Phenotypic and functional properties of γδ T Cells from patients with Guillain Barre syndrome

被引:17
作者
Borsellino, G
Poccia, F
Placido, R
Tramonti, D
Mancino, G
Luchetti, S
Galgani, S
Bonetti, B
Bach, S
Cipriani, B
Brosnan, CF
Battistini, L
机构
[1] IRCCS Santa Lucia, Lab Neuroimmunol, I-00179 Rome, Italy
[2] IRCCS L Spallanzani, Int Ctr AIDS & Emerging Infect, I-00149 Rome, Italy
[3] Osped S Camillo Roma, Dept Neurosci Lancisi, Rome, Italy
[4] Univ Verona, Dept Neurol, I-37100 Verona, Italy
[5] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10467 USA
关键词
Guillain Barre syndrome; gamma-delta T cells; cytokines;
D O I
10.1016/S0165-5728(99)00165-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this study we have examined the phenotypic and functional properties of circulating gamma delta T cells in patients with Guillain Barre syndrome (GBS), in normal healthy controls, and in patients with active multiple sclerosis (MS). Cells expressing the V delta 2 T cell receptor showed elevated expression of the C-lectin receptor NKRP1A in both GBS and MS, suggestive of an activated state. However, in patients with GBS these cells failed to respond to pyrenil-pyrophosphate derivatives and V delta 2 + T cell clones derived from these patients released lower levels of IFN gamma than V delta 2 + clones derived from controls and MS patients. In contrast, in patients with GBS the V delta 1 + subset was expanded, showed elevated expression of NKRP1A and V delta 1 + clones derived from these patients secreted high levels of IL-4. Our findings of expanded NKRP-1A +, IL-4-producing V delta 1 T cells in the GBS patients suggests the possibility that these cells are activated by the recognition of non-protein antigens in an MHC-unrestricted manner and contribute to the humoral response to glycolipids that is a hallmark of this disease. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:199 / 207
页数:9
相关论文
共 54 条
[1]   ASSESSMENT OF CURRENT DIAGNOSTIC-CRITERIA FOR GUILLAIN-BARRE-SYNDROME [J].
ASBURY, AK ;
CORNBLATH, DR .
ANNALS OF NEUROLOGY, 1990, 27 :S21-S24
[2]  
Battistini L, 1996, J NEUROIMMUNOL, V67, P145
[3]   MULTIPLE-SCLEROSIS - LIMITED DIVERSITY OF THE V-DELTA-2-J-DELTA-3 T-CELL RECEPTOR IN CHRONIC ACTIVE LESIONS [J].
BATTISTINI, L ;
SELMAJ, K ;
KOWAL, C ;
OHMEN, J ;
MODLIN, RL ;
RAINE, CS ;
BROSNAN, CF .
ANNALS OF NEUROLOGY, 1995, 37 (02) :198-203
[4]  
Battistini L, 1997, J IMMUNOL, V159, P3723
[5]   Stimulation of peripheral blood lymphocytes with Campylobacter jejuni generates a gamma delta T cell response in patients with Guillain-Barre syndrome [J].
BenSmith, A ;
Goodall, JC ;
Gaston, JSH ;
Winer, JB .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1997, 109 (01) :121-126
[6]   Isolation and characterisation of T lymphocytes from sural nerve biopsies in patients with Guillain-Barre syndrome and chronic inflammatory demyelinating polyneuropathy [J].
BenSmith, A ;
Gaston, JSH ;
Barber, PC ;
Winer, JB .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1996, 61 (04) :362-368
[7]  
BOULLIER S, 1995, J IMMUNOL, V154, P1418
[8]   Mechanisms of immune injury in multiple sclerosis [J].
Brosnan, CF ;
Raine, CS .
BRAIN PATHOLOGY, 1996, 6 (03) :243-257
[9]   CD1d-mediated recognition of an α-galactosylceramide by natural killer T cells is highly conserved through mammalian evolution [J].
Brossay, L ;
Chioda, M ;
Burdin, N ;
Koezuka, Y ;
Casorati, G ;
Dellabona, P ;
Kronenberg, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (08) :1521-1528
[10]   Recognition by gamma/delta T cells [J].
Chien, YH ;
Jores, R ;
Crowley, MP .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :511-532