Center for Infectious Diseases, Tulane University Health Sciences Center, New Orleans, LA 70112, USA ; Department of Tropical Medicine, Tulane University Health Sciences Center, New Orleans, LA 70112, USA ; Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30333, USA.
Center for Gene Therapy, Tulane University Health Sciences Center, New Orleans, LA 70112, USA ; Department of Biology, University of Mary Hardin-Baylor, 900 College Street, Box 8432, Belton, TX 76513, USA.
J Immunol Res. 2015;2015:162639. doi: 10.1155/2015/162639. Epub 2015 Sep 30.
To examine human gene expression during uncomplicated P. falciparum malaria, we obtained three samples (acute illness, treatment, and recovery) from 10 subjects and utilized each subject's recovery sample as their baseline. At the time of acute illness (day 1), subjects had upregulation of innate immune response, cytokine, and inflammation-related genes (IL-1β, IL-6, TNF, and IFN-γ), which was more frequent with parasitemias >100,000 per μL and body temperatures ≥ 39°C. Apoptosis-related genes (Fas, BAX, and TP53) were upregulated acutely and for several days thereafter (days 1-3). In contrast, the expression of immune-modulatory (transcription factor 7, HLV-DOA, and CD6) and apoptosis inhibitory (c-myc, caspase 8, and Fas Ligand G) genes was downregulated initially and returned to normal with clinical recovery (days 7-10). These results indicate that the innate immune response, cytokine, and apoptosis pathways are upregulated acutely in uncomplicated malaria with concomitant downregulation of immune-modulatory and apoptosis inhibitory genes.
为了研究无并发症恶性疟原虫感染期间人类基因的表达情况,我们从 10 名受试者中获取了三个样本(急性感染期、治疗期和恢复期),并将每个受试者的恢复期样本作为其基线。在急性感染期(第 1 天),受试者中先天免疫反应、细胞因子和炎症相关基因(IL-1β、IL-6、TNF 和 IFN-γ)的表达上调,当寄生虫血症>100,000 个/μL 且体温≥39°C 时更为常见。凋亡相关基因(Fas、BAX 和 TP53)在急性感染期及其后数天(第 1-3 天)被上调。相比之下,免疫调节(转录因子 7、HLV-DOA 和 CD6)和凋亡抑制(c-myc、caspase 8 和 Fas Ligand G)基因的表达最初被下调,并在临床恢复期(第 7-10 天)恢复正常。这些结果表明,无并发症疟疾中先天免疫反应、细胞因子和凋亡途径在急性感染期被上调,同时免疫调节和凋亡抑制基因被下调。