Arévalo-Herrera Myriam, Vásquez-Jiménez Juan M, Lopez-Perez Mary, Vallejo Andrés F, Amado-Garavito Andrés B, Céspedes Nora, Castellanos Angélica, Molina Karen, Trejos Johanna, Oñate José, Epstein Judith E, Richie Thomas L, Herrera Sócrates
Malaria Vaccine and Drug Development Center (MVDC), Cali, Colombia.
Faculty of Health, Universidad del Valle, Cali, Colombia.
PLoS Negl Trop Dis. 2016 Oct 19;10(10):e0005070. doi: 10.1371/journal.pntd.0005070. eCollection 2016 Oct.
Immunizing human volunteers by mosquito bite with radiation-attenuated Plasmodium falciparum sporozoites (RAS) results in high-level protection against infection. Only two volunteers have been similarly immunized with P. vivax (Pv) RAS, and both were protected. A phase 2 controlled clinical trial was conducted to assess the safety and protective efficacy of PvRAS immunization.
METHODOLOGY/PRINCIPAL FINDINGS: A randomized, single-blinded trial was conducted. Duffy positive (Fy+; Pv susceptible) individuals were enrolled: 14 received bites from irradiated (150 ± 10 cGy) Pv-infected Anopheles mosquitoes (RAS) and 7 from non-irradiated non-infected mosquitoes (Ctl). An additional group of seven Fy- (Pv refractory) volunteers was immunized with bites from non-irradiated Pv-infected mosquitoes. A total of seven immunizations were carried out at mean intervals of nine weeks. Eight weeks after last immunization, a controlled human malaria infection (CHMI) with non-irradiated Pv-infected mosquitoes was performed. Nineteen volunteers completed seven immunizations (12 RAS, 2 Ctl, and 5 Fy-) and received a CHMI. Five of 12 (42%) RAS volunteers were protected (receiving a median of 434 infective bites) compared with 0/2 Ctl. None of the Fy- volunteers developed infection by the seventh immunization or after CHMI. All non-protected volunteers developed symptoms 8-13 days after CHMI with a mean pre-patent period of 12.8 days. No serious adverse events related to the immunizations were observed. Specific IgG1 anti-PvCS response was associated with protection.
Immunization with PvRAS was safe, immunogenic, and induced sterile immunity in 42% of the Fy+ volunteers. Moreover, Fy- volunteers were refractory to Pv malaria.
Identifier: NCT01082341.
通过蚊虫叮咬用辐射减毒的恶性疟原虫子孢子(RAS)免疫人类志愿者可产生高水平的感染防护作用。仅有两名志愿者用间日疟原虫(Pv)RAS进行了类似免疫,且两人均受到了保护。开展了一项2期对照临床试验以评估PvRAS免疫的安全性和保护效力。
方法/主要发现:进行了一项随机、单盲试验。招募达菲阳性(Fy+;对Pv易感)个体:14人接受经辐照(150±10厘戈瑞)的感染Pv的按蚊叮咬(RAS组),7人接受未辐照的未感染蚊虫叮咬(对照组)。另外一组7名Fy-(对Pv难治)志愿者接受未辐照的感染Pv的蚊虫叮咬免疫。共进行了7次免疫,平均间隔9周。末次免疫后8周,用未辐照的感染Pv的蚊虫进行了一次受控人类疟疾感染(CHMI)。19名志愿者完成了7次免疫(12名RAS组、2名对照组和5名Fy-组)并接受了CHMI。12名RAS组志愿者中有5名(42%)受到保护(接受的感染性叮咬中位数为434次),而对照组为0/2。Fy-组志愿者在第7次免疫或CHMI后均未发生感染。所有未受保护的志愿者在CHMI后8 - 13天出现症状,平均潜伏期为12.8天。未观察到与免疫相关的严重不良事件。特异性IgG1抗PvCS反应与保护相关。
用PvRAS免疫是安全的、具有免疫原性的,并在42%的Fy+志愿者中诱导了无菌免疫力。此外,Fy-组志愿者对Pv疟疾难治。
标识符:NCT01082341。