Low T L, Thurman G B, Chincarini C, McClure J E, Marshall G D, Hu S K, Goldstein A L
Ann N Y Acad Sci. 1979;332:33-48. doi: 10.1111/j.1749-6632.1979.tb47095.x.
Thymosin fraction 5 contains several distinct hormonal-like factors which are effective in partially or fully inducing and maintaining immune function. Several of the peptide components of fraction 5 have been purified, sequenced and studied in assay systems designed to measure T-cell differentiation and function. These studied indicate that a number of the purified peptides act on different subpopulations of T-cells (see Figure 1). Thymosin beta 3 and beta 4 peptides act on terminal deoxynucleotidyl transferase (TdT) negative precursor T-cells to induce TdT positive cells. Thymosin alpha 1 induces the formation of functional helper cells and conversion of Lyt- cells to Lyt 1+, 2+, 3+ cells. Thymosin alpha 7 induces the formation of functional suppressor T-cells and also converts Lyt- cells to Lyt 1+, 2+, 3+ cells. These studies have provided further evidence that the thymus secretes a family of distinct peptides which act at various sites of the maturation sequence of T-cells to induce and maintain immune function. Phase I and Phase II clinical studied with thymosin in the treatment of primary immunodeficiency diseases, autoimmune diseases, and cancer point to a major role of the endocrine thymus in the maintenance of immune balance and in the treatment of diseases characterized by thymic malfunction. It is becoming increasingly clear that immunological maturation is a process involving a complex number of steps and that a single factor initiating a single cellular event might not be reflected in any meaningful immune reconstitution unless it is the only peptide lacking. Given the complexity of the maturation sequence of T-cells and the increasing numbers of T-cell subpopulations that are being identified, it would be surprising if a single thymic factor could control all of the steps and populations involved. Rather, it would appear that the control of T-cell maturation and function involves a complex number of thymic-specific factors and other molecules that rigidly control the intermediary steps in the differentiation process.
胸腺素组分5含有几种不同的类激素因子,它们在部分或完全诱导和维持免疫功能方面有效。组分5的几种肽成分已被纯化、测序,并在旨在测量T细胞分化和功能的测定系统中进行了研究。这些研究表明,许多纯化的肽作用于T细胞的不同亚群(见图1)。胸腺素β3和β4肽作用于末端脱氧核苷酸转移酶(TdT)阴性的前体T细胞,以诱导TdT阳性细胞。胸腺素α1诱导功能性辅助细胞的形成,并使Lyt-细胞转化为Lyt 1+、2+、3+细胞。胸腺素α7诱导功能性抑制性T细胞的形成,并也使Lyt-细胞转化为Lyt 1+、2+、3+细胞。这些研究提供了进一步的证据,表明胸腺分泌一族不同的肽,它们作用于T细胞成熟序列的各个位点,以诱导和维持免疫功能。用胸腺素治疗原发性免疫缺陷疾病、自身免疫性疾病和癌症的I期和II期临床试验表明,内分泌胸腺在维持免疫平衡以及治疗以胸腺功能障碍为特征的疾病中起主要作用。越来越清楚的是,免疫成熟是一个涉及许多复杂步骤的过程,除非它是唯一缺乏的肽,否则启动单个细胞事件的单一因子可能不会在任何有意义的免疫重建中得到体现。鉴于T细胞成熟序列的复杂性以及正在识别的T细胞亚群数量不断增加,如果单一的胸腺因子能够控制所有涉及的步骤和群体,那将是令人惊讶的。相反,似乎T细胞成熟和功能 的控制涉及许多胸腺特异性因子和其他分子,它们严格控制分化过程中的中间步骤。