HERVs, immunity, and autoimmunity: understanding the connection

• Published in: PeerJ (San Francisco, CA) Vol. 7; p. e6711
• Main Author: Greenig, Matthew
• Format: Journal Article
• Language: English
• Published: United States PeerJ. Ltd 05.04.2019; PeerJ, Inc; PeerJ Inc
• Subjects: Allergy and Clinical Immunology; Autoimmune disease; Autoimmune diseases; Autoimmunity; Cell division; Deoxyribonucleic acid; DNA; Endogenous retrovirus; Genes; Genetic research; Genomes; HERV; Immune system; Immunology; Leukemia; Lupus; Medical research; Molecular Biology; Molecular modelling; Multiple sclerosis; Mutation; Novels; Proteins; Retroviruses; Systemic lupus erythematosus; Vertebrates; Virology; Viruses; United States > US; HERV; Multiple sclerosis; Endogenous retrovirus; Systemic lupus erythematosus; Endogenous viral element; Autoimmune disease; Paleovirology; Immune system
• ISSN: 2167-8359; 2167-8359
• DOI: 10.7717/peerj.6711

Since their discovery in the 1960s, further investigation into endogenous retroviruses (ERVs) has challenged the conventional view of viral sequences as exclusively parasitic elements. Once presumed to be a group of passive genetic relics, it is becoming increasingly clear that this view of ERVs, while generally accurate, is incorrect in many specific cases. Research has identified ERV genes that appear to be co-opted by their mammalian hosts, but the biological function of ERV elements in humans remains a controversial subject. One area that has attracted some attention in this domain is the role of co-opted ERV elements in mammalian immune systems. The relationship between ERVs and human autoimmune diseases has also been investigated, but has historically been treated as a separate topic. This review will summarize the current evidence concerning the phenotypic significance of ERVs, both in the healthy immune system and in manifestations of autoimmunity. Furthermore, it will evaluate the relationship between these fields of study, and propose previously-unexplored molecular mechanisms through which human endogenous retroviruses might contribute to certain autoimmune pathologies. Investigation into these novel mechanisms could further our understanding of the molecular basis of autoimmune disease, and may one day provide new targets for treatment.