首页> 美国卫生研究院文献>Clinical and Experimental Immunology >Regulation of the immune response in Plasmodium falciparum malaria. III. Proliferative response to antigen in vitro and subset composition of T cells from patients with acute infection or from immune donors.
【2h】

Regulation of the immune response in Plasmodium falciparum malaria. III. Proliferative response to antigen in vitro and subset composition of T cells from patients with acute infection or from immune donors.

机译:恶性疟原虫疟疾免疫应答的调节。三急性感染患者或免疫供体对T细胞抗原的体外增殖反应。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

T cells from patients with acute Plasmodium falciparum malaria were investigated for their proliferative responses in vitro to malarial antigen. Of 26 patients, 14 had acute and short lived (less than or equal to 8 days) disease episodes, most of them for the first time, while 12 had been ill for more than 8 days at the time of the blood samples were taken. The lymphocytes from the first group gave a weak, and apparently P. falciparum specific proliferation, peaking after 3-4 days, but waning within 5-6 days, suggesting the induction of suppression. No such responses were obtained with control antigen consisting of normal RBC membranes. The P. falciparum antigen-induced proliferative response was completely lacking in the second group of patients. Since both groups responded equally to T cell mitogen, the results are indicative of a malaria specific non-responsiveness. In contrast T cells from a group of apparently immune donors living in highly endemic P. falciparum malaria areas developed strong and long lasting proliferative responses to P. falciparum antigen with a peak on days 5-6. T cells from acutely infected P. vivax patients did not respond to either the P. falciparum antigen or to the control antigen. The cellular basis of the proliferative responses were investigated by surface marker studies with monoclonal antibodies. Within the T cell preparations, the T4+/T8+ cell ratio was close to normal for both the immune donors and for those with acute P. vivax infection. In contrast, this ratio was depressed for both groups of patients with acute P. falciparum infection. However, this was due to reduced number of circulating T4+ cells in the patients with short disease episodes whereas it was due to increased numbers of T8+ cells, probably including suppressor cells, in those who were ill for more than 8 days.
机译:研究了来自急性恶性疟原虫疟疾患者的T细胞在体外对疟疾抗原的增殖反应。在26例患者中,有14例患有急性和短暂的(少于或等于8天)疾病发作,其中大多数是首次发病,而在采集血样时有12例病了超过8天。第一组淋巴细胞产生的恶性疟原虫特异性增殖较弱,明显,在3-4天后达到峰值,但在5-6天内逐渐减弱,提示诱导了抑制作用。使用由正常RBC膜组成的对照抗原无法获得此类反应。在第二组患者中完全缺乏恶性疟原虫抗原诱导的增殖反应。由于两组对T细胞促分裂原的反应均等,结果表明疟疾特异性无反应。相反,来自生活在高度流行的恶性疟原虫疟疾地区的一组显然具有免疫力的供体的T细胞对恶性疟原虫抗原产生强而持久的增殖反应,并在第5-6天达到峰值。来自急性感染间日疟原虫患者的T细胞对恶性疟原虫抗原或对照抗原均无反应。通过使用单克隆抗体的表面标记研究研究了增殖反应的细胞基础。在T细胞制剂中,免疫供体和急性间日疟原虫感染者的T4 + / T8 +细胞比率均接近正常。相比之下,两组急性恶性疟原虫感染患者的这一比率均降低。但是,这是由于疾病发作时间短的患者循环中的T4 +细胞数量减少,而病期超过8天的患者中T8 +细胞(可能包括抑制细胞)数量增加。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号