绵羊肝脏组织病理学和免疫组化评估

IF 2.7 2区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE Animals Pub Date : 2024-06-20 DOI:10.3390/ani14121833
Guillem Herrera-Torres, María T Ruiz-Campillo, María J Bautista, Francisco J Martínez-Moreno, Rafael Zafra, Leandro Buffoni, Pablo J Rufino-Moya, Álvaro Martínez-Moreno, Verónica Molina-Hernández, José Pérez
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引用次数: 0

摘要

法氏囊病是家畜的一种重要经济疾病。由于目前的抗蠕虫药疗法已难以为继,因此全球都在关注保护性疫苗的开发。要设计出有效的疫苗,就必须更好地了解宿主与寄生虫之间的相互作用。迄今为止,很少有研究通过比较感染和再感染动物来评估宿主与寄生虫之间的相互作用。本研究评估了感染和再感染肝包虫病的绵羊在急性和慢性感染阶段的肝脏显微病变。组织病理学研究显示,在感染初期,初感组(PI)和再感组(RI)都存在与幼虫迁移相关的坏死灶(NF1)。在 PI 组的感染晚期和 RI 组的感染早期和晚期,在肿大的胆管附近发现了广泛的坏死/出血灶(NF2),其中一些含有成虫,这表明寄生虫可能在进食时引起了 NF2。免疫组化研究显示,与 UC 组相比,PI 组和 RI 组的 Foxp3+ T 细胞都有所增加,与 PI 组相比,RI 组 NF1 附近的浸润也有所增加,这表明肝蝇会诱导 Foxp3 T 细胞扩增,以促进寄生虫的存活。此外,在 PI 组和 RI 组中,以及在感染的急性和慢性阶段,都发现 iNOS 的表达较差,同时 CD163 的表达较强,这表明肝脏病变中巨噬细胞的 M2 激活明显,这可能与愈合过程有关,也可能有利于寄生虫的存活。PI 和 RI 动物的主要区别在于嗜酸性粒细胞和 Foxp3+ T 细胞的浸润更为严重,而 RI 并未改变巨噬细胞的 M2 激活,这种激活在原始感染的早期阶段就已出现。
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Liver Histopathological and Immunohistochemical Evaluation from Fasciola hepatica Experimentally Infected and Reinfected Sheep.

Fasciolosis is an important economic disease of livestock. There is a global interest in the development of protective vaccines since the current anthelmintic therapy is no longer sustainable. A better knowledge of the host-parasite interaction is needed to design effective vaccines. To date, few studies have evaluated host-parasite interaction by comparing infected and reinfected animals. The present study evaluates the microscopical hepatic lesions in sheep infected and reinfected with Fasciola hepatica during the acute and chronic stages of infection. The histopathological study revealed the presence of necrotizing foci (NF1) associated with larvae migration during the early stages of infection in the primoinfected (PI) and reinfected (RI) groups. In the late stages of infection of the PI group and at the early and late stages of infection in the RI groups, extensive necrotizing/hemorrhagic foci (NF2) were found in the vicinity of enlarged bile ducts, some containing adult flukes, suggesting parasites may have caused NF2 while feeding. The immunohistochemical study revealed an increase in Foxp3+ T cells in both PI and RI groups with respect to the UC group and in the infiltrates adjacent to NF1 in the RI groups with respect to the PI group, suggesting the F. hepatica induce Foxp3 T cell expansion to facilitate parasite survival. In addition, in both the PI and RI groups, and during acute and chronic stages of the infection, a poor expression of iNOS was found accompanied by a strong expression of CD163, suggesting a marked M2 activation of macrophages in the hepatic lesions, which may be related with healing processes, and it also may facilitate parasite survival. The main differences between PI and RI animals were the more severe infiltration of eosinophils and Foxp3+ T cells, whereas RI did not modify M2 activation of macrophages which occurs since the early stages of primoinfection.

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来源期刊
Animals
Animals Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
4.90
自引率
16.70%
发文量
3015
审稿时长
20.52 days
期刊介绍: Animals (ISSN 2076-2615) is an international and interdisciplinary scholarly open access journal. It publishes original research articles, reviews, communications, and short notes that are relevant to any field of study that involves animals, including zoology, ethnozoology, animal science, animal ethics and animal welfare. However, preference will be given to those articles that provide an understanding of animals within a larger context (i.e., the animals'' interactions with the outside world, including humans). There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental details and/or method of study, must be provided for research articles. Articles submitted that involve subjecting animals to unnecessary pain or suffering will not be accepted, and all articles must be submitted with the necessary ethical approval (please refer to the Ethical Guidelines for more information).
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