循环可溶性因子和t细胞亚群作为人皮肤利什曼病治疗反应的免疫学预测因子

Amanda B Figueiredo, Katia L P Morais, Israel T Silva, Lorhenn B L Maia, Jaqueline R Buttura, Bruna D F Barros, Natalia S Alves, Flavio Pignataro-Oshiro, Samara M M Shimon, Andrea Teixeira-Carvalho, Lucas Almeida, Edgar Carvalho, Paulo Machado, Jenefer M Blackwell, Lea Castellucci, Walderez O Dutra, Kenneth J Gollob
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引用次数: 0

摘要

人类皮肤利什曼病是由巴西利什曼原虫引起的一种被忽视的热带病,由于治疗反应不同,提出了治疗挑战。目前的治疗方法经常遇到有限的疗效和治疗失败,需要更深入地了解免疫发病机制和预测标志物。方法探讨影响人类皮肤利什曼病治疗反应的免疫学因素,重点关注宿主-寄生虫复杂的免疫相互作用。我们在治疗干预前评估了同一个体的血液和病变,并对患者进行了60天的随访以确定治疗效果。我们采用多参数流式细胞术方法分析外周血可溶性因子和t细胞亚群,并对病变活检进行RNA测序分析。结果:我们的研究确定了一组循环可溶性因子作为治疗结果的无创预测指标。此外,我们揭示了循环CD8+粘膜相关不变T (MAIT)细胞与病变病理增加之间的关联,以及难治性患者中CD8+ MAIT细胞相关病变的基因标记。这些发现强调了量身定制的干预措施和新的免疫调节策略的潜力,以提高治疗效果,并解决这种使人衰弱的疾病无反应病例的挑战。
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Circulating Soluble Factors and T-Cell Subsets as Immunological Predictors of Therapy Response in Human Cutaneous Leishmaniasis
Background Human cutaneous leishmaniasis, a neglected tropical disease caused by Leishmania braziliensis, presents treatment challenges due to varying therapeutic responses. Current therapies often encounter limited efficacy and treatment failure, demanding a deeper understanding of immunopathogenesis and predictive markers. Methods We explored the immunological determinants influencing therapy response in human cutaneous leishmaniasis, focusing on the intricate host–parasite immune interactions. We evaluated blood and lesions from the same individuals before therapeutic intervention and followed the patients for 60 days to determine treatment efficacy. We employed multiparameter flow cytometry methods for peripheral blood analysis of soluble factors and T-cell subpopulations, and RNA sequencing for analysis of lesion biopsies. Results Our investigation identified a combined set of circulating soluble factors as promising noninvasive predictive markers for treatment outcomes. Additionally, we reveal an association between circulating CD8+ mucosal-associated invariant T (MAIT) cells with increased lesion pathology, and a gene signature in lesions associated with CD8+ MAIT cells in refractory patients. Conclusions These findings highlight the potential for tailored interventions and novel immunomodulatory strategies to enhance treatment efficacy and address challenges in unresponsive cases of this debilitating disease.
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