Idiotype-specific T cells in multiple myeloma: Targets for an immunotherapeutic intervention?

被引:24
作者
Yi, Q
Osterborg, A
机构
[1] Immunological Research Laboratory, Department of Medicine, Karolinska Hospital
[2] Department of Oncology, Karolinska Hospital
关键词
multiple myeloma; T cells; idiotype; M-component;
D O I
10.1007/BF02988835
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this paper, the results of some recent studies on idiotype-specific T cells in human multiple myeloma (MM) and monoclonal gammopathy of undetermined significance (MGUS) are discussed. By using different in vitro measurements such as H-3-thymidine incorporation and ELISPOT assay, idiotype-specific T cells have been demonstrated in most of MM and MGUS patients. Based on the cytokine-secretion profiles, idiotype-specific T cells were found to comprise both Th1 and Th2 cells. A Th1 type immunity was found preferentially in indolent disease and a Th2-like response predominated in advanced MM, suggesting a specific T-cell regulation of the tumor B-cell clone. The mode of T-cell recognition of id determinants on M-components has been studied. We found that idiotype-specific T cells recognized processed id determinants presented by MHC class II (HLA-DR) molecules on APC. B cells were much more efficient APC than monocytes. With the aim to induce or to amplify an idiotype-specific T-cell response, we have immunized MM patients with the autologous M-component precipitated in aluminum. Three out of the five patients showed an induction of specific cellular and humoral immunity. Nevertheless, the role for such immunity in controlling the tumor clone remains to be established.
引用
收藏
页码:1 / 7
页数:7
相关论文
共 70 条
[1]   TREATMENT FOR MULTIPLE MYELOMA - COMBINATION CHEMOTHERAPY WITH DIFFERENT MELPHALAN DOSE REGIMENS [J].
ALEXANIAN, R ;
HAUT, A ;
KHAN, AU ;
LANE, M ;
MCKELVEY, EM ;
MIGLIORE, PJ ;
STUCKEY, WJ ;
WILSON, HE .
JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1969, 208 (09) :1680-+
[2]  
BAKKUS MHC, 1992, BLOOD, V80, P2326
[3]   EVIDENCE THAT THE CLONOGENIC CELL IN MULTIPLE-MYELOMA ORIGINATES FROM A PRE-SWITCHED BUT SOMATICALLY MUTATED B-CELL [J].
BAKKUS, MHC ;
VANRIET, I ;
VANCAMP, B ;
THIELEMANS, K .
BRITISH JOURNAL OF HAEMATOLOGY, 1994, 87 (01) :68-74
[4]  
BERENSON J, 1987, BLOOD, V70, P1550
[5]   Modulation of anti-idiotypic immune response by immunization with the autologous M-component protein in multiple myeloma patients [J].
Bergenbrant, S ;
Yi, Q ;
Osterborg, A ;
Bjorkholm, M ;
Osby, E ;
Mellstedt, H .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 92 (04) :840-846
[6]  
BERGMANN L, 1985, SCAND J HAEMATOL, V34, P170
[7]   INTERLEUKIN-3 AND INTERLEUKIN-6 SYNERGISTICALLY PROMOTE THE PROLIFERATION AND DIFFERENTIATION OF MALIGNANT PLASMA-CELL PRECURSORS IN MULTIPLE-MYELOMA [J].
BERGUI, L ;
SCHENA, M ;
GAIDANO, G ;
RIVA, M ;
CALIGARISCAPPIO, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (02) :613-618
[8]  
BILLADEAU D, 1992, BLOOD, V80, P1818
[9]   THE BONE-MARROW OF MULTIPLE-MYELOMA PATIENTS CONTAINS B-CELL POPULATIONS AT DIFFERENT STAGES OF DIFFERENTIATION THAT ARE CLONALLY RELATED TO THE MALIGNANT PLASMA-CELL [J].
BILLADEAU, D ;
AHMANN, G ;
GREIPP, P ;
VANNESS, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (03) :1023-1031
[10]   IDIOTOPE-SPECIFIC T-CELL CLONES THAT RECOGNIZE SYNGENEIC IMMUNOGLOBULIN FRAGMENTS IN THE CONTEXT OF CLASS-II MOLECULES [J].
BOGEN, B ;
MALISSEN, B ;
HAAS, W .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1986, 16 (11) :1373-1378