HLA-G and IL-10 expression in human cancer - different stories with the same message

被引:93
作者
Urosevic, M [1 ]
Dummer, R [1 ]
机构
[1] Univ Zurich Hosp, Dept Dermatol, CH-8091 Zurich, Switzerland
关键词
HLA-G; interleukin-10; lung cancer; cutaneous lymphoma;
D O I
10.1016/S1044-579X(03)00024-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immune evasion in cancer may result from structural and functional alterations of human leukocyte antigen (HLA) class I molecules and/or local release of immunosuppressive cytokines, such as interleukin (IL)-10. In lung cancer, both of these mechanisms seem to often take place. resulting in the impaired tumor recognition and the progression of the disease. In primary cutaneous lymphomas on the other side, the shift towards immunosuppressive T helper (T-h)2 cytokine profile and the secretion of IL-10 appears to occur more frequently than the loss of HLA class I molecules. In addition to down-regulation of HLA class I expression, IL-10 appears to be one of the factors responsible for the up-regulation of FILA-G, another molecule involved in the immunescape. It is possible that the expression of HLA-G itself may account for induction of T(h)2-skewing state and the production of IL-10, thence establishing a vicious circle of immune abrogation in cancer. This article reviews the current literature on this topic and provides new insights into the role of HLA-G and IL-10 in cancer. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:337 / 342
页数:6
相关论文
共 63 条
[1]   Tetrameric complexes of human histocompatibility leukocyte antigen (HLA)-G bind to peripheral blood myelomonocytic cells [J].
Allan, DSJ ;
Colonna, M ;
Lanier, LL ;
Churakova, TD ;
Abrams, JS ;
Ellis, SA ;
McMichael, AJ ;
Braud, VM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (07) :1149-1155
[2]   Cytokines and cutaneous T-cell lymphomas [J].
Asadullah, K ;
Docke, WD ;
Volk, HD ;
Sterry, W .
EXPERIMENTAL DERMATOLOGY, 1998, 7 (06) :314-320
[3]   HLA-G suppresses proliferation of CD4+ T-lymphocytes [J].
Bainbridge, DRJ ;
Ellis, SA ;
Sargent, IL .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2000, 48 (01) :17-26
[4]   LIRs/ILTs/MIRs, inhibitory and stimulatory Ig-superfamily receptors expressed in myeloid and lymphoid cells [J].
Borges, L ;
Cosman, D .
CYTOKINE & GROWTH FACTOR REVIEWS, 2000, 11 (03) :209-217
[5]   Structure and function of major histocompatibility complex (MHC) class I specific receptors expressed on human natural killer (NK) cells [J].
Borrego, F ;
Kabat, J ;
Kim, DK ;
Lieto, L ;
Maasho, K ;
Peña, J ;
Solana, R ;
Coligan, JE .
MOLECULAR IMMUNOLOGY, 2002, 38 (09) :637-660
[6]   The human major histocompatibility complex class Ib molecule HLA-E binds signal sequence-derived peptides with primary anchor residues at positions 2 and 9 [J].
Braud, V ;
Jones, EY ;
McMichael, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (05) :1164-1169
[7]   HLA-G: a tolerance molecule from the major histocompatibility complex [J].
Carosella, ED ;
Rouas-Freiss, N ;
Paul, P ;
Dausset, J .
IMMUNOLOGY TODAY, 1999, 20 (02) :60-62
[8]   Immune stimulatory potential of B7.1 and B7.2 retrovirally transduced melanoma cells:: suppression by interleukin 10 [J].
Dummer, R ;
Yue, FY ;
Pavlovic, J ;
Geertsen, R ;
Döhring, C ;
Moelling, K ;
Burg, G .
BRITISH JOURNAL OF CANCER, 1998, 77 (09) :1413-1419
[9]   Sezary syndrome T-cell clones display T-helper 2 cytokines and express the accessory factor-1 (Interferon-gamma receptor beta-chain) [J].
Dummer, R ;
Heald, PW ;
Nestle, FO ;
Ludwig, E ;
Laine, E ;
Hemmi, S ;
Burg, G .
BLOOD, 1996, 88 (04) :1383-1389
[10]   Pathogenesis of cutaneous lymphomas [J].
Dummer, R ;
Willers, J ;
Kamarashev, J ;
Urosevic, M ;
Döbbeling, U ;
Burg, G .
SEMINARS IN CUTANEOUS MEDICINE AND SURGERY, 2000, 19 (02) :78-86