HLA-G in B-chronic lymphocytic leukaemia:: Clinical relevance and functional implications

被引:27
作者
Rebmann, Vera [1 ]
Nueckel, Holger [2 ]
Duehrsen, Ulrich [2 ]
Grosse-Wilde, Hans [1 ]
机构
[1] Univ Klinikum Essen, Inst Immunol, D-45122 Essen, Germany
[2] Univ Klinikum Essen, Zentrum Innere Med, Abt Hamatol, Essen, Germany
关键词
HLA-G; sHLA-G; B-CLL; immune escape mechanism;
D O I
10.1016/j.semcancer.2007.06.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
HLA-G appears to be involved in regulatory functions counteracting the cellular immune response of T and NK cells by several pathways. We here summarize the HLA-G expression patterns in leukaemia with emphasis on the clinical relevance of this expression for disease progression. Especially in patients with B-chronic lymphocytic leukaemia (B-CLL) the HLA-G expression on B-CLL cells was strongly associated with a reduced treatment-free survival. The corresponding immunological parameters point to a broad immunosuppression in these patients. Thus, HLA-G seems to contribute to the impaired immune response in B-CLL supporting disease progression. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:430 / 435
页数:6
相关论文
共 58 条
[1]   Distribution of HLA-G alternative mRNAs including soluble forms in normal lymphocytes and in lymphoid cell-derived leukemia [J].
Amiot, L ;
Onno, M ;
Drenou, B ;
leMarchand, B ;
Lamy, T ;
Semana, G ;
Fauchet, R .
EUROPEAN JOURNAL OF IMMUNOGENETICS, 1996, 23 (04) :311-320
[2]   HLA-G and lymphoproliferative disorders [J].
Amiot, L ;
Le Friec, G ;
Sebti, Y ;
Drénou, B ;
Pangault, C ;
Guilloux, V ;
Leleu, X ;
Bernard, M ;
Facon, T ;
Fauchet, R .
SEMINARS IN CANCER BIOLOGY, 2003, 13 (05) :379-385
[3]   HLA-G class I gene expression in normal and malignant hematopoietic cells [J].
Amiot, L ;
Onno, M ;
Drénou, B ;
Monvoisin, C ;
Fauchet, R .
HUMAN IMMUNOLOGY, 1998, 59 (08) :524-528
[4]   HLA-G transcription studies during the different stages of normal and malignant hematopoiesis (vol 47, pg 408, 1996). [J].
Amiot, L ;
Onno, M ;
Renard, I ;
Drenou, B ;
Guillaudeux, T ;
LeBouteiller, P ;
Fauchet, R .
TISSUE ANTIGENS, 1996, 48 (05) :608-614
[5]  
APPS R, 2007, EUR J IMMUNOL
[6]   HLA-G and NK receptor are expressed in psoriatic skin - A possible pathway for regulating infiltrating T cells? [J].
Aractingi, S ;
Briand, N ;
Le Danff, C ;
Viguier, M ;
Bachelez, H ;
Michel, L ;
Dubertret, L ;
Carosella, ED .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 159 (01) :71-77
[7]   HLA-G polymorphism and evolution [J].
Arnaiz-Villena, A. ;
Martinez-Laso, J. ;
Serrano-Vela, J. I. ;
Reguera, R. ;
Moscoso, J. .
TISSUE ANTIGENS, 2007, 69 :156-159
[8]   Disulfide bond-mediated dimerization of HLA-G on the cell surface [J].
Boyson, JE ;
Erskine, R ;
Whitman, MC ;
Chiu, M ;
Lau, JM ;
Koopman, LA ;
Valter, MM ;
Angelisova, P ;
Horejsi, V ;
Strominger, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (25) :16180-16185
[9]   CD40-activated B-cell chronic lymphocytic leukemia cells for tumor immunotherapy: Stimulation of allogeneic versus autologous T cells generates different types of effector cells [J].
Buhmann, R ;
Nolte, A ;
Westhaus, D ;
Emmerich, B ;
Hallek, M .
BLOOD, 1999, 93 (06) :1992-2002
[10]  
Bukur J, 2003, CANCER RES, V63, P4107