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恶性疟原虫感染性子孢子的体外生产

In vitro production of infectious Plasmodium falciparum sporozoites.

作者信息

Eappen Abraham G, Li Tao, Marquette Meghan, Chakravarty Sumana, Kc Natasha, Zanghi Gigliola, Hoffman Benjamin U, Hettiarachchi Hashani, Patil Asha, Abebe Yonas, Tran Christiane, Yossef Alemtaye A, McWilliams Ian, Morrison Robert D, Rathakrishnan Ayyappan, Inbar Ehud, Aly Ahmed S I, De La Vega Patricia, Belmonte Maria, Sedegah Martha, Wai Tint, Campo Joseph J, King Harley, Kappe Stefan H I, Li MingLin, Billingsley Peter F, Sim B Kim Lee, Hoffman Stephen L

机构信息

Sanaria, Rockville, MD, USA.

Protein Potential, Rockville, MD, USA.

出版信息

Nature. 2022 Dec;612(7940):534-539. doi: 10.1038/s41586-022-05466-7. Epub 2022 Dec 7.

Abstract

An effective vaccine is needed for the prevention and elimination of malaria. The only immunogens that have been shown to have a protective efficacy of more than 90% against human malaria are Plasmodium falciparum (Pf) sporozoites (PfSPZ) manufactured in mosquitoes (mPfSPZ). The ability to produce PfSPZ in vitro (iPfSPZ) without mosquitoes would substantially enhance the production of PfSPZ vaccines and mosquito-stage malaria research, but this ability is lacking. Here we report the production of hundreds of millions of iPfSPZ. iPfSPZ invaded human hepatocytes in culture and developed to mature liver-stage schizonts expressing P. falciparum merozoite surface protein 1 (PfMSP1) in numbers comparable to mPfSPZ. When injected into FRGhuHep mice containing humanized livers, iPfSPZ invaded the human hepatocytes and developed to PfMSP1-expressing late liver stage parasites at 45% the quantity of cryopreserved mPfSPZ. Human blood from FRGhuHep mice infected with iPfSPZ produced asexual and sexual erythrocytic-stage parasites in culture, and gametocytes developed to PfSPZ when fed to mosquitoes, completing the P. falciparum life cycle from infectious gametocyte to infectious gametocyte without mosquitoes or primates.

摘要

预防和消除疟疾需要一种有效的疫苗。唯一已被证明对人类疟疾具有超过90%保护效力的免疫原是在蚊子体内产生的恶性疟原虫(Pf)子孢子(mPfSPZ)。在无蚊条件下体外生产PfSPZ(iPfSPZ)的能力将极大地提高PfSPZ疫苗的产量并推动蚊期疟疾研究,但目前尚缺乏这种能力。在此,我们报告了数亿个iPfSPZ的生产情况。iPfSPZ在培养物中侵入人肝细胞,并发育为表达恶性疟原虫裂殖子表面蛋白1(PfMSP1)的成熟肝期裂殖体,其数量与mPfSPZ相当。当将iPfSPZ注射到含有人类肝脏的FRGhuHep小鼠体内时,iPfSPZ侵入人肝细胞,并发育为表达PfMSP1的晚期肝期寄生虫,其数量为冷冻保存的mPfSPZ的45%。来自感染iPfSPZ的FRGhuHep小鼠的人血在培养物中产生了无性和有性红细胞期寄生虫,当将配子体喂给蚊子时,它们发育为PfSPZ,从而在无蚊或灵长类动物的情况下完成了从感染性配子体到感染性配子体的恶性疟原虫生命周期。

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