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Apoptotic cell infusion treats ongoing collagen-induced arthritis, even in the presence of methotrexate, and is synergic with anti-TNF therapy
被引:32
|作者:
Bonnefoy, Francis
[1
,2
,3
,4
,5
]
Daoui, Anna
[1
,2
,3
,4
,5
]
Valmary-Degano, Severine
[6
]
Toussirot, Eric
[7
,8
]
Saas, Philippe
[1
,2
,3
,4
,5
,7
]
Perruche, Sylvain
[1
,2
,3
,4
,5
,9
]
机构:
[1] INSERM, UMR1098, F-25000 Besancon, France
[2] Univ Bourgogne Franche Comte, SFR FED4234, F-25000 Besancon, France
[3] EFS Bourgogne Franche Comte, F-25000 Besancon, France
[4] LabEX LipSTIC, ANR LABX 0021 11, F-25000 Besancon, France
[5] Besancon Univ Hosp, FHU INCREASE, F-25000 Besancon, France
[6] Besancon Univ Hosp, Dept Pathol, F-25000 Besancon, France
[7] Besancon Univ Hosp, Clin Invest Ctr Biotherapy, INSERM CIC1431, F-25000 Besancon, France
[8] Besancon Univ Hosp, Dept Rheumatol, F-25000 Besancon, France
[9] INSERM, UMR1098, Etab Francais Sang BFC, 8 Rue Dr JFX Girod, F-25000 Besancon, France
关键词:
REGULATORY T-CELLS;
TGF-BETA;
RHEUMATOID-ARTHRITIS;
SUPPRESSIVE ACTIVITY;
ADOPTIVE TRANSFER;
PROTECT MICE;
DISEASE;
INDUCTION;
TRANSPLANTATION;
INFLAMMATION;
D O I:
10.1186/s13075-016-1084-0
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background: Apoptotic cell-based therapies have been proposed to treat chronic inflammatory diseases. The aim of this study was to investigate the effect of intravenous (i.v.) apoptotic cell infusion in ongoing collagen-induced arthritis (CIA) and the interaction of this therapy with other treatments used in rheumatoid arthritis (RA), including methotrexate (MTX) or anti-TNF therapy. Methods: The effects of i.v. apoptotic cell infusion were evaluated in a CIA mouse model in DBA/1 mice immunized with bovine type II collagen. The number and functions of antigen-presenting cells (APC), regulatory CD4(+) T cells (Treg), and circulating anti-collagen auto-antibodies were analyzed in CIA mice. Results: Treatment of arthritic mice with i.v. apoptotic cell infusion significantly reduced the arthritis clinical score. This therapeutic approach modified T cell responses against the collagen auto-antigen with selective induction of collagen-specific Treg. In addition, we observed that APC from apoptotic-cell-treated animals were resistant to toll-like receptor ligand activation and favored ex vivo Treg induction, indicating APC reprogramming. Apoptotic cell injection-induced arthritis modulation was dependent on transforming growth factor (TGF)-beta, as neutralizing anti-TGF-beta antibody prevented the effects of apoptotic cells. Methotrexate did not interfere, while anti-TNF therapy was synergic with apoptotic-cell-based therapy. Conclusion: Overall, our data demonstrate that apoptotic-cell-based therapy is efficient in treating ongoing CIA, compatible with current RA treatments, and needs to be evaluated in humans in the treatment of RA.
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