急性基孔肯雅病患者的先天免疫反应。

IF 5.5 3区 医学 Q1 IMMUNOLOGY Medical Microbiology and Immunology Pub Date : 2023-08-01 DOI:10.1007/s00430-023-00771-y
Wallace Pitanga Bezerra, Raíza Nara Cunha Moizéis, Amanda Costa Ayres Salmeron, Hannaly Wana Bezerra Pereira, Josélio Maria Galvão de Araújo, Paulo Marcos Matta Guedes, José Veríssimo Fernandes, Manuela Sales Lima Nascimento
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引用次数: 0

摘要

基孔肯雅病(CHIKD)是一种高发病率的虫媒病毒病,主要由关节痛引起。炎症介质包括IL-6、IL-1β、GM-CSF等与CHIKD的发病机制有关,而I型干扰素可能与更好的结果相关。模式识别受体的作用尚未得到充分的研究。在这里,我们评估了rna特异性PRRs及其接头分子和下游细胞因子在急性CHIKD患者中的表达。在症状出现后第3 ~ 5天招募28例患者进行临床检查、外周血采集和PBMC qRT-PCR分析,与健康对照组进行比较(n = 20)。我们观察到急性CHIKD的常见症状,发烧、关节痛、头痛和肌痛是最常见的。与未感染的对照组相比,急性CHIKV感染上调了受体TLR3、RIG-I和MDA5的表达,也上调了接头分子TRIF的表达。在细胞因子表达方面,我们发现IL-6、IL-12、IFN-α、IFN-β和IFN-γ上调,这些因子与炎症或抗病毒反应直接相关。TLR3-TRIF轴与IL-6、IFN-α高表达相关。有趣的是,在CHIKD急性患者中,MDA5、IL-12和IFN-α的高表达与较低的病毒载量有关。总之,这些发现有助于完成急性CHIKD期间先天免疫激活的图景,同时证实了强烈抗病毒反应的诱导。在了解CHIKD的免疫病理和病毒清除机制方面,下一步的工作对于开发有效的治疗方法以减轻这种使人衰弱的疾病的严重程度至关重要。
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Innate immune response in patients with acute Chikungunya disease.

Chikungunya disease (CHIKD) is an arbovirose that presents with high morbidity, mainly due to arthralgia. Inflammatory mediators including IL-6, IL-1β, GM-CSF and others have been implicated in the pathogenesis of CHIKD, whilst type I interferons can be associated with better outcomes. The role of pattern recognition receptors has been studied incompletely. Here, we evaluated the expression of RNA-specific PRRs, their adaptor molecules and downstream cytokines in acute CHIKD patients. Twenty-eight patients were recruited during the 3rd-5th day after the symptoms onset for clinical examination, peripheral blood collection and qRT-PCR analysis of PBMC to compare to the healthy control group (n = 20). We observed common symptoms of acute CHIKD, with fever, arthralgia, headache and myalgia being the most frequent. Compared with uninfected controls, acute CHIKV infection upregulates the expression of the receptors TLR3, RIG-I and MDA5, and also the adaptor molecule TRIF. Regarding cytokine expression, we found an upregulation of IL-6, IL-12, IFN-α, IFN-β and IFN-γ, which are related directly to the inflammatory or antiviral response. The TLR3-TRIF axis correlated with high expression of IL-6 and IFN-α. Interestingly, greater expression of MDA5, IL-12 and IFN-α was related to lower viral loads in CHIKD acute patients. Together, these findings help to complete the picture of innate immune activation during acute CHIKD, while confirming the induction of strong antiviral responses. Drawing the next steps in the understanding of the immunopathology and virus clearance mechanisms of CHIKD should be of utter importance in the aid of the development of effective treatment to reduce the severity of this debilitating disease.

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来源期刊
CiteScore
10.60
自引率
0.00%
发文量
29
审稿时长
1 months
期刊介绍: Medical Microbiology and Immunology (MMIM) publishes key findings on all aspects of the interrelationship between infectious agents and the immune system of their hosts. The journal´s main focus is original research work on intrinsic, innate or adaptive immune responses to viral, bacterial, fungal and parasitic (protozoan and helminthic) infections and on the virulence of the respective infectious pathogens. MMIM covers basic, translational as well as clinical research in infectious diseases and infectious disease immunology. Basic research using cell cultures, organoid, and animal models are welcome, provided that the models have a clinical correlate and address a relevant medical question. The journal also considers manuscripts on the epidemiology of infectious diseases, including the emergence and epidemic spreading of pathogens and the development of resistance to anti-infective therapies, and on novel vaccines and other innovative measurements of prevention. The following categories of manuscripts will not be considered for publication in MMIM: submissions of preliminary work, of merely descriptive data sets without investigation of mechanisms or of limited global interest, manuscripts on existing or novel anti-infective compounds, which focus on pharmaceutical or pharmacological aspects of the drugs, manuscripts on existing or modified vaccines, unless they report on experimental or clinical efficacy studies or provide new immunological information on their mode of action, manuscripts on the diagnostics of infectious diseases, unless they offer a novel concept to solve a pending diagnostic problem, case reports or case series, unless they are embedded in a study that focuses on the anti-infectious immune response and/or on the virulence of a pathogen.
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