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恶性疟原虫疟疾中免疫反应的调节。III. 急性感染患者或免疫供体T细胞体外对抗原的增殖反应及亚群组成

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.

作者信息

Troye-Blomberg M, Romero P, Patarroyo M E, Björkman A, Perlmann P

出版信息

Clin Exp Immunol. 1984 Nov;58(2):380-7.

Abstract

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.

摘要

对急性恶性疟原虫疟疾患者的T细胞进行了体外增殖反应研究,以检测其对疟疾抗原的反应。26名患者中,14名经历了急性且短暂(小于或等于8天)的疾病发作,其中大多数是首次发作,而12名患者在采集血样时已患病超过8天。第一组患者的淋巴细胞产生了微弱且明显针对恶性疟原虫的增殖反应,在3 - 4天后达到峰值,但在5 - 6天内减弱,提示有抑制作用的诱导。由正常红细胞膜组成的对照抗原未引发此类反应。第二组患者完全缺乏恶性疟原虫抗原诱导的增殖反应。由于两组对T细胞有丝分裂原的反应相同,结果表明存在疟疾特异性无反应性。相比之下,来自生活在恶性疟原虫高度流行地区的一组明显具有免疫力的供体的T细胞,对恶性疟原虫抗原产生了强烈且持久的增殖反应,在第5 - 6天达到峰值。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进行表面标志物研究,对增殖反应的细胞基础进行了研究。在T细胞制剂中,免疫供体和急性感染间日疟原虫的患者的T4 + /T8 +细胞比值均接近正常。相比之下,两组急性恶性疟原虫感染患者的这一比值均降低。然而,疾病发作短暂的患者中循环T4 +细胞数量减少导致了这种情况,而患病超过8天的患者中T8 +细胞数量增加,可能包括抑制细胞,导致了这种情况。

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