宠物肿瘤及其免疫治疗进展

肿瘤是人类和宠物的常见病,恶性肿瘤对人类和宠物的健康构成严重危害。人类和宠物肿瘤病理改变极为相似,研究宠物肿瘤在比较医学和人类肿瘤上均具有重要学术价值。本文仅就临床常见15种宠物肿瘤病理特点和免疫治疗研究进展作一简述,供临床宠物肿瘤病理诊断和免疫治疗参考。     

宠物与人类健康

本文围绕宠物与人类健康主题,阐述了宠物对人类健康的积极作用;宠物对人类健康的负面影响,并对保障我国宠物业健康发展提出建议。     

宠物和实验动物

宠物在我国已经成为一个日渐壮大的产业和庞大的群体。宠物与人类朝夕相处,最容易成为动物源性疾病的传染源,对人类健康造成潜在威胁。为了人类自身和宠物健康,我们必须对宠物投入更多的关注。宠物和实验动物作为两种不同用途的动物,存在众多的相似点。我国已经建立了相对完善的实验动物生产、使用、质量保障和福利的管理体系。实验动物的管理体系也许可以为宠物的生产、饲养、质量保证和福利的管理体系提供借鉴。     

宠物会引发人类传染病吗?

Q:宠物会引发人类传染病,你知道吗?A:动物是各种病原体的储存库,绝大多数动物是人畜共患病的传染源和贮存宿主。人们身边的宠物能携带某些疾病的病原,它自己不生病,但能将多种疾病传播给人类。随着人们生活水平的提高及人口老龄化,豢养宠物已成为一种生活上的享受和乐趣。特别是豢养犬、猫,各种禽类、鸟类等很多见。有些人与宠物同居一堂,餐具不分,甚至带着宠物同床睡觉。这说明宠物已直接进入家庭生活,对人类健康造成的隐患也越来越多。     

野生动物与宠物

动物可分为野生动物和家养动物,越来越多的野生动物被人们当作宠物来饲养。野生动物作为宠物的危害是巨大的。野生动物对人类的危害主要包括直接攻击人类,携带病原威胁人类以及对环境设施造成的破坏。人类对野生动物的危害包括野生动物驯养繁殖、疾病传播等方面。野生动物对家养动物的危害包括直接危害和疾病危害。因此,野生动物不适合作为宠物饲养,不仅仅是因为它们原本的生活习性,对野生动物资源的破坏,更重要的是病原体可能跨越种间障碍而威胁人类的安全。     

宠物狂犬病及其防控

本文对狂犬病在犬、猫等宠物中的流行情况;宠物狂犬病及其危害;宠物狂犬病的预防及国外宠物狂犬病的防控经验等进行了综述,为保证宠物和人类健康、有效防控宠物狂犬病提供参考。     

宠物重要人兽共患病毒病

随着人们生活水平的不断提高,城市家庭饲养宠物日益增多,宠物已经成为人们日常生活中接触最多的动物。然而,许多宠物是人兽共患疾病的重要传染源,随着人类与各种动物间＂零＂距离的接触,各种宠物携带的人兽共患病也悄然传入人类,给人们身体健康和公共卫生安全带来了严重的威胁。近年来,许多学者对犬、猫、鸟、鼠和其他宠物易感的人兽共患病毒病开展了许多研究工作,本文对狂犬病、戊型肝炎、禽流感、淋巴细胞脉络膜脑膜炎、流行性出血热、西尼罗热等一些严重危害的宠物人兽共患病毒病进行了概述。     

宠物化学药物研究

为正确导向宠物化学药物的发展,提高研制水平,避免＂超级细菌＂的产生,保护人类医疗资源,本文简述了宠物化学药物的研究现状,剖析了宠物化学药物的研究过程中存在的问题,提出了我国宠物化学药物创新发展战略,并展望了宠物化学药物的发展前景。科学使用宠物专用化学药物不仅促进宠物产业乃至整个畜牧业的健康发展,而且对降低耐药性产生,保护人类健康也具有重要的公共卫生学意义。     

我国宠物业现状、机遇与挑战

我国宠物业是一个朝阳产业,发展速度快,问题多,整体水平不高,以市场化为主。宠物业的发展应当是全面的,逐步走向成熟。我们在宠物饲养观念、宠物在社会生活中的作用研究、宠物疾病防治、宠物与人共患疾病的关注度、宠物医疗、宠物药品、宠物食品、宠物医学教育等全方位面临机会和挑战。今后,中国大陆的宠物业在宠物疫苗研制、新宠物药品研发、新中兽药研制和推广、高质量宠物食品和处方食品生产、高水平的宠物医疗机构的扩展、和宠物与人类比较医学上必将得到很大的发展机会。     

结核病动物模型研究进展

结核病是由结核分枝杆菌感染引起的传染病,是危害人类健康的主要传染病之一。动物模型已经成为研究人类传染病的标准化工具。虽然对于结核分枝杆菌而言并没有真正意义的动物资源,但由于不同种类的动物,对分枝杆菌的敏感性不一样,因此可以成为结核病研究的有利工具。结核病最常用的实验动物模型包括小鼠、兔和豚鼠。每种动物有其自身特点,但并不能完全模拟人类疾病。通过建立结核病的动物模型,可以大大增加我们对疾病的病因、毒力和发病机制的理解。除了这三种模型外,非人灵长类也常被用于结核病的研究。本文总结了这几种结核病模型的研究状况。     

结核分枝杆菌感染动物模型的研究进展

人类结核病位居单一病原引起死亡的严重传染病之首,结核分枝杆菌是其主要病原.尽管结核分枝杆菌可引起许多种动物感染并患病,但人类是其主要宿主.动物模型作为研究人类疾病的标准化工具,虽然不能完全模拟人类结核病的整个过程,但可成为研究结核病的有用工具,有助于研究其发病机制、治疗过程及宿主对病原的免疫病理学反应.由于不同种类动物...     

结核分枝杆菌感染实验模型

结核分枝杆菌是引起人结核病的主要病原,全世界约有1/3人口感染结核分枝杆菌。尽管该病原可感染并引起许多动物疾病,但人类是其中心宿主。为研究结核分枝杆菌的致病机理及宿主对本病原的保护性和免疫病理学反应,选择合适的动物模型非常必要。本文阐述了结核病研究中常用的实验模型及各种模型的优缺点。实验模型的合理应用将促进我们对结核病的认识,从中获取的资料将有助于我们发现更好的预防和治疗方案。     

From the mouths of monkeys: detection of Mycobacterium tuberculosis complex DNA from buccal swabs of synanthropic macaques

Although the Mycobacterium tuberculosis complex (MTBC) infects a third of all humans, little is known regarding the prevalence of mycobacterial infection in nonhuman primates (NHP). For more than a century, tuberculosis has been regarded as a serious infectious threat to NHP species. Advances in the detection of MTBC open new possibilities for investigating the effects of this poorly understood pathogen in diverse populations of NHP. Here, we report results of a cross-sectional study using well-described molecular methods to detect a nucleic acid sequence (IS6110) unique to the MTBC. Sample collection was focused on the oral cavity, the presumed route of transmission of MTBC. Buccal swabs were collected from 263 macaques representing 11 species in four Asian countries and Gibraltar. Contexts of contact with humans included free ranging, pets, performing monkeys, zoos, and monkey temples. Following DNA isolation from buccal swabs, the polymerase chain reaction (PCR) amplified IS6110 from 84 (31.9%) of the macaques. In general, prevalence of MTBC DNA was higher among NHP in countries where the World Health Organization reports higher prevalence of humans infected with MTBC. This is the first demonstration of MTBC DNA in the mouths of macaques. Further research is needed to establish the significance of this finding at both the individual and population levels. PCR of buccal samples holds promise as a method to elucidate the mycobacterial landscape among NHP, particularly macaques that thrive in areas of high human MTBC prevalence.     

Paleopathological and biomolecular study of tuberculosis in a medieval skeletal collection from England

Nine human skeletons of medieval date from a rural English burial site show signs of skeletal tuberculosis. They were subject to polymerase chain reaction (PCR) assays aimed at detecting traces of DNA from infecting mycobacteria, with the purpose both of confirming the paleopathological diagnosis of tuberculosis and determining in individual cases whether disease was due to M. tuberculosis or M. bovis. In all nine cases, evidence for M. tuberculosis complex DNA was found, and in all instances it appeared that disease was due to M. tuberculosis rather than M. bovis. The significance of the findings for understanding tuberculous infection in rural agrarian communities in medieval England is discussed.     

Identification of Mycobacterium marinum virulence genes using signature-tagged mutagenesis and the goldfish model of mycobacterial pathogenesis

Mycobacterium marinum, a causative agent of fish tuberculosis, is one of the most closely related Mycobacterium species (outside the M. tuberculosis complex) to M. tuberculosis, the etiologic agent of human tuberculosis. Signature-tagged mutagenesis was used to identify genes of M. marinum required for in vivo survival in a goldfish model of mycobacterial pathogenesis. Screening the first 1008 M. marinum mutants led to the identification of 40 putative virulence mutants. DNA sequence analysis of these 40 mutants identified transposon insertions in 35 unique loci. Twenty-eight out of 33 (85%) loci encoding putative virulence genes have homologous genes in M. tuberculosis.     

结核分枝杆菌在动物中的流行与传播

结核分枝杆菌(Mycobacterium tuberculosis)是一种重要的人兽共患病病原菌,人类是其主要宿主。千百年来,由于动物与人类关系密切,动物也成为结核分枝杆菌的重要宿主,且感染结核分枝杆菌的动物还能成为传染源,将其传播至人类和其他动物。关于动物感染结核分枝杆菌已有大量报道,包括大象、非人灵长类动物、貘、海狮、犬、猫、牛、鸟等。本文就结核分枝杆菌在野生动物、家畜中的流行与传播进行介绍,总结其在动物间传播的主要途径。     

分枝杆菌枝菌酸合成及其调控

结核病是危害人类健康的重要传染病,每年200多万人死于结核病。耐(多)药菌株的出现、与HIV共感染以及人口老龄化等原因与全球结核病的卷土重来密切相关。枝菌酸是存在于结核分枝杆菌、其他分枝杆菌和许多放线菌的细胞壁中的关键组分,与结核分枝杆菌的致病、毒力和免疫逃避都有关系。枝菌酸在抗结核研究中有着极其重要的地位。结核分枝杆菌枝菌酸的生物合成途径一直是很重要的抗结核药物靶标,异烟肼、乙胺丁醇等抗结核药物都是以此为靶标。深入研究枝菌酸的合成、调控有助于发现更多的药物靶标,为开发结核病控制新措施提供基础。本文综述了结核分枝杆菌枝菌酸的结构与分类、生物合成途径及其调控、作为抗结核药物靶标的前景与应用,以期对枝菌酸有更深入的了解并为新型抗结核药物靶标的发现提供基础。     

巨噬细胞凋亡对结核分枝杆菌感染的机制研究进展

结核病是一种严重危害人类健康的慢性传染性疾病,主要由结核分枝杆菌感染导致,结核分枝杆菌进入人体后,与免疫防御的第一道屏障—巨噬细胞发生反应,部分菌株在细胞内长期生存、繁殖,是导致结核病转归的决定性因素。感染早期,结核分枝杆菌的繁殖受到巨噬细胞凋亡的抑制,随着高效价、高毒力菌株繁殖速度的增加,抗巨噬细胞凋亡作用不断增强,使自身繁殖得到有效保护,为菌株的生长提供了充足、适宜的胞内环境。因此,调控结核分枝杆菌对巨噬细胞凋亡进程的抑制作用,是预防和治疗结核病的关键。     

Negotiated Bonds: The Practice of Childfree Pet Parenting

The American Pet Products Association reports a decade-long increase of pet spending, estimated to reach over $69 billion in 2017. In some cases, these owners apply traditional parenting practices while nurturing their pets. Relatedly, a growing number of pet owners identify themselves as “pet parents.” This study is the first known work to investigate how identity plays a role in the growing population of pet parents. While previous research into the pet parenting phenomenon has sought to quantify the demographics, spending, and frequency of this population, less work seeks to understand what pet parenting looks like in practice. Sampling a population of childfree pet parents, the current study utilized semi-structured interviews and identified two common themes in their daily practice of the identity: 1) Despite the use of parent–child terms and strategies, childfree pet parents are acutely aware of the differences between raising children and raising pets, and 2) pet parents ascribe agency to their pet, identifying individual pet wants and needs to fulfill. This may further inform future research on human–animal relationships by establishing a human identity that connects directly to pet practices in the United States, asking us to consider the lived experiences of this growing population and their pets including spending, lifestyle, and attachment concerns.     

Antitubercular activity of trifluoperazine, a calmodulin antagonist

Trifluoperazine, a calmodulin antagonist, completely inhibited the growth of mycobacteria. The minimum inhibitory concentrations in shake cultures in a synthetic medium containing 0.2% Tween 80 were 5 and 8 micrograms/ml, respectively, for the human pathogenic strain Mycobacterium tuberculosis H37Rv and M. tuberculosis resistant to isoniazid. When added to a growing culture of M. tuberculosis H37Rv on the 10th day (mid exponential phase), trifluoperazine 50 micrograms/ml further arrested growth of this organism. It is suggested that trifluoperazine or similar calmodulin antagonists might be useful as antitubercular drugs.