Bangwen Eugene, Berens-Riha Nicole, de Vrij Nicky, Ceulemans Ann, Brosius Isabel, De Vos Elise, Pham Thao-Thy, Bottieau Emmanuel, van Griensven Johan, Netongo Palmer Masumbe, Van Esbroeck Marjan, Vercauteren Koen, Van Dijck Christophe, Adriaensen Wim, Liesenborghs Laurens
Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Virology, Antiviral Drug & Vaccine Research Group, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
J Med Virol. 2025 Apr;97(4):e70320. doi: 10.1002/jmv.70320.
Previous studies indicated Clade I monkeypox virus infection to be associated with marked elevation of proinflammatory cytokines. This remains unexplored for Clade II-associated disease, which has different clinical manifestations and prognosis. We used a 65-plex cytokine, chemokine, and growth factor (CCG) panel to analyze serum samples of 100 male acute Clade IIb mpox patients and 26 healthy controls in Belgium. Cluster analyses revealed no strong or distinct CCG profiles distinguishing mpox patients from controls but suggested trends in certain cytokine modulation. Individual CCG analyses found elevated levels of cytokines (MIF, CD30, IL2R, IL18, APRIL, and TNFRII), chemokines (CCL4, CCL8, CCL22, CCL24, CXCL9, CXCL10, CXCL11, CXCL12, and CXCL13), and growth factors (HGF and VEGFA) in patients, while CCL11 and CXCL5 were significantly suppressed. We detected no differences in key proinflammatory cytokines, IL-1α, IL-1β, IL-6, IL-8 or anti-inflammatory cytokines, IL-4, IL-10, IL-13. In patients living with HIV, comparison with pre-outbreak samples showed an increase in CXCL13 and a decrease in CXCL5, CCL2, CCL24, HGF, SCF, and TWEAK. The absence of discriminatory CCG profiles in Clade IIb mpox patients compared to healthy controls suggests there may be limited clinical applications of those markers.
先前的研究表明,I 分支猴痘病毒感染与促炎细胞因子的显著升高有关。对于具有不同临床表现和预后的 II 分支相关疾病,这一点尚未得到探索。我们使用了一个包含 65 种细胞因子、趋化因子和生长因子(CCG)的检测板,对比利时 100 名男性急性 IIb 分支猴痘患者和 26 名健康对照的血清样本进行了分析。聚类分析显示,没有强烈或明显的 CCG 谱能够区分猴痘患者和对照组,但提示了某些细胞因子调节的趋势。个体 CCG 分析发现,患者体内细胞因子(MIF、CD30、IL2R、IL18、APRIL 和 TNFRII)、趋化因子(CCL4、CCL8、CCL22、CCL24、CXCL9、CXCL10、CXCL11、CXCL12 和 CXCL13)和生长因子(HGF 和 VEGFA)水平升高,而 CCL11 和 CXCL5 则受到显著抑制。我们未检测到关键促炎细胞因子 IL-1α、IL-1β、IL-6、IL-8 或抗炎细胞因子 IL-4、IL-10、IL-13 存在差异。在感染 HIV 的患者中,与暴发前样本相比,CXCL13 升高,而 CXCL5、CCL2、CCL24、HGF、SCF 和 TWEAK 降低。与健康对照相比,IIb 分支猴痘患者缺乏可区分的 CCG 谱,这表明这些标志物的临床应用可能有限。