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CTLA-4 Expression Inversely Correlates with Kidney Function and Serum Immunoglobulin Concentration in Patients with Primary Glomerulonephritides

机译:CTLA-4表达与初级肾小球酮糖苷患者中的肾功能和血清免疫球蛋白浓度与肾功能和血清免疫球蛋白浓度相关联

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摘要

Major causes of chronic kidney disease are primary proliferative and nonproliferative glomerulonephritides (PGN and NPGN). However, the pathogenesis of PGN and NPGN is still not fully understood. Cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) is a T-cell membrane receptor that plays a key role in T-cell inhibition. Despite its role in autoimmunological diseases, little is known about the involvement of CTLA-4 in the pathogenesis of PGN and NPGN. The objective of this study was to determine the role of CTLA-4 in the pathogenesis of PGN and NPGN by evaluating the frequencies of T and B lymphocytes expressing CTLA-4 and the serum concentration of the sCTLA-4 isoform in patients with PGN and NPGN in relation to clinical parameters. The study included peripheral blood (PB) samples from 40 PGN and NPGN patients and 20 healthy age- and sex-matched volunteers (control group). The viable PB lymphocytes were labeled with fluorochrome-conjugated monoclonal anti-CTLA-4 antibodies and analyzed using flow cytometry. The serum concentration of sCTLA-4 was measured using ELISA. The frequencies and absolute counts of CD4(+)/CTLA-4(+) T lymphocytes, CD8(+)/CTLA-4(+) T lymphocytes and CD19(+)/CTLA-4(+) B lymphocytes and the serum sCTLA-4 concentration were lower in PGN and NPGN patients that in the control group. Reduced sCTLA-4 expression was associated with a lower concentration of serum immunoglobulins. Our results indicate that deregulation of CTLA-4 expression may result in continuous activation of T cells and contribute to the pathogenesis of PGN and NPGN.
机译:慢性肾脏疾病的主要病因是伯增殖和非增殖性肾小球肾炎(PGN和NPGN)。然而,PGN和NPGN的发病机制还没有完全理解。细胞毒性T淋巴细胞相关抗原-4(CTLA-4)是在T细胞的抑制中起关键作用的T细胞的膜受体。尽管其在自身免疫疾病中的作用,知之甚少CTLA-4的PGN和NPGN的发病机制中的参与。本研究的目的是通过评估的T表达CTLA-4的频率和B淋巴细胞和sCTLA-4同种型的患者PGN和NPGN血清浓度,以确定CTLA-4的在PGN和NPGN的发病中的作用有关临床参数。该研究包括40名PGN和NPGN患者和20名健康年龄和性别匹配的志愿者(对照组)的外周血(PB)样​​品。活PB淋巴细胞标记有荧光染料缀合的单克隆抗CTLA-4抗体,并使用流式细胞术分析。 sCTLA-4的血清浓度用ELISA测定。频率和CD4(+)/ CTLA-4(+)T淋巴细胞,CD8(+)的绝对计数/ CTLA-4(+)T淋巴细胞和CD19(+)/ CTLA-4(+)B淋巴细胞和血清sCTLA-4浓度在对照组中PGN和NPGN患者比。降低sCTLA-4表达与血清免疫球蛋白的浓度较低相关联。我们的研究结果表明,CTLA-4表达的失调可导致T细胞的激活连续而有助于PGN和NPGN的发病机制。

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