Clonality analysis of lymphoproliferative disorders in patients with Sjogren's syndrome

被引:20
作者
Dong, L.
Masaki, Y. [1 ]
Takegami, T.
Jin, Z.-X.
Huang, C.-R.
Fukushima, T.
Sawaki, T.
Kawanami, T.
Saeki, T.
Kitagawa, K.
Sugai, S.
Okazaki, T.
Hirose, Y.
Umehara, H.
机构
[1] Kanazawa Med Univ, Dept Hematol & Immunol, Daigaku, Uchinada, Ishikawa 9200293, Japan
[2] Kanazawa Med Univ, Dept Mol Oncol & Virol, Uchinada, Ishikawa 9200293, Japan
[3] Kanazawa Med Univ, Dept Ophthalmol, Uchinada, Ishikawa 9200293, Japan
[4] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Hematol & Immunol, Wuhan 430074, Peoples R China
[5] Nagaokoa Red Cross Hosp, Nagaoka, Niigata, Japan
[6] Tottori Univ, Fac Med, Yonago, Tottori, Japan
关键词
clonality; lymphoproliferative disorders; Sjogren's syndrome;
D O I
10.1111/j.1365-2249.2007.03486.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The aim of this study was to clarify the nature of the clonal lymphocyte infiltration in Sjogren's syndrome (SS) patients associated with lymphoproliferative disorders. We examined B cell clonality in lymphoproliferative tissues from six primary SS patients associated with lymphoproliferative disorders or lymphoma by cloning and sequencing of the gene rearrangement of the immunoglobulin heavy chain complementarity determining region 3 (IgVH-CDR3). Three patients with sequential observation showed progressional clonal expansion with the presence of the same subclone in different tissues during the course of disease. Among them, one patient developed mucosa-associated lymphoid tissue (MALT) lymphoma in glandular parotid. The other three SS patients concomitant with malignant B cells lymphomas showed different clonal expansion of B cells between nodal sites and salivary glands. The cloanality analysis indicated that monoclonal B cell population could spread from one glandular site to another site during the course of SS, suggesting that the malignant clone may arise from the general abnormal microenvironment, not restricted to the glandular tissue, in some SS patients.
引用
收藏
页码:279 / 284
页数:6
相关论文
共 32 条
[1]   Simultaneous phenotypically distinct but clonally identical mucosa-associated lymphoid tissue and follicular lymphoma in a patient with Sjogren's syndrome [J].
Aiello, A ;
Du, MQ ;
Diss, TC ;
Pang, HZ ;
Pezzella, F ;
Papini, D ;
Giardini, R ;
Pilotti, S ;
Pan, LX ;
Isaacson, PG .
BLOOD, 1999, 94 (07) :2247-2251
[2]   Clonal salivary gland infiltrates associated with myoepithelial sialadenitis (Sjogren's syndrome) begin as nonmalignant antigen-selected expansions [J].
Bahler, DW ;
Swerdlow, SH .
BLOOD, 1998, 91 (06) :1864-1872
[3]   Among B cell non-Hodgkin's lymphomas, MALT lymphomas express a unique antibody repertoire with frequent rheumatoid factor reactivity [J].
Bende, RJ ;
Aarts, WM ;
Riedl, RG ;
de Jong, D ;
Pals, ST ;
van Noesel, CJM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (08) :1229-1241
[4]   SJOGRENS-SYNDROME - A CLINICAL, PATHOLOGICAL, AND SEROLOGICAL STUDY OF 62 CASES [J].
BLOCH, KJ ;
BUCHANAN, WW ;
WOHL, MJ ;
BUNIM, JJ .
MEDICINE, 1992, 71 (06) :386-401
[5]  
BLOCH KJ, 1992, MEDICINE, V71, P401
[6]  
De Re V, 2002, EUR J IMMUNOL, V32, P903, DOI 10.1002/1521-4141(200203)32:3<903::AID-IMMU903>3.0.CO
[7]  
2-D
[8]   The relevance of VDJ PCR protocols in detecting B-cell clonal expansion in lymphomas and other lymphoproliferative disorders [J].
De Re, V ;
DeVita, S ;
Carbone, A ;
Ferraccioli, G ;
Gloghini, A ;
Marzotto, A ;
Pivetta, B ;
Dolcetti, R ;
Boiocchi, M .
TUMORI JOURNAL, 1995, 81 (06) :405-409
[9]   Characterization of prelymphomatous stages of B cell lymphoproliferation in Sjogren's syndrome [J].
DeVita, S ;
Boiocchi, M ;
Sorrentino, D ;
Carbone, A ;
Avellini, C ;
Dolcetti, R ;
Marzotto, A ;
Gloghini, A ;
Bartoli, E ;
Beltrami, CA ;
Ferraccioli, G .
ARTHRITIS AND RHEUMATISM, 1997, 40 (02) :318-331
[10]   A SINGLE NEOPLASTIC CLONE IN SEQUENTIAL BIOPSY SPECIMENS FROM A PATIENT WITH PRIMARY GASTRIC-MUCOSA-ASSOCIATED LYMPHOID-TISSUE LYMPHOMA AND SJOGRENS-SYNDROME [J].
DISS, TC ;
PENG, HZ ;
WOTHERSPOON, AC ;
PAN, LX ;
SPEIGHT, PM ;
ISAACSON, PG .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (03) :172-175