Changes in activated T cells in the blood correlate with disease activity in multiple sclerosis

被引:88
作者
Khoury, SJ
Guttmann, CRG
Orav, EJ
Kikinis, R
Jolesz, FA
Weiner, HL
机构
[1] Ctr Neurol Dis, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Radiol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
关键词
D O I
10.1001/archneur.57.8.1183
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To determine whether changes in activation markers on peripheral blood T cells correlate with disease activity in patients with multiple sclerosis. Design: In a prospective longitudinal study during 1 year, we analyzed the change in percentage of activated T lymphocytes in the peripheral blood of 40 patients with multiple sclerosis in relation to clinical findings and changes on brain magnetic resonance imaging (MRI) scans. The patients underwent repeated imaging of the brain (mean number of MRIs for each patient, 22) at the time blood samples were obtained as well as at monthly neurological examinations, and at the time of scoring on the Kurtzke Expanded Disability Status Scale (EDSS) and ambulation index scale. Results: A change in the percentage of cells expressing the activation markers interleukin 2 receptor (CD25), class II major histocompatibility complex (MHC) (13) or surface dipeptidyl peptidase (CD26) correlated significantly with a change in lesion volume or a change in number of gadolinium-enhancing lesions as detected on MRI. Changes in CD25(+) cells and in CD4(+) cells expressing class II MHC also correlated with changes in disability as measured by EDSS in patients with relapsing-remitting disease, and changes in CD4(+)CD25(+) cells correlated with the occurrence of attacks in patients with relapsing-remitting disease. These correlations are dependent on measurement of changes between time points sampled at 1- or 2-week intervals. Conclusion: There is a linkage between peripheral T-lymphocyte activation as measured by cell surface markers and disease activity in patients with multiple sclerosis.
引用
收藏
页码:1183 / 1189
页数:7
相关论文
共 49 条
[1]  
ANTEL J, 1986, J IMMUNOL, V137, P3436
[2]   Increased interleukin 12 production in progressive multiple sclerosis: Induction by activated CD4(+) T cells via CD40 ligand [J].
Balashov, KE ;
Smith, DR ;
Khoury, SJ ;
Hafler, DA ;
Weiner, HL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (02) :599-603
[3]   INHIBITION OF T-CELL RESPONSES BY ACTIVATED HUMAN CD8+ T-CELLS IS MEDIATED BY INTERFERON-GAMMA AND IS DEFECTIVE IN CHRONIC PROGRESSIVE MULTIPLE-SCLEROSIS [J].
BALASHOV, KE ;
KHOURY, SJ ;
HAFLER, DA ;
WEINER, HL .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (06) :2711-2719
[4]  
BAXEVANIS CN, 1990, J IMMUNOL, V144, P4166
[5]   ABSENCE OF A CORRELATION BETWEEN LYMPHOCYTE-T SUBSETS AND CLINICAL ACTIVITY IN RELAPSING-REMITTING MULTIPLE-SCLEROSIS [J].
CAPRA, R ;
MATTIOLI, F ;
VIGNOLO, LA ;
BETTINZIOLI, M ;
CATTANEO, R ;
FRANCESCHINI, F .
JOURNAL OF NEUROIMMUNOLOGY, 1989, 22 (01) :41-45
[6]   LOSS OF FUNCTIONAL SUPPRESSION IS LINKED TO DECREASES IN CIRCULATING SUPPRESSOR INDUCER (CD4+2H4+) T-CELLS IN MULTIPLE-SCLEROSIS [J].
CHOFFLON, M ;
WEINER, HL ;
MORIMOTO, C ;
HAFLER, DA .
ANNALS OF NEUROLOGY, 1988, 24 (02) :185-191
[7]   DECREASE OF SUPPRESSOR INDUCER (CD4+2H4+) T-CELLS IN MULTIPLE-SCLEROSIS CEREBROSPINAL-FLUID [J].
CHOFFLON, M ;
WEINER, HL ;
MORIMOTO, C ;
HAFLER, DA .
ANNALS OF NEUROLOGY, 1989, 25 (05) :494-499
[8]   Elevated interleukin-12 in progressive multiple sclerosis correlates with disease activity and is normalized by pulse cyclophosphamide therapy [J].
Comabella, M ;
Balashov, K ;
Issazadeh, S ;
Smith, D ;
Weiner, HL ;
Khoury, SJ .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (04) :671-678
[9]   CD26, let it cut or cut it down [J].
De Meester, I ;
Korom, S ;
Van Damme, J ;
Scharpé, S .
IMMUNOLOGY TODAY, 1999, 20 (08) :367-375
[10]   LYMPHOCYTE-T SUBPOPULATIONS IN PERIPHERAL-BLOOD OF PATIENTS WITH MULTIPLE-SCLEROSIS, PATIENTS WITH OTHER NEUROLOGICAL DISEASES AND HEALTHY CONTROLS [J].
DEGRAAF, J ;
MINDERHOUD, JM ;
TEELKEN, AW .
CLINICAL NEUROLOGY AND NEUROSURGERY, 1986, 88 (03) :181-187