TY - JOUR
T1 - Autoantibodies to REG, a beta-cell regeneration factor, in diabetic patients
AU - Shervani, N. J.
AU - Takasawa, S.
AU - Uchigata, Y.
AU - Akiyama, T.
AU - Nakagawa, K.
AU - Noguchi, N.
AU - Takada, H.
AU - Takahashi, I.
AU - Yamauchi, A.
AU - Ikeda, T.
AU - Iwamoto, Y.
AU - Nata, K.
AU - Okamoto, Hiroshi
PY - 2004/11
Y1 - 2004/11
N2 - Background: Regenerating gene (Reg) product, Reg, acts as an autocrine/paracrine growth factor for beta-cell regeneration. The presence of autoimmunity against REG may affect the operative of the regenerative mechanisms in beta cells of Type 1 and Type 2 diabetes patients. We screened sera from Type 1 and Type 2 diabetes subjects for anti-REG autoantibodies, searched for correlations in the general characteristics of the subjects with the presence of anti-REG autoimmunity, and tested the attenuation of REG-induced beta-cell proliferation by the autoanitibodies. Material and methods: We examined the occurrence of anti-REG autoantibodies in patients' sera (265 Type 1, 368 Type 2 diabetes patients, and 75 unrelated control subjects) by Western blot analysis, and evaluated inhibitory effects of the sera on REG-stimulated beta-cell proliferation by a 5′-Bromo-2′-deoxyuridine (BrdU) incorporation assay in vitro. Results: Anti-REG autoantibodies were found in 24.9% of Type 1, 14-9% of Type 2 and 2.7% of control subjects (P = 0.0004). There were significant differences between the autoantibody positive and negative groups in the duration of disease in the Type 1 subjects (P = 0.0035), and the age of onset in the Type 2 subjects (P = 0.0274). The patient sera containing anti-REG autoantibodies significantly attenuated the BrdU incorporation by REG (35.6 ± 4.06% of the control), whereas the nondiabetic sera without anti-REG autoantibodies scarcely reduced the incorporation (88.8 ± 5.10%). Conclusion: Anti-REG autoantibodies, which retard beta-cell proliferation in vitro, are found in some diabetic patients. Thus, autoimmunity to REG may be associated with the development/acceleration of diabetes in at least some patients.
AB - Background: Regenerating gene (Reg) product, Reg, acts as an autocrine/paracrine growth factor for beta-cell regeneration. The presence of autoimmunity against REG may affect the operative of the regenerative mechanisms in beta cells of Type 1 and Type 2 diabetes patients. We screened sera from Type 1 and Type 2 diabetes subjects for anti-REG autoantibodies, searched for correlations in the general characteristics of the subjects with the presence of anti-REG autoimmunity, and tested the attenuation of REG-induced beta-cell proliferation by the autoanitibodies. Material and methods: We examined the occurrence of anti-REG autoantibodies in patients' sera (265 Type 1, 368 Type 2 diabetes patients, and 75 unrelated control subjects) by Western blot analysis, and evaluated inhibitory effects of the sera on REG-stimulated beta-cell proliferation by a 5′-Bromo-2′-deoxyuridine (BrdU) incorporation assay in vitro. Results: Anti-REG autoantibodies were found in 24.9% of Type 1, 14-9% of Type 2 and 2.7% of control subjects (P = 0.0004). There were significant differences between the autoantibody positive and negative groups in the duration of disease in the Type 1 subjects (P = 0.0035), and the age of onset in the Type 2 subjects (P = 0.0274). The patient sera containing anti-REG autoantibodies significantly attenuated the BrdU incorporation by REG (35.6 ± 4.06% of the control), whereas the nondiabetic sera without anti-REG autoantibodies scarcely reduced the incorporation (88.8 ± 5.10%). Conclusion: Anti-REG autoantibodies, which retard beta-cell proliferation in vitro, are found in some diabetic patients. Thus, autoimmunity to REG may be associated with the development/acceleration of diabetes in at least some patients.
KW - Anti-REG autoantibodies
KW - Beta-cell regeneration
KW - REG
KW - Type 1 diabetes mellitus
KW - Type 2 diabetes mellitus
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U2 - 10.1111/j.1365-2362.2004.01419.x
DO - 10.1111/j.1365-2362.2004.01419.x
M3 - Article
C2 - 15530148
AN - SCOPUS:8744228847
SN - 0014-2972
VL - 34
SP - 752
EP - 758
JO - Archiv fur klinische Medizin
JF - Archiv fur klinische Medizin
IS - 11
ER -