*Sandra Rotman Centre for Global Health, UHN, Toronto, Ontario, Canada; †Toronto General Research Institute, UHN, Toronto, Ontario, Canada; ‡Maple Leaf Research and Women's College Research Institute, Toronto, Ontario, Canada; and §Tropical Disease Unit, Division of Infectious Diseases, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
J Acquir Immune Defic Syndr. 2015 Feb 1;68(2):128-32. doi: 10.1097/QAI.0000000000000427.
Malaria-specific immune responses are altered in HIV/malaria-coinfected individuals and are associated with higher parasite burdens and more severe clinical disease. Monocyte/macrophage phagocytosis is a major mechanism of malaria parasite clearance. We hypothesized that phagocytosis of malaria-parasitized erythrocytes is impaired in coinfected individuals and could contribute to the increased parasite burdens observed. We show that nonopsonic phagocytosis of Plasmodium falciparum parasitized erythrocytes is impaired in monocytes isolated from HIV-infected individuals. The observed defects in phagocytic capacity were rescued after 6 months of antiretroviral therapy, demonstrating the importance of HIV treatment and immune reconstitution in the context of coinfection.
疟疾特异性免疫应答在 HIV/疟疾合并感染个体中发生改变,并与更高的寄生虫载量和更严重的临床疾病相关。单核细胞/巨噬细胞吞噬作用是清除疟原虫的主要机制。我们假设在合并感染个体中,疟原虫感染的红细胞吞噬作用受损,这可能导致观察到的寄生虫载量增加。我们表明,从 HIV 感染者中分离的单核细胞对疟原虫感染的红细胞的非调理吞噬作用受损。在接受抗逆转录病毒治疗 6 个月后,观察到的吞噬能力缺陷得到了挽救,这表明在合并感染的情况下,HIV 治疗和免疫重建的重要性。