Corrales J J, Orfao A, Miralles J M, López-Berges M C, García L C, González M, Mories M T, San Miguel J
Departamento de Medicina, Universidad de Salamanca, Spain.
Clin Investig. 1993 Jul;71(7):552-8. doi: 10.1007/BF00208480.
The origin of sporadic multinodular goiter is still uncertain. To obtain information on a number of unexplored immunological features, the distribution and characterization of T, B, and natural killer lymphocyte subsets were studied in the peripheral blood of 15 patients with multinodular goiter; 8 patients with Graves' disease (for reference purposes with a well-characterized autoimmune disease) and 29 age- and sex-matched healthy controls, combining double-staining immunofluorescence technique with monoclonal antibodies and flow cytometry. Although in both thyroid diseases increased CD3+ HLA-DR+ activated T cells (P < 0.01) were detected, in Graves' disease this was associated with decreased numbers of CD8 cells (P < 0.05) and an increased CD4/CD8 ratio (P < 0.01). These abnormalities were absent in multinodular goiter, which displayed increased CD8+ CD57+ cytotoxic/suppressor cells (P < 0.01). There was an increase in the percentage of natural killer cells expressing CD16 and CD57 antigens in multinodular goiter but not in Graves' disease. The B-cell associated antigens CD19 and CD19+ CD5+ were significantly increased in Graves' disease (P < 0.01), while the multinodular goiter patients exhibited only an increased number of B cells coexpressing the CD5 antigen (CD19+ CD5+), which was unrelated to the titers of anti-microsomal and antithyroglobulin autoantibodies. Our results point to the presence of several abnormalities of peripheral T, B, and natural killer lymphocytes in sporadic multinodular goiter, with a distribution pattern quite different from that observed in Graves' disease.(ABSTRACT TRUNCATED AT 250 WORDS)
散发性多结节性甲状腺肿的病因仍不明确。为获取一些未被探索的免疫学特征信息,我们采用单克隆抗体双染免疫荧光技术结合流式细胞术,研究了15例多结节性甲状腺肿患者、8例格雷夫斯病患者(作为具有明确自身免疫性疾病特征的对照)以及29名年龄和性别匹配的健康对照者外周血中T、B和自然杀伤淋巴细胞亚群的分布及特征。尽管在这两种甲状腺疾病中均检测到CD3 + HLA - DR + 活化T细胞增多(P < 0.01),但在格雷夫斯病中,这与CD8细胞数量减少(P < 0.05)及CD4/CD8比值升高(P < 0.01)相关。这些异常在多结节性甲状腺肿中不存在,多结节性甲状腺肿表现为CD8 + CD57 + 细胞毒性/抑制细胞增多(P < 0.01)。多结节性甲状腺肿中表达CD16和CD57抗原的自然杀伤细胞百分比增加,而格雷夫斯病中未增加。格雷夫斯病中B细胞相关抗原CD19和CD19 + CD5 + 显著增加(P < 0.01),而多结节性甲状腺肿患者仅表现为共表达CD5抗原的B细胞(CD19 + CD5 + )数量增加,这与抗微粒体和抗甲状腺球蛋白自身抗体滴度无关。我们的结果表明散发性多结节性甲状腺肿外周T、B和自然杀伤淋巴细胞存在多种异常,其分布模式与格雷夫斯病明显不同。(摘要截选至250字)