| Literature DB >> 12604315 |
Ryuji Suzuki1, Akira Shimada, Taro Maruyama, Osamu Funae, Jiro Morimoto, Keiichi Kodama, Yoichi Oikawa, Akira Kasuga, Koichi Matsubara, Takao Saruta, Shosaku Narumi.
Abstract
We have recently reported that in patients with anti-glutamic acid decarboxylase (GAD) 65(+)diabetes with residual beta-cell function, most with a 'high-titer' (>10U/ml) required insulin within 5 years, whereas most with a 'low-titer' (1.3-9.9U/ml) did not need insulin for over 15-20 years after the onset. We therefore examined T-cell function to evaluate the difference between the high-titer and low-titer groups. Interleukin (IL)-10 production upon polyclonal activation was significantly lower in the high-titer group than in the low-titer group. The serum level of interferon-inducible protein-10 (IP-10) was higher in the high-titer than the low-titer group. Although GAD65-reactive CD4(+)cells in the periphery were detected in both groups, a significant positive correlation between serum IP-10 level and the number of GAD65-reactive CD4(+)cells was observed only in the high-titer group. Therefore, it has been speculated that the co-existence of GAD65-reactive IFN-gamma-producing CD4(+)cells and a high serum IP-10 level may be important for rapid disease progression as seen in the high-titer group. Based upon these results, T-cell function is considered to be different between the high-titer and low-titer groups in anti-GAD65(+)diabetes with residual beta-cell function, supporting our previous findings regarding the clinical outcome of insulin-dependence in the two groups.Entities:
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Year: 2003 PMID: 12604315 DOI: 10.1016/s0896-8411(02)00093-8
Source DB: PubMed Journal: J Autoimmun ISSN: 0896-8411 Impact factor: 7.094