Avramović V, Petrović V, Jović M, Vlahović P
Institute of Histology and Embryology, Faculty of Medicine University of Niš, Serbia;
Centre for Medical Biochemistry, Clinical Centre Niš, Serbia.
Acta Otorhinolaryngol Ital. 2015 Oct;35(4):277-84.
During chronic tonsillitis, the relationship between proliferation and apoptosis of lymphocytes in tonsillar follicles can be disturbed, which gives rise to attenuation of tonsil immunocompetence and diminishing its contribution in systemic immunity. In this study, we have quantified the cells expressing the markers of proliferation and apoptosis in the follicles of the palatine tonsil. Six tonsils from patients aged 10-29 years with hypertrophic tonsillitis and five tonsils from patients aged 18-22 years with recurrent tonsillitis were studied. The sections of paraffin blocks of tonsillar tissue were stained by the immunohistochemical LSAB/HRP method with the utilisation of antibodies for: Ki-67 antigen-cell marker of proliferation; Bcl-2 and survivin anti-apoptotic factors and Fas/CD95, caspase-3 and Bax pro-apoptotic factors. The size of lymphoid follicles, i.e. mean follicle area and number of lymphoid follicle immunopositive cells per mm2 of a slice area, i.e. numerical areal density were determined by the quantitative image analysis. The localisation of Ki-67, Bcl-2, survivin, Fas/CD95, caspase-3 and Bax- immunopositive cells inside the palatine tonsil was similar in both types of tonsillitis. The number of Ki-67 immunopositive cells was significantly (p < 0.01) larger in the tonsils with hypertrophic tonsillitis (14681.4 ± 1460.5) in comparison to those with recurrent tonsillitis (12491.4 ± 2321.6), although the number of survivin and caspase-3 immunopositive cells was significantly (p < 0.05) larger in recurrent tonsillitis (survivin, 406.9 ± 98.4; caspase-3, 350.4 ± 119.4) when compared to those with hypertrophic tonsillitis (survivin, 117.4 ± 14.5; caspase-3, 210 ± 24). Our results show that the rate of the proliferation and apoptosis of follicular lymphocytes is different in various types of tonsillitis. This suggests that the immunological potential of the palatine tonsil varies in patients with hypertrophic and recurrent tonsillitis, which in practice poses a dilemma over the choice of conservative or surgical treatment.
在慢性扁桃体炎期间,扁桃体滤泡中淋巴细胞的增殖与凋亡之间的关系可能受到干扰,这会导致扁桃体免疫能力减弱,其在全身免疫中的作用降低。在本研究中,我们对腭扁桃体滤泡中表达增殖和凋亡标志物的细胞进行了定量分析。研究了6例年龄在10 - 29岁的肥厚性扁桃体炎患者的扁桃体以及5例年龄在18 - 22岁的复发性扁桃体炎患者的扁桃体。利用针对以下抗体,通过免疫组织化学LSAB/HRP方法对扁桃体组织石蜡块切片进行染色:Ki-67抗原——增殖细胞标志物;Bcl-2和生存素抗凋亡因子以及Fas/CD95、半胱天冬酶-3和Bax促凋亡因子。通过定量图像分析确定淋巴滤泡的大小,即平均滤泡面积以及每平方毫米切片面积中淋巴滤泡免疫阳性细胞的数量,即数值面积密度。在两种类型的扁桃体炎中,腭扁桃体内部Ki-67、Bcl-2、生存素、Fas/CD95、半胱天冬酶-3和Bax免疫阳性细胞的定位相似。与复发性扁桃体炎患者(12491.4 ± 2321.6)相比,肥厚性扁桃体炎患者的扁桃体中Ki-67免疫阳性细胞数量显著更多(p < 0.01)(14681.4 ± 1460.5),不过与肥厚性扁桃体炎患者(生存素,117.4 ± 14.5;半胱天冬酶-3,210 ± 24)相比,复发性扁桃体炎患者的生存素和半胱天冬酶-3免疫阳性细胞数量显著更多(p < 0.05)(生存素,406.9 ± 98.4;半胱天冬酶-3,350.4 ± 119.4)。我们的数据表明,不同类型的扁桃体炎中滤泡淋巴细胞的增殖和凋亡速率不同。这表明肥厚性和复发性扁桃体炎患者腭扁桃体的免疫潜能不同,这在实际中给保守治疗还是手术治疗的选择带来了困境。