Soulard Valérie, Bosson-Vanga Henriette, Lorthiois Audrey, Roucher Clémentine, Franetich Jean-François, Zanghi Gigliola, Bordessoulles Mallaury, Tefit Maurel, Thellier Marc, Morosan Serban, Le Naour Gilles, Capron Frédérique, Suemizu Hiroshi, Snounou Georges, Moreno-Sabater Alicia, Mazier Dominique
1] Sorbonne Universités, UPMC Univ Paris 06, CR7, Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), 91 Bd de l'hôpital, F-75013 Paris, France [2] INSERM, U1135, CIMI-PARIS, 91 Bd de l'hôpital, F-75013 Paris, France [3] CNRS, ERL 8255, CIMI-PARIS, 91 Bd de l'hôpital, F-75013 Paris, France.
1] Sorbonne Universités, UPMC Univ Paris 06, CR7, Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), 91 Bd de l'hôpital, F-75013 Paris, France [2] INSERM, U1135, CIMI-PARIS, 91 Bd de l'hôpital, F-75013 Paris, France [3] CNRS, ERL 8255, CIMI-PARIS, 91 Bd de l'hôpital, F-75013 Paris, France [4] Université FHB, UFR SPB, Departement de Parasitologie-Mycologie, BP V 34 Abidjan, Ivory Coast.
Nat Commun. 2015 Jul 24;6:7690. doi: 10.1038/ncomms8690.
Experimental studies of Plasmodium parasites that infect humans are restricted by their host specificity. Humanized mice offer a means to overcome this and further provide the opportunity to observe the parasites in vivo. Here we improve on previous protocols to achieve efficient double engraftment of TK-NOG mice by human primary hepatocytes and red blood cells. Thus, we obtain the complete hepatic development of P. falciparum, the transition to the erythrocytic stages, their subsequent multiplication, and the appearance of mature gametocytes over an extended period of observation. Furthermore, using sporozoites derived from two P. ovale-infected patients, we show that human hepatocytes engrafted in TK-NOG mice sustain maturation of the liver stages, and the presence of late-developing schizonts indicate the eventual activation of quiescent parasites. Thus, TK-NOG mice are highly suited for in vivo observations on the Plasmodium species of humans.
感染人类的疟原虫的实验研究受到其宿主特异性的限制。人源化小鼠提供了一种克服这一限制的方法,并进一步提供了在体内观察疟原虫的机会。在此,我们改进了先前的方案,以实现人原代肝细胞和红细胞对TK-NOG小鼠的高效双重植入。因此,我们在延长的观察期内获得了恶性疟原虫完整的肝脏发育、向红细胞阶段的转变、其随后的增殖以及成熟配子体的出现。此外,使用来自两名卵形疟原虫感染患者的子孢子,我们表明植入TK-NOG小鼠的人肝细胞维持了肝脏阶段的成熟,晚期发育裂殖体的存在表明静止疟原虫最终被激活。因此,TK-NOG小鼠非常适合对人类疟原虫物种进行体内观察。