Cytokine profile in collagen-induced arthritis:: Differences between syngeneic and allogeneic pregnancy

被引:2
作者
Almeida Gonzalez, D. [1 ]
Cabrera de Leon, A. [1 ,2 ,3 ]
Vazquez Moncholi, C. [1 ]
Brito Diaz, B. [1 ]
Rodriguez Perez, M. C. [1 ]
Aguirre-Jaime, A. [1 ]
Dominguez Coello, S. [1 ]
Gonzalez Hernandez, A. [1 ]
机构
[1] Hosp La Candelaria, Res Unit, Santa Cruz de Tenerife, Canary Islands, Spain
[2] Hosp San Juan Dios, Santa Cruz de Tenerife 38009, Canary Islands, Spain
[3] Univ La Laguna, Sch Med, Canary Isl, Spain
关键词
arthritis; pregnancy; allogeneic; syngeneic; cytokines;
D O I
10.1007/s00011-007-7197-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: To identify the differences in cytokine profile between allogeneic and syngeneic pregnancy in mice with collagen-induced arthritis (CIA). Methods: Mice (strain B10.RIII) were injected with bovine collagen. Females were mated with males of the same strain (syngeneic pregnancy) or with males of strain B10. Q (allogeneic pregnancy). Concentrations of cytokines were measured during pregnancy and after delivery, and the onset and evolution of arthritis was followed in all female animals throughout the study period. Results: In female mice that developed CIA, cytokine concentrations were lower in allogeneic pregnancies than syngeneic pregnancies. When paired cytokine concentrations were compared in each animal during and after pregnancy, MCP-1 was lower during gestation than after delivery in both groups of pregnant mice, IL-6 was lower during gestation than after delivery only in allogeneic pregnancies, and IL-10 was lower during gestation than after delivery in allogeneic pregnancies, whereas in syngeneic pregnancies IL-10 was higher during gestation than after delivery. Conclusions: Allogeneic pregnancy was associated with less arthritis because of lower concentrations of proinflammatory cytokines (IL-6 and others), not because of an increase in the concentration of antiinflammatory cytokines (IL-10).
引用
收藏
页码:266 / 271
页数:6
相关论文
共 25 条
  • [1] Regulatory T cells mediate maternal tolerance to the fetus
    Aluvihare, VR
    Kallikourdis, M
    Betz, AG
    [J]. NATURE IMMUNOLOGY, 2004, 5 (03) : 266 - 271
  • [2] Identification of new quantitative trait loci in mice with collagen-induced arthritis
    Bauer, K
    Yu, XH
    Wernhoff, P
    Koczan, D
    Thiesen, HJ
    Ibrahim, SM
    [J]. ARTHRITIS AND RHEUMATISM, 2004, 50 (11): : 3721 - 3728
  • [3] Mechanisms of disease - The many roles of chemokines and chemokine receptors in inflammation
    Charo, IF
    Ransohoff, RM
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (06) : 610 - 621
  • [4] Involvement of lymphocytes with a Th1 cytokine profile in bone cell damage associated with MMP-9 production in collagen-induced arthritis
    Chen, J
    Zhang, XM
    Xu, Q
    [J]. INFLAMMATION RESEARCH, 2004, 53 (12) : 670 - 679
  • [5] Mechanisms of disease: Cytokine pathways and joint inflammation in rheumatoid arthritis.
    Choy, EHS
    Panayi, GS
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (12) : 907 - 916
  • [6] Ellingsen T, 2001, J RHEUMATOL, V28, P41
  • [7] Tryptophan-derived catabolites are responsible for inhibition of T and natural killer cell proliferation induced by indoleamine 2,3-dioxygenase
    Frumento, G
    Rotondo, R
    Tonetti, M
    Damonte, G
    Benatti, U
    Ferrara, GB
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (04) : 459 - 468
  • [8] González DA, 2004, J RHEUMATOL, V31, P30
  • [9] Blockade of lymphotoxin pathway exacerbates autoimmune arthritis by enhancing the Th1 response
    Han, SH
    Zhang, XJ
    Marinova, E
    Ozen, Z
    Bheekha-Escura, R
    Guo, LJ
    Wansley, D
    Booth, G
    Fu, YX
    Zheng, B
    [J]. ARTHRITIS AND RHEUMATISM, 2005, 52 (10): : 3202 - 3209
  • [10] Chemokines in joint disease: the key to inflammation?
    Haringman, JJ
    Ludikhuize, J
    Tak, PP
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2004, 63 (10) : 1186 - 1194