Characterisation of T and B lymphocytes infiltrating abdominal aortic aneurysms

被引:103
作者
Ocana, E
Bohórquez, JC
Pérez-Requena, J
Brieva, JA
Rodríguez, C
机构
[1] Hosp Univ Puerta del Mar, Serv Immunol, Cadiz 110009, Spain
[2] Hosp Univ Puerta del Mar, Serv Cirugia Vasc, Cadiz, Spain
[3] Hosp Univ Puerta del Mar, Serv Anat Patol, Cadiz, Spain
关键词
abdominal aortic aneurysms; infiltrating B and T lymphocytes; phenotype; flow cytometry; inflammation;
D O I
10.1016/S0021-9150(03)00282-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cellular infiltrates consisting mainly of lymphocytes are commonly present in the arterial wall in abdominal aortic aneurysm (AAA). However, despite this, the precise nature of these populations has to date not been described in detail. The aim of this study was to perform an exhaustive phenotypic characterisation of the infiltrating lymphocytes in order to define the inflammatory process that develops in AAA. For this purpose, AAA-infiltrating lymphocytes from 25 fresh aneurysm wall samples and, as a control, peripheral blood (PB) lymphocytes from the same patients were purified. The expression of lineage specific markers, maturation molecules, activation antigens and adhesion molecules on T and B lymphocytes was examined by triple-colour immunofluorescence and flow cytometry analysis. The phenotype of AAA-infiltrating lymphocytes was compared with that of PB of the patients with AAA. The results reveal that AAA-infiltrating B and T lymphocytes consist of activated memory cells, with specific homing properties. In addition, they express molecules of B-T co-stimulation and, occasionally, exhibit phenotypical features indicative of the ectopic formation of lymphoid structures. These findings are discussed in the light of the similarities shared with the lymphoid infiltration occurring in other chronic autoimmune/inflammatory disorders. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:39 / 48
页数:10
相关论文
共 30 条
[1]   CD27: a memory B-cell marker [J].
Agematsu, K ;
Hokibara, S ;
Nagumo, H ;
Komiyama, A .
IMMUNOLOGY TODAY, 2000, 21 (05) :204-206
[2]   ELASTASE-INDUCED EXPERIMENTAL ANEURYSMS IN RATS [J].
ANIDJAR, S ;
SALZMANN, JL ;
GENTRIC, D ;
LAGNEAU, P ;
CAMILLERI, JP ;
MICHEL, JB .
CIRCULATION, 1990, 82 (03) :973-981
[3]   Differential regulation of matrix metalloproteinase activities in abdominal aortic aneurysms [J].
Annabi, B ;
Shédid, D ;
Ghosn, P ;
Kenigsberg, RL ;
Desrosiers, RR ;
Bojanowski, MW ;
Beaulieu, É ;
Nassif, E ;
Moumdjian, R ;
Béliveau, R .
JOURNAL OF VASCULAR SURGERY, 2002, 35 (03) :539-546
[4]   Differential gene expression in human abdominal aorta: Aneurysmal versus occlusive disease [J].
Armstrong, PJ ;
Johanning, JM ;
Calton, WC ;
Delatore, JR ;
Franklin, DP ;
Han, DC ;
Carey, DJ ;
Elmore, JR .
JOURNAL OF VASCULAR SURGERY, 2002, 35 (02) :346-355
[5]   SIBLING RISKS OF ABDOMINAL AORTIC-ANEURYSM [J].
BAIRD, PA ;
SADOVNICK, AD ;
YEE, IML ;
COLE, CW ;
COLE, L .
LANCET, 1995, 346 (8975) :601-604
[6]   Vascular-associated lymphoid tissue (VALT) involvement in aortic aneurysm [J].
Bobryshev, YV ;
Lord, RSA .
ATHEROSCLEROSIS, 2001, 154 (01) :15-21
[7]   Stromelysin-1 (matrix metalloproteinase-3) and tissue inhibitor of metalloproteinase-3 are overexpressed in the wall of abdominal aortic aneurysms [J].
Carrell, TWG ;
Burnand, KG ;
Wells, GMA ;
Clements, JM ;
Smith, A .
CIRCULATION, 2002, 105 (04) :477-482
[8]  
CROFT M, 1994, J IMMUNOL, V152, P2675
[9]   Mechanisms of abdominal aortic aneurysm formation. [J].
Daugherty A. ;
Cassis L.A. .
Current Atherosclerosis Reports, 2002, 4 (3) :222-227
[10]   Regulation of lymphocyte traffic by adhesion molecules [J].
Fabbri, M ;
Bianchi, E ;
Fumagalli, L ;
Pardi, R .
INFLAMMATION RESEARCH, 1999, 48 (05) :239-246