Effect of cyclophosphamide on leukocytic infiltration in the brain of MRL/1pr mice

被引:41
作者
Farrell, M
Sakic, B
Szechtman, H
Denburg, JA
机构
[1] MCMASTER UNIV,DEPT MED,HAMILTON,ON L8N 3Z5,CANADA
[2] MCMASTER UNIV,DEPT PSYCHIAT,HAMILTON,ON L8N 3Z5,CANADA
[3] MCMASTER UNIV,DEPT BIOMED SCI,HAMILTON,ON L8N 3Z5,CANADA
关键词
neuropsychiatric lupus; behavioural immunology; autoimmune mice; cyclophosphamide; CD45; CD45R; choroid plexus;
D O I
10.1177/096120339700600310
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Neuropsychiatric manifestations are a poorly understood and potentially life-threatening complication of systemic lupus erythematosus (SLE). MRL/lpr mice spontaneously develop a lupus-like syndrome which is similar to the human disease in many respects, including behavioural abnormalities. Our previous findings indicated that the age at which infiltration of immune cells into the choroid plexus is first observed coincides with the appearance of behavioural dysfunction in MRL/lpr mice. This present study quantified leukocyte infiltration in relation to prolonged administration of cyclophosphamide (CY), a treatment effective in preventing some behavioural deficits. Compared to MRL +/+ controls, saline-treated MRL/lpr mice had significantly more CD45-positive cells (leukocytes) and CD45R-positive (B) cells in the choroid plexus and in the brain parenchyma. A six week course of CY (100 mg/kg i.p.) significantly reduced the infiltration of CD45, but not of CD45R-positive cells into the choroid plexus of the MRL/lpr substrain. In addition, the presence of leukocytes correlated positively with measures on one behavioural test (floating in the forced swim test) but not on another test (novel object test). These findings suggest that CY treatment has a differential effect on the infiltration of leukocyte subtypes and strengthen the hypothesis that some abnormal behaviour in MRL/lpr mice may be related to the presence of immunocompetent cells in the brain.
引用
收藏
页码:268 / 274
页数:7
相关论文
共 42 条
  • [1] CONGENIC AUTOIMMUNE MURINE MODELS OF CENTRAL NERVOUS-SYSTEM DISEASE IN CONNECTIVE-TISSUE DISORDERS
    ALEXANDER, EL
    MURPHY, ED
    ROTHS, JB
    ALEXANDER, GE
    [J]. ANNALS OF NEUROLOGY, 1983, 14 (02) : 242 - 248
  • [2] THE ACUTE INFLAMMATORY RESPONSE TO LIPOPOLYSACCHARIDE IN CNS PARENCHYMA DIFFERS FROM THAT IN OTHER BODY-TISSUES
    ANDERSSON, PB
    PERRY, VH
    GORDON, S
    [J]. NEUROSCIENCE, 1992, 48 (01) : 169 - 186
  • [3] DERIVATION OF THE SLEDAI - A DISEASE-ACTIVITY INDEX FOR LUPUS PATIENTS
    BOMBARDIER, C
    GLADMAN, DD
    UROWITZ, MB
    CARON, D
    CHANG, CH
    [J]. ARTHRITIS AND RHEUMATISM, 1992, 35 (06): : 630 - 640
  • [4] PULSE CYCLOPHOSPHAMIDE FOR SEVERE NEUROPSYCHIATRIC LUPUS
    BOUMPAS, DT
    YAMADA, H
    PATRONAS, NJ
    SCOTT, D
    KLIPPEL, JH
    BALOW, JE
    [J]. QUARTERLY JOURNAL OF MEDICINE, 1991, 81 (296): : 975 - 984
  • [5] Coffman R L, 1982, Immunol Rev, V69, P5
  • [6] LPR AND GLD - SINGLE GENE MODELS OF SYSTEMIC AUTOIMMUNITY AND LYMPHOPROLIFERATIVE DISEASE
    COHEN, PL
    EISENBERG, RA
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1991, 9 : 243 - 269
  • [7] DENBURG JA, 1993, RHEUM REV, V2, P123
  • [8] DENBURG JA, 1995, SCAN J RHEUMATOL, V12, P263
  • [9] DENBURG SD, 1993, RHEUM DIS CLIN N AM, V19, P815
  • [10] LYMPHOCYTE ADHESION TO BRAIN CAPILLARY ENDOTHELIAL-CELLS IN-VITRO
    DEVRIES, HE
    MOOR, ACE
    BLOMROOSEMALEN, MCM
    DEBOER, AG
    BREIMER, DD
    VANBERKEL, TJC
    KUIPER, J
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1994, 52 (01) : 1 - 8