Chizzolini C, Dupont A, Akue J P, Kaufmann M H, Verdini A S, Pessi A, Del Giudice G
Centre International de Recherches Médicales, Franceville, Gabon.
Am J Trop Med Hyg. 1988 Aug;39(2):150-6. doi: 10.4269/ajtmh.1988.39.150.
The magnitude of the antibody response to three distinct and defined antigens of Plasmodium falciparum was assessed in 144 inhabitants of the Kassa district (Haut Ogooué Province, Gabon), a region where malaria is mesoendemic. Antibodies against a polypeptide consisting of 40 (Asn-Ala-Asn-Pro) repeats of P. falciparum circumsporozoite protein [(NANP)40] were detected by ELISA. Antibodies against the fusion peptide 31.1, which consists of the N-terminal portion of the 190-200 kDa glycoprotein, were also detected by ELISA. Antibodies against ring-infected erythrocyte surface antigens (RESA), mainly the P. falciparum 155 kDa antigen (Pf 155), were detected by IFA on glutaraldehyde-fixed P. falciparum infected red blood cells (IRBC). In addition, a standard IFA employing air-dried P. falciparum IRBC was used to detect antibodies against intraerythrocytic asexual forms. Parasitemia and spleen enlargement were also recorded. The frequency of sera positive for specific antibodies increased with age for all the antigens tested. Plateau antibody levels were reached at different ages for the different antigens. Individual antibody responses varied in titer to the different antigens. Subjects with parasite-negative thick smears showed higher titers of anti-31.1 as well as an increased frequency of anti-RESA antibodies compared to subjects having positive smears. No differences in the titer and in the prevalence of anti-(NANP)40 antibodies were found between these groups. The results suggest that the antibody response against asexual blood stage antigens, especially anti-RESA and anti-31.1, may play a role in controlling parasitemia.
在加蓬上奥果韦省卡萨区这个疟疾为中度流行的地区,对144名居民评估了其对恶性疟原虫三种不同且明确的抗原的抗体反应强度。通过酶联免疫吸附测定(ELISA)检测针对由40个恶性疟原虫环子孢子蛋白[(NANP)40]重复序列(天冬酰胺 - 丙氨酸 - 天冬酰胺 - 脯氨酸)组成的多肽的抗体。针对融合肽31.1(由190 - 200 kDa糖蛋白的N端部分组成)的抗体也通过ELISA进行检测。通过间接荧光抗体试验(IFA)在戊二醛固定的恶性疟原虫感染红细胞(IRBC)上检测针对环状感染红细胞表面抗原(RESA)的抗体,主要是恶性疟原虫155 kDa抗原(Pf 155)。此外,使用空气干燥的恶性疟原虫IRBC进行标准IFA来检测针对红细胞内无性体的抗体。同时记录了疟原虫血症和脾脏肿大情况。对于所有测试抗原,特异性抗体血清阳性频率随年龄增加。不同抗原在不同年龄达到抗体水平平台期。个体对不同抗原的抗体反应滴度各不相同。与涂片阳性的受试者相比,厚涂片疟原虫阴性的受试者抗31.1抗体滴度更高,抗RESA抗体频率也增加。这些组之间抗-(NANP)40抗体的滴度和流行率没有差异。结果表明,针对无性血液阶段抗原的抗体反应,尤其是抗RESA和抗31.1抗体,可能在控制疟原虫血症中发挥作用。