Medical Technology Program, School of Allied Health Sciences, Walailak University, Tha Sala, Nakhon Si Thammarat, Thailand.
Department of Medical Technology, University of Santo Tomas, Manila, Philippines.
PLoS Negl Trop Dis. 2023 Jan 30;17(1):e0011061. doi: 10.1371/journal.pntd.0011061. eCollection 2023 Jan.
Few data exist on the distinct cytokine profiles of individuals with malaria coinfections and other diseases. This study focuses on data collation of distinct cytokine profiles between individuals with malaria coinfections and monoinfections to provide evidence for further diagnostic or prognostic studies.
We searched five medical databases, including Embase, MEDLINE, PubMed, Ovid, and Scopus, for articles on cytokines in malaria coinfections published from January 1, 1983 to May 3, 2022, after which the distinct cytokine patterns between malaria coinfection and monoinfection were illustrated in heat maps.
Preliminary searches identified 2127 articles, of which 34 were included in the systematic review. Distinct cytokine profiles in malaria coinfections with bacteremia; HIV; HBV; dengue; filariasis; intestinal parasites; and schistosomiasis were tumor necrosis factor (TNF), interferon (IFN)-γ, IFN-α, interleukin (IL)-1, IL-1 receptor antagonist (Ra), IL-4, IL-7, IL-12, IL-15, IL-17; TNF, IL-1Ra, IL-4, IL-10, IL-12, IL-18, CCL3, CCL5, CXCL8, CXCL9, CXCL11, granulocyte colony-stimulating factor (G-CSF); TNF, IFN-γ, IL-4, IL-6, IL-10, IL-12, CCL2; IFN-γ, IL-1, IL-4, IL-6, IL-10, IL-12, IL-13, IL-17, CCL2, CCL3, CCL4, G-CSF; IL-1Ra, IL-10, CXCL5, CXCL8, CXCL10; TNF, IL-2, IL-4, IL-6, IL-10; and TNF, IFN-γ, IL-4, IL-5, IL-10, transforming growth factor-β, CXCL8, respectively.
This systematic review provides information on distinct cytokine profiles of malaria coinfections and malaria monoinfections. Further studies should investigate whether specific cytokines for each coinfection type could serve as essential diagnostic or prognostic biomarkers for malaria coinfections.
关于疟疾合并感染和其他疾病患者的细胞因子特征,目前数据有限。本研究旨在比较疟疾合并感染和单纯感染患者的细胞因子特征,为进一步的诊断或预后研究提供证据。
我们检索了 Embase、MEDLINE、PubMed、Ovid 和 Scopus 这五个医学数据库,以获取 1983 年 1 月 1 日至 2022 年 5 月 3 日发表的疟疾合并感染细胞因子相关文献,并用热图展示疟疾合并感染和单纯感染的细胞因子特征。
初步检索得到 2127 篇文献,其中 34 篇纳入系统评价。伴有菌血症、HIV、HBV、登革热、丝虫病、肠道寄生虫和血吸虫病的疟疾合并感染的特征性细胞因子分别为肿瘤坏死因子(TNF)、干扰素(IFN)-γ、IFN-α、白细胞介素(IL)-1、IL-1 受体拮抗剂(Ra)、IL-4、IL-7、IL-12、IL-15、IL-17;TNF、IL-1Ra、IL-4、IL-10、IL-12、IL-18、CCL3、CCL5、CXCL8、CXCL9、CXCL11、粒细胞集落刺激因子(G-CSF);TNF、IFN-γ、IL-4、IL-6、IL-10、IL-12、IL-18、CCL2;IFN-γ、IL-1、IL-4、IL-6、IL-10、IL-12、IL-13、IL-17、CCL2、CCL3、CCL4、G-CSF;IL-1Ra、IL-10、CXCL5、CXCL8、CXCL10;TNF、IL-2、IL-4、IL-6、IL-10;TNF、IFN-γ、IL-4、IL-5、IL-10、转化生长因子-β、CXCL8。
本系统评价提供了疟疾合并感染和单纯感染患者的细胞因子特征信息。进一步的研究应探讨每种合并感染类型的特定细胞因子是否可作为疟疾合并感染的重要诊断或预后生物标志物。