Ateba-Ngoa Ulysse, Jones Sophie, Zinsou Jeannot Fréjus, Honkpehedji Josiane, Adegnika Ayola Akim, Agobe Jean-Claude Dejon, Massinga-Loembe Marguerite, Mordmüller Benjamin, Bousema Teun, Yazdanbakhsh Maria
Department of Parasitology, Leiden University Medical Center, Leiden, The Netherlands. Institut für Tropenmedizin, Universität Tübingen, Tübingen, Germany. Centre de Recherches Médicales de Lambaréné, Lambaréné, Gabon.
Department of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Am J Trop Med Hyg. 2016 Aug 3;95(2):394-400. doi: 10.4269/ajtmh.15-0703. Epub 2016 Jun 6.
Infections with helminths and Plasmodium spp. overlap in their geographical distribution. It has been postulated that helminth infections may influence malarial transmission by altering Plasmodium falciparum gametocytogenesis. This cross-sectional study assessed the effect of helminth infections on P. falciparum gametocyte carriage and on humoral immune responses to sexual stage antigens in Gabon. Schistosoma haematobium and filarial infections as well as P. falciparum asexual forms and gametocyte carriage were determined. The antibody responses measured were to sexual (Pfs230, Pfs48/45) and asexual P. falciparum antigens (AMA1, MSP1, and GLURP). A total of 287 subjects were included. The prevalence of microscopically detectable P. falciparum asexual parasites was higher in S. haematobium-infected subjects in comparison to their uninfected counterparts (47% versus 26%, P = 0.003), but this was not different when filarial infections were considered. Plasmodium falciparum gametocyte carriage was similar between Schistosoma- or filaria-infected and uninfected subjects. We observed a significant decrease of Pfs48/45 immunoglobulin G titer in S. haematobium-infected subjects (P = 0.037), whereas no difference was seen for Pfs230 antibody titer, nor for antibodies to AMA1, MSP1, or GLURP. Our findings suggest an effect of S. haematobium on antibody responses to some P. falciparum gametocyte antigens that may have consequences for transmission-blocking immunity.
蠕虫感染和疟原虫感染在地理分布上存在重叠。据推测,蠕虫感染可能通过改变恶性疟原虫的配子体生成来影响疟疾传播。这项横断面研究评估了加蓬蠕虫感染对恶性疟原虫配子体携带情况以及对性阶段抗原的体液免疫反应的影响。测定了埃及血吸虫和丝虫感染情况以及恶性疟原虫的无性形式和配子体携带情况。所检测的抗体反应针对的是恶性疟原虫的性抗原(Pfs230、Pfs48/45)和无性抗原(AMA1、MSP1和GLURP)。总共纳入了287名受试者。与未感染埃及血吸虫的受试者相比,显微镜下可检测到的恶性疟原虫无性寄生虫在感染埃及血吸虫的受试者中的患病率更高(47%对26%,P = 0.003),但在考虑丝虫感染时情况并无差异。感染血吸虫或丝虫的受试者与未感染的受试者之间,恶性疟原虫配子体携带情况相似。我们观察到感染埃及血吸虫的受试者中Pfs48/45免疫球蛋白G滴度显著降低(P = 0.037),而Pfs230抗体滴度以及针对AMA1、MSP1或GLURP的抗体滴度并无差异。我们的研究结果表明,埃及血吸虫对某些恶性疟原虫配子体抗原的抗体反应有影响,这可能对传播阻断免疫产生影响。