Literature DB >> 10724086

BCG vaccine prevents insulitis in low dose streptozotocin-induced diabetic mice.

S H Baik1, I B Park, K M Choi, Y H Kim, N H Kim, S J Kim, G G Song, D S Choi.   

Abstract

Autoimmune type 1 diabetes mellitus is caused by the immunologic destruction of pancreatic beta-cells; therefore, there have been many attempts at immunologic modulation as a block or prevention of the underlying process. The aim of this study is to investigate the effect of BCG vaccination on low dose streptozotocin-induced diabetic (LDSD) mice. The mice were pretreated with BCG 7 days before starting low dose streptozotocin (STZ), observed body weight and blood glucose for 2 months, then analyzed the severity of the STZ-induced insulitis after the animals were sacrificed. In this experiment, the mean body weights in the BCG-STZ group on days 1, 19, 33, 47, and 61 of the experiment were 37.5 +/- 3.6, 37.3 +/- 3.6, 37.5 +/- 3.5, 39.4 +/- 3.9, and 39.3 +/- 4.5 (g), respectively. Those in the STZ group were 37.7 +/- 3.5, 38.3 +/- 4.5, 38.4 +/- 3.9, 36.2 +/- 4.5, and 36.3 +/- 4.0 (g), respectively (P < 0.05). The mean blood glucose levels in the BCG-STZ group on days 1, 19, 33, 47, and 61 were 106.5 +/- 8, 150 +/- 37, 147 +/- 54, 143 +/- 60, and 142 +/- 66 (mg/dl), respectively. Those in the STZ group were 103 +/- 12, 196 +/- 90, 261 +/- 236, 236 +/- 91, and 224 +/- 89 (mg/dl), respectively (P < 0.05). The numbers developing grade 0, I, II, III, and IV insulitis in the BCG-treated group were 63, 48, 33, 4, and 2, respectively, and in the control group were 16, 23, 31, 45, and 35, respectively. This study indicates that BCG vaccination reduces the development of insulitis and overt diabetes in LDSD mice.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10724086     DOI: 10.1016/s0168-8227(99)00079-0

Source DB:  PubMed          Journal:  Diabetes Res Clin Pract        ISSN: 0168-8227            Impact factor:   5.602


  5 in total

1.  Caspase-3-dependent beta-cell apoptosis in the initiation of autoimmune diabetes mellitus.

Authors:  Nicole Liadis; Kiichi Murakami; Mohamed Eweida; Alisha R Elford; Laura Sheu; Herbert Y Gaisano; Razqallah Hakem; Pamela S Ohashi; Minna Woo
Journal:  Mol Cell Biol       Date:  2005-05       Impact factor: 4.272

2.  Altered monocyte cyclo-oxygenase response in non-obese diabetic mice.

Authors:  H Beyan; L R Buckley; S A Bustin; N Yousaf; P Pozzilli; R D Leslie
Journal:  Clin Exp Immunol       Date:  2008-11-24       Impact factor: 4.330

3.  Bacille Calmette-Guérin/DNAhsp65 prime-boost is protective against diabetes in non-obese diabetic mice but not in the streptozotocin model of type 1 diabetes.

Authors:  L C da Rosa; F Chiuso-Minicucci; S F G Zorzella-Pezavento; T G D França; L L W Ishikawa; P M Colavite; B Balbino; L C B Tavares; C L Silva; C Marques; M R V Ikoma; A Sartori
Journal:  Clin Exp Immunol       Date:  2013-09       Impact factor: 4.330

4.  Reactivation of latent tuberculosis through modulation of resuscitation promoting factors by diabetes.

Authors:  Arpana Verma; Maninder Kaur; Lakshya Veer Singh; Divya Aggarwal; Indu Verma; Bishan D Radotra; Sadhna Sharma
Journal:  Sci Rep       Date:  2021-10-05       Impact factor: 4.379

5.  BCG and BCG/DNAhsp65 vaccinations promote protective effects without deleterious consequences for experimental autoimmune encephalomyelitis.

Authors:  Sofia Fernanda Gonçalves Zorzella-Pezavento; Clara Pires Fujiara Guerino; Fernanda Chiuso-Minicucci; Thais Graziela Donegá França; Larissa Lumi Watanabe Ishikawa; Ana Paula Masson; Célio Lopes Silva; Alexandrina Sartori
Journal:  Clin Dev Immunol       Date:  2013-10-29
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.