Shanks G Dennis, Waller Michael
Australian Defence Force Malaria and Infectious Diseases Institute, Enoggera, Australia.
University of Queensland, School of Public Health, Brisbane, Australia.
Am J Trop Med Hyg. 2022 Feb 28;106(4):1237-1239. doi: 10.4269/ajtmh.21-1274. Print 2022 Apr 6.
Latent Plasmodium vivax parasites in the liver known as hypnozoites activate causing malaria relapses months after the original infection. The putative initiation signal is unknown. Plasmodium falciparum infections appear to trigger P. vivax relapses and initiation of relapse may be triggered by hemolysis or fever. The U.S. Army hospital records from the Korean War (> 500,000 individual records) were used to determine whether there was an association between blood transfusion and vivax malaria relapse. Importantly, blood for transfusion was collected in the United States, so the risk of transmission of malaria parasites was minimal. Blood transfusion (largely for combat trauma) was a risk factor for subsequent vivax malaria (relative risk 2.54, 95% CI 2.15-2.99, P < 0.0001). As expected, blood transfusion was not a risk factor for subsequent dysentery, but transfusion was a risk factor for subsequent hepatitis. Blood transfusion causing an increased heme delivery to the liver and a subsequent redox signal within hepatocytes may partially explain hypnozoite activation leading to relapses of vivax malaria.
肝脏中潜伏的间日疟原虫寄生虫(即休眠子)被激活,导致在初次感染数月后出现疟疾复发。假定的起始信号尚不清楚。恶性疟原虫感染似乎会引发间日疟原虫复发,而复发的起始可能由溶血或发热触发。利用朝鲜战争时期美国陆军医院的记录(超过50万份个人记录)来确定输血与间日疟复发之间是否存在关联。重要的是,用于输血的血液是在美国采集的,因此疟原虫传播的风险极小。输血(主要用于治疗战斗创伤)是随后发生间日疟的一个风险因素(相对风险为2.54,95%置信区间为2.15 - 2.99,P < 0.0001)。正如预期的那样,输血不是随后发生痢疾的风险因素,但输血是随后发生肝炎的风险因素。输血导致肝脏血红素输送增加以及随后肝细胞内的氧化还原信号,这可能部分解释了休眠子激活导致间日疟复发的现象。