Intradermal administration of GAD & evaluation of diabetes incidence in mice: Possible relevance for skin tests in humans

Citation
Pe. Beales et al., Intradermal administration of GAD & evaluation of diabetes incidence in mice: Possible relevance for skin tests in humans, AUTOIMMUN, 32(2), 2000, pp. 109-113
Citations number
17
Categorie Soggetti
Immunology
Journal title
AUTOIMMUNITY
ISSN journal
08916934 → ACNP
Volume
32
Issue
2
Year of publication
2000
Pages
109 - 113
Database
ISI
SICI code
0891-6934(2000)32:2<109:IAOG&E>2.0.ZU;2-O
Abstract
In vitro cell mediated reactivity to Glutamic Acid Decarboxylase (GAD) has been reported in man and in the non-obese diabetic (NOD) mouse. The demonst ration of such reactivity in vivo using GAD in a simple intradermal skin te st would be useful for mass screening of subjects at risk of Type 1 diabete s. Such a skin test could be simply applied to the forearm, then signs of l ocal reaction would indicate patients at risk. However, in order to safely apply a skin test of this type it must be certain that administration of th e antigen does not itself provoke or start the process leading to diabetes in susceptible individuals. In the present study the NOD mouse model was used. GAD and two peptides of GAD, which may have relevance to the disease process, were applied intrader mally to these mice to determine whether a local reaction could be seen and to see if the diabetes rate was altered. Moreover, Balb/c mice, which can be considered to be at zero risk of developing the disease, were also injec ted with the same GAD and GAD peptides, No significant differences were seen in the diabetes incidence of the treat ment groups compared to the control groups in either the NOD or Balb/c mice although a local swelling was seen in female NOD mice susceptible to diabe tes after GAD administration in the footpad. We conclude that the administration of GAD and/or GAD peptides does not pro voke or accelerate diabetes incidence in the NOD mouse and that an intrader mal skin-test with GAD may be suitable for preliminary trials aimed at larg e scale screening of humans for their potential to develop type 1 diabetes.