Jongo Said Abdallah, Church L W Preston, Nchama Vicente Urbano Nsue Ndong, Hamad Ali, Chuquiyauri Raul, Kassim Kamaka Ramadhani, Athuman Thabit, Deal Anna, Natasha K C, Mtoro Ali, Mpina Maxmillian, Nyakarungu Elizabeth, Bidjimi Gertrudis Owono, Owono Marta Alene, Mayé Escolástica Raquel Mansogo, Mangue Martín Eká Ondó, Okomo Genaro Nsué Nguema, Pasialo Beltrán Ekuá Ntutumu, Mandumbi Dolores Mbang Ondó, Mikue María-Silvia A López, Mochomuemue Fortunata Lobede, Obono Mariano Obiang, Besahá Juan Carlos Momo, Bijeri José Raso, Abegue Gabriel Mbá, Veri Yolanda Rimoy, Bela Ines Toichoa, Chochi Federico Comsil, Lima Sánchez José Enrique, Pencelli Vanessa, Gayozo Griselda, Nlang José Antonio Esono Mbá, Schindler Tobias, James Eric R, Abebe Yonas, Lemiale Laurence, Stabler Thomas C, Murshedkar Tooba, Chen Mei-Chun, Schwabe Christopher, Ratsirarson Josea, Rivas Matilde Riloha, Ayekaba Mitoha Ondo'o, Milang Diosdado Vicente Nsué, Falla Carlos Cortés, Phiri Wonder P, García Guillermo A, Maas Carl D, Nlavo Bonifacio Manguire, Tanner Marcel, Billingsley Peter F, Kim Lee Sim B, Daubenberger Claudia, Hoffman Stephen L, Abdulla Salim, Richie Thomas L
Bagamoyo Research and Training Center, Ifakara Health Institute, Bagamoyo, Tanzania.
Sanaria Inc., Rockville, Maryland.
Am J Trop Med Hyg. 2022 Feb 7;106(4):1215-1226. doi: 10.4269/ajtmh.21-0942. Print 2022 Apr 6.
Plasmodium falciparum sporozoite (PfSPZ) Vaccine is composed of radiation-attenuated, aseptic, purified cryopreserved PfSPZ. Multiple clinical trials empirically assessing two to six doses have shown multi-dose priming (two to four doses the first week) to be optimal for protection in both 4- and 16-week regimens. In this randomized, double-blind, normal saline (NS) placebo-controlled trial, four groups (G) of 18- to 32-year-old Equatoguineans received multi-dose priming regimens with or without a delayed final dose at 4 or 16 weeks. The regimens were G1: days 1, 3, 5, 7, and 113; G2: days 1, 3, 5, and 7; G3: days 1, 3, 5, 7, and 29; and G4: days 1, 8, and 29. All doses were 9 × 105 PfSPZ. Tolerability, safety, immunogenicity, and vaccine efficacy (VE) against homologous controlled human malaria infection (CHMI) 6-7 weeks after vaccination were assessed to down-select the best regimen. All four regimens were safe and well tolerated, with no significant differences in adverse events (AEs) between vaccinees (N = 84) and NS controls (N = 20) or between regimens. Out of 19 controls, 13 developed Pf parasitemia by quantitative polymerase chain reaction (qPCR) after CHMI. Only the vaccine regimen administered on study days 1, 8, and 29 gave significant protection (7/21 vaccinees versus 13/19 controls infected, VE 51.3%, P = 0.03, Barnard's test, two-tailed). There were no significant differences in antibodies against Pf circumsporozoite protein (PfCSP), a major SPZ antigen, between protected and nonprotected vaccinees or controls pre-CHMI. The six controls not developing Pf parasitemia had significantly higher antibodies to blood stage antigens Pf exported protein 1 (PfEXP1) and Pf merozoite surface protein 1 (PfMSP1) than the controls who developed parasitemia, suggesting naturally acquired immunity against Pf limited infections in controls. This study identified a safe, protective, 4-week, multi-dose prime vaccination regimen for assessment in future trials of PfSPZ Vaccine.
恶性疟原虫子孢子(PfSPZ)疫苗由经辐射减毒、无菌、纯化并冷冻保存的PfSPZ组成。多项经验性评估两至六剂疫苗的临床试验表明,多剂次启动免疫(第一周两至四剂)对于4周和16周免疫方案中的保护作用而言是最佳的。在这项随机、双盲、生理盐水(NS)安慰剂对照试验中,四组年龄在18至32岁的赤道几内亚人接受了多剂次启动免疫方案,在4周或16周时有的方案有延迟的最后一剂,有的则没有。这些方案分别为:G1:第1、3、5、7和113天;G2:第1、3、5和7天;G3:第1、3、5、7和29天;以及G4:第1、8和29天。所有剂量均为9×105个PfSPZ。评估了疫苗接种后6至7周时针对同源性受控人类疟疾感染(CHMI)的耐受性、安全性、免疫原性和疫苗效力(VE),以筛选出最佳方案。所有四种方案均安全且耐受性良好,疫苗接种者(N = 84)与NS对照组(N = 20)之间或各方案之间的不良事件(AE)无显著差异。在19名对照组中,13名在CHMI后通过定量聚合酶链反应(qPCR)出现了Pf寄生虫血症。只有在研究第1、8和29天接种的疫苗方案提供了显著的保护作用(21名疫苗接种者中有7名感染,而19名对照组中有13名感染,VE为51.3%,P = 0.03,Barnard检验,双侧)。在CHMI前,受保护和未受保护的疫苗接种者或对照组之间,针对主要子孢子抗原Pf环子孢子蛋白(PfCSP)的抗体没有显著差异。6名未出现Pf寄生虫血症的对照组针对血期抗原Pf输出蛋白1(PfEXP1)和Pf裂殖子表面蛋白1(PfMSP1)的抗体明显高于出现寄生虫血症的对照组,这表明对照组中存在针对Pf有限感染的自然获得性免疫力。本研究确定了一种安全、具有保护作用的4周多剂次启动疫苗接种方案,以供未来PfSPZ疫苗试验评估。