VISAVET Health Surveillance Centre, Complutense University of Madrid, Madrid, Spain.
Department of Animal Health, Faculty of Veterinary, Complutense University of Madrid, Madrid, Spain.
Vet Q. 2024 Dec;44(1):1-13. doi: 10.1080/01652176.2024.2331525. Epub 2024 Mar 27.
Despite the great interest in the development of a vaccine against African swine fever (ASF) in wild boar, the immunological mechanisms that induce animal protection are still unknown. For this purpose, tertiary lymphoid organs (TLOs) of wild boar were characterised and compared with mucosa-associated lymphoid tissues (MALTs) by histopathology, histomorphometry and immunohistochemistry (CD3, CD79, PAX5, LYVE1, fibronectin). In addition, real-time polymerase chain reaction (qPCR) and immunohistochemistry (p72) were used to evaluate the presence of ASF virus (ASFV) in blood and tissues samples, respectively. TLOs were observed in animals infected with a low-virulent ASFV isolate (LVI), animals co-infected with low and high-virulent ASFV isolates (LVI-HVI) and animals infected only with the high virulence isolate (HVI). TLOs in LVI and LVI-HVI groups were located adjacent to the mucosa and presented a similar structure to MALT. Immunoexpresion of p72 observed in the inflammatory cells adjacent to TLOs/MALTs confirmed its development and reactivity generated by ASF attenuated isolates. Immunohistochemical evaluation, based on cellular composition (T and B lymphocytes), and histomorphometrical study revealed a more pronounced maturation of TLOs/MALTs in the LVI-HVI group. It is currently unclear whether these formations play a protective role by contributing to local immunity in chronic inflammatory diseases. However, the structural similarities between TLOs and MALTs and the location of TLOs close to the mucosa suggest that they may perform a similar function, facilitating a local protective response. Nevertheless, further investigations are warranted to assess the cellular and humoral dynamics of these lymphoid organs induced by attenuated isolates.
尽管人们对开发针对野猪非洲猪瘟(ASF)的疫苗非常感兴趣,但诱导动物保护的免疫机制仍不清楚。为此,通过组织病理学、组织形态计量学和免疫组织化学(CD3、CD79、PAX5、LYVE1、纤维连接蛋白)对野猪的三级淋巴器官(TLO)进行了表征,并与黏膜相关淋巴组织(MALT)进行了比较。此外,实时聚合酶链反应(qPCR)和免疫组织化学(p72)分别用于评估血液和组织样本中 ASF 病毒(ASFV)的存在。在感染低毒力 ASFV 分离株(LVI)的动物、感染低毒力和高毒力 ASFV 分离株的动物(LVI-HVI)以及仅感染高毒力分离株的动物(HVI)中观察到 TLO。LVI 和 LVI-HVI 组中的 TLO 位于黏膜附近,具有与 MALT 相似的结构。在 TLO/MALT 附近的炎症细胞中观察到的 p72 的免疫表达证实了其由 ASF 减毒分离株产生的发育和反应性。基于细胞组成(T 和 B 淋巴细胞)的免疫组织化学评估和组织形态计量学研究表明,LVI-HVI 组中 TLO/MALT 的成熟度更为明显。目前尚不清楚这些形成物是否通过为慢性炎症性疾病中的局部免疫做出贡献而发挥保护作用。然而,TLO 与 MALTs 之间的结构相似性以及 TLO 靠近黏膜的位置表明它们可能具有相似的功能,促进局部保护反应。然而,需要进一步研究来评估减毒分离株诱导这些淋巴器官的细胞和体液动力学。