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We are analyzing https://link.springer.com/article/10.1007/s10067-025-07528-3.

Title:
Luminex-based pilot study identifies novel serum autoantibodies associated with disease activity in patients with lupus nephritis | Clinical Rheumatology
Description:
Objective To explore the associations of novel serum autoantibodies with disease activity and organ injuries in patients with lupus nephritis (LN). Method This study included 75 patients with active LN (5 class II, 37 class IV, and 33 class V). Indirect immunofluorescence was used to measure serum anti-dsDNA; ELISA was used to measure serum anti-PLA2R and anti-C1q, and the Luminex method was used to measure 58 novel serum autoantibodies, with a median fluorescence intensity (MFI)/threshold β‰₯ 1.5 as the antibody positivity cutoff. Results The positivity rates for 11 novel antibodies (anti-PLA2R, anti-P2RY11, anti-DEXI, anti-HARS, anti-TUBA1B, anti-KRT8, anti-TUBB, anti-NCL, anti-HSPB1, anti-AGRN, and anti-LGALS8) were highly associated with SLE activity and were inconsistent with those for anti-dsDNA and anti-C1q. Anti-TUBA1B and anti-AGRN positivity may independently influence LN with extrarenal organ involvement (OR = 6.73, 95% CI = 1.19 ~ 38.09; OR = 6.11, 95% CI = 1.32 ~ 28.25, respectively). The positivity rate for anti-PLA2R as detected by the Luminex platform was 40%, whereas the rate among those detected by ELISA was 12.7%. Twenty-one patients who achieved renal remission were retested, and the positivity rates of anti-PLA2R (42.9% vs. 9.5%, P = 0.014), anti-KRT8 (47.6% vs. 4.8%, P = 0.001), and anti-AGRN (38.1% vs. 4.8%, P = 0.008) also significantly decreased from baseline. Conclusion On the basis of Luminex technology, the present study revealed multiple novel autoantibodies related to SLE activity and organ injury, especially anti-PLA2R, anti-KRT8, and anti-AGRN, thereby providing novel serological markers for the assessment of activity in patients with LN. Anti-TUBA1B and anti-AGRN are strongly associated with extrarenal involvement. Key Points β€’ The Luminex method is highly sensitive and high-throughput for detecting serum autoantibodies. β€’ LN patients with anti-TUBA1B and anti-AGRN positivity are more likely to be complicated by extrarenal organ involvement. β€’ Serum anti-PLA2R, anti-KRT8, and anti-AGRN reflect the activity of SLE and provide novel serological markers for the evaluation of LN patients negative for anti-dsDNA and anti-C1q.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Education
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Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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Keywords {πŸ”}

pubmed, article, google, scholar, lupus, cas, central, nephritis, liu, patients, systemic, erythematosus, zhang, activity, study, autoantibodies, kidney, clinical, antibodies, httpsdoiorgs, immunol, serum, disease, wang, membranous, data, research, yang, antiplar, positivity, antiagrn, access, deng, organ, anticq, antibody, author, front, httpsdoiorgfimmu, int, cell, national, authors, privacy, cookies, content, information, manuscript, huan, zhou,

Topics {βœ’οΈ}

ifn-gamma-induced il-6 production month download article/chapter single-center retrospective study tlr-mediated syk activation tubulin alpha-1b chain antiphospholipid antibody positivity luminex technology systemic lupus erythematosus anti-dsdna igg1 correlates national key research full article pdf acute kidney injury bioinformatics-based analysis cabral-marques phospholipase a2 receptor measure serum anti-dsdna privacy choices/manage cookies severe lupus nephritis measure serum anti-pla2r secretory phospholipase a2 lupus nephritis development membranous lupus nephritis autoantibody-induced pathology active lupus nephritis modified national institutes genes encoding agrin organ injury achieved renal remission language polishing services weixin hu huan zhang participated related subjects de miranda gc article zhang detecting serum autoantibodies holds exclusive rights check access instant access anti-histone antibodies european economic area median fluorescence intensity regulating intracellular glycosyltransferases subsequent vascular events interferon signaling pathway normalize blood ifnΞ± improving global outcomes current diagnostic modalities altered vesicle trafficking heat shock proteins protein-coupled receptors

Schema {πŸ—ΊοΈ}

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         headline:Luminex-based pilot study identifies novel serum autoantibodies associated with disease activity in patients with lupus nephritis
         description:To explore the associations of novel serum autoantibodies with disease activity and organ injuries in patients with lupus nephritis (LN). This study included 75 patients with active LN (5 class II, 37 class IV, and 33 class V). Indirect immunofluorescence was used to measure serum anti-dsDNA; ELISA was used to measure serum anti-PLA2R and anti-C1q, and the Luminex method was used to measure 58 novel serum autoantibodies, with a median fluorescence intensity (MFI)/threshold β‰₯ 1.5 as the antibody positivity cutoff. The positivity rates for 11 novel antibodies (anti-PLA2R, anti-P2RY11, anti-DEXI, anti-HARS, anti-TUBA1B, anti-KRT8, anti-TUBB, anti-NCL, anti-HSPB1, anti-AGRN, and anti-LGALS8) were highly associated with SLE activity and were inconsistent with those for anti-dsDNA and anti-C1q. Anti-TUBA1B and anti-AGRN positivity may independently influence LN with extrarenal organ involvement (OR = 6.73, 95% CI = 1.19 ~ 38.09; OR = 6.11, 95% CI = 1.32 ~ 28.25, respectively). The positivity rate for anti-PLA2R as detected by the Luminex platform was 40%, whereas the rate among those detected by ELISA was 12.7%. Twenty-one patients who achieved renal remission were retested, and the positivity rates of anti-PLA2R (42.9% vs. 9.5%, P = 0.014), anti-KRT8 (47.6% vs. 4.8%, P = 0.001), and anti-AGRN (38.1% vs. 4.8%, P = 0.008) also significantly decreased from baseline. On the basis of Luminex technology, the present study revealed multiple novel autoantibodies related to SLE activity and organ injury, especially anti-PLA2R, anti-KRT8, and anti-AGRN, thereby providing novel serological markers for the assessment of activity in patients with LN. Anti-TUBA1B and anti-AGRN are strongly associated with extrarenal involvement.
         datePublished:2025-06-11T00:00:00Z
         dateModified:2025-06-11T00:00:00Z
         pageStart:1
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            Autoantibodies
            Luminex technology
            Lupus nephritis
            Organ injury
            SLE activity
            Systemic lupus erythematosus
            Rheumatology
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      headline:Luminex-based pilot study identifies novel serum autoantibodies associated with disease activity in patients with lupus nephritis
      description:To explore the associations of novel serum autoantibodies with disease activity and organ injuries in patients with lupus nephritis (LN). This study included 75 patients with active LN (5 class II, 37 class IV, and 33 class V). Indirect immunofluorescence was used to measure serum anti-dsDNA; ELISA was used to measure serum anti-PLA2R and anti-C1q, and the Luminex method was used to measure 58 novel serum autoantibodies, with a median fluorescence intensity (MFI)/threshold β‰₯ 1.5 as the antibody positivity cutoff. The positivity rates for 11 novel antibodies (anti-PLA2R, anti-P2RY11, anti-DEXI, anti-HARS, anti-TUBA1B, anti-KRT8, anti-TUBB, anti-NCL, anti-HSPB1, anti-AGRN, and anti-LGALS8) were highly associated with SLE activity and were inconsistent with those for anti-dsDNA and anti-C1q. Anti-TUBA1B and anti-AGRN positivity may independently influence LN with extrarenal organ involvement (OR = 6.73, 95% CI = 1.19 ~ 38.09; OR = 6.11, 95% CI = 1.32 ~ 28.25, respectively). The positivity rate for anti-PLA2R as detected by the Luminex platform was 40%, whereas the rate among those detected by ELISA was 12.7%. Twenty-one patients who achieved renal remission were retested, and the positivity rates of anti-PLA2R (42.9% vs. 9.5%, P = 0.014), anti-KRT8 (47.6% vs. 4.8%, P = 0.001), and anti-AGRN (38.1% vs. 4.8%, P = 0.008) also significantly decreased from baseline. On the basis of Luminex technology, the present study revealed multiple novel autoantibodies related to SLE activity and organ injury, especially anti-PLA2R, anti-KRT8, and anti-AGRN, thereby providing novel serological markers for the assessment of activity in patients with LN. Anti-TUBA1B and anti-AGRN are strongly associated with extrarenal involvement.
      datePublished:2025-06-11T00:00:00Z
      dateModified:2025-06-11T00:00:00Z
      pageStart:1
      pageEnd:12
      sameAs:https://doi.org/10.1007/s10067-025-07528-3
      keywords:
         Autoantibodies
         Luminex technology
         Lupus nephritis
         Organ injury
         SLE activity
         Systemic lupus erythematosus
         Rheumatology
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                     name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, The First School of Clinical Medicine, Southern Medical University, Nanjing, China
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                     name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
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                  address:
                     name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
                     type:PostalAddress
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                     name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
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         name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
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         name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
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      name:Jiayi Deng
      affiliation:
            name:Nanjing University
            address:
               name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
               type:PostalAddress
            type:Organization
      name:Yang Liu
      affiliation:
            name:Southern Medical University
            address:
               name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, The First School of Clinical Medicine, Southern Medical University, Nanjing, China
               type:PostalAddress
            type:Organization
      name:Wen Xia
      affiliation:
            name:Nanjing University
            address:
               name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
               type:PostalAddress
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      name:Lulu Zhuang
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               name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
               type:PostalAddress
            type:Organization
      name:Haitao Zhang
      affiliation:
            name:Nanjing University
            address:
               name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
               type:PostalAddress
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      name:Weixin Hu
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            name:Nanjing University
            address:
               name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
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      name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, The First School of Clinical Medicine, Southern Medical University, Nanjing, China
      name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
      name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
      name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
      name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
      name:National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
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