Pseudo-spikes are common in histologically benign lymphoid tissues

被引:50
作者
Lee, SC
Berg, KD
Backe, FK
Griffin, CA
Eshleman, JR
机构
[1] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
关键词
D O I
10.1016/S1525-1578(10)60630-7
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
T cell receptor gene rearrangement is a classic marker of T cell clonality and is a useful adjunct in the diagnosis of T cell lymphomas and leukemias. Rearranged V-J gene segments amplified by polymerase chain reaction (PCR) are traditionally analyzed by polyacrylamide gel electrophoresis, We and others have analyzed TCR-gamma PCR products using capillary gel electrophoresis, which produces single nucleotide resolution and provides improved diagnostic sensitivity over conventional methods. However, with this marked increase in resolution and sensitivity, it is necessary to re-define normal variation of TCR-gamma gene rearrangement in control tissues to allow appropriate interpretation of monoclonality if present. Using DNA capillary gel electrophoresis, we examined the spectrum of normal patterns for TCR-gamma in a variety of T-cell-rich, histologically benign tissue types, including spleen, lymph node, tonsil, and blood, and compared this with the patterns in T cell lymphoma samples. We defined relative peak heights as h(1)/h(2), where h(1) represents the peak height of the largest peak above the normally distributed population, and h(2) represents the peak height of the normally distributed curve. We found spikes in almost 20% of histologically benign samples with relative peak heights that were more than 0.5 and up to 1.5, We designated these as pseudo-spikes, because they may be mistaken for monoclonal spikes. In contrast, the relative peak height of the T cell lymphoma samples that showed clonal rearrangement was much higher than that of the pseudo-spikes, being at least 2 in 11/11 and at least 3 in 10/11 cases. Our data suggest that peaks with relative height of at least 3 represent a true clonal population in diagnostic samples. Peaks with relative heights of less than 1.5 may be insignificant, while peaks with relative heights between 1.5 to 3 may warrant further evaluation. Although capillary gel electrophoresis is superior in assessing T cell clonality, caution must be exercised when interpreting results, because pseudo-spikes appear to be common in benign tissues with lymphoid populations and are not necessarily indicative of clonal malignant T cell-population.
引用
收藏
页码:145 / 152
页数:8
相关论文
共 27 条
[1]   IMPROVED POLYMERASE CHAIN-REACTION DETECTION OF CLONAL T-CELL LYMPHOID NEOPLASMS [J].
BENHATTAR, J ;
DELACRETAZ, F ;
MARTIN, P ;
CHAUBERT, P ;
COSTA, J .
DIAGNOSTIC MOLECULAR PATHOLOGY, 1995, 4 (02) :108-112
[2]  
Caignard A, 1996, INT J CANCER, V66, P564, DOI 10.1002/(SICI)1097-0215(19960516)66:4<564::AID-IJC23>3.0.CO
[3]  
2-6
[4]  
DAVIS MM, 1988, NATURE, V335, P744, DOI 10.1038/335744b0
[5]   T-CELL ANTIGEN RECEPTOR GENES AND T-CELL RECOGNITION [J].
DAVIS, MM ;
BJORKMAN, PJ .
NATURE, 1988, 334 (6181) :395-402
[6]   THE POLYMERASE CHAIN-REACTION IN THE DEMONSTRATION OF MONOCLONALITY IN T-CELL LYMPHOMAS [J].
DISS, TC ;
WATTS, M ;
PAN, LX ;
BURKE, M ;
LINCH, D ;
ISAACSON, PG .
JOURNAL OF CLINICAL PATHOLOGY, 1995, 48 (11) :1045-1050
[7]  
Ebert MPA, 1998, AM J GASTROENTEROL, V93, P2141
[8]   Multiplex PCR for rapid detection of T-cell receptor-gamma chain gene rearrangements in patients with lymphoproliferative diseases [J].
Fodinger, M ;
Buchmayer, H ;
Schwarzinger, I ;
Simonitsch, I ;
Winkler, K ;
Jager, U ;
Knobler, R ;
Mannhalter, C .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 94 (01) :136-139
[9]   A SENSITIVE METHOD OF SCREENING FOR DOMINANT T-CELL CLONES BY AMPLIFICATION OF T-CELL GAMMA-GENE REARRANGEMENTS WITH THE POLYMERASE CHAIN-REACTION [J].
GOUDIE, RB ;
KARIM, SN ;
MILLS, K ;
ALCORN, M ;
LEE, FD .
JOURNAL OF PATHOLOGY, 1990, 162 (03) :191-196
[10]   Clonal dominance of human autologous cytotoxic T lymphocytes against gastric carcinoma: Molecular stability of the CDR3 structure of the TCR alpha beta gene [J].
Ikeda, H ;
Sato, N ;
Matsuura, A ;
Sasaki, A ;
Takahashi, S ;
Kozutsumi, D ;
Kobata, T ;
Okumura, K ;
Wada, Y ;
Hirata, K ;
Kikuchi, K .
INTERNATIONAL IMMUNOLOGY, 1996, 8 (01) :75-82