Malaria Group, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, P.O. Box No. 10504, New Delhi 110067, India.
Trans R Soc Trop Med Hyg. 2010 May;104(5):371-3. doi: 10.1016/j.trstmh.2010.01.002. Epub 2010 Jan 29.
The precise function of Plasmodium falciparum histidine-rich protein II (HRPII) is not known, but in vitro studies have indicated its immunomodulatory function. The host immune response to HRPII was measured and compared with the response to P. falciparum merozoite surface protein 1 (MSP1) in four groups of study subjects (healthy malaria-naïve adults, uncomplicated malaria patients, asymptomatic parasite carriers and aparasitemic endemic adults; n=15 in each group). Serum antibody concentrations, lymphocyte proliferation and IFN-( and IL-4 responses were significantly higher with MSP1 than with HRPII stimulation in all three malaria-exposed groups (P<0.001), suggesting a strong immunomodulatory role for HRPII.
疟原虫富组氨酸蛋白 II(HRPII)的确切功能尚不清楚,但体外研究表明其具有免疫调节功能。在四组研究对象(健康无疟疾的成年人、无并发症的疟疾患者、无症状寄生虫携带者和地方性无寄生虫成年人;每组 15 人)中,测量了宿主对 HRPII 的免疫反应,并与疟原虫裂殖子表面蛋白 1(MSP1)的反应进行了比较。在所有三种疟疾暴露组中,MSP1 刺激的血清抗体浓度、淋巴细胞增殖和 IFN-和 IL-4 反应均明显高于 HRPII 刺激(P<0.001),这表明 HRPII 具有很强的免疫调节作用。