Enriched CD161high CCR6+ γδ T Cells in the Cerebrospinal Fluid of Patients With Multiple Sclerosis

被引:66
作者
Schirmer, Lucas [1 ]
Rothhammer, Veit [1 ]
Hemmer, Bernhard [1 ]
Korn, Thomas [1 ]
机构
[1] Tech Univ Munich, Dept Neurol, Klinikum Rechts Isar, D-81675 Munich, Germany
关键词
RECEPTOR; DIFFERENTIATION; LYMPHOCYTES; REPERTOIRE; PHENOTYPE; CD161; AGE;
D O I
10.1001/2013.jamaneurol.409
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To investigate the expression of CD161 (KLRB1) and CCR6 on human gamma delta T cells in blood and cerebrospinal fluid (CSF) of patients with a clinically isolated syndrome (CIS) and multiple sclerosis (MS) in relapse. Design: Flow cytometry analysis of CD161 and CCR6 expression and intracellular cytokine staining for interleukin 17 and interferon-gamma on human gamma delta T cells in blood and CSF samples. Setting: Department of Neurology, Klinikum rechts der Isar, Technische Universitat Munchen, a tertiary referral center. Patients: Twenty-six patients with CIS/MS in active relapse, 10 patients with other autoimmune disorders, 12 patients with neuroinfectious diseases, and 15 patients with noninflammatory neurological diseases. Main Outcome Measures: Frequencies of CD161(high) and CCR6(+) gamma delta T cells in blood and CSF samples of patients with CIS/MS in relapse and control patients. Results: gamma delta T cells were increased in both blood and CSF of patients with CIS/MS in relapse as compared with controls with noninflammatory disease. The fraction of CD161(high) CCR6(+) gamma delta T cells was significantly higher in the CSF of patients with CIS/ MS in relapse than of those with systemic autoimmune disorders or controls with noninflammatory disease. The CD161(high) CCR6(+) doublepositive gamma delta T-cell population was further enriched in the CSF in relation to blood in patients with CIS/MS in relapse but not in patients with infectious disease or the other control groups. The CD161(high) CCR6(+) gamma delta T-cell population was characterized by its capacity to produce interleukin 17. Conclusion: Interleukin 17-producing CD161(high) CCR6(+) gamma delta T cells might contribute to the compartmentalized inflammatory process in the central nervous system of patients with MS. JAMA Neurol. 2013;70(3):345-351. Published online December 17, 2012. doi: 10.1001/2013.jamaneurol.409
引用
收藏
页码:345 / 351
页数:7
相关论文
共 28 条
[1]   Surface phenotype and antigenic specificity of human interleukin 17-producing T helper memory cells [J].
Acosta-Rodriguez, Eva V. ;
Rivino, Laura ;
Geginat, Jens ;
Jarrossay, David ;
Gattorno, Marco ;
Lanzavecchia, Antonio ;
Sallusto, Federica ;
Napolitani, Giorgio .
NATURE IMMUNOLOGY, 2007, 8 (06) :639-646
[2]   CD161highCD8+T cells bear pathogenetic potential in multiple sclerosis [J].
Annibali, Viviana ;
Ristori, Giovanni ;
Angelini, Daniela F. ;
Serafini, Barbara ;
Mechelli, Rosella ;
Cannoni, Stefania ;
Romano, Silvia ;
Paolillo, Andrea ;
Abderrahim, Hadi ;
Diamantini, Adamo ;
Borsellino, Giovanna ;
Aloisi, Francesca ;
Battistini, Luca ;
Salvetti, Marco .
BRAIN, 2011, 134 :542-554
[3]   Phenotypical and functional characterization of T helper 17 cells in multiple sclerosis [J].
Brucklacher-Waldert, Verena ;
Sturner, Klarissa ;
Kolster, Manuela ;
Wolthausen, Julia ;
Tolosa, Eva .
BRAIN, 2009, 132 :3329-3341
[4]   Differentiation, phenotype, and function of interleukin-17-producing human Vγ9Vδ2 T cells [J].
Caccamo, Nadia ;
La Mendola, Carmela ;
Orlando, Valentina ;
Meraviglia, Serena ;
Todaro, Matilde ;
Stassi, Giorgio ;
Sireci, Guido ;
Fournie, Jean Jacques ;
Dieli, Francesco .
BLOOD, 2011, 118 (01) :129-138
[5]  
Cai YH, 2011, IMMUNITY, V35, P596, DOI 10.1016/j.immuni.2011.08.001
[6]   Impact of age, gender, and race on circulating γδ T cells [J].
Cairo, Cristiana ;
Armstrong, Cheryl L. ;
Cummings, Jean Saville ;
Deetz, Carl O. ;
Tan, Ming ;
Lu, Changwan ;
Davis, Charles E. ;
Pauza, C. David .
HUMAN IMMUNOLOGY, 2010, 71 (10) :968-975
[7]   Human interleukin 17-producing cells originate from a CD161+CD4+ T cell precursor [J].
Cosmi, Lorenzo ;
De Palma, Raffaele ;
Santarlasci, Veronica ;
Maggi, Laura ;
Capone, Manuela ;
Frosali, Francesca ;
Rodolico, Gabriella ;
Querci, Valentina ;
Abbate, Gianfranco ;
Angeli, Roberta ;
Berrino, Liberato ;
Fambrini, Massimiliano ;
Caproni, Marzia ;
Tonelli, Francesco ;
Lazzeri, Elena ;
Parronchi, Paola ;
Liotta, Francesco ;
Maggi, Enrico ;
Romagnani, Sergio ;
Annunziato, Francesco .
JOURNAL OF EXPERIMENTAL MEDICINE, 2008, 205 (08) :1903-1916
[8]   Development of Interleukin-17-Producing γδ T Cells Is Restricted to a Functional Embryonic Wave [J].
Haas, Jan D. ;
Ravens, Sarina ;
Dueber, Sandra ;
Sandrock, Inga ;
Oberdoerfer, Linda ;
Kashani, Elham ;
Chennupati, Vijaykumar ;
Foehse, Lisa ;
Naumann, Ronald ;
Weiss, Siegfried ;
Krueger, Andreas ;
Foerster, Reinhold ;
Prinz, Immo .
IMMUNITY, 2012, 37 (01) :48-59
[9]   CCR6 and NK1.1 distinguish between IL-17A and IFN-γ-producing γδ effector T cells [J].
Haas, Jan D. ;
Malinarich Gonzalez, Frano H. ;
Schmitz, Susanne ;
Chennupati, Vijaykumar ;
Foehse, Lisa ;
Kremmer, Elisabeth ;
Foerster, Reinhold ;
Prinz, Immo .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2009, 39 (12) :3488-3497
[10]   Risk alleles for multiple sclerosis identified by a genomewide study [J].
Hafler, David A. ;
Compston, Alastair ;
Sawcer, Stephen ;
Lander, Eric S. ;
Daly, Mark J. ;
De Jager, Philip L. ;
de Bakker, Paul I. W. ;
Gabriel, Stacey B. ;
Mirel, Daniel B. ;
Ivinson, Adrian J. ;
Pericak-Vance, Margaret A. ;
Gregory, Simon G. ;
Rioux, John D. ;
McCauley, Jacob L. ;
Haines, Jonathan L. ;
Barcellos, Lisa F. ;
Cree, Bruce ;
Oksenberg, Jorge R. ;
Hauser, Stephen L. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (09) :851-862