Xi Cheng, Xue Bai, Wen-Ya Shang, Li Wei, Jun-Ya Jia, Tie-Kun Yan, Qiu-Hua Gu
{"title":"新月体性肾小球肾炎患者肾组织树突状细胞亚群图谱。","authors":"Xi Cheng, Xue Bai, Wen-Ya Shang, Li Wei, Jun-Ya Jia, Tie-Kun Yan, Qiu-Hua Gu","doi":"10.1007/s11255-024-04175-6","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Dendritic cells (DCs) have been speculated to be involved in the pathogenesis of glomerular diseases. However, the numbers and distribution of DC subsets in the kidneys of patients with crescentic glomerulonephritis (CrGN) have not been clearly elucidated.</p><p><strong>Methods: </strong>A total of 26 patients with biopsy-proven CrGN were enrolled. Indirect immunofluorescence staining was used to quantify DC subsets in renal specimens. Double staining of HLA with CD11C, BDCA2 and CD209 respectively was performed to detect DC subsets. The correlation between DC subsets infiltrated in the kidney and clinical and pathological parameters was investigated.</p><p><strong>Results: </strong>DC subsets were predominantly present in the kidney interstitium, particularly in the peri-glomerular area. The numbers of CD11C<sup>+</sup>DCs, BDCA2<sup>+</sup>DCs and CD209<sup>+</sup>DCs increased in the patients with CrGN and varied among different types of CrGN. Though significant correlation between DC subsets and the percentage of crescents had not been identified, a notable increase in the number of CD11C<sup>+</sup>DCs were observed with the chronic development of crescents. Furthermore, patients with severe tubulointerstitial injury exhibited significantly more infiltrations of CD11C<sup>+</sup>DCs, BDCA2<sup>+</sup>DCs and CD209<sup>+</sup>DCs. Moreover, the numbers of CD11C<sup>+</sup>DCs and BDCA2<sup>+</sup>DCs were found to correlate with the level of serum C3.</p><p><strong>Conclusions: </strong>Patients with CrGN showed increased kidney infiltration of DC subsets, primarily localized in the renal interstitium and peri-glomerular region. The correlation between DC subsets and fibrosis of crescent and severe tubulointerstitial injury implied a potential involvement of DCs in the development of CrGN.</p>","PeriodicalId":14454,"journal":{"name":"International Urology and Nephrology","volume":" ","pages":"263-273"},"PeriodicalIF":1.8000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Profiling dendritic cells subsets in renal tissue of patients with crescentic glomerulonephritis.\",\"authors\":\"Xi Cheng, Xue Bai, Wen-Ya Shang, Li Wei, Jun-Ya Jia, Tie-Kun Yan, Qiu-Hua Gu\",\"doi\":\"10.1007/s11255-024-04175-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Dendritic cells (DCs) have been speculated to be involved in the pathogenesis of glomerular diseases. However, the numbers and distribution of DC subsets in the kidneys of patients with crescentic glomerulonephritis (CrGN) have not been clearly elucidated.</p><p><strong>Methods: </strong>A total of 26 patients with biopsy-proven CrGN were enrolled. Indirect immunofluorescence staining was used to quantify DC subsets in renal specimens. Double staining of HLA with CD11C, BDCA2 and CD209 respectively was performed to detect DC subsets. The correlation between DC subsets infiltrated in the kidney and clinical and pathological parameters was investigated.</p><p><strong>Results: </strong>DC subsets were predominantly present in the kidney interstitium, particularly in the peri-glomerular area. The numbers of CD11C<sup>+</sup>DCs, BDCA2<sup>+</sup>DCs and CD209<sup>+</sup>DCs increased in the patients with CrGN and varied among different types of CrGN. Though significant correlation between DC subsets and the percentage of crescents had not been identified, a notable increase in the number of CD11C<sup>+</sup>DCs were observed with the chronic development of crescents. Furthermore, patients with severe tubulointerstitial injury exhibited significantly more infiltrations of CD11C<sup>+</sup>DCs, BDCA2<sup>+</sup>DCs and CD209<sup>+</sup>DCs. Moreover, the numbers of CD11C<sup>+</sup>DCs and BDCA2<sup>+</sup>DCs were found to correlate with the level of serum C3.</p><p><strong>Conclusions: </strong>Patients with CrGN showed increased kidney infiltration of DC subsets, primarily localized in the renal interstitium and peri-glomerular region. The correlation between DC subsets and fibrosis of crescent and severe tubulointerstitial injury implied a potential involvement of DCs in the development of CrGN.</p>\",\"PeriodicalId\":14454,\"journal\":{\"name\":\"International Urology and Nephrology\",\"volume\":\" \",\"pages\":\"263-273\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Urology and Nephrology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s11255-024-04175-6\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/7/29 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"UROLOGY & NEPHROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Urology and Nephrology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11255-024-04175-6","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/29 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景:树突状细胞(DC)被推测与肾小球疾病的发病机制有关。然而,新月体性肾小球肾炎(CrGN)患者肾脏中DC亚群的数量和分布尚未明确阐明:方法:共招募了26名经活检证实患有新月体性肾小球肾炎(CrGN)的患者。采用间接免疫荧光染色法量化肾脏标本中的 DC 亚群。HLA与CD11C、BDCA2和CD209分别进行双重染色,以检测DC亚群。研究了肾脏中浸润的 DC 亚群与临床和病理参数之间的相关性:结果:DC亚群主要存在于肾间质,尤其是肾小球周围区域。在 CrGN 患者中,CD11C+DCs、BDCA2+DCs 和 CD209+DCs 的数量增加,且在不同类型的 CrGN 中存在差异。虽然尚未发现 DC 亚群与新月体百分比之间存在明显的相关性,但观察到 CD11C+DCs 的数量随着新月体的慢性发展而明显增加。此外,严重肾小管间质损伤患者的 CD11C+DC、BDCA2+DC 和 CD209+DC 的浸润明显增多。此外,CD11C+DCs 和 BDCA2+DCs 的数量还与血清 C3 水平相关:结论:CrGN 患者肾脏中的 DC 亚群浸润增加,主要分布在肾间质和肾小球周围区域。DC亚群与新月体纤维化和严重肾小管间质损伤之间的相关性意味着DC可能参与了CrGN的发病。
Profiling dendritic cells subsets in renal tissue of patients with crescentic glomerulonephritis.
Background: Dendritic cells (DCs) have been speculated to be involved in the pathogenesis of glomerular diseases. However, the numbers and distribution of DC subsets in the kidneys of patients with crescentic glomerulonephritis (CrGN) have not been clearly elucidated.
Methods: A total of 26 patients with biopsy-proven CrGN were enrolled. Indirect immunofluorescence staining was used to quantify DC subsets in renal specimens. Double staining of HLA with CD11C, BDCA2 and CD209 respectively was performed to detect DC subsets. The correlation between DC subsets infiltrated in the kidney and clinical and pathological parameters was investigated.
Results: DC subsets were predominantly present in the kidney interstitium, particularly in the peri-glomerular area. The numbers of CD11C+DCs, BDCA2+DCs and CD209+DCs increased in the patients with CrGN and varied among different types of CrGN. Though significant correlation between DC subsets and the percentage of crescents had not been identified, a notable increase in the number of CD11C+DCs were observed with the chronic development of crescents. Furthermore, patients with severe tubulointerstitial injury exhibited significantly more infiltrations of CD11C+DCs, BDCA2+DCs and CD209+DCs. Moreover, the numbers of CD11C+DCs and BDCA2+DCs were found to correlate with the level of serum C3.
Conclusions: Patients with CrGN showed increased kidney infiltration of DC subsets, primarily localized in the renal interstitium and peri-glomerular region. The correlation between DC subsets and fibrosis of crescent and severe tubulointerstitial injury implied a potential involvement of DCs in the development of CrGN.
期刊介绍:
International Urology and Nephrology publishes original papers on a broad range of topics in urology, nephrology and andrology. The journal integrates papers originating from clinical practice.