Expression of inhibitory receptor ILT3 on neoplastic B cells is associated with lymphoid tissue involvement in chronic lymphocytic leukemia

被引:53
作者
Colovai, Adriana. I.
Tsao, Lawrence
Wang, Su
Lin, Hana
Wang, Chuan
Seki, Tetsunori
Fisher, Julie G.
Menes, Manuel
Bhagat, Govind
Alobeid, Bachir
Suciu-Foca, Nicole
机构
[1] Columbia Univ, Dept Pathol, New York, NY USA
[2] Columbia Univ, Dept Surg, New York, NY USA
[3] Columbia Univ, Div Hematol & Med Oncol, Dept Med, New York, NY USA
关键词
chronic lymphocytic leukemia; immunoglobulin-like transcript; flow cytometry;
D O I
10.1002/cyto.b.20164
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
T cell responses against leukemia-associated antigens have been reported in chronic lymphocytic leukemia (CLL). However, the relentless accumulation of CLL B cells in some patients indicates that antitumor immune responses are inefficient. Inhibitory receptors from the Ig-like transcript (ILT) family, such as ILT3 and ILT4, are crucial to the tolerogenic activity of antigen presenting cells. In this study, we examined the expression of ILT3 on CD5+ B cells obtained from 47 patients with CLL. Using flow cytometry and RT-PCR, we found that B CLL cells from 23 of 47 patients expressed ILT3 protein and mature ILT3 mRNA. ILT3 protein and mRNA were not found in normal B cells obtained from donors without CLL. Expression of ILT4 in normal and B CLL cells showed a pattern similar to ILT3. The frequency of ILT3 positive CLL B cells was higher in patients with lymphoid tissue involvement, suggesting that ILT3 may have prognostic value in CLL. Our findings indicate that expression of ILT3 and ILT4 on CLL B cells represents a phenotypic abnormality that may play a role in tolerization of tumor-specific T cells. (c) 2007 Clinical Cytometry Society.
引用
收藏
页码:354 / 362
页数:9
相关论文
共 31 条
[1]  
Andersen MH, 2001, CANCER RES, V61, P869
[2]  
Bartik MM, 1998, SEMIN ONCOL, V25, P27
[3]   LIR-1 expression on lymphocytes, and cytomegalovirus disease in lung-transplant recipients [J].
Berg, L ;
Riise, GC ;
Cosman, D ;
Bergström, T ;
Olofsson, S ;
Kärre, W ;
Carbone, E .
LANCET, 2003, 361 (9363) :1099-1101
[4]   Reduced frequencies and suppressive function of CD4+CD25hi regulatory T cells in patients with chronic lymphocytic leukemia after therapy with fludarabine [J].
Beyer, M ;
Kochanek, M ;
Darabi, K ;
Popov, A ;
Jensen, M ;
Endl, E ;
Knolle, PA ;
Thomas, RK ;
von Bergwelt-Baildon, M ;
Bebey, S ;
Hallek, M ;
Schultze, JL .
BLOOD, 2005, 106 (06) :2018-2025
[5]   Perspectives on the use of new diagnostic tools in the treatment of chronic lymphocytic leukemia [J].
Binet, JL ;
Caligaris-Cappio, F ;
Catovsky, D ;
Cheson, B ;
Davis, T ;
Dighiero, G ;
Döhner, H ;
Hallek, M ;
Hillmen, P ;
Keating, M ;
Montserrat, E ;
Kipps, TJ ;
Rai, K .
BLOOD, 2006, 107 (03) :859-861
[6]   The LILR family: modulators of innate and adaptive immune pathways in health and disease [J].
Brown, D ;
Trowsdale, J ;
Allen, R .
TISSUE ANTIGENS, 2004, 64 (03) :215-225
[7]   Acquired CD40-ligand deficiency in chronic lymphocytic leukemia [J].
Cantwell, M ;
Hua, T ;
Pappas, J ;
Kipps, TJ .
NATURE MEDICINE, 1997, 3 (09) :984-989
[8]  
Casado LF, 2001, HAEMATOLOGICA, V86, P457
[9]   A novel inhibitory receptor (ILT3) expressed on monocytes, macrophages, and dendritic cells involved in antigen processing [J].
Cella, M ;
Dohring, C ;
Samaridis, J ;
Dessing, M ;
Brockhaus, M ;
Lanzavecchia, A ;
Colonna, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (10) :1743-1751
[10]   Tolerization of dendritic cells by TS cells:: the crucial role of inhibitory receptors ILT3 and ILT4 [J].
Chang, CC ;
Ciubotariu, R ;
Manavalan, JS ;
Yuan, J ;
Colovai, AI ;
Piazza, F ;
Lederman, S ;
Colonna, M ;
Cortesini, R ;
Dalla-Favera, R ;
Suciu-Foca, N .
NATURE IMMUNOLOGY, 2002, 3 (03) :237-243