A very recent paper which looks at the connections between autoimmune thyroid diseases. Surely many here have had questions over the years. Especially those who switched between the forms.
Autoimmune thyroid diseases as a cost of physiological autoimmune surveillance
Tomer Milo
Yael Korem Kohanim
Yoel Toledano
Uri Alon
Open Access Published: April 13, 2023
DOI: doi.org/10.1016/j.it.2023.0...
Highlights
Graves’ disease (GD) and Hashimoto’s thyroiditis (HT) are common human thyroid autoimmune diseases with opposite clinical manifestations.
GD and HT originate from T cells that are autoreactive to thyroid-stimulating hormone (TSH) receptor antigens and to thyroglobulin (Tg)/thyroid peroxidase (TPO) antigens, respectively.
The two diseases exhibit shared risk factors and incidence curves, and can interconvert.
The autoimmune surveillance theory provides a rationale for a putative shared etiology between the two diseases based on a physiological circuit of a mutant removal mechanism.
Autoreactive T cells are suggested to weed out hypersecreting mutants in the thyroid, with the cost of triggering a humoral response, leading to GD or HT in susceptible individuals.
Significance
The origin of the two autoimmune diseases of the thyroid (Graves’ disease and Hashimoto's thyroiditis) remains insufficiently understood. Despite their opposite clinical manifestations of hyper- and hypothyroidism, we propose a shared origin based on a physiological autoimmune surveillance mechanism against hypersecreting mutant cells, which may explain observed links between these diseases.
Abstract
Graves' disease (GD) and Hashimoto's thyroiditis (HT) are common autoimmune diseases of the thyroid gland, causing hyperthyroidism and hypothyroidism, respectively. Despite their opposing clinical manifestation, they have several enigmatic links. Here, we propose that GD and HT have the same fundamental origin: both diseases are the cost of a beneficial physiological process called autoimmune surveillance of hypersecreting mutants. Autoreactive T cells selectively eliminate mutant cells that hypersecrete the hormones and threaten to become toxic nodules. These T cells can trigger a humoral response in susceptible individuals, leading to the production of antibodies against thyroid antigens. This shared origin can explain similarities in incidence and risk factors between HT and GD, despite their opposite clinical phenotypes.
Keywords
physiological autoimmunity
Graves' disease
Hashimoto's thyroiditis
thyroid autoimmune diseases
autoimmune etiology
systems immunology
cell.com/trends/immunology/...
Note the thanks to Johannes Dietrich!