Department of Biology and Medical Parasitology, Pomeranian Medical University in Szczecin, 70-204, Szczecin, Poland.
Department of Histology and Embryology, Pomeranian Medical University in Szczecin, 70-204, Szczecin, Poland.
Parasit Vectors. 2018 Sep 20;11(1):517. doi: 10.1186/s13071-018-3108-x.
Acanthamoebiasis is most often found in patients with immune deficiency, with infections facilitated by the intake of immunosuppressive drugs. The host immune response to Acanthamoeba spp. infection is poorly understood. Thus, in this study, we aimed to examine the course of Acanthamoeba spp. infection taking into account the host's immunological status, including assessment of the hematological parameters, cytokine analysis, immunophenotypic changes in spleen populations, and histological spleen changes, which could help clarify some aspects of the immune response to acanthamoebiasis. In our experimental study, we used Acanthamoeba strain AM 22 isolated from the bronchoaspirate of a patient with acute myeloid leukaemia (AML) and atypical pneumonia symptoms.
Acanthamoeba spp. affected the hematological parameters in immunocompetent and immunosuppressed mice and induced a change in spleen weight during infection. Moreover, analysis of anti-inflammatory (IL-4 and IL-10) and pro-inflammatory (IL-17A and IFN-γ) cytokines produced by splenocytes stimulated with concanavalin A demonstrated that Acanthamoeba spp. induced a selective Th1, Th2 and Th17 response at later stages of the infection in immunocompetent hosts. In the case of hosts with low immunity, Acanthamoeba elicited robust Th1 cell-mediated immunity without the participation of Th17. We observed suppression of CD8+ and CD4+ T lymphocytes and CD3+CD4-CD8- double-negative (DN) T lymphocyte populations in the beginning, and in the case of CD3+/CD4+/CD8+ double-positive (DP) T cells in the final phase of Acanthamoeba spp. infection in hosts with low immunity. Also, CD4+T lymphocytes and CD3+/CD4+ and CD3+/CD8+ lymphocyte counts during each stage of acanthamoebiasis were shown to be upregulated.
We demonstrated that analysis of the immune response and pathogenesis mechanisms of clinical isolates of Acanthamoeba spp. in an animal model not only has purely cognitive significance but above all, may help in the development of effective methods of pharmacological therapy especially in patients with low immunity.
棘阿米巴病最常发生于免疫功能低下的患者,免疫抑制药物的摄入可促进感染。宿主对棘阿米巴属感染的免疫反应知之甚少。因此,在这项研究中,我们旨在研究棘阿米巴属感染的过程,同时考虑宿主的免疫状态,包括评估血液学参数、细胞因子分析、脾群体免疫表型变化和组织学脾变化,这有助于阐明对棘阿米巴病的免疫反应的某些方面。在我们的实验研究中,我们使用了从患有急性髓细胞白血病(AML)和非典型肺炎症状的患者支气管吸出物中分离出的棘阿米巴菌株 AM 22。
棘阿米巴属影响免疫功能正常和免疫抑制的小鼠的血液学参数,并在感染过程中引起脾重变化。此外,分析用刀豆蛋白 A 刺激的脾细胞产生的抗炎(IL-4 和 IL-10)和促炎(IL-17A 和 IFN-γ)细胞因子表明,棘阿米巴属在免疫功能正常的宿主感染后期诱导了选择性的 Th1、Th2 和 Th17 反应。在免疫力低下的宿主中,棘阿米巴属引起强烈的 Th1 细胞介导的免疫反应,而没有 Th17 的参与。我们观察到在感染的开始时,CD8+和 CD4+T 淋巴细胞以及 CD3+CD4-CD8-双阴性(DN)T 淋巴细胞群受到抑制,而在免疫力低下的宿主中,棘阿米巴属感染的最后阶段,CD3+/CD4+/CD8+双阳性(DP)T 细胞受到抑制。此外,在棘阿米巴病的每个阶段,CD4+T 淋巴细胞和 CD3+/CD4+和 CD3+/CD8+淋巴细胞计数均上调。
我们证明了在动物模型中分析棘阿米巴属临床分离株的免疫反应和发病机制不仅具有纯粹的认知意义,而且最重要的是,可能有助于开发特别是在免疫力低下的患者中有效的药物治疗方法。