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Introductory Chapter: Immunization - Vaccine Adjuvant Delivery System and Strategies 导论章:免疫-疫苗佐剂输送系统和策略
Pub Date : 2018-11-05 DOI: 10.5772/INTECHOPEN.81981
Ning Wang, Ting Wang
Immunization plays a key role in maintaining human health as it saves millions of lives in the most economical way from lethal pathogens and other fatal diseases each year, thanks to the advanced development of model vaccines, which are biological preparations containing an antigenic agent that resembles a disease-causing microorganism to stimulate the host’s immune system, thus providing active acquired immunity to a particular disease and destroying it [1, 2]. Since Jenner’s pioneering inoculations in the late eighteenth century, vaccines have been successfully developed to combat various diseases and each year saved numerous lives from, mostly, lethal infections and now also certain cancers [3, 4]. Especially, taking advantage of the tools discovered in microbiology and immunology, vaccines have recently obtained great achievements as demonstrated by their successful performances in conquering some formidable pathogens, such as smallpox and rabies, which are used to claim many lives. However, the list of pathogens for which there exist no vaccines is still long, and, in particular, many pathogens, such as human immunodeficiency virus (HIV), herpes simplex virus (HSV), and Ebola virus (EBV), are still posing a big threat to human life, therefore needing urgently the effective products to cope with their infections [5].
免疫在维持人类健康方面发挥着关键作用,因为由于模型疫苗的先进发展,它每年以最经济的方式从致命病原体和其他致命疾病中拯救数百万人的生命。模型疫苗是一种生物制剂,含有一种类似于致病微生物的抗原剂,可以刺激宿主的免疫系统,从而提供对特定疾病的主动获得性免疫并摧毁它[1,2]。自从詹纳在18世纪晚期开创性地接种疫苗以来,疫苗已经成功地发展用于对抗各种疾病,每年都挽救了许多人的生命,其中大多数是致命的感染,现在也包括某些癌症[3,4]。特别是,利用在微生物学和免疫学中发现的工具,疫苗最近取得了巨大的成就,这表明它们在征服一些可怕的病原体方面取得了成功,例如天花和狂犬病,这些病原体夺去了许多人的生命。然而,没有疫苗的病原体名单仍然很长,特别是许多病原体,如人类免疫缺陷病毒(HIV)、单纯疱疹病毒(HSV)、埃博拉病毒(EBV),仍然对人类生命构成很大威胁,因此迫切需要有效的产品来应对它们的感染。
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引用次数: 0
Practical Finance Strategies in Immunization 实用的免疫财务策略
Pub Date : 2018-11-05 DOI: 10.5772/INTECHOPEN.78719
L. Zaremba
My first goal is to present the basic immunization problem (BIP) as it is understood in finance. BIP relies on a construction of such a bond portfolio (BP), meaning a selection of individual bonds, that the single liability to pay L dollars q years from now will be discharged by means of BP (a patient will return to health at time q ), no matter what random shift a(t) (a particular disease) will occur in the future. What kind of a function is a shift of interest rates is critically important because both present and future values of BP depend solely on underlying interest rates. Having identified shifts (diseases) against which a BP is immunized, the natural question arises how to find among such immunized (immune) portfolios the best ones. In the context of finance, it means bond portfolios with maximal unanticipated rate of return. My second goal is to trigger interest among medical scientists by suggesting that certain finance notions, such as duration and convexity of a bond portfolio, might give extra insight to medical researchers working in the immunization area both into BIP and into similar problems in medicine. A considerable attention is also paid to certain mathematical notions (base of a linear space, a Hilbert space, triangular functions) because of their successful applications to problem-solving occurring in bond portfolio immunization.
我的第一个目标是介绍金融学中所理解的基本免疫问题(BIP)。BIP依赖于这样一个债券组合(BP)的构建,即单个债券的选择,无论未来发生什么随机变化a(t)(特定疾病),从现在起q年后支付L美元的单一负债将通过BP(患者将在q时间恢复健康)来解除。利率变动是什么样的函数至关重要,因为BP的现在和未来价值都完全取决于基础利率。在确定了BP可以免疫的变化(疾病)之后,自然会出现如何在这些免疫(免疫)组合中找到最佳组合的问题。在金融领域,它是指具有最大意外收益率的债券组合。我的第二个目标是,通过提出某些金融概念(如债券投资组合的持续时间和凸性),可能会让免疫领域的医学研究人员对BIP和医学领域的类似问题有更多的了解,从而引发医学科学家的兴趣。由于某些数学概念(线性空间的基,希尔伯特空间,三角函数)成功地应用于债券投资组合免疫问题的解决,因此也给予了相当大的关注。
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引用次数: 0
Polymeric Nanoparticles Engineered as a Vaccine Adjuvant-Delivery System 聚合纳米颗粒工程作为疫苗佐剂递送系统
Pub Date : 2018-11-05 DOI: 10.5772/INTECHOPEN.81084
B. Liu, Zhangbao Wu, Ting Liu, Ruifeng Qian, Tingni Wu, Qingchuan Liu, Aizong Shen
Global immunization saves millions of human lives each year through using vaccines, which include whole microbe-based products and the subunit ones formulated with just the components of antigens able to stimulate immune system to establish specific immunity against diseases. Subunit vaccines show numerous advantages, such as defined components, high safety profile, and production without the use of dangerous pathogens, but also limited capacity in eliciting immunity due to the lack of other components than antigens, including the immunostimulatory elements of pathogen- associated molecular patterns which are able to activate the innate immunoreponses. Recently, nanoparticles (NPs) formulated with polymeric materials, such as poly(lactic- co-glycolic acid), viral proteins, chitosan, hyaluronic acid, and polystyrene, with some bearing intrinsic adjuvanticity, are widely employed as vaccine adjuvant-delivery sys- tems (VADSs) and show great potential in developing subunit vaccines. Particularly, the polymeric NPs engineered with functional materials possess many features, such as targeting delivery, lysosome escape, anti-damaging protection, and ability to guide immune reactions toward a Th1 (T helper type 1) and Th2 pathway, which are crucial for establishing humoral and cellular immunity. This chapter describes polymeric NP-based VADSs designed for developing subunit vaccines able to elicit Ag-specific immunity at both systemic and mucosal levels via different vaccination routes. cell line expression system [28]. The researchers demonstrated that mice vaccinated by intranasal prime followed by two sub-cheek boosts with VLPs adjuvanted with liposomes entrapping TLR3 ligand dsRNA were stimulated to secrete high titers of Abs against the Ags, with predominant IgG2c over IgG and produce a significantly increased germinal center B cells and T follicular cells, suggesting that the VLP-based VADS is superior for induction of a Th1-biased immune response, while prolonging lymph node germinal centers, T follicular cells, and generating neutralizing antibodies, and thus is rather suitable for making HIV vaccines [26].
全球免疫每年通过使用疫苗挽救数百万人的生命,其中包括基于整个微生物的产品和仅由抗原成分配制的亚基产品,这些抗原成分能够刺激免疫系统建立针对疾病的特异性免疫。亚单位疫苗具有许多优点,如成分明确、安全性高、生产时不使用危险病原体,但由于缺乏抗原以外的其他成分,包括能够激活先天免疫反应的病原体相关分子模式的免疫刺激成分,其激发免疫的能力也有限。近年来,由聚乳酸-羟基乙酸、病毒蛋白、壳聚糖、透明质酸和聚苯乙烯等高分子材料配制的纳米颗粒(NPs)具有一定的内在佐剂性,被广泛用作疫苗佐剂递送系统(vads),在亚单位疫苗的开发中显示出巨大的潜力。特别是,用功能材料设计的聚合物NPs具有许多特性,如靶向递送,溶酶体逃逸,抗损伤保护,以及引导免疫反应向Th1 (T辅助型1)和Th2途径的能力,这对于建立体液和细胞免疫至关重要。本章描述了基于聚合np的vads,设计用于开发亚单位疫苗,能够通过不同的接种途径在全身和粘膜水平引发ag特异性免疫。细胞系表达系统[28]。研究人员证明,通过鼻内启动疫苗接种小鼠,然后用脂质体包裹TLR3配体dsRNA佐剂VLPs两次脸颊下刺激,可分泌高滴度的针对Ags的抗体,其中IgG2c多于IgG,并产生显著增加的生发中心B细胞和T滤泡细胞,这表明基于vlp的VADS在诱导th1偏向性免疫应答方面更优越,同时延长淋巴结生发中心。T滤泡细胞,并产生中和抗体,因此非常适合制作HIV疫苗[26]。
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引用次数: 6
Vaccine Adjuvant Delivery Systems Constructed Using Biocompatible Nanoparticles Formed through Self-Assembly of Small Molecules 利用小分子自组装形成的生物相容性纳米颗粒构建疫苗佐剂递送系统
Pub Date : 2018-11-05 DOI: 10.5772/INTECHOPEN.79905
Ting Liu, Ruifeng Qian, Qingchuan Liu, Tingni Wu, Jia-Li Chen
Subunit vaccines are playing a critical role in controlling numerous diseases and attract - ing more and more research interests due to their numerous advantages over conventional whole microbe-based vaccines. However, subunit vaccines are weak immunogens and thus have limited capacity in eliciting the humoral and cellular immunity against pathogens. Recently, nanoparticles (NPs) formed with certain small molecules through self-assembly have been employed as an effective carrier for subunit vaccines to play roles of adjuvant, delivery and stabilization of antigens, thus engendering a vaccine adjuvant-delivery system (VADS), which shows promises to overcome the hurdles in developing subunit vaccines. In particular, the small molecule-self-assembled NPs as a VADS can not only deliver vaccine ingredients to immune cells but also influence the immunoresponse toward a Th1 (type 1 T helper cell) and Th2 balanced pathway to establish both humoral and cellular immunity. This chapter describes the innovative VADSs based on the small molecule-self-assembled NPs, such as metal NPs (mNPs), emulsions, liposomes, and ISCOMs, which are elaborately designed for the development of subunit vaccines. interfacial Emulsions, based on structural of three classical types of single emulsions, double emulsions and Pickering emulsions: single emulsions oil-in-water (O/W) type denoting oil droplets emulsified in a bulk aqueous phase, vice versa, the (W/O) emulsions O/W/O
亚单位疫苗与传统的全微生物疫苗相比具有许多优点,在控制多种疾病方面发挥着关键作用,并吸引了越来越多的研究兴趣。然而,亚单位疫苗是弱免疫原,因此在激发对病原体的体液和细胞免疫方面能力有限。近年来,一些小分子通过自组装形成的纳米颗粒(NPs)被用作亚单位疫苗的有效载体,发挥抗原的佐剂、递送和稳定作用,从而产生了疫苗佐剂递送系统(VADS),有望克服亚单位疫苗开发中的障碍。特别是,作为VADS的小分子自组装NPs不仅可以将疫苗成分传递给免疫细胞,还可以影响对Th1(1型T辅助细胞)和Th2平衡通路的免疫应答,从而建立体液和细胞免疫。本章描述了基于小分子自组装NPs的创新性vads,如金属NPs (mNPs)、乳剂、脂质体和ISCOMs,它们被精心设计用于亚单位疫苗的开发。界面乳液,基于单乳液、双乳液和Pickering乳液三种经典的结构类型:单乳液水包油(O/W)型表示油滴在体水相中乳化,反之为(W/O)型O/W/O
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引用次数: 0
Preventing Vaccine Failure in Poultry Flocks 预防禽群疫苗失效
Pub Date : 2018-11-05 DOI: 10.5772/INTECHOPEN.79330
A. Sharif, T. Ahmad
Poultry sector is very useful for humans in terms of production of food items like meat and eggs. Pakistan has a developing poultry sector and is the second important sector after the textile industry. The poultry sector is encountered with many challenges; among them is the high incidence of disease outbreaks that result in colossal economic losses. The diseases of commercial and rural poultry include Newcastle disease (ND), infec- tious bursal disease (IBD), fowl pox, Marek’s disease, infectious bronchitis (IB), avian influenza, hydropericardium syndrome, etc. The disease outbreaks have also occurred in vaccinated flocks. Better understanding of the causes of vaccine failure will result in iden tifying prophylactic measures regarding disease outbreaks in poultry flocks. This chapter overviews the common causes of vaccine failure and further highlights the procedures for successful immunization.
家禽业在生产肉类和蛋类等食品方面对人类非常有用。巴基斯坦的家禽业正在发展,是仅次于纺织业的第二大重要产业。家禽业面临许多挑战;其中之一是疾病爆发的高发生率,造成巨大的经济损失。商品家禽和农村家禽的疾病包括新城疫、传染性法氏囊病、禽痘、马雷克氏病、传染性支气管炎、禽流感、心包积液综合征等。在接种疫苗的鸡群中也发生了疾病暴发。更好地了解疫苗失败的原因将有助于确定针对禽群疾病暴发的预防措施。本章概述了疫苗失败的常见原因,并进一步强调了成功免疫的程序。
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引用次数: 18
Vaccines Developed for Cancer Immunotherapy 癌症免疫治疗疫苗的开发
Pub Date : 2018-11-05 DOI: 10.5772/INTECHOPEN.80889
Aizong Shen, Ruifeng Qian, Ting Liu, Qingchuan Liu, Bin Liu, Zhangbao Wu
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引用次数: 0
期刊
Immunization - Vaccine Adjuvant Delivery System and Strategies
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