Dosenko V Ie, Goldenberg D I
A.A. Bogomoletz National Medical University, Kiev.
Fiziol Zh (1994). 2001;47(6):71-84.
In the review data about origin, spreading in the organism, differentiation, physiologic sense, role in diversity of pathologic processes, and also pharmaco- and immunocorrection's probable foundations of T-lymphocyte's new population with T cell receptor (TcR) gamma delta (TL gamma delta) are resumed. In the phylogenesis TL gamma delta are supposed to be older than T lymphocytes with TcR alpha beta. The conclusion is based upon domination of this lymphocyte population at gestation's early stage and huge representation of pseudogenes in the DNA region that encodes TcR structure of TL gamma delta. A morphological and functional resemblance of the given population with natural killer cells is underlined. It is paid attention to wide representation of TL gamma delta in the periphery tissues, poverty of TcR diapason that may evidence about postdifferentiation's process of TL gamma delta to be accomplished due to TcR genes rearrangement. This process appears to supply the enhancement of antigen-specific TL gamma delta in foreign agent's inculcation. A maturation process and probable mechanisms of these lymphocytes education in thymus is described. A classification of TL gamma delta depending on TcR structure and cytokine profile of the lymphocytes that subdivides them on T-helper/cytotoxic (Vg9/Vd2 phenotype) and cytotoxic/suppressor (Vd1 or Vd3 phenotype) was proposed. In the review the role of TL gamma delta in mucous immunity supporting and possible participating in systemic regulation of the immune response is emphasized. A physiologic role of TL gamma delta, namely ability to identify non-protein antigens (lipopolysaccharides, polyphosphates, glycolipids) and heat shock proteins, is also described. Evidences about uncertainty of incomplete phagocytosis phenomenon in vivo in case of TL gamma delta's normal function are given. Particularly it is made out that these lymphocytes are able to activate inducible NO-synthase in the macrophages that enhances their phagocytic activity in tens time. A function of these lymphocytes in defense against infection of bacterial, viral, protozoa, fungal origin, and also in tumor growth and autoimmune diseases is represented. Methods of specific therapeutic influence upon TL gamma delta, both pharmacological (pamidronat, 2,3-diphosphoglyceric acid) and immunologic profile (monoclonal antibodies conjugated with cytotoxic agent) are given.
本综述总结了有关具有γδT细胞受体(TcR)的T淋巴细胞新亚群(TLγδ)的起源、在机体中的扩散、分化、生理意义、在多种病理过程中的作用,以及药物和免疫校正可能的基础等方面的研究数据。在系统发生过程中,TLγδ被认为比具有αβTcR的T淋巴细胞更为古老。这一结论基于该淋巴细胞亚群在妊娠早期的主导地位以及编码TLγδTcR结构的DNA区域中假基因的大量存在。文中强调了该亚群与自然杀伤细胞在形态和功能上的相似性。还提到了TLγδ在外周组织中的广泛分布、TcR范围的有限性,这可能表明TLγδ的分化后过程是通过TcR基因重排完成的。这一过程似乎在接触外来病原体时增强了抗原特异性TLγδ。文中描述了这些淋巴细胞在胸腺中的成熟过程和可能的发育机制。提出了根据TcR结构和淋巴细胞细胞因子谱对TLγδ进行分类的方法,将其分为辅助性/细胞毒性(Vγ9/Vδ2表型)和细胞毒性/抑制性(Vδ1或Vδ3表型)。综述中强调了TLγδ在支持黏膜免疫以及可能参与免疫反应的全身调节中的作用。还描述了TLγδ的生理作用,即识别非蛋白质抗原(脂多糖、多磷酸盐、糖脂)和热休克蛋白的能力。文中给出了关于TLγδ正常功能情况下体内不完全吞噬现象不确定性的证据。特别指出这些淋巴细胞能够激活巨噬细胞中的诱导型一氧化氮合酶,从而使其吞噬活性提高数十倍。阐述了这些淋巴细胞在抵御细菌、病毒、原生动物、真菌来源的感染以及在肿瘤生长和自身免疫性疾病中的作用。给出了对TLγδ进行特异性治疗干预的方法,包括药理学方法(帕米膦酸盐、2,3 - 二磷酸甘油酸)和免疫学方法(与细胞毒性剂偶联的单克隆抗体)。