Bach J F
J Immunopharmacol. 1979;1(3):277-310. doi: 10.3109/08923977909026377.
The thymus produces several polypeptides, which induce lymphocyte differentiation in vitro and in vivo. Several of these polypeptides have been chemically characterized, and three of them have been sequenced and synthesised (alpha 1 thymosin, thymopoietin and the serum thymic factor). Thymic hormones do not act identically on all T-cell subsets: they alter preferentially post-thymic precursor cells, and among mature T cells cytotoxic cells and suppressor cells. Their mode of action at the cellular level involves binding to specific cellular receptors and interaction with adenyl cyclase. Preliminary clinical trials with crude extracts have provided promising results in immunodeficient and cancer patients. The differentiation of T cells from stem cells has been the matter of considerable investigation over the last two decades, since it has been realized that the thymus and its products, the thymus-derived cells (T cells) play a central role in the generation of effector cells in cell-mediated immunity and in the regulation of the various categories of immune responses. That the thymus could act by the intermediate of humoral substances was precociously suggested by MILLER and OSOBA before the observation that thymuses grafted within a cell-impermeable Millipore diffusion chamber restored the immunocompetence of neonatally thymectomized (Tx) mice (1). However, although this experiment was ultimately confirmed by using chambers with well-controlled impermeability (2), MILLER did not pursue the idea of the humoral function of the thymus. Probably, the striking results obtained by DAVIES (3) and other workers, indicating direct migration of functional T cells from the thymus and the poor results initially obtained in trying to reconstitute the immune system of neonatally Tx mice by cell-free thymic extracts contributed to this disappointment. A new impetus was given to the subject in the early 70's when in vitro tests of lymphocyte function became available and when purified extracts of the thymus proved capable of restoring antigen-specific and non-specific immunocompetence of Tx mice. More recently, completely defined synthetic thymic hormones have been obtained. The question is no longer to decide whether thymic hormones exist, but rather to elucidate their biological significance and potential clinical applications. The multiplicity of available factors has created some confusion. It will be the aim of these few pages to review critically the various factors reported in the literature, giving particular emphasis to their pharmacology and their potential use in the modulation of immune responses.
胸腺产生多种多肽,这些多肽在体内外均可诱导淋巴细胞分化。其中几种多肽已进行化学特性鉴定,并且其中三种已完成测序和合成(α1胸腺素、胸腺生成素和血清胸腺因子)。胸腺激素对所有T细胞亚群的作用并非完全相同:它们优先作用于胸腺后的前体细胞,以及成熟T细胞中的细胞毒性细胞和抑制性细胞。它们在细胞水平的作用方式包括与特定细胞受体结合以及与腺苷酸环化酶相互作用。对粗提物进行的初步临床试验在免疫缺陷患者和癌症患者中取得了有前景的结果。在过去二十年中,T细胞从干细胞的分化一直是大量研究的课题,因为人们已经认识到胸腺及其产物,即胸腺衍生细胞(T细胞)在细胞介导免疫中效应细胞的产生以及各类免疫反应的调节中起着核心作用。早在观察到移植到细胞不可渗透的微孔扩散室中的胸腺可恢复新生期胸腺切除(Tx)小鼠的免疫能力之前,MILLER和OSOBA就已早熟地提出胸腺可能通过体液物质发挥作用(1)。然而,尽管该实验最终通过使用具有良好控制的不可渗透性的扩散室得到了证实(2),但MILLER并未继续深入研究胸腺的体液功能这一想法。可能是DAVIES(3)和其他研究人员获得的显著结果,表明功能性T细胞从胸腺直接迁移,以及最初试图通过无细胞胸腺提取物重建新生期Tx小鼠免疫系统时得到的不佳结果导致了这种失望。在70年代早期,当淋巴细胞功能的体外检测方法问世,并且胸腺的纯化提取物被证明能够恢复Tx小鼠的抗原特异性和非特异性免疫能力时,这个课题获得了新的推动力。最近,已经获得了完全确定的合成胸腺激素。问题不再是确定胸腺激素是否存在,而是阐明它们的生物学意义和潜在的临床应用。现有因子的多样性造成了一些混乱。这几页的目的将是批判性地回顾文献中报道的各种因子,特别强调它们的药理学以及它们在调节免疫反应中的潜在用途。