Thyroid-infiltrating B lymphocytes in Graves' disease are related to marginal zone and memory B cell compartments

被引:29
作者
Segundo, C
Rodríguez, C
García-Poley, A
Aguilar, M
Gavilán, I
Bellas, C
Brieva, JA
机构
[1] Hosp Univ Puerta Del Mar, Serv Inmunol, Cadiz 11009, Spain
[2] Hosp Univ Puerta Del Mar, Serv Cirurgia, Cadiz 11009, Spain
[3] Hosp Univ Puerta Del Mar, Serv Endocrinol, Cadiz 11009, Spain
[4] Hosp Ramon y Cajal, Serv Anat Patol, E-28034 Madrid, Spain
关键词
D O I
10.1089/105072501750302813
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
B lymphocytes that infiltrate the thyroid (Thy-B cells) in Graves' patients appear to be implicated in the patho-physiology of this disorder. The goal of the present study was to examine the nature of these Thy-B cells. To this end, Thy-B lymphocytes were isolated from surgical thyroidal samples, and their phenotype was determined by using mouse monoclonal antibodies (mAb) directed against a wide variety of surface markers, followed by flow cytometry multicolor analysis. The results show that most Thp-B cells (congruent to 60%) exhibited IgM(+) IgD(low) (to-) surface immunoglobulin (Ig) profile, whereas the minor cell fraction (congruent to 30%) consisted of switched IgG(+) memory B lymphocytes. Thy-B cells expressed low levels of CD5, CD23, and CD62L, which distinguished them from the resting B-cell pool, the major B-cell subset in the blood. In addition, they lacked CD38, CD10, and CD71, characteristic molecules for the germinal center B lymphocytes. In addition, Thy B lymphocytes showed peculiar patterns both of adhesion molecules (CD62L(-), CD44(intermediate)), and of activation molecules (CD69(+), CD80(+), and, in part, CD95(+)). Taken together, these results suggest that the Thy-B lymphocyte subset consists of a combination of IgM(+) B cells resembling marginal zone B lymphocytes, and isotype-su itched memory B cells.
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页码:525 / 530
页数:6
相关论文
共 33 条
[1]   CD5 B cells in autoimmune and non immune-mediated thyroid dysfunctions. [J].
Afeltra, A ;
Ferri, GM ;
Amoroso, A ;
Leri, O ;
Pellegrino, C ;
Guido, F ;
Garzia, P ;
Paggi, A .
ENDOCRINE RESEARCH, 1997, 23 (1-2) :81-94
[2]   Death receptors: Signaling and modulation [J].
Ashkenazi, A ;
Dixit, VM .
SCIENCE, 1998, 281 (5381) :1305-1308
[3]  
ATHERTON MC, 1985, IMMUNOLOGY, V55, P271
[4]   HUMAN-B LYMPHOCYTES - PHENOTYPE, PROLIFERATION, AND DIFFERENTIATION [J].
BANCHEREAU, J ;
ROUSSET, F .
ADVANCES IN IMMUNOLOGY, 1992, 52 :125-262
[5]   CD5+ B cells in Graves' disease: Correlation with disease activity [J].
Corrales, JJ ;
Orfao, A ;
Lopez, A ;
Mories, MT ;
Miralles, JM ;
Ciudad, J .
HORMONE AND METABOLIC RESEARCH, 1996, 28 (06) :280-285
[6]   Subepithelial B cells in the human palatine tonsil .1. Morphologic, cytochemical and phenotypic characterization [J].
Dono, M ;
Burgio, VL ;
Tacchetti, C ;
Favre, A ;
Zupo, S ;
Taborelli, G ;
Chiorazzi, N ;
Grossi, CE ;
Ferrarini, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (09) :2035-2042
[7]   ANALYSIS OF MUTATIONS IN IMMUNOGLOBULIN HEAVY-CHAIN VARIABLE REGION GENES OF MICRODISSECTED MARGINAL ZONE (MGZ) B-CELLS SUGGESTS THAT THE MGZ OF HUMAN SPLEEN IS A RESERVOIR OF MEMORY B-CELLS [J].
DUNNWALTERS, DK ;
ISAACSON, PG ;
SPENCER, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (02) :559-566
[8]  
DURANDY A, 1990, J IMMUNOL, V144, P60
[9]   CD40 and B cell antigen receptor dual triggering of resting B lymphocytes turns on a partial germinal center phenotype [J].
Galibert, L ;
Burdin, N ;
deSaintVis, B ;
Garrone, P ;
VanKooten, C ;
Banchereau, J ;
Rousset, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (01) :77-85
[10]  
KANSAS GS, 1985, J IMMUNOL, V134, P2995