Gilbreath M J, Pavanand K, MacDermott R P, Phisphumvithi P, Permpanich B, Wimonwattrawatee T
J Clin Microbiol. 1983 Feb;17(2):296-304. doi: 10.1128/jcm.17.2.296-304.1983.
To assess general cytotoxic effector cell capabilities by peripheral blood mononuclear cells from patients with active malaria infections, we examined antibody-dependent cellular cytotoxicity, spontaneous cell-mediated cytotoxicity, and lectin-induced cellular cytotoxicity by using human and chicken erythrocyte, Chang cell line, and K562 cell line targets. By using human erythrocyte and Change cell line targets, we found that Thai adults naturally infected with malaria had significantly impaired lectin-induced cellular cytotoxicity. In addition, spontaneous cell-mediated cytotoxicity was deficient with K562 but not with Chang cell line targets. Finally, no change in antibody-dependent cellular cytotoxicity was observed when chicken erythrocyte or Chang cell line targets were used. These observations, coupled with our previous observations of a physical loss of peripheral blood T cells, the presence of lymphocytotoxic serum antibodies, and defective T suppressor cell generation in patients with malaria, indicate that major alterations in the cellular immune system occur in patients with active malaria infections.
为了通过来自活动性疟疾感染患者的外周血单个核细胞评估一般细胞毒性效应细胞的能力,我们使用人和鸡红细胞、Chang细胞系和K562细胞系靶标检测了抗体依赖性细胞毒性、自发细胞介导的细胞毒性和凝集素诱导的细胞毒性。通过使用人红细胞和Chang细胞系靶标,我们发现自然感染疟疾的泰国成年人凝集素诱导的细胞毒性显著受损。此外,针对K562靶标,自发细胞介导的细胞毒性不足,但针对Chang细胞系靶标则不然。最后,当使用鸡红细胞或Chang细胞系靶标时,未观察到抗体依赖性细胞毒性的变化。这些观察结果,再加上我们之前对疟疾患者外周血T细胞物理性减少、淋巴细胞毒性血清抗体的存在以及T抑制细胞生成缺陷的观察结果,表明活动性疟疾感染患者的细胞免疫系统发生了重大改变。