Characterization of a New Monoclonal Antibody Against PAX5/BASP in 1525 Paraffin-embedded Human and Animal Tissue Samples

被引:16
作者
Agostinelli, Claudio [1 ]
Sabattini, Elena [1 ]
Gjorret, Jakob Oemar [4 ]
Righi, Simona [1 ]
Rossi, Maura [1 ]
Mancini, Manuela [1 ]
Piccaluga, Pier Paolo [1 ]
Bacci, Francesco [1 ]
Marafioti, Teresa [5 ]
Bettini, Giuliano [2 ]
Falini, Brunangelo [3 ]
Pileri, Stefano A. [1 ]
机构
[1] Univ Bologna, St Orsola Malpighi Hosp, Interdept Ctr Canc Res Giorgio Prodi, Pathol & Haematopathol Unit,Dept Haematol & Clin, I-40138 Bologna, Italy
[2] Univ Bologna, St Orsola Malpighi Hosp, Interdept Ctr Canc Res Giorgio Prodi, Pathol & Haematopathol Unit,Dept Vet Publ Hlth &, I-40138 Bologna, Italy
[3] Univ Perugia, Inst Haematol, Lab Haematopathol, I-06100 Perugia, Italy
[4] Dako Denmark AS, Glostrup, Denmark
[5] Univ Coll London Hosp, Dept Pathol, London, England
关键词
PAX5; PAX2; immunohistochemistry; tissue microarray; normal tissues; tumors; PATHOLOGISTS VIEW POINT; RENAL-CELL CARCINOMA; REED-STERNBERG CELLS; B-CELL; PAX5; EXPRESSION; ACTIVATOR PROTEIN; PROSTATE-CANCER; GENE; LYMPHOMA; MARKER;
D O I
10.1097/PAI.0b013e3181e79013
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Introduction: We describe the newly generated DAK-PAX5 monoclonal antibody raised against a fixation-resistant epitope of the human PAX5/BSAP molecule. Materials and Methods: Following Western-blot, absorption, and chess-board titration tests, and optimization of antigen-retrieval and detection methods, DAK-Pax5 was used in parallel with a reference antibody (clone 24) on tissue microarrays (TMAs) constructed from normal human and animal tissues and from hematologic and nonhematologic human malignancies. Such TMAs were also tested with an anti-PAX2 antibody. Results: DAK-Pax5 reacted with normal human and animal B-cells and with 460/473 B-cell non-Hodgkin lymphomas (BNHLs). All plasmacytomas/plasmablastic tumors (n = 13) and T/NK-cell neoplasms (n = 264) turned out consistently negative as did acute myelogenous leukaemias (n = 19) except 2 carrying t(8;21). Positivity was found in 6/6 and 155/169 lymphocyte predominant and classical HLs, respectively, although the staining intensity varied through cases. Among 521 nonhematologic malignancies, DAK-Pax5 reacted with 22/399 carcinomas (4/11 neuroendocrine, 2/4 Merkel-cell, 4/21 prostatic, 1/11 urothelial, 1/26 renal, 2/12 cervical squamous-cell, 3/13 ovarian, and 5/75 colonic). When compared with clone 24, DAK-Pax5 produced a stronger positivity in most if not all B-NHLs and HLs. No cross-reactivity with the anti-PAX2 antibody was recorded. Discussion: DAK-Pax5 represents a new reliable tool for diagnostics and research.
引用
收藏
页码:561 / 572
页数:12
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