Th1-like cytokine production profile and individual specific alterations in TCRBV-gene usage of T cells from newly diagnosed type 1 diabetes patients after stimulation with β-cell antigens

被引:23
作者
Kallan, AA
Duinkerken, G
de Jong, R
van den Elsen, P
Hutton, JC
Martin, S
Roep, BO
de Vries, RRP
机构
[1] Univ Leiden Hosp, Dept Immunohaematol, NL-2300 RC Leiden, Netherlands
[2] Univ Leiden Hosp, Blood Bank, NL-2300 RC Leiden, Netherlands
[3] Univ Colorado, Barbara Davis Ctr Childhood Diabet, Denver, CO 80202 USA
[4] Univ Dusseldorf, Diabet Res Inst, D-4000 Dusseldorf, Germany
基金
英国惠康基金;
关键词
cytokine production; TCRBV-gene usage; beta-cell antigens; T cells; type; 1; diabetes;
D O I
10.1006/jaut.1997.0167
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 order to study cytokine production profile (IFN-gamma, IL-4 and TNF-alpha) and TCRBV-gene usage of peripheral autoreactive T cells from IDDM patients, we have generated antigen-specific T cell lines with either tetanus toroid, insulinoma membranes or a single beta-cell protein, recombinant ICA69, which has been shown to be a target of both autoantibodies and T cells in IDDM. By semi-quantitative polymerase chain reaction (PCR) analysis, we have determined the composition of the T cell receptor repertoire of these T cell lines and compared this with the general peripheral repertoire. T cell responses against beta-cell antigens and tetanus toroid (TT) were shown to be associated with IFN-gamma and TNF-alpha production, suggestive of a Th1-like phenotype of the T-cell lines. The production of IFN-gamma was significantly higher in T-cell lines generated with ISG compared to those generated with TT. The cytokine production profiles of the T-cell lines generated with ICA69 did not provide an obvious explanation for the inverse relation between cellular and humoral responses to this protein observed earlier. Upon stimulation with beta-cell antigens, outgrowth of T cells using a restricted set of TCRBV elements was observed in newly diagnosed IDDM patients. However, this skewing in TCRBV-gene expression was patient-specific rather than antigen-associated, since the T-cell repertoire that is used for the recognition of these antigens was, overall, heterogeneous. (C) 1997 Academic Press Limited.
引用
收藏
页码:589 / 598
页数:10
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