Pichyangkul S, Saengkrai P, Yongvanitchit K, Stewart A, Heppner D G
Department of Immunology and Medicine, US Army Medical Component, AFRIMS, Bangkok, Thailand.
J Infect Dis. 1997 Jul;176(1):233-41. doi: 10.1086/514029.
A soluble Plasmodium falciparum antigen that specifically stimulates gammadelta T cells has been found associated predominantly with schizonts rather than ring forms, trophozoites, or gametocytes. This schizont-associated antigen (SAA) is resistant to protease digestion, is anionic at pH 8.5, is heat- and pH-resistant, and contains a phosphate group(s) that is crucial for biologic activity. Partially purified SAA induced proliferative responses and interferon-gamma production by gammadelta T cells. These stimulatory effects were greatly enhanced by monocyte-derived cytokines, interleukin (IL)-10, IL-12, and IL-1beta, but not by tumor necrosis factor-alpha. Taken together, these results suggest that concurrent stimulation of gammadelta T cells by SAA and by cytokines released from activated monocytes (IL-10, IL-12, IL-1beta) may represent the major mechanism underlying the selective activation of gammadelta T cells that is consistently observed in clinical cases of P. falciparum infection.
一种特异性刺激γδ T细胞的可溶性恶性疟原虫抗原,已被发现主要与裂殖体相关,而非环状体、滋养体或配子体。这种与裂殖体相关的抗原(SAA)对蛋白酶消化具有抗性,在pH 8.5时呈阴离子性,耐热且耐pH变化,并且含有对生物活性至关重要的一个或多个磷酸基团。部分纯化的SAA可诱导γδ T细胞的增殖反应和干扰素-γ产生。这些刺激作用被单核细胞衍生的细胞因子白细胞介素(IL)-10、IL-12和IL-1β极大增强,但未被肿瘤坏死因子-α增强。综上所述,这些结果表明,SAA与活化单核细胞释放的细胞因子(IL-10、IL-12、IL-1β)对γδ T细胞的同时刺激,可能代表了在恶性疟原虫感染临床病例中始终观察到的γδ T细胞选择性激活的主要机制。