Departamento de Análises Clínicas e Toxicológicas, Faculdade de Ciências Farmacêuticas, Universidade de São Paulo, São Paulo, Brazil.
PLoS One. 2013;8(2):e56061. doi: 10.1371/journal.pone.0056061. Epub 2013 Feb 14.
A recent clinical trial in African children demonstrated the potential utility of merozoite surface protein (MSP)-3 as a vaccine against Plasmodium falciparum malaria. The present study evaluated the use of Plasmodium vivax MSP-3 (PvMSP-3) as a target antigen in vaccine formulations against malaria caused by P. vivax. Recombinant proteins representing MSP-3α and MSP-3β of P. vivax were expressed as soluble histidine-tagged bacterial fusions. Antigenicity during natural infection was evaluated by detecting specific antibodies using sera from individuals living in endemic areas of Brazil. A large proportion of infected individuals presented IgG antibodies to PvMSP-3α (68.2%) and at least 1 recombinant protein representing PvMSP-3β (79.1%). In spite of the large responder frequency, reactivity to both antigens was significantly lower than was observed for the immunodominant epitope present on the 19-kDa C-terminal region of PvMSP-1. Immunogenicity of the recombinant proteins was studied in mice in the absence or presence of different adjuvant formulations. PvMSP-3β, but not PvMSP-3α, induced a TLR4-independent humoral immune response in the absence of any adjuvant formulation. The immunogenicity of the recombinant antigens were also tested in formulations containing different adjuvants (Alum, Salmonella enterica flagellin, CpG, Quil A,TiterMax® and incomplete Freunds adjuvant) and combinations of two adjuvants (Alum plus flagellin, and CpG plus flagellin). Recombinant PvMSP-3α and PvMSP-3β elicited higher antibody titers capable of recognizing P. vivax-infected erythrocytes harvested from malaria patients. Our results confirm that P. vivax MSP-3 antigens are immunogenic during natural infection, and the corresponding recombinant proteins may be useful in elucidating their vaccine potential.
最近一项在非洲儿童中进行的临床试验表明,裂殖子表面蛋白(MSP)-3 作为预防恶性疟原虫疟疾的疫苗具有潜在的应用价值。本研究评估了用间日疟原虫 MSP-3(PvMSP-3)作为间日疟原虫疟疾疫苗制剂的靶抗原。表达了代表间日疟原虫 MSP-3α和 MSP-3β的重组蛋白,作为可溶性组氨酸标记的细菌融合蛋白。通过检测来自巴西流行地区个体的血清中特异性抗体来评估自然感染期间的抗原性。很大一部分感染个体对 PvMSP-3α(68.2%)和至少 1 种代表 PvMSP-3β的重组蛋白呈现 IgG 抗体。尽管反应频率很高,但与 PvMSP-1 19kDa C 端区域上存在的免疫显性表位相比,两种抗原的反应性均显著降低。在没有或存在不同佐剂配方的情况下,研究了重组蛋白在小鼠中的免疫原性。在没有任何佐剂配方的情况下,PvMSP-3β而不是 PvMSP-3α诱导了 TLR4 非依赖性体液免疫反应。还在含有不同佐剂(明矾、沙门氏菌鞭毛蛋白、CpG、Quil A、TiterMax®和不完全弗氏佐剂)和两种佐剂(明矾加鞭毛蛋白和 CpG 加鞭毛蛋白)的配方中测试了重组抗原的免疫原性。重组 PvMSP-3α和 PvMSP-3β引发了更高的抗体滴度,能够识别从疟疾患者中采集的感染疟原虫的红细胞。我们的结果证实,间日疟原虫 MSP-3 抗原在自然感染期间具有免疫原性,相应的重组蛋白可能有助于阐明其疫苗潜力。