HLA-DP allele-specific T cell responses to beryllium account for DP-associated susceptibility to chronic beryllium disease

被引:78
作者
Lombardi, G
Germain, C
Uren, J
Fiorillo, MT
du Bois, RM
Jones-Williams, W
Saltini, C
Sorrentino, R
Lechler, R
机构
[1] Hammersmith Hosp, ICSM, Dept Immunol, London W12 0NN, England
[2] Univ La Sapienza, Dept Cell Biol & Dev, I-00161 Rome, Italy
[3] Royal Brompton Hosp, London SW3 6LY, England
[4] Univ Wales, Coll Med, Dept Med, Cardiff CF1 3NS, S Glam, Wales
[5] Univ Roma Tor Vergata, Div Res Dis, Rome, Italy
[6] L Spallanzani Hosp, Inst Res & Clin Care, Rome, Italy
关键词
D O I
10.4049/jimmunol.166.5.3549
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Occupational exposure to small molecules, such as metals, is frequently associated with hypersensitivity reactions, Chronic beryllium (Be) disease (CBD) is a multisystem granulomatous disease that primarily affects the lung, and occurs in similar to3% of individuals exposed to this element. Immunogenetic studies have demonstrated a strong association between CBD and possession of alleles of HLA-DP containing glutamic acid (Glu) at position 69 in the HLA-DP beta -chain. T cell clones were raised from three patients with CBD in whom exposure occurred 10 and 30 years previously. Of 25 Be-specific clones that were obtained, all were restricted by HLA-DP alleles with Glu at DP beta 69, Furthermore, the proliferative responses of the clones were absolutely dependent upon DP beta Glu(69) in that a single amino acid substitution at this position abolished the response. As befits a disease whose pathogenesis involves a delayed type hypersensitivity response, the large majority of Be-specific clones secreted IFN-gamma (Th1) and little or no IL-4 (Th2) cytokines, This study provides insights into the molecular basis of DP2-associated susceptibility to CBD.
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页码:3549 / 3555
页数:7
相关论文
共 43 条
[1]   A SPECIFIC HLA-DP-BETA ALLELE IS ASSOCIATED WITH PAUCIARTICULAR JUVENILE RHEUMATOID-ARTHRITIS BUT NOT ADULT RHEUMATOID-ARTHRITIS [J].
BEGOVICH, AB ;
BUGAWAN, TL ;
NEPOM, BS ;
KLITZ, W ;
NEPOM, GT ;
ERLICH, HA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (23) :9489-9493
[2]   3-DIMENSIONAL STRUCTURE OF THE HUMAN CLASS-II HISTOCOMPATIBILITY ANTIGEN HLA-DR1 [J].
BROWN, JH ;
JARDETZKY, TS ;
GORGA, JC ;
STERN, LJ ;
URBAN, RG ;
STROMINGER, JL ;
WILEY, DC .
NATURE, 1993, 364 (6432) :33-39
[3]   A COMBINATION OF A PARTICULAR HLA-DP-BETA ALLELE AND AN HLA-DQ HETERODIMER CONFERS SUSCEPTIBILITY TO CELIAC-DISEASE [J].
BUGAWAN, TL ;
ANGELINI, G ;
LARRICK, J ;
AURICCHIO, S ;
FERRARA, GB ;
ERLICH, HA .
NATURE, 1989, 339 (6224) :470-473
[4]  
CARTHY D, 1995, REV RHUM, V62, P163
[5]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P56
[6]   REASSESSMENT OF HLA ASSOCIATION WITH CELIAC-DISEASE IN SPECIAL REFERENCE TO THE DP ASSOCIATION [J].
COLONNA, M ;
MANTOVANI, W ;
CORAZZA, GR ;
BARBONI, P ;
GASBARRINI, G ;
FERRARA, GB ;
TOSI, R ;
TANIGAKI, N .
HUMAN IMMUNOLOGY, 1990, 29 (04) :263-274
[7]  
Drénou B, 1999, J IMMUNOL, V163, P4115
[8]   HLA-DP VARIATION AS ADDITIONAL RISK FACTOR IN IDDM [J].
EASTEAL, S ;
KOHONENCORISH, MRJ ;
ZIMMET, P ;
SERJEANTSON, SW .
DIABETES, 1990, 39 (07) :855-857
[9]   EPIDEMIOLOGICAL ASPECTS OF BERYLLIUM-INDUCED NONMALIGNANT LUNG-DISEASE - A 30-YEAR UPDATE [J].
EISENBUD, M ;
LISSON, J .
JOURNAL OF OCCUPATIONAL AND ENVIRONMENTAL MEDICINE, 1983, 25 (03) :196-202
[10]   STUDIES ON THE HUMAN T-CELL RECEPTOR ALPHA/BETA VARIABLE REGION GENES .2. IDENTIFICATION OF 4 ADDITIONAL V-BETA SUBFAMILIES [J].
FERRADINI, L ;
ROMANROMAN, S ;
AZOCAR, J ;
MICHALAKI, H ;
TRIEBEL, F ;
HERCEND, T .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1991, 21 (04) :935-942