INFECTION OF HUMAN SYNOVIAL-CELLS BY HUMAN T-CELL LYMPHOTROPIC VIRUS TYPE-I - PROLIFERATION AND GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR PRODUCTION BY SYNOVIAL-CELLS

被引:42
作者
SAKAI, M
EGUCHI, K
TERADA, K
NAKASHIMA, M
YAMASHITA, I
IDA, H
KAWABE, Y
AOYAGI, T
TAKINO, H
NAKAMURA, T
NAGATAKI, S
机构
[1] NAGASAKI UNIV,SCH MED,DEPT INTERNAL MED 1,1-7-1 SAKAMOTO,NAGASAKI 852,JAPAN
[2] URESHINO NATL HOSP,DEPT ORTHOPED,SAGA 84303,JAPAN
关键词
HUMAN T-CELL LYMPHOTROPIC VIRUS TYPE-I (HTLV-I); CHRONIC INFLAMMATORY ARTHROPATHY; SYNOVIAL CELLS; GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR;
D O I
10.1172/JCI116789
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The present study was performed to clarify the relationship between human T cell lymphotropic virus type I (HTLV-I) infection and chronic inflammatory arthropathy. To determine the ability of HTLV-I to infect synovial cells and the effect on synovial cell proliferation, synovial cells were cocultured with the HTLV-I-producing T cell lines (MT-2 or HCT-1). After coculture with HTLV-I-infected T cells, the synovial cells expressed HTLV-I-specific core antigens, and HTLV-I proviral DNA was detected from the synovial cells by polymerase chain reaction. These cocultured synovial cells with HTLV-I-infected T cells proliferated more actively than the synovial cells cocultured with uninfected T cells. This stimulatory effect of HTLV-I-infected T cells on synovial cell proliferation seems necessary to contact each other. After being cocultured with MT-2 cells, synovial cells proliferated more actively than control cells even after several passages. Furthermore, HTLV-1-infected synovial cells produced significant amounts of granulocyte/macrophage colony-stimulating factor. These results suggest that HTLV-1 can infect synovial cells, resulting their active proliferation and may be involved in the pathogenesis of proliferative synovitis similar to that found in rheumatoid arthritis.
引用
收藏
页码:1957 / 1966
页数:10
相关论文
共 43 条
[1]  
ALVAROGRACIA JM, 1991, J IMMUNOL, V146, P3365
[2]   CYTOKINES AND CYTOKINE INHIBITORS OR ANTAGONISTS IN RHEUMATOID-ARTHRITIS [J].
AREND, WP ;
DAYER, JM .
ARTHRITIS AND RHEUMATISM, 1990, 33 (03) :305-315
[3]  
Bois P., 1987, R5389 CEA
[4]   CONSTITUTIVE PRODUCTION OF INFLAMMATORY AND MITOGENIC CYTOKINES BY RHEUMATOID SYNOVIAL FIBROBLASTS [J].
BUCALA, R ;
RITCHLIN, C ;
WINCHESTER, R ;
CERAMI, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (03) :569-574
[5]  
CHAN JY, 1986, P NATL ACAD SCI USA, V83, P8869
[6]   THE CHI-GENE IS ESSENTIAL FOR HTLV REPLICATION [J].
CHEN, ISY ;
SLAMON, DJ ;
ROSENBLATT, JD ;
SHAH, NP ;
QUAN, SG ;
WACHSMAN, W .
SCIENCE, 1985, 229 (4708) :54-58
[7]  
EGUCHI K, 1991, J RHEUMATOL, V18, P297
[8]   HTLV-I ASSOCIATED ARTHRITIS - CHARACTERISTICS OF AN HTLV-I VIRUS-INFECTED T-CELL LINE FROM SYNOVIAL-FLUID [J].
EGUCHI, K ;
NAKAMURA, T ;
MINE, M ;
IDA, H ;
KAWAKAMI, A ;
MIGITA, K ;
NAGASATO, K ;
KURATA, A ;
FUKUDA, T ;
NAGATAKI, S .
ANNALS OF THE RHEUMATIC DISEASES, 1992, 51 (05) :673-677
[9]  
EGUCHI K, 1992, J RHEUMATOL, V19, P1925
[10]  
FREI K, 1986, J IMMUNOL, V137, P3521