B7-H1 (PD-L1, CD274) suppresses host immunity in T-cell lymphoproliferative disorders

被引:179
作者
Wilcox, Ryan A. [1 ]
Feldman, Andrew L. [2 ]
Wada, David A. [3 ]
Yang, Zhi-Zhang [1 ]
Comfere, Nneka I. [3 ]
Dong, Haidong [4 ]
Kwon, Eugene D. [5 ]
Novak, Anne J. [1 ]
Markovic, Svetomir N. [1 ]
Pittelkow, Mark R. [3 ]
Witzig, Thomas E. [1 ]
Ansell, Stephen M. [1 ]
机构
[1] Mayo Clin, Div Hematol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Dermatol, Rochester, MN 55905 USA
[4] Mayo Clin, Dept Immunol, Rochester, MN 55905 USA
[5] Mayo Clin, Dept Urol, Rochester, MN 55905 USA
基金
美国国家卫生研究院;
关键词
ABSOLUTE LYMPHOCYTE COUNT; LEUKOCYTE ANTIGEN-DR; PROGNOSTIC MARKER; TYROSINE KINASE; EXPRESSION; IDENTIFICATION; MONOCYTES; PREDICTS; RECEPTOR; SURVIVAL;
D O I
10.1182/blood-2009-04-216671
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Stromal elements present within the tumor microenvironment may suppress host immunity and promote the growth of malignant lymphocytes in B cell-derived non-Hodgkin lymphoma (NHL). In contrast, little is known about the microenvironment's role in T cell-derived NHL. B7-H1 (PD-L1, CD274), a member of the B7 family of costimulatory/coinhibitory ligands expressed by both malignant cells and stromal cells within the tumor microenvironment, has emerged as an important immune modulator capable of suppressing host immunity. Therefore, B7-H1 expression and function were analyzed in cutaneous and peripheral T-cell NHL. B7-H1 was expressed by tumor cells, monocytes, and monocyte-derived cells within the tumor microenvironment in T-cell NHL and was found to inhibit T-cell proliferation and promote the induction of FoxP3(+) regulatory T cells. Collectively, the data presented provide the first evidence implicating B7-H1 in the suppression of host immunity in T-cell lymphoproliferative disorders and suggest that the targeting of B7-H1 may represent a novel therapeutic approach. (Blood. 2009; 114: 2149-2158)
引用
收藏
页码:2149 / 2158
页数:10
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