Panarese Alessandra, D'Andrea Vito, Pironi Daniele, Filippini Angelo
Ann Ital Chir. 2014 Nov-Dec;85(6):617-8.
Dear Sir The thymus plays a crucial role in the context of cellmediated immunity in the differentiation of T lymphocytes, not only during the embryogenesis and fetal period but also during the adulthood, even after its involution 1,2,3. It has been proved, indeed, that thymectomy in adult rat entails a decrease of the T-lymphocite response to mitogens and eventually its abolition 4,5,6. The removal of the thymus can decrease the activity of T-helper cells but in the same time it might enhance the activity of T-suppressor whose function is depressed in autoimmune diseases 7. The therapeutic role of thymectomy is proved in Myasthenia Gravis even if the exact mechanism underlying its effect remains largely unknown. The role of thymectomy as a treatment of autoimmune diseases other than Myasthenia Gravis (i.e. sistemic lupus erythematosus, rheumatoid arthritis, autoimmune hemolytic anemia, multiple sclerosis) has been investigated but the results of these studies are questionable 7. Our aim is to evaluate the role of thymectomy in order to clarify whether it may be regarded not just as therapeuytic, but, on the contrary, as a factor paving the way to the onset of autoimmune diseases. Therefore, the relevant literature has been taken into account along our study. Thymus has an important role in regulating immune reaction through its control on T-cell differentiation of both T-helper and T-suppressor/cytotoxic cells. That is the reason why thymectomy produces a shift in autoimmune diseases with disregulation of the immune networks2. After thymectomy, indeed, an induction and an acceleration of autoimmune processes has been observed. A relevant work focusing on those mechanisms was written by Gerli et al1 . In their work, the authors consider the long term immunologic effects of therapeutic thymectomy in patients with Myasthenia Gravis comparing 16 patients with Myasthenia Gravis and previous Thymectomy (at least 8 years before), 6 patients with Myasthenia Gravis and recent Thymectomy (<1year) and 13 with Myasthenia Gravis non Thymectomized and 32 healthy subjects used as control. The study shows that the long term thymectomized patients had mild T-cell lymphopenia and an expansion of CD4+ and CD8+ cells. These serologic abnormalities were not detectable in not and recently thymectomized patients. Myasthenia Gravis and SLE are autoimmune disorders. They have positivity for antinuclear antibodies (ANA) and thymus hyperplasia. SLE is characterized by an alteration of the immune system that involves B cells and T lymphocites, resulting in polyclonal B cell activation and autoantybody production. The thymus deletes self-reactive T-cells with high avidity T-cell receptors for self antigens expressed in the thymus 8,9. This, hence, means that thymus has a protective role against autoimmunity. The prevalence of SLE in pts with Myasthenia Gravis has been reported 0,2%-2,7% 10. Cases in which the SLE has developed after thymectomy for Myasthenia Gravis have been reported in the literature, but there are also cases in which SLE developed before thymectomy in pts with both SLE and MG. Iwadate at al reported from a review of the literature in a period of 40 years (1963- 2004) 21 patients in whom LES developed after thymectomy. Their ages ranged from 11 to 66 years (mean 40.4 years) with SLE developing from 2 months to 13 years (mean 4.9 years) after thymectomy. Polyarthritis was the most common manifestation of SLE 11. The proof that thymectomy can facilitate the development of SLE can be traced in the cases reported by the literature. The prevalence of SLE among patients with thymoma varies between 1,5 and 10% 12. Boonen et al identified in a period of 20 years (1975-1998) 18 new cases of thymoma and SLE. In 39% of the patients SLE was diagnosed before detection of thymoma. In 33% of the patients, thymoma and SLE was found simultaneously and in 28% SLE was discovered after thymoma. In five cases thymectomy had no clear effect on SLE. In two cases an exacerbation was reported and in one case SLE was attenuated 11,13. However, Vaiopoulos et al 14 described in a series of 28 patients with both LES and Myasthenia Gravis, 17 cases in which LES developed before thymectomy.
Thymectomy may thus be a precipitating factor for the development of SLE due to the loss of central tolerance and the overproduction of antibodies. Therefore, after a thymectomy, it is important to perform a timely follow up of the patient.
尊敬的先生 胸腺在细胞介导的免疫中对T淋巴细胞的分化起着关键作用,不仅在胚胎发生期和胎儿期如此,在成年期甚至在其退化后也是如此1,2,3。事实上,已经证明成年大鼠胸腺切除会导致T淋巴细胞对有丝分裂原的反应降低,最终使其消失4,5,6。胸腺切除可降低辅助性T细胞的活性,但同时可能增强抑制性T细胞的活性,而抑制性T细胞的功能在自身免疫性疾病中受到抑制7。胸腺切除在重症肌无力中的治疗作用已得到证实,但其确切作用机制仍大多未知。胸腺切除作为重症肌无力以外的自身免疫性疾病(即系统性红斑狼疮、类风湿性关节炎、自身免疫性溶血性贫血、多发性硬化症)的治疗方法已被研究,但这些研究结果存在疑问7。我们的目的是评估胸腺切除的作用,以阐明它是否不仅可被视为一种治疗方法,相反,是否是导致自身免疫性疾病发生的一个因素。因此,在我们的研究中考虑了相关文献。胸腺通过控制辅助性T细胞和抑制性/细胞毒性T细胞的T细胞分化,在调节免疫反应中起重要作用。这就是胸腺切除会导致自身免疫性疾病中免疫网络失调而发生转变的原因2。事实上,胸腺切除后,已观察到自身免疫过程的诱导和加速。Gerli等人1撰写了一篇关于这些机制的相关论文。在他们的论文中,作者比较了16例重症肌无力且之前已进行胸腺切除(至少8年前)的患者、6例重症肌无力且近期进行胸腺切除(<1年)的患者、13例未进行胸腺切除的重症肌无力患者以及32名作为对照的健康受试者,研究了治疗性胸腺切除对重症肌无力患者的长期免疫学影响。研究表明,长期胸腺切除的患者有轻度T细胞淋巴细胞减少以及CD4+和CD8+细胞的扩增。在未进行胸腺切除和近期进行胸腺切除的患者中未检测到这些血清学异常。重症肌无力和系统性红斑狼疮是自身免疫性疾病。它们抗核抗体(ANA)呈阳性且胸腺增生。系统性红斑狼疮的特征是免疫系统改变,涉及B细胞和T淋巴细胞,导致多克隆B细胞活化和自身抗体产生。胸腺会清除对胸腺中表达的自身抗原有高亲和力T细胞受体的自身反应性T细胞8,9。因此,这意味着胸腺对自身免疫有保护作用。据报道,重症肌无力患者中系统性红斑狼疮的患病率为0.2% - 2.7% 10。文献中报道了重症肌无力患者胸腺切除后发生系统性红斑狼疮的病例,但也有系统性红斑狼疮和重症肌无力患者在胸腺切除前就已发生系统性红斑狼疮的病例。Iwadate等人对40年(1963 - 2004年)的文献进行回顾,报告了21例胸腺切除后发生系统性红斑狼疮的患者。他们的年龄在11至66岁之间(平均40.4岁),系统性红斑狼疮在胸腺切除后2个月至13年(平均4.9年)发生。多关节炎是系统性红斑狼疮最常见的表现11。文献报道的病例可证明胸腺切除可促进系统性红斑狼疮的发生。胸腺瘤患者中系统性红斑狼疮的患病率在1.5%至10%之间12。Boonen等人在20年(1975 - 1998年)期间确定了18例新的胸腺瘤和系统性红斑狼疮病例。在39%的患者中,系统性红斑狼疮在胸腺瘤检测之前被诊断出来。在33%的患者中,胸腺瘤和系统性红斑狼疮同时被发现,在28%的患者中,系统性红斑狼疮在胸腺瘤之后被发现。在5例中,胸腺切除对系统性红斑狼疮没有明显影响。在2例中报告病情加重,在1例中系统性红斑狼疮病情减轻11,13。然而,Vaiopoulos等人14在一系列28例同时患有系统性红斑狼疮和重症肌无力的患者中描述,17例系统性红斑狼疮在胸腺切除前就已发生。
胸腺切除可能因中枢耐受性丧失和抗体过度产生而成为系统性红斑狼疮发生的一个促发因素。因此,胸腺切除后,对患者进行及时随访很重要。