Nacher M, Gay F, Singhasivanon P, Krudsood S, Treeprasertsuk S, Mazier D, Vouldoukis I, Looareesuwan S
Unité INSERM 511, Immunobiologie Cellulaire et Moléculaire des Infections Parasitaires, Faculté de médecine Pitié-Salpétrière, 91 boulevard de l'Hôpital, 75634 Paris, Cedex 13, France; Faculty of Tropical Medicine, Hospital for Tropical Di.
Parasite Immunol. 2000 Mar;22(3):107-13. doi: 10.1046/j.1365-3024.2000.00284.x.
Following reports of increased IgE in severe malaria and hypothesizing that helminth coinfections could modify its outcome, we conducted a retrospective case-control study to establish whether helminths affect the evolution of Plasmodium falciparum malaria. Some 182 severe cases, 315 mild controls and 40 controls with circulating schizonts were examined for intestinal helminths. Comparing cerebral malaria with mild controls, Ascaris lumbricoides was associated with a protective adjusted odds ratio (OR) of 0.58 (0. 32-1.03) P = 0.06, for coinfection with Ascaris and Necator americanus, OR = 0.39 (0.17-0.88) P = 0.02. Protection followed a dose-effect trend (P = 0.008). When comparing cerebral malaria cases and controls with circulating schizonts the OR was 0.25 (0.009-0.67) P = 0.006. We hypothesized that Ascaris infected patients may have had decreased cyto-adherence, possibly through endothelial cell receptor downregulation and/or decreased splenic clearance leading to the absence of selection of virulent P. falciparum strains. IgE-anti-IgE immune complexes resulting from helminth preinfection may have an important role in influencing clinical presentation of severe malaria, and in establishing malaria tolerance, through the CD23/NO pathway.
在有报告称严重疟疾患者体内IgE水平升高,且推测蠕虫共感染可能会改变其病情转归之后,我们开展了一项回顾性病例对照研究,以确定蠕虫是否会影响恶性疟原虫疟疾的病程。对约182例重症病例、315例轻症对照以及40例有循环裂殖体的对照进行了肠道蠕虫检查。将脑型疟疾患者与轻症对照进行比较,感染蛔虫时校正优势比(OR)为0.58(0.32 - 1.03),P = 0.06;同时感染蛔虫和美洲板口线虫时,OR = 0.39(0.17 - 0.88),P = 0.02。保护作用呈现剂量效应趋势(P = 0.008)。将脑型疟疾病例与有循环裂殖体的对照进行比较时,OR为0.25(0.009 - 0.67),P = 0.006。我们推测,感染蛔虫的患者可能细胞黏附性降低,这可能是由于内皮细胞受体下调和/或脾脏清除功能降低,导致毒力强的恶性疟原虫菌株未被选择。蠕虫预感染产生的IgE - 抗IgE免疫复合物可能通过CD23/NO途径在影响严重疟疾的临床表现以及建立疟疾耐受性方面发挥重要作用。