Pregnancy-induced expansion of regulatory T-lymphocytes may mediate protection to multiple sclerosis activity

被引:58
作者
Sánchez-Ramón, S
Navarro, J
Aristimuño, C
Rodríguez-Mahou, M
Bellón, JM
Fernández-Cruz, E
de Andrés, C
机构
[1] Gregorio Maranon Univ, Gen Hosp, Dept Immunol, Madrid 28007, Spain
[2] Gregorio Maranon Univ, Gen Hosp, Dept Neurol, Madrid 28007, Spain
[3] Gregorio Maranon Univ, Gen Hosp, Dept Prevent Med, Madrid 28007, Spain
关键词
multiple sclerosis; pregnancy; regulatory T-lymphocytes; tolerance;
D O I
10.1016/j.imlet.2004.09.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pregnancy represents a physiological transitory state of immune tolerance to avoid the rejection of the foetus, and concomitantly of stabilisation of many autoimmune diseases, such as multiple sclerosis (MS). Alterations in regulatory T-lymphocytes (T-Reg) are known to be involved in organ-specific autoimmune disease pathophysiology. Our goal was to quantify CD4(+)CD25(+) and CD4(+)CD25(hi+) T-Reg and activated (CD4(+)HLA-DR(+)CD38(+)) T-lymphocytes during pregnancy and puerperium in 13 MS patients in comparison with healthy pregnant and non-pregnant women. During pregnancy, it progressive parallel increase in CD4(+)CD25(+) T-lymphocytes in healthy pregnants as well as MS pregnant patients was observed. The proportion of T-Reg was significantly higher in all pregnants than in non-pregnant women (p=0.01), whereas no differences were observed neither in the percentages of total nor activated CD4(+) T-lymphocytes. In MS patients, CD4(+)CD25(+) T-lymphocytes significantly decreased when comparing the third trimester with the puerperal period proportions (p=0.01), whereas CD4(+)CD25(hi+) T-lymphocytes significantly increased (p=0.002). Our findings are consistent with the expansion of circulating regulatory CD4(+)CD25(+) T-lymphocytes pool with suppressive activity during normal pregnancy and in MS. A different pattern of CD4(+)CD25(hi+) T-lymphocytes between healthy pregnants and MS women, which may represent relevant factors in the activity course of MS. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:195 / 201
页数:7
相关论文
共 39 条
[1]   Th1/Th2 cytokine patterns and clinical profiles during and after pregnancy in women with multiple sclerosis [J].
Al-Shammri, S ;
Rawoot, P ;
Azizieh, F ;
AbuQoora, A ;
Hanna, M ;
Saminathan, TR ;
Raghupathy, R .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2004, 222 (1-2) :21-27
[2]   Regulatory T cells mediate maternal tolerance to the fetus [J].
Aluvihare, VR ;
Kallikourdis, M ;
Betz, AG .
NATURE IMMUNOLOGY, 2004, 5 (03) :266-271
[3]   Phenotype, localization, and mechanism of suppression of CD4+CD25+ human thymocytes [J].
Annunziato, F ;
Cosmi, L ;
Liotta, F ;
Lazzeri, E ;
Manetti, R ;
Vanini, V ;
Romagnani, P ;
Maggi, E ;
Romagnani, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (03) :379-387
[4]   An essential role for interleukin 10 in the function of regulatory T cells that inhibit intestinal inflammation [J].
Asseman, C ;
Mauze, S ;
Leach, MW ;
Coffman, RL ;
Powrie, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (07) :995-1003
[5]   Regulatory T cells under scrutiny [J].
Bach, JF .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (03) :189-198
[6]   CD4+CD25high regulatory cells in human peripheral blood [J].
Baecher-Allan, C ;
Brown, JA ;
Freeman, GJ ;
Hafler, DA .
JOURNAL OF IMMUNOLOGY, 2001, 167 (03) :1245-1253
[7]   Quantitative alterations of the functionally distinct subsets of CD4 and CD8 T lymphocytes in asymptomatic HIV infection: Changes in the expression of CD45RO, CD45RA, CD11b, CD38, HLA-DR, and CD25 antigens [J].
Benito, JM ;
Zabay, JM ;
Gil, J ;
Bermejo, M ;
Escudero, A ;
Sanchez, E ;
FernandezCruz, E .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY, 1997, 14 (02) :128-135
[8]  
Confavreux C, 1999, REV NEUROL-FRANCE, V155, P186
[9]   Rate of pregnancy-related relapse in multiple sclerosis [J].
Confavreux, C ;
Hutchinson, M ;
Hours, MM ;
Cortinovis-Tourniaire, P ;
Moreau, T .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (05) :285-291
[10]   Ex vivo isolation and characterization of CD4+CD25+ T cells with regulatory properties from human blood [J].
Dieckmann, D ;
Plottner, H ;
Berchtold, S ;
Berger, T ;
Schuler, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (11) :1303-1310