多价和多病原体病毒载体疫苗。

Q2 Biochemistry, Genetics and Molecular Biology Clinical and Vaccine Immunology Pub Date : 2017-01-05 Print Date: 2017-01-01 DOI:10.1128/CVI.00298-16
Katharina B Lauer, Ray Borrow, Thomas J Blanchard
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引用次数: 0

摘要

抗原的呈现和传递对于诱导免疫以及理想的终生保护至关重要。重组病毒载体--在兽用疫苗应用中被证明是安全和成功的--是传递外来蛋白的理想载体,通过模拟自然感染诱导具有保护性抗体水平的免疫反应。病毒载体的一些例子包括腺病毒、麻疹病毒或痘病毒。作为疫苗载体的必要条件如下:将编码序列稳定插入基因组、诱导保护性免疫反应、经证实的安全记录以及大规模生产的潜力。由于需要开发新的传染病疫苗、提高疫苗的可及性、降低医疗成本并简化超负荷的免疫计划,人们产生了将来自相同或不同病原体的抗原组合在一起的想法。有些疫苗需要一种病原体或不同病原体血清型/血清群的多种抗原组合(多价疫苗或多价疫苗)才能提供有效保护。未来的多价候选疫苗很可能是疟疾和艾滋病毒等复杂疾病所必需的。其他新战略则建议将不同病原体的抗原组合在一起,以同时预防几种疾病(多病或多病原体疫苗)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Multivalent and Multipathogen Viral Vector Vaccines.

The presentation and delivery of antigens are crucial for inducing immunity and, desirably, lifelong protection. Recombinant viral vectors-proven safe and successful in veterinary vaccine applications-are ideal shuttles to deliver foreign proteins to induce an immune response with protective antibody levels by mimicking natural infection. Some examples of viral vectors are adenoviruses, measles virus, or poxviruses. The required attributes to qualify as a vaccine vector are as follows: stable insertion of coding sequences into the genome, induction of a protective immune response, a proven safety record, and the potential for large-scale production. The need to develop new vaccines for infectious diseases, increase vaccine accessibility, reduce health costs, and simplify overloaded immunization schedules has driven the idea to combine antigens from the same or various pathogens. To protect effectively, some vaccines require multiple antigens of one pathogen or different pathogen serotypes/serogroups in combination (multivalent or polyvalent vaccines). Future multivalent vaccine candidates are likely to be required for complex diseases like malaria and HIV. Other novel strategies propose an antigen combination of different pathogens to protect against several diseases at once (multidisease or multipathogen vaccines).

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来源期刊
Clinical and Vaccine Immunology
Clinical and Vaccine Immunology 医学-传染病学
CiteScore
2.88
自引率
0.00%
发文量
0
审稿时长
1.5 months
期刊介绍: Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.
期刊最新文献
Correction for Nishimori et al., “Identification of an Atypical Enzootic Bovine Leukosis in Japan by Using a Novel Classification of Bovine Leukemia Based on Immunophenotypic Analysis” GI-19007, a Novel Saccharomyces cerevisiae-Based Therapeutic Vaccine against Tuberculosis. High-Definition Mapping of Four Spatially Distinct Neutralizing Epitope Clusters on RiVax, a Candidate Ricin Toxin Subunit Vaccine. Progress toward Development of a Vaccine against Congenital Cytomegalovirus Infection. Stable Chromosomal Expression of Shigella flexneri 2a and 3a O-Antigens in the Live Salmonella Oral Vaccine Vector Ty21a.
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