Bahrami Fariborz, Masoudzadeh Nasrin, Van Veen Suzanne, Persson Josefine, Lari Arezou, Sarvnaz Hamzeh, Taslimi Yasaman, Östensson Malin, Andersson Björn, Sharifi Iraj, Goyonlo Vahid Mashayekhi, Ottenhoff Tom Hm, Haks Mariëlle C, Harandi Ali M, Rafati Sima
Department of Immunology, Pasteur Institute of Iran, Tehran, Iran.
Department of Immunotherapy and Leishmania Vaccine Research, Pasteur Institute of Iran, Tehran, Iran.
Mol Immunol. 2022 Sep;149:165-173. doi: 10.1016/j.molimm.2022.07.008. Epub 2022 Jul 26.
Cutaneous leishmaniasis (CL) is a neglected tropical disease with severe morbidity and socioeconomic sequelae. A better understanding of underlying immune mechanisms that lead to different clinical outcomes of CL could inform the rational design of intervention measures. While transcriptomic analyses of CL lesions were recently reported by us and others, there is a dearth of information on the expression of immune-related genes in the blood of CL patients. Herein, we investigated immune-related gene expression in whole blood samples collected from individuals with different clinical stages of CL along with healthy volunteers in an endemic CL region where Leishmania (L.) tropica is prevalent. Study participants were categorized into asymptomatic (LST+) and healthy uninfected (LST-) groups based on their leishmanin skin test (LST). Whole blood PAXgene samples were collected from volunteers, who had healed CL lesions, and patients with active L. tropica cutaneous lesions. Quality RNA extracted from 57 blood samples were subjected to Dual-color reverse-transcription multiplex ligation-dependent probe amplification (dcRT-MLPA) assay for profiling 144 immune-related genes. Results show significant changes in the expression of genes involved in interferon signaling pathway in the blood of active CL patients, asymptomatics and healed individuals. Nonetheless, distinct profiles for several immune-related genes were identified in the healed, the asymptomatic, and the CL patients compared to the healthy controls. Among others, IFI16 and CCL11 were found as immune transcript signatures for the healed and the asymptomatic individuals, respectively. These results warrant further exploration to pinpoint novel blood biomarkers for different clinical stages of CL.
皮肤利什曼病(CL)是一种被忽视的热带疾病,具有严重的发病率和社会经济后果。更好地了解导致CL不同临床结果的潜在免疫机制,可为合理设计干预措施提供依据。虽然我们和其他人最近报道了CL病变的转录组分析,但关于CL患者血液中免疫相关基因表达的信息却很匮乏。在此,我们调查了在热带利什曼原虫(L. tropica)流行的CL流行地区,从不同临床阶段的CL患者以及健康志愿者采集的全血样本中免疫相关基因的表达情况。根据利什曼原虫皮肤试验(LST),研究参与者被分为无症状(LST+)和健康未感染(LST-)组。从已治愈CL病变的志愿者和患有活动性热带利什曼原虫皮肤病变的患者中采集全血PAXgene样本。从57份血液样本中提取的高质量RNA进行双色逆转录多重连接依赖探针扩增(dcRT-MLPA)分析,以分析144个免疫相关基因。结果显示,活动性CL患者、无症状者和已治愈个体血液中参与干扰素信号通路的基因表达有显著变化。尽管如此,与健康对照相比,在已治愈者、无症状者和CL患者中发现了几种免疫相关基因的不同表达谱。其中,IFI16和CCL11分别被发现是已治愈者和无症状个体的免疫转录特征。这些结果值得进一步探索,以确定CL不同临床阶段的新型血液生物标志物。