and requires extensive validation processes. Moreover, these vaccines often demonstrate suboptimal efficacy against emerging viral strains. As a response to these challenges, multi-epitope vaccines have gained significant interest for their potential to activate B-cell and T-cell responses, providing prolonged immunological activity against pathogens. These vaccines feature a targeted approach, offering chemical stability, non-infectious properties, rapid and cost-effective production, enhanced safety, and the potential to elicit a robust immune response. Several studies employing immunoinformatics have confirmed the efficacy of multi-epitope vaccines, designed to provide comprehensive immune protection against MPXV. These vaccines promise to deliver a strong immune response, better coverage against various viral strains and variants, and improved stability and effectiveness. In addition, they are expected to be non-allergenic, non-toxic, and highly antigenic. While promising results have been reported regarding the use of these vaccines for monkeypox, further research on their efficacy, delivery systems, and additional preclinical and clinical trials is crucial to maximize their benefits for humanity.</p>","PeriodicalId":49194,"journal":{"name":"Human Cell","volume":"38 5","pages":"126"},"PeriodicalIF":3.4000,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multi-epitope vaccines: charting a new frontier in monkeypox prevention and control.\",\"authors\":\"Pooja Tiwary, Krishil Oswal, Ryan Varghese, Harsh Anchan, Mitul Oswal\",\"doi\":\"10.1007/s13577-025-01255-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Monkeypox is a viral zoonotic infection that has emerged as a significant public health threat recently. The world has experienced a global outbreak of the Monkeypox virus (MPXV), with 124,753 confirmed cases in 128 countries and a total of 272 fatalities as of February 13, 2025. This alarming increase in cases demands immediate attention to the underlying causes of the surge. The World Health Organization (WHO) has endorsed the use of the MVA-BN vaccine, which was previously approved for smallpox prevention. However, there are currently no antiviral treatments approved by the FDA for MPXV. In addition, the emergence of mutations in MPXV strains poses challenges for the development and effectiveness of viable vaccines. Developing conventional vaccines is typically expensive, time-consuming, and requires extensive validation processes. Moreover, these vaccines often demonstrate suboptimal efficacy against emerging viral strains. As a response to these challenges, multi-epitope vaccines have gained significant interest for their potential to activate B-cell and T-cell responses, providing prolonged immunological activity against pathogens. These vaccines feature a targeted approach, offering chemical stability, non-infectious properties, rapid and cost-effective production, enhanced safety, and the potential to elicit a robust immune response. Several studies employing immunoinformatics have confirmed the efficacy of multi-epitope vaccines, designed to provide comprehensive immune protection against MPXV. These vaccines promise to deliver a strong immune response, better coverage against various viral strains and variants, and improved stability and effectiveness. In addition, they are expected to be non-allergenic, non-toxic, and highly antigenic. While promising results have been reported regarding the use of these vaccines for monkeypox, further research on their efficacy, delivery systems, and additional preclinical and clinical trials is crucial to maximize their benefits for humanity.</p>\",\"PeriodicalId\":49194,\"journal\":{\"name\":\"Human Cell\",\"volume\":\"38 5\",\"pages\":\"126\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-07-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Human Cell\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s13577-025-01255-2\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s13577-025-01255-2","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
Multi-epitope vaccines: charting a new frontier in monkeypox prevention and control.
Monkeypox is a viral zoonotic infection that has emerged as a significant public health threat recently. The world has experienced a global outbreak of the Monkeypox virus (MPXV), with 124,753 confirmed cases in 128 countries and a total of 272 fatalities as of February 13, 2025. This alarming increase in cases demands immediate attention to the underlying causes of the surge. The World Health Organization (WHO) has endorsed the use of the MVA-BN vaccine, which was previously approved for smallpox prevention. However, there are currently no antiviral treatments approved by the FDA for MPXV. In addition, the emergence of mutations in MPXV strains poses challenges for the development and effectiveness of viable vaccines. Developing conventional vaccines is typically expensive, time-consuming, and requires extensive validation processes. Moreover, these vaccines often demonstrate suboptimal efficacy against emerging viral strains. As a response to these challenges, multi-epitope vaccines have gained significant interest for their potential to activate B-cell and T-cell responses, providing prolonged immunological activity against pathogens. These vaccines feature a targeted approach, offering chemical stability, non-infectious properties, rapid and cost-effective production, enhanced safety, and the potential to elicit a robust immune response. Several studies employing immunoinformatics have confirmed the efficacy of multi-epitope vaccines, designed to provide comprehensive immune protection against MPXV. These vaccines promise to deliver a strong immune response, better coverage against various viral strains and variants, and improved stability and effectiveness. In addition, they are expected to be non-allergenic, non-toxic, and highly antigenic. While promising results have been reported regarding the use of these vaccines for monkeypox, further research on their efficacy, delivery systems, and additional preclinical and clinical trials is crucial to maximize their benefits for humanity.
期刊介绍:
Human Cell is the official English-language journal of the Japan Human Cell Society. The journal serves as a forum for international research on all aspects of the human cell, encompassing not only cell biology but also pathology, cytology, and oncology, including clinical oncology. Embryonic stem cells derived from animals, regenerative medicine using animal cells, and experimental animal models with implications for human diseases are covered as well.
Submissions in any of the following categories will be considered: Research Articles, Cell Lines, Rapid Communications, Reviews, and Letters to the Editor. A brief clinical case report focusing on cellular responses to pathological insults in human studies may also be submitted as a Letter to the Editor in a concise and short format.
Not only basic scientists but also gynecologists, oncologists, and other clinical scientists are welcome to submit work expressing new ideas or research using human cells.