Pandolfi Franco, Cianci Rossella, Cammarota Giovanni, Pagliari Danilo, Landolfi Raffaele, Conti Pio, Theoharides Theoharis C
Institute of Internal Medicine, Catholic University, Largo F. Vito 1, 00186 Rome, Italy.
Ann Clin Lab Sci. 2010 Winter;40(1):3-9.
In recent years, the field of primary immunodeficienciency diseases (PID) has experienced remarkable progress with the identification of a number of new genes associated with specific diseases. Yet the diagnosis of PID remains difficult. In fact, this field requires continuous updating because once a novel molecule related to the immune function is discovered, the corresponding PID will soon be described. Since comprehensive reviews on the classification of PID are available, we concentrate here on reviewing some controversial and new issues, mainly those related to the role of T-cells and innate immunity. We will consider common variable immunodeficiency as an example of a PID where several immune pathways are impaired. We will also discuss the restricted usage of the T-cell receptor repertoire in PID. Innate immunity and Toll-like receptors (TLR) are new major players in this field. We will therefore discuss the association of TLR with the function of Bruton tyrosine kinase (Btk) that is essential in the development of B-cells and in the pathogenesis of X-linked agammaglobulinemia. Finally, we will discuss the role of mast-cells. These cells were once thought to be relevant almost exclusively to the pathogenesis of allergy. Now we know that mast cells are involved in initiating the adaptive response and may contribute to ineffective immune responses.
近年来,原发性免疫缺陷病(PID)领域取得了显著进展,发现了许多与特定疾病相关的新基因。然而,PID的诊断仍然困难。事实上,由于一旦发现与免疫功能相关的新分子,相应的PID很快就会被描述出来,所以这个领域需要不断更新。鉴于已有关于PID分类的全面综述,我们在此集中探讨一些有争议的新问题,主要是与T细胞和固有免疫作用相关的问题。我们将以常见变异型免疫缺陷为例,说明一种多种免疫途径受损的PID。我们还将讨论PID中T细胞受体库的有限使用情况。固有免疫和Toll样受体(TLR)是该领域新的主要参与者。因此,我们将讨论TLR与布鲁顿酪氨酸激酶(Btk)功能的关联,Btk在B细胞发育和X连锁无丙种球蛋白血症的发病机制中至关重要。最后,我们将讨论肥大细胞的作用。这些细胞曾被认为几乎只与过敏发病机制相关。现在我们知道肥大细胞参与启动适应性反应,可能导致免疫反应无效。