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Characterization of Thymus-dependent and Thymus-independent Immunoglobulin Isotype Responses in Mice Using Enzyme-linked Immunosorbent Assay
Published on: September 7, 2018
Antigenicity and immunogenicity of the C-terminal peptide of human thyroglobulin
Rabii Ameziane El Hassani1, Valérie Estienne, Stéphanie Blanchin
1Unité 555 de l'Institut National de la Santé et de la Recherche Médicale, Faculté de Médecine Timone, 27 Boulevard Jean Moulin, Université de la Méditerranée, F-13385 Marseille Cedex 5, France.
Abstract:
Thyroglobulin (Tg) is cleaved into several peptides during thyroid hormone synthesis, an oxidative process. P40, an iodinated C-terminal peptide from human Tg, has a molecular weight of about 40 kDa and contains two hormonogenic sites. P40 is the smallest peptide that is still recognized by monoclonal antibodies from mice immunized with human Tg directed against its immunodominant region. Since P40 also contains several T-cell epitopes, it is a good candidate for studying the primary events involved in the process of hormone synthesis leading to thyroid autoimmunity. The present results show that P40 is recognized by Tg antibodies from patients with thyroid disorders and induces Tg antibodies in CBA mice. P40 may therefore be involved in the autoimmune process, thus providing a useful tool for diagnostic and therapeutic purposes.

