Fredeking Terry M, Zavala-Castro Jorge E, González-Martínez Pedro, Moguel-Rodríguez William, Sanchez Ernesto C, Foster Michael J, Diaz-Quijano Fredi A
Departamento de Epidemiologia, Faculdade de Saude Publica da Universidade de Sao Paulo, Av. Dr. Arnaldo, 715, Cerqueira Cesar, CEP 01246-904, Sao Paulo, SP, Brazil.
Recent Pat Antiinfect Drug Discov. 2015;10(1):51-8. doi: 10.2174/1574891x10666150410153839.
To determine the effect of doxycycline treatment on cytokine levels, including tumor necrosis factor (TNF) and interleukin 6 (IL-6), and mortality in dengue patients at high risk of complication.
A group of dengue hemorrhagic fever patients (n=231) were randomized to receive either standard supportive care or supportive care in addition to oral doxycycline twice daily for 7 days. Dengue virus infection was confirmed by PCR using multiple primers. Serum samples were obtained at days 0, 3, 5 and 7 and tested for levels of TNF and IL-6.
Doxycycline-treated group presented a 46% lower mortality than that observed in the untreated group (11.2% [13/116] vs 20.9% [24/115], respectively, p=0.05). Moreover, administration of doxycycline resulted in a significant (p<0.01) decrease in levels of TNF and IL-6 versus controls in the tests performed during follow-up (day 3, 5 and 7). Patients who died in both groups possessed significantly (p<0.01) higher levels of TNF and IL-6 compared to those who survived at all-time points.
The above findings suggest that doxycycline can provide a clinical benefit to dengue patients at high risk of complications. This effect could be mediated by decreasing pro-inflammatory cytokine levels.
确定强力霉素治疗对细胞因子水平(包括肿瘤坏死因子(TNF)和白细胞介素6(IL-6))的影响,以及对有并发症高风险的登革热患者死亡率的影响。
一组登革出血热患者(n = 231)被随机分为两组,一组接受标准支持治疗,另一组除标准支持治疗外,每天口服两次强力霉素,持续7天。使用多种引物通过PCR确认登革病毒感染。在第0、3、5和7天采集血清样本,检测TNF和IL-6水平。
强力霉素治疗组的死亡率比未治疗组低46%(分别为11.2% [13/116] 和20.9% [24/115],p = 0.05)。此外,在随访期间(第3、5和7天)进行的测试中,与对照组相比,强力霉素的使用导致TNF和IL-6水平显著降低(p < 0.01)。与在所有时间点存活的患者相比,两组中死亡的患者TNF和IL-6水平均显著更高(p < 0.01)。
上述研究结果表明,强力霉素可为有并发症高风险的登革热患者带来临床益处。这种效果可能是通过降低促炎细胞因子水平来介导的。