National Clinical Research Center for Infectious Diseases, The First Affiliated Hospital, College of Medicine, Zhejiang University, Qingchun Rd, Hangzhou, China.
The State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, College of Medicine, Zhejiang University, Qingchun Rd, Hangzhou, China.
Mediators Inflamm. 2019 Dec 31;2019:2053958. doi: 10.1155/2019/2053958. eCollection 2019.
Serum cytokines/chemokines play important roles in cryptococcal meningitis, but it is unclear whether cytokines/chemokines in cerebrospinal fluid (CSF) contribute to high intracranial pressure (HICP) in HIV-associated cryptococcal meningitis (HCM).
CSF cytokines/chemokines were assayed in 17 HIV-uninfected patients, 26 HIV-infected patients without CNS infection, and 39 HCM patients at admission. Principal component analysis and correlation and logistic regression analyses were used to assess the relationships between these parameters.
The CSF Th1, Th2, and macrophage cytokines showed an obvious increase in HCM patients as compared to the HIV-uninfected patients and HIV-infected patients without CNS infection. CSF IL-6, GM-CSF, and IL-8 were positively correlated with CSF fungal burden. Serum CD4 count, CSF Th1 cytokines (TNF-, TNF-, IL-12, IL-1, IL-12, IL-1, TNF-, TNF-, IL-12, IL-1, and IL-12) and Th2 cytokines (IL-4 and IL-10) contribute to HICP.
Overall, the present findings indicated that both pro- and anti-inflammatory cytokines of Th1, Th2, and macrophage origin contributed to the development of HCM. Specifically, the chemokine and cytokine cascade caused by skewing of the Th1-Th2 balance and reduced CD4 count were found to be important contributors to HICP. . Our research suggested that chemokine and cytokine cascade caused by skewing of the Th1-Th2 balance in HIV-infected patients played more important role than Cryptococcus numbers and size in CSF on the development of high intracranial pressure in HIV-associated cryptococcal meningitis, providing a new understanding of mechanisms of HCM.
血清细胞因子/趋化因子在隐球菌性脑膜炎中发挥重要作用,但尚不清楚脑脊液(CSF)中的细胞因子/趋化因子是否有助于 HIV 相关隐球菌性脑膜炎(HCM)中的颅内压升高(HICP)。
在入院时检测了 17 名未感染 HIV 的患者、26 名未感染 HIV 且无中枢神经系统感染的患者和 39 名 HCM 患者的 CSF 细胞因子/趋化因子。使用主成分分析和相关性及逻辑回归分析来评估这些参数之间的关系。
与未感染 HIV 的患者和未感染 HIV 且无中枢神经系统感染的患者相比,HCM 患者的 CSF Th1、Th2 和巨噬细胞细胞因子明显增加。CSF IL-6、GM-CSF 和 IL-8 与 CSF 真菌负荷呈正相关。血清 CD4 计数、CSF Th1 细胞因子(TNF-α、TNF-β、IL-12、IL-1β、IL-1β、TNF-β、TNF-α、IL-1β、TNF-β、IL-1β 和 IL-12)和 Th2 细胞因子(IL-4 和 IL-10)有助于 HICP。
总的来说,目前的研究结果表明,Th1、Th2 和巨噬细胞来源的促炎和抗炎细胞因子均有助于 HCM 的发展。具体而言,发现由 Th1-Th2 平衡倾斜和 CD4 计数减少引起的趋化因子和细胞因子级联反应是 HICP 的重要原因。我们的研究表明,HIV 感染患者中 Th1-Th2 平衡倾斜引起的趋化因子和细胞因子级联反应在 HIV 相关隐球菌性脑膜炎中对颅内压升高的发展比 CSF 中隐球菌数量和大小更为重要,为理解 HCM 的发病机制提供了新的认识。