CLONAL HISTORY OF A HUMAN FOLLICULAR LYMPHOMA AS REVEALED IN THE IMMUNOGLOBULIN VARIABLE REGION GENES

被引:92
作者
ZHU, D
HAWKINS, RE
HAMBLIN, TJ
STEVENSON, FK
机构
[1] SOUTHAMPTON UNIV HOSP,TENOVUS LAB,MOLEC IMMUNOL GRP,SOUTHAMPTON SO9 4XY,HANTS,ENGLAND
[2] MRC,MOLEC BIOL LAB,CAMBRIDGE,CAMBS,ENGLAND
关键词
VARIABLE REGION GENES; LYMPHOMA; B CELLS; IMMUNOGLOBULIN; ANTIGEN SELECTION;
D O I
10.1111/j.1365-2141.1994.tb04780.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The variable region genes used to encode the immunoglobulin expressed by tumour cells of a patient with follicular lymphoma have been identified and sequenced. Initially, a lymph node biopsy was analysed and revealed usage of V-H and V(k)appa genes which had numerous substitutions as compared with the closest germ line genes. The pattern of mutations in VH was consistent with a role for positive selection by antigen. In addition, there was evidence in both V-H and V(k)appa sequences for clonal heterogeneity. After 5 years, which included treatment with chemotherapy, the patient relapsed with tumour cells present in the blood. Analysis of the V-genes used by the emerging tumour revealed a single homogeneous sequence for both V-H and V-L. which, in each case, matched closely one of the sequences in the original lymph node biopsy. These results indicate that selection, possibly mediated by antigen, can operate on a cell destined to give rise to lymphoma, and that intraclonal variation can occur after the neoplastic event. However, in this case, late relapse in the blood is dominated by a single clone.
引用
收藏
页码:505 / 512
页数:8
相关论文
共 28 条
[1]   CLONAL EVOLUTION OF A FOLLICULAR LYMPHOMA - EVIDENCE FOR ANTIGEN SELECTION [J].
BAHLER, DW ;
LEVY, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (15) :6770-6774
[2]   THE DEVELOPMENT OF B-CELLS AND THE B-CELL REPERTOIRE IN THE MICROENVIRONMENT OF THE GERMINAL CENTER [J].
BEREK, C .
IMMUNOLOGICAL REVIEWS, 1992, 126 :5-19
[3]   PASSENGER TRANSGENES REVEAL INTRINSIC SPECIFICITY OF THE ANTIBODY HYPERMUTATION MECHANISM - CLUSTERING, POLARITY, AND SPECIFIC HOT-SPOTS [J].
BETZ, AG ;
RADA, C ;
PANNELL, R ;
MILSTEIN, C ;
NEUBERGER, MS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (06) :2385-2388
[4]   USE OF FAMILY SPECIFIC LEADER REGION PRIMERS FOR PCR AMPLIFICATION OF THE HUMAN HEAVY-CHAIN VARIABLE REGION GENE REPERTOIRE [J].
CAMPBELL, MJ ;
ZELENETZ, AD ;
LEVY, S ;
LEVY, R .
MOLECULAR IMMUNOLOGY, 1992, 29 (02) :193-203
[5]   THE ROLE OF CLONAL SELECTION IN THE PATHOGENESIS OF AN AUTOREACTIVE HUMAN B-CELL LYMPHOMA [J].
FRIEDMAN, DF ;
CHO, EA ;
GOLDMAN, J ;
CARMACK, CE ;
BESA, EC ;
HARDY, RR ;
SILBERSTEIN, LE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 174 (03) :525-537
[6]   IMMUNOLOGICAL MEMORY [J].
GRAY, D .
ANNUAL REVIEW OF IMMUNOLOGY, 1993, 11 :49-77
[7]   A GENETIC APPROACH TO IDIOTYPIC VACCINATION [J].
HAWKINS, RE ;
WINTER, G ;
HAMBLIN, TJ ;
STEVENSON, FK ;
RUSSELL, SJ .
JOURNAL OF IMMUNOTHERAPY, 1993, 14 (04) :273-278
[8]   INTRACLONAL GENERATION OF ANTIBODY MUTANTS IN GERMINAL-CENTERS [J].
JACOB, J ;
KELSOE, G ;
RAJEWSKY, K ;
WEISS, U .
NATURE, 1991, 354 (6352) :389-392
[9]   CHROMOSOMAL TRANSLOCATIONS IN LYMPHOID MALIGNANCIES REVEAL NOVEL PROTOONCOGENES [J].
KORSMEYER, SJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1992, 10 :785-807
[10]   B-CELLS OF CHRONIC LYMPHATIC-LEUKEMIA EXPRESS V-GENES IN UNMUTATED FORM [J].
KUPPERS, R ;
GAUSE, A ;
RAJEWSKY, K .
LEUKEMIA RESEARCH, 1991, 15 (06) :487-&