Diagnostic role of BIOMED-2 multiplex polymerase chain reaction for antigen receptor genes rearrangement in lymphoproliferative disorders.
- Author:
Yan-Ling LIU
1
;
Mei HUANG
;
Deng-Ju LI
;
Yi XIAO
;
Yi TANG
;
Fan-Kai MENG
;
Jin-Niu DENG
;
Han-Ying SUN
;
Wen-Li LIU
;
Jian-Feng ZHOU
Author Information
- Publication Type:Journal Article
- MeSH: Female; Gene Rearrangement, B-Lymphocyte, Light Chain; Gene Rearrangement, T-Lymphocyte; Humans; Lymphoproliferative Disorders; diagnosis; genetics; Male; Polymerase Chain Reaction; methods; Sensitivity and Specificity
- From: Chinese Journal of Hematology 2009;30(4):251-254
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo establish a sensitive and effective method for detection of immunoglobulin and T-cell receptor (Ig/TCR) gene rearrangement,and to explore its role in diagnosis and differential diagnosis of lymphoproliferative disorders.
METHODSFifty-eight lymphoid tissue samples from 54 patients with lymphoproliferations were evaluated by the novel BIOMED-2 multiplex polymerase chain reaction (PCR) for antigen receptor genes rearrangement.
RESULTSMultiplex PCR demonstrated monoclonal Ig/TCR gene rearrangements in 22 of 25 (88.0%) B-cell malignancies and 8 of 15 (53.3%) T-cell malignancies. Among 17 benign lymphoproliferations confirmed histopathologically, polyclonal rearrangements were detected in 14 cases (82.4%). In total, the clonality analysis and the final clinico-histopathological diagnosis were concordant in 77.2%. Combination detection of Iglambda and TCR delta gene rearrangements did not increase the detection rate of monoclonal rearrangement of Ig/TCR, but might help to the detection of Iglambda+ or TCR delta+ lymphomas.
CONCLUSIONThe novel BIOMED-2 multiplex PCR strategy is a rapid, reliable and sensitive approach to detecting clonality in suspected lymphoproliferations, especially in atypical cases.