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Determining Immune System Suppression versus CNS Protection for Pharmacological Interventions in Autoimmune Demyelination
Published on: September 12, 2016
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HERVs, immunity, and autoimmunity: understanding the connection.
1Department of Life Sciences, Imperial College London, London, United Kingdom.
Peerj
|April 16, 2019
Summary
Human endogenous retroviruses (ERVs) are not just parasitic relics; some are co-opted by hosts. This review explores ERVs' roles in immunity and autoimmune diseases, proposing novel mechanisms for their contribution to pathology.
Area of Science:
- Immunology
- Genetics
- Molecular Biology
Background:
- Endogenous retroviruses (ERVs) were once considered solely parasitic genetic elements.
- Emerging evidence suggests some ERV genes are co-opted by mammalian hosts, challenging this view.
- The biological functions of ERVs in humans, particularly in immunity and autoimmunity, are still debated.
Purpose of the Study:
- To review the phenotypic significance of ERVs in healthy immune systems and autoimmune diseases.
- To evaluate the interconnectedness of ERV function in immunity and autoimmunity.
- To propose novel molecular mechanisms linking human endogenous retroviruses to autoimmune pathologies.
Main Methods:
- Literature review of current evidence on ERV functions.
- Analysis of the relationship between ERVs, immunity, and autoimmunity.
- Hypothesizing molecular mechanisms of ERV involvement in autoimmune disease.
Main Results:
- ERV elements have roles beyond parasitic functions, including potential co-option by host systems.
- A link exists between ERVs and both normal immune function and autoimmune conditions.
- Specific molecular pathways through which ERVs may influence autoimmunity are proposed.
Conclusions:
- Human endogenous retroviruses have complex roles in host biology, impacting immunity and autoimmunity.
- Understanding ERV involvement in autoimmune diseases may reveal new therapeutic targets.
- Further research into ERV-mediated molecular mechanisms is crucial for advancing autoimmune disease treatment.
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