Literature DB >> 20697266

Characterization of a new monoclonal antibody against PAX5/BASP in 1525 paraffin-embedded human and animal tissue samples.

Claudio Agostinelli1, Elena Sabattini, Jakob Oemar Gjørret, Simona Righi, Maura Rossi, Manuela Mancini, Pier Paolo Piccaluga, Francesco Bacci, Teresa Marafioti, Giuliano Bettini, Brunangelo Falini, Stefano A Pileri.   

Abstract

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 micro-arrays (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 (B-NHLs). 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.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20697266     DOI: 10.1097/PAI.0b013e3181e79013

Source DB:  PubMed          Journal:  Appl Immunohistochem Mol Morphol        ISSN: 1533-4058


  7 in total

1.  T-cell-derived Hodgkin lymphoma has motility characteristics intermediate between Hodgkin and anaplastic large cell lymphoma.

Authors:  Julia Bein; Nadine Flinner; Björn Häupl; Aastha Mathur; Olga Schneider; Marwa Abu-Ayyad; Martin-Leo Hansmann; Matthieu Piel; Thomas Oellerich; Sylvia Hartmann
Journal:  J Cell Mol Med       Date:  2022-05-19       Impact factor: 5.295

Review 2.  Overview of PAX gene family: analysis of human tissue-specific variant expression and involvement in human disease.

Authors:  Brian Thompson; Emily A Davidson; Wei Liu; Daniel W Nebert; Elspeth A Bruford; Hongyu Zhao; Emmanouil T Dermitzakis; David C Thompson; Vasilis Vasiliou
Journal:  Hum Genet       Date:  2020-07-29       Impact factor: 4.132

3.  Pathobiology of anaplastic large cell lymphoma.

Authors:  Pier Paolo Piccaluga; Anna Gazzola; Claudia Mannu; Claudio Agostinelli; Francesco Bacci; Elena Sabattini; Carlo Sagramoso; Roberto Piva; Fernando Roncolato; Giorgio Inghirami; Stefano A Pileri
Journal:  Adv Hematol       Date:  2011-02-06

4.  Pathobiology of ALK-negative anaplastic large cell lymphoma.

Authors:  Stefano A Pileri; Claudio Agostinelli; Francesco Bacci; Elena Sabattini; Carlo Sagramoso; Brunangelo Falini; Pier Paolo Piccaluga
Journal:  Pediatr Rep       Date:  2011-06-22

Review 5.  Pathobiology of hodgkin lymphoma.

Authors:  Claudio Agostinelli; Stefano Pileri
Journal:  Mediterr J Hematol Infect Dis       Date:  2014-06-05       Impact factor: 2.576

6.  Immunophenotyping of Sheep Paraffin-Embedded Peripheral Lymph Nodes.

Authors:  Eleonora Melzi; Mara S Rocchi; Gary Entrican; Marco Caporale; Massimo Palmarini
Journal:  Front Immunol       Date:  2018-12-11       Impact factor: 7.561

7.  Ocular mycobacterial lesions in cats.

Authors:  Jordan L Mitchell; Laura MacDougall; Melanie J Dobromylskyj; Ken Smith; Renata Stavinohova; Danièlle A Gunn-Moore; Jayne C Hope; Emma Scurrell
Journal:  Vet Pathol       Date:  2022-05-19       Impact factor: 3.157

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.