Report from the 1st International NOD Mouse T-Cell Workshop and the follow-up mini-workshop

被引:27
作者
Kaufman, DL
Tisch, R
Sarvetnick, N
Chatenoud, L
Harrison, LC
Haskins, K
Quinn, A
Sercarz, E
Singh, B
von Herrath, M
Wegmann, D
Wen, L
Zekzer, D
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
[2] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC USA
[3] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[4] Hop Necker Enfants Malad, INSERM, Paris, France
[5] PO Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Melbourne, Vic, Australia
[6] Univ Colorado, Hlth Sci Ctr, Dept Immunol, Denver, CO USA
[7] La Jolla Inst Allergy & Immunol, San Diego, CA USA
[8] Univ Western Ontario, Dept Microbiol, London, ON, Canada
[9] Scripps Res Inst, Dept Virol, La Jolla, CA 92037 USA
[10] Univ Colorado, Hlth Sci Ctr, Barbara Davis Ctr Childhood Diabet, Denver, CO 80262 USA
[11] Yale Univ, Dept Internal Med, New Haven, CT 06510 USA
[12] Sankyo, La Jolla, CA USA
关键词
D O I
10.2337/diabetes.50.11.2459
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A workshop on autoreactive T-cell responses in NOD mice was held to optimize autoreactive T-cell detection methodologies. Using different proliferation assay protocols, 1 of the 11 participating laboratories detected spontaneous T-cell responses to GAD(524-543) and insulin(9-23) in their NOD mice. Two other laboratories were able to detect autoreactive responses when using enzyme-linked immunospot assay (ELISPOT) and enzyme-linked immunosorbent assay (ELISA) analysis of cytokines in culture supernatants, suggesting that these assays provided greater sensitivity. To address the divergent findings, a follow-up mini-workshop tested NOD mice from four different colonies side-by-side for T-cell proliferative responses to an expanded panel of autoantigens, using the protocol that had enabled detection of responses in the 1st International NOD Mouse T-Cell Workshop. Under these assay conditions, 16 of 16 NOD mice displayed proliferative responses to whole GAD65, 13 of 16 to GAD(524-543), 9 of 16 to GAD(217-236), 7 of 16 to insulin(9-23), and 5 of 16 to HSP277. Thus, spontaneous proliferative T-cell responses can be consistently detected to some P-cell autoantigens and peptides thereof. Overall, the results suggest that more sensitive assays (e.g., ELISPOT, ELISA analysis of cytokines in supernatants, or tetramer staining) may be preferred for the detection of autoreactive T-cells.
引用
收藏
页码:2459 / 2463
页数:5
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