Routine immunohistochemical staining in membranous nephropathy: in situ detection of phospholipase A2 receptor and thrombospondin type 1 containing 7A domain

被引:17
|
作者
L'Imperio, Vincenzo [1 ]
Pieruzzi, Federico [2 ]
Sinico, Renato Alberto [2 ]
Nebuloni, Manuela [3 ,4 ]
Granata, Antonio [5 ]
Smith, Andrew [6 ]
Radice, Antonella [7 ]
Pagni, Fabio [1 ,4 ]
机构
[1] Univ Milano Bicocca, San Gerardo Hosp, Dept Med & Surg, Pathol, Monza, Italy
[2] Univ Milano Bicocca, Dept Med & Surg, Nephrol Unit, Monza, Italy
[3] Univ Milan, Dept Biomed & Clin Sci L Sacco, Milan, Italy
[4] Univ Milan, Res Ctr Renal Immunopathol, Milan, Italy
[5] San Giovanni Dio Hosp, Dept Nephrol, Agrigento, Italy
[6] Univ Milano Bicocca, Dept Med & Surg, Prote & Metabol Unit, Monza, Italy
[7] San Carlo Borromeo Hosp, Microbiol & Virol Dept, Milan, Italy
关键词
PLA2R; Membranous nephropathy; THSD7A; A(2) RECEPTOR; CLASSIFICATION CRITERIA; RENAL BIOPSIES; GLOMERULONEPHRITIS; CHILDREN; CANCER; GLOMERULOPATHY; ASSOCIATION; ANTIBODIES; IDENTIFICATION;
D O I
10.1007/s40620-018-0489-z
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Membranous nephropathy (MN) can be idiopathic (iMN) or manifest as a result of systemic underlying conditions as a secondary epiphenomenon. For the prognostic and predictive consequences of this discrimination, the routine use of reliable markers is crucial. This large MN series aimed to evaluate the routine and standardized immunohistochemical (IHC) employment of a panel of 3 biomarkers-phospholipase A2 receptor (PLA2R), thrombospondin type-1 domain-containing 7A (THSD7A), and immunoglobulin (Ig)G4-in the differential diagnosis of MN forms, contributing to the validation of the technique and the correct interpretation of reproducible patterns of reactivity. We classified 95 patients with a biopsy proven diagnosis of MN as primary (n = 72) or secondary (n = 23) cases based on clinical data. After performing an IHC assay directed against PLA2R, THSD7A and IgG4 antigens, samples were interpreted by three different nephropathologists to assess the positivity/negativity of the staining according to new interpretation criteria. Useful interpretation criteria were introduced to exclude false positive patterns of reactivity and to identify only true granular membranous or mesangial deposits in MN. The IHC directed against PLA2R resulted positive in 51 iMN cases and negative in 21, while 4/23 secondary forms were considered positive. Based on these data the technique showed a sensitivity of 71% and specificity of 83%. On the other hand, the IHC analysis for IgG4 resulted positive in 44 cases of iMN and negative in 28 cases, while only 4/23 secondary forms were positive (same cases positive to PLA2R). Finally, THSD7A was found to be positive only in 1 case, which was negative to PLA2R and IgG4. The combination of the results allowed a classification of the series into two major groups: "double-positive" (PLA2R+/IgG4+/THSD7A-) and "triple-negative" (PLA2R-/IgG4-/THSD7A-) cases. Based on these data, the diagnostic performance of the three biomarkers used in a "tandem fashion" can reach 79% sensitivity and 83% specificity, significantly reducing the risk of a false-positive or false-negative result and improving the routine characterization of this frequent glomerulonephritis.
引用
收藏
页码:543 / 550
页数:8
相关论文
共 50 条
  • [31] Clinical characteristics of thrombospondin type-1 domain-containing 7A-associated membranous nephropathy
    Suzuki, Tomo
    Han, Wei
    Watanabe, Shiika
    Terashita, Maho
    Nakata, Mayumi
    Ichikawa, Daisuke
    Shirai, Sayuri
    Shibagaki, Yugo
    RENAL FAILURE, 2020, 42 (01) : 966 - 968
  • [32] Progress on the M-type phospholipase A2 receptor in idiopathic membranous nephropathy
    Wang Chao
    Lu Huan
    Yang Cui
    Luo Yuezhong
    CHINESE MEDICAL JOURNAL, 2014, 127 (10) : 1960 - 1963
  • [33] Progress on the M-type phospholipase A2 receptor in idiopathic membranous nephropathy
    Wang Chao
    Lu Huan
    Yang Cui
    Luo Yuezhong
    中华医学杂志(英文版), 2014, 127 (10) : 1960 - 1963
  • [34] Presence of M-type Phospholipase A2 Receptor Antibody in Membranous Nephropathy
    Oto, Ozgur Akin
    Yazici, Halil
    Caliskan, Yasar
    Artan, Ayse Serra
    Sever, Mehmet Sukru
    Cebeci, Egemen
    Ozturk, Savas
    Turkmen, Aydin
    TURKISH JOURNAL OF NEPHROLOGY, 2020, 29 (04): : 258 - 263
  • [35] Compared staining of the phospholipase A2 receptor in the glomeruli of Chinese adults and children with idiopathic membranous nephropathy
    Zhang, Dan
    Wu, Ying
    Zhang, Chong
    Zhang, Wenzhu
    Zou, Jun
    Jiang, Gengru
    PATHOLOGY RESEARCH AND PRACTICE, 2019, 215 (05) : 952 - 956
  • [36] An Indirect Immunofluorescence Method Facilitates Detection of Thrombospondin Type 1 Domain-Containing 7A-Specific Antibodies in Membranous Nephropathy
    Hoxha, Elion
    Beck, Laurence H., Jr.
    Wiech, Thorsten
    Tomas, Nicola M.
    Probst, Christian
    Mindorf, Swantje
    Meyer-Schwesinger, Catherine
    Zahner, Gunther
    Stahl, Phillip R.
    Schoepper, Ruth
    Panzer, Ulf
    Harendza, Sigrid
    Helmchen, Udo
    Salant, David J.
    Stahl, Rolf A. K.
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2017, 28 (02): : 520 - 531
  • [37] M-type phospholipase A2 receptor (PLA2R) glomerular staining in pediatric idiopathic membranous nephropathy
    Kanda, Shoichiro
    Horita, Shigeru
    Yanagihara, Takeshi
    Shimizu, Akira
    Hattori, Motoshi
    PEDIATRIC NEPHROLOGY, 2017, 32 (04) : 713 - 717
  • [38] M-type phospholipase A2 receptor (PLA2R) glomerular staining in pediatric idiopathic membranous nephropathy
    Shoichiro Kanda
    Shigeru Horita
    Takeshi Yanagihara
    Akira Shimizu
    Motoshi Hattori
    Pediatric Nephrology, 2017, 32 : 713 - 717
  • [39] Anti-Phospholipase A2 Receptor-1 Autoantibodies and Membranous Nephropathy
    Beck, Laurence H.
    PODOCYTOPATHY, 2014, 183 : 132 - 144
  • [40] Spontaneous Remission of Thrombospondin Type-1 Domain-Containing-Associated Membranous Nephropathy
    Watanabe, Shiika
    Suzuki, Tomo
    Han, Wei
    Nakata, Mayumi
    Koitabashi, Kenichiro
    Ichikawa, Daisuke
    Kamijo-Ikemori, Atsuko
    Koike, Junki
    Shibagaki, Yugo
    INTERNAL MEDICINE, 2021, 60 (19) : 3125 - 3128