Hodgkin's disease: A disorder of dysregulated cellular cross-talk

被引:18
作者
Pinto, A
Gattei, V
Zagonel, V
Aldinucci, D
Degan, M
De Iuliis, A
Rossi, FM
Mazzocco, FT
Godeas, C
Rupolo, M
Poletto, D
Gloghini, A
Carbone, A
Gruss, HJ
机构
[1] Ctr Riferimento Oncol, IRCCS, Dept Med Oncol, Leukemia Unit, I-33081 Aviano, Italy
[2] Univ Ulm, Med Ctr, Dept Hematol & Oncol Internal Med 3, D-89069 Ulm, Germany
关键词
human lymphomas; Hodgkin's disease; cell contact-dependent interactions; cytokine network;
D O I
10.1007/BF02678551
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hodgkin's disease (HD) is a peculiar type of human malignant lymphoma characterized by a very low frequency of tumor cells, the so called Hodgkin and Reed-Sternberg (H-RS) cells, embedded in a hyperplastic background of non-neoplastic (reactive) cells recruited and activated by H-RS cells-derived cytokines. H-RS cells can be functionally regarded as antigen-presenting cells (APC) able to elicit an intense, but anergic and ineffective, T-cell mediated immune response along with a hyperplastic inflammatory reaction which involves several cell types including T-and B-cells, neutrophils, eosinophils, plasma cells, fibroblasts and stromal cells. In tissues involved by HD, malignant H-RS cells and their reactive neighboring cells are able to cross-talk via a complex network of cytokine- and cell contact-dependent interactions. As a result of such interactions, mediated by specific surface receptors and adhesion molecules on both tumor and non-neoplastic cells, H-RS cells may receive several proliferative and anti-apoptotic signals favoring the cellular expansion and tumor cell survival in HD. The ineffective T-cell immune response elicited by the abnormal APC function of H-RS cells may further contribute to the biologic and clinical progression of HD. Innovative therapeutic strategies aimed at blocking the pathways of dysregulated cellular cross-talk among H-RS cells and bystander reactive cell populations might be beneficial in the teatment of HD patients.
引用
收藏
页码:309 / 320
页数:12
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