Cargando…

Natural Autoimmunity to the Thyroid Hormone Monocarboxylate Transporters MCT8 and MCT10

The monocarboxylate transporters 8 (MCT8) and 10 (MCT10) are important for thyroid hormone (TH) uptake and signaling. Reduced TH activity is associated with impaired development, weight gain and discomfort. We hypothesized that autoantibodies (aAb) to MCT8 or MCT10 are prevalent in thyroid disease a...

Descripción completa

Detalles Bibliográficos
Autores principales: Porst, Theresa, Johannes, Jörg, Gluschke, Hans, Köhler, Richard, Mehl, Sebastian, Kühnen, Peter, Renko, Kostja, Minich, Waldemar B., Wiegand, Susanna, Schomburg, Lutz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147215/
https://www.ncbi.nlm.nih.gov/pubmed/33946552
http://dx.doi.org/10.3390/biomedicines9050496
_version_ 1783697578498457600
author Porst, Theresa
Johannes, Jörg
Gluschke, Hans
Köhler, Richard
Mehl, Sebastian
Kühnen, Peter
Renko, Kostja
Minich, Waldemar B.
Wiegand, Susanna
Schomburg, Lutz
author_facet Porst, Theresa
Johannes, Jörg
Gluschke, Hans
Köhler, Richard
Mehl, Sebastian
Kühnen, Peter
Renko, Kostja
Minich, Waldemar B.
Wiegand, Susanna
Schomburg, Lutz
author_sort Porst, Theresa
collection PubMed
description The monocarboxylate transporters 8 (MCT8) and 10 (MCT10) are important for thyroid hormone (TH) uptake and signaling. Reduced TH activity is associated with impaired development, weight gain and discomfort. We hypothesized that autoantibodies (aAb) to MCT8 or MCT10 are prevalent in thyroid disease and obesity. Analytical tests for MCT8-aAb and MCT10-aAb were developed and characterized with commercial antiserum. Serum samples from healthy controls, thyroid patients and young overweight subjects were analyzed, and prevalence of the aAb was compared. MCT8-aAb were additionally tested for biological effects on thyroid hormone uptake in cell culture. Positive MCT8-aAb and MCT10-aAb were detected in all three clinical cohorts analyzed. MCT8-aAb were most prevalent in thyroid patients (11.9%) as compared to healthy controls (3.8%) and overweight adolescents (4.2%). MCT8-aAb positive serum reduced T4 uptake in cell culture in comparison to MCT8-aAb negative control serum. Prevalence of MCT10-aAb was highest in the group of thyroid patients as compared to healthy subjects or overweight adolescents (9.0% versus 4.5% and 6.3%, respectively). We conclude that MCT8 and MCT10 represent autoantigens in humans, and that MCT8-aAb may interfere with regular TH uptake and signaling. The increased prevalence of MCT8-aAb and MCT10-aAb in thyroid disease suggests that their presence may be of pathophysiological relevance. This hypothesis deserves an analysis in large prospective studies.
format Online
Article
Text
id pubmed-8147215
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-81472152021-05-26 Natural Autoimmunity to the Thyroid Hormone Monocarboxylate Transporters MCT8 and MCT10 Porst, Theresa Johannes, Jörg Gluschke, Hans Köhler, Richard Mehl, Sebastian Kühnen, Peter Renko, Kostja Minich, Waldemar B. Wiegand, Susanna Schomburg, Lutz Biomedicines Article The monocarboxylate transporters 8 (MCT8) and 10 (MCT10) are important for thyroid hormone (TH) uptake and signaling. Reduced TH activity is associated with impaired development, weight gain and discomfort. We hypothesized that autoantibodies (aAb) to MCT8 or MCT10 are prevalent in thyroid disease and obesity. Analytical tests for MCT8-aAb and MCT10-aAb were developed and characterized with commercial antiserum. Serum samples from healthy controls, thyroid patients and young overweight subjects were analyzed, and prevalence of the aAb was compared. MCT8-aAb were additionally tested for biological effects on thyroid hormone uptake in cell culture. Positive MCT8-aAb and MCT10-aAb were detected in all three clinical cohorts analyzed. MCT8-aAb were most prevalent in thyroid patients (11.9%) as compared to healthy controls (3.8%) and overweight adolescents (4.2%). MCT8-aAb positive serum reduced T4 uptake in cell culture in comparison to MCT8-aAb negative control serum. Prevalence of MCT10-aAb was highest in the group of thyroid patients as compared to healthy subjects or overweight adolescents (9.0% versus 4.5% and 6.3%, respectively). We conclude that MCT8 and MCT10 represent autoantigens in humans, and that MCT8-aAb may interfere with regular TH uptake and signaling. The increased prevalence of MCT8-aAb and MCT10-aAb in thyroid disease suggests that their presence may be of pathophysiological relevance. This hypothesis deserves an analysis in large prospective studies. MDPI 2021-04-30 /pmc/articles/PMC8147215/ /pubmed/33946552 http://dx.doi.org/10.3390/biomedicines9050496 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Porst, Theresa
Johannes, Jörg
Gluschke, Hans
Köhler, Richard
Mehl, Sebastian
Kühnen, Peter
Renko, Kostja
Minich, Waldemar B.
Wiegand, Susanna
Schomburg, Lutz
Natural Autoimmunity to the Thyroid Hormone Monocarboxylate Transporters MCT8 and MCT10
title Natural Autoimmunity to the Thyroid Hormone Monocarboxylate Transporters MCT8 and MCT10
title_full Natural Autoimmunity to the Thyroid Hormone Monocarboxylate Transporters MCT8 and MCT10
title_fullStr Natural Autoimmunity to the Thyroid Hormone Monocarboxylate Transporters MCT8 and MCT10
title_full_unstemmed Natural Autoimmunity to the Thyroid Hormone Monocarboxylate Transporters MCT8 and MCT10
title_short Natural Autoimmunity to the Thyroid Hormone Monocarboxylate Transporters MCT8 and MCT10
title_sort natural autoimmunity to the thyroid hormone monocarboxylate transporters mct8 and mct10
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147215/
https://www.ncbi.nlm.nih.gov/pubmed/33946552
http://dx.doi.org/10.3390/biomedicines9050496
work_keys_str_mv AT porsttheresa naturalautoimmunitytothethyroidhormonemonocarboxylatetransportersmct8andmct10
AT johannesjorg naturalautoimmunitytothethyroidhormonemonocarboxylatetransportersmct8andmct10
AT gluschkehans naturalautoimmunitytothethyroidhormonemonocarboxylatetransportersmct8andmct10
AT kohlerrichard naturalautoimmunitytothethyroidhormonemonocarboxylatetransportersmct8andmct10
AT mehlsebastian naturalautoimmunitytothethyroidhormonemonocarboxylatetransportersmct8andmct10
AT kuhnenpeter naturalautoimmunitytothethyroidhormonemonocarboxylatetransportersmct8andmct10
AT renkokostja naturalautoimmunitytothethyroidhormonemonocarboxylatetransportersmct8andmct10
AT minichwaldemarb naturalautoimmunitytothethyroidhormonemonocarboxylatetransportersmct8andmct10
AT wiegandsusanna naturalautoimmunitytothethyroidhormonemonocarboxylatetransportersmct8andmct10
AT schomburglutz naturalautoimmunitytothethyroidhormonemonocarboxylatetransportersmct8andmct10