Molecular Mimicry is a concept in immunology and endocrinology describing a situation where a foreign antigen, typically a component of an invading pathogen like a virus or bacteria, shares structural similarities with a specific self-antigen found in the host’s body. This structural cross-reactivity can lead to the immune system mistakenly targeting and attacking the host’s own tissues, representing a critical pathway in the development of certain autoimmune diseases. It fundamentally signifies a breakdown in immunological self-tolerance.
Origin
The phenomenon was first described and formally named in the mid-20th century as researchers sought to understand the etiology of post-infectious autoimmune conditions, such as the development of rheumatic fever following a streptococcal infection. The term literally describes the foreign molecule “mimicking” the structure of a host molecule, effectively deceiving the immune system. This discovery provided a mechanistic, tangible link between environmental infectious triggers and the eventual onset of autoimmune pathology.
Mechanism
The mechanism involves the initial activation of T-cells or B-cells by the foreign, microbial antigen, which subsequently recognize the structurally similar self-antigen due to the molecular resemblance at the receptor binding site. For example, a bacterial protein might mimic a protein found on the thyroid gland or the adrenal cortex. This immune confusion initiates an autoimmune cascade, leading to chronic inflammation and functional destruction of the endocrine gland, resulting in conditions like Hashimoto’s thyroiditis or Addison’s disease.
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