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白细胞介素-2受体在逆转录病毒相关成人T细胞白血病中的表达

Interleukin-2 receptor expression in retrovirus associated adult T-cell leukemia.

作者信息

Waldmann T A, Leonard W J, Depper J M, Krönke M, Goldman C K, Oh T, Greene W C

出版信息

Princess Takamatsu Symp. 1984;15:259-68.

PMID:6100644
Abstract

Interleukin-2 (IL-2) is a lymphokine synthesized by some T cells following activation. Resting T cells do not express IL-2 receptors but receptors are rapidly expressed on T cells following the interaction of antigens, mitogens, or monoclonal antibodies with the antigen specific T-cell receptor complex. Using anti-Tac a monoclonal antibody that recognizes the IL-2 receptor, the receptor has been purified. The receptor is a 33 kdalton peptide that is post-translationally glycosylated to a 55 kdalton mature form. Mature receptors contain both N-linked and O-linked sugars and are both sulfated and phosphorylated. Using an oligonucleotide probe, based on the N-terminal amino acid sequence, cDNAs encoding this receptor have been cloned, sequenced and expressed. The addition of anti-Tac to in vitro culture systems blocks the IL-2 induced DNA synthesis of IL-2 dependent T-cell lines and inhibits soluble auto- and alloantigen induced T-cell proliferation. Furthermore, it prevents the generation of cytotoxic and suppressor effector T cells. The anti-receptor antibody also inhibits lectin stimulated immunoglobulin synthesis and the sequential expression of late appearing activation antigens on T cells. Normal resting T cells and most leukemic T-cell populations do not express IL-2 receptors however the leukemic cells of all patients with human T-cell leukemia/lymphoma virus (HTLV-I) associated, adult T-cell leukemia (ATL) examined expressed the Tac antigen. In HTLV-I infected cells the 42 kdalton long open reading frame (LOR) protein encoded in part, by the pX region of HTLV-I may act as a transacting transcriptional activator that induces transcription of the IL-2 receptor gene thus providing an explanation for the constant association of HTLV-I infection of lymphoid cells and IL-2 receptor expression. The constant display of large numbers of IL-2 receptors which may be aberrant in the ATL cells may play a role in the uncontrolled growth of these leukemic T cells. Patients with the Tac positive ATL are being treated with an anti-Tac monoclonal antibody directed towards this growth factor receptor.

摘要

白细胞介素-2(IL-2)是某些T细胞激活后合成的一种淋巴因子。静止的T细胞不表达IL-2受体,但在抗原、丝裂原或单克隆抗体与抗原特异性T细胞受体复合物相互作用后,T细胞上会迅速表达受体。利用抗Tac(一种识别IL-2受体的单克隆抗体),该受体已被纯化。该受体是一种33千道尔顿的肽,经翻译后糖基化成为55千道尔顿的成熟形式。成熟受体含有N-连接和O-连接的糖类,且都经过硫酸化和磷酸化。基于N端氨基酸序列,利用寡核苷酸探针,已克隆、测序并表达了编码该受体的cDNA。将抗Tac添加到体外培养系统中,可阻断IL-2诱导的IL-2依赖性T细胞系的DNA合成,并抑制可溶性自身抗原和同种异体抗原诱导的T细胞增殖。此外,它还可阻止细胞毒性和抑制性效应T细胞的产生。抗受体抗体还可抑制凝集素刺激的免疫球蛋白合成以及T细胞上晚期出现的激活抗原的顺序表达。正常静止T细胞和大多数白血病T细胞群体不表达IL-2受体,然而,所有检测过的与人类T细胞白血病/淋巴瘤病毒(HTLV-I)相关的成人T细胞白血病(ATL)患者的白血病细胞均表达Tac抗原。在HTLV-I感染的细胞中,HTLV-I的pX区域部分编码的42千道尔顿长开放阅读框(LOR)蛋白可能作为一种反式作用转录激活因子,诱导IL-2受体基因的转录,从而解释了淋巴细胞HTLV-I感染与IL-2受体表达之间的持续关联。ATL细胞中大量可能异常的IL-2受体持续呈现,可能在这些白血病T细胞的失控生长中起作用。Tac阳性的ATL患者正在接受针对这种生长因子受体的抗Tac单克隆抗体治疗。

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