Khattab Ayman, Reinhardt Christina, Staalsoe Trine, Fievet Nadine, Kremsner Peter G, Deloron Philippe, Hviid Lars, Klinkert Mo-Quen
Bernhard-Nocht Institute for Tropical Medicine, Hamburg, Germany.
Malar J. 2004 Jul 8;3:21. doi: 10.1186/1475-2875-3-21.
Pregnancy-associated malaria (PAM) is caused by Plasmodium falciparum-infected erythrocytes that can sequester in placental intervillous space by expressing particular variant surface antigens (VSA) that can mediate adhesion to chondroitin sulfate A (CSA) in vitro. IgG antibodies with specificity for the VSA expressed by these parasites (VSAPAM) are associated with protection from maternal anaemia, prematurity and low birth weight, which is the greatest risk factor for death in the first month of life.
In this study, the development of anti-VSAPAM antibodies in a group of 151 women who presented to the maternity ward of Albert Schweitzer Hospital in Lambaréné, Gabon for delivery was analysed using flow cytometry assays. Plasma samples from placenta infected primiparous women were also investigated for their capacity to inhibit parasite binding to CSA in vitro.
In the study cohort, primiparous as well as secundiparous women had the greatest risk of infection at delivery as well as during pregnancy. Primiparous women with infected placentas at delivery showed higher levels of VSAPAM-specific IgG compared to women who had no malaria infections at delivery. Placental isolates of Gabonese and Senegalese origin tested on plasma samples from Gabon showed parity dependency and gender specificity patterns. There was a significant correlation of plasma reactivity as measured by flow cytometry between different placental isolates. In the plasma of infected primiparous women, VSAPAM-specific IgG measured by flow cytometry could be correlated with anti-adhesion antibodies measured by the inhibition of CSA binding.
Recognition of placental parasites shows a parity- and sex- dependent pattern, like that previously observed in laboratory strains selected to bind to CSA. Placental infections at delivery in primiparous women appear to be sufficient to induce functional antibodies which can both recognize the surface of the infected erythrocytes as well as block their binding to CSA. The correlation between serum reactivities of placental field isolates from different geographic locations and collected at different times is indicative of the conserved nature of the antigen(s) mediating PAM.
妊娠相关疟疾(PAM)由感染恶性疟原虫的红细胞引起,这些红细胞可通过表达特定的变异表面抗原(VSA)而滞留于胎盘绒毛间隙,这些VSA在体外可介导与硫酸软骨素A(CSA)的黏附。对这些寄生虫表达的VSA具有特异性的IgG抗体(VSAPAM)与预防产妇贫血、早产和低出生体重相关,而低出生体重是出生后第一个月死亡的最大风险因素。
在本研究中,使用流式细胞术分析了151名到加蓬兰巴雷内阿尔贝特·施韦泽医院产科病房分娩的女性体内抗VSAPAM抗体的产生情况。还研究了来自胎盘感染初产妇的血浆样本在体外抑制寄生虫与CSA结合的能力。
在研究队列中,初产妇和经产妇在分娩时以及怀孕期间感染风险最高。与分娩时未感染疟疾的女性相比,分娩时胎盘感染的初产妇显示出更高水平的VSAPAM特异性IgG。对来自加蓬的血浆样本进行检测的加蓬和塞内加尔来源的胎盘分离株显示出胎次依赖性和性别特异性模式。不同胎盘分离株之间通过流式细胞术测量的血浆反应性存在显著相关性。在感染初产妇的血浆中,通过流式细胞术测量的VSAPAM特异性IgG可与通过抑制CSA结合测量的抗黏附抗体相关联。
胎盘寄生虫的识别呈现出胎次和性别依赖性模式,类似于先前在选择与CSA结合的实验室菌株中观察到的模式。初产妇分娩时的胎盘感染似乎足以诱导功能性抗体,这些抗体既能识别感染红细胞的表面,又能阻断其与CSA的结合。来自不同地理位置且在不同时间收集的胎盘现场分离株的血清反应性之间的相关性表明介导PAM的抗原具有保守性。