Are human endogenous retroviruses triggers of autoimmune diseases? Unveiling associations of three diseases and viral loci

Research output: Contribution to journalJournal articleResearchpeer-review

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Are human endogenous retroviruses triggers of autoimmune diseases? Unveiling associations of three diseases and viral loci. / Nexø, Bjørn A; Villesen, Palle; Nissen, Kari K; Lindegaard, Hanne M; Rossing, Peter; Petersen, Thor; Tarnow, Lise; Hansen, Bettina; Lorenzen, Tove; Hørslev-Petersen, Kim; Jensen, Sara B; Bahrami, Shervin; Lajer, Maria; Schmidt, Kathrine L M; Parving, Hans-Henrik; Junker, Peter; Laska, Magdalena J.

In: Immunologic Research, Vol. 64, No. 1, 02.2016, p. 55-63.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Nexø, BA, Villesen, P, Nissen, KK, Lindegaard, HM, Rossing, P, Petersen, T, Tarnow, L, Hansen, B, Lorenzen, T, Hørslev-Petersen, K, Jensen, SB, Bahrami, S, Lajer, M, Schmidt, KLM, Parving, H-H, Junker, P & Laska, MJ 2016, 'Are human endogenous retroviruses triggers of autoimmune diseases? Unveiling associations of three diseases and viral loci', Immunologic Research, vol. 64, no. 1, pp. 55-63. https://doi.org/10.1007/s12026-015-8671-z

APA

Nexø, B. A., Villesen, P., Nissen, K. K., Lindegaard, H. M., Rossing, P., Petersen, T., Tarnow, L., Hansen, B., Lorenzen, T., Hørslev-Petersen, K., Jensen, S. B., Bahrami, S., Lajer, M., Schmidt, K. L. M., Parving, H-H., Junker, P., & Laska, M. J. (2016). Are human endogenous retroviruses triggers of autoimmune diseases? Unveiling associations of three diseases and viral loci. Immunologic Research, 64(1), 55-63. https://doi.org/10.1007/s12026-015-8671-z

Vancouver

Nexø BA, Villesen P, Nissen KK, Lindegaard HM, Rossing P, Petersen T et al. Are human endogenous retroviruses triggers of autoimmune diseases? Unveiling associations of three diseases and viral loci. Immunologic Research. 2016 Feb;64(1):55-63. https://doi.org/10.1007/s12026-015-8671-z

Author

Nexø, Bjørn A ; Villesen, Palle ; Nissen, Kari K ; Lindegaard, Hanne M ; Rossing, Peter ; Petersen, Thor ; Tarnow, Lise ; Hansen, Bettina ; Lorenzen, Tove ; Hørslev-Petersen, Kim ; Jensen, Sara B ; Bahrami, Shervin ; Lajer, Maria ; Schmidt, Kathrine L M ; Parving, Hans-Henrik ; Junker, Peter ; Laska, Magdalena J. / Are human endogenous retroviruses triggers of autoimmune diseases? Unveiling associations of three diseases and viral loci. In: Immunologic Research. 2016 ; Vol. 64, No. 1. pp. 55-63.

Bibtex

@article{1b421ddf16b544fc81708aa894fc1a58,
title = "Are human endogenous retroviruses triggers of autoimmune diseases? Unveiling associations of three diseases and viral loci",
abstract = "Autoimmune diseases encompass a plethora of conditions in which the immune system attacks its own tissue, identifying them as foreign. Multiple factors are thought to contribute to the development of immune response to self, including differences in genotypes, hormonal milieu, and environmental factors. Viruses including human endogenous retroviruses have long been linked to the occurrence of autoimmunity, but never proven to be causative factors. Endogenous viruses are retroviral sequences embedded in the host germline DNA and transmitted vertically through successive generations in a Mendelian manner. In this study by means of genetic epidemiology, we have searched for the involvement of endogenous retroviruses in three selected autoimmune diseases: multiple sclerosis, type 1 diabetes mellitus, and rheumatoid arthritis. We found that at least one human endogenous retroviral locus was associated with each of the three diseases. Although there was a significant overlap, most loci only occurred in one of the studied disease. Remarkably, within each disease, there was a statistical interaction (synergy) between two loci. Additional synergy between retroviral loci and human lymphocyte antigens is reported for multiple sclerosis. We speculate the possibility that recombinants or mixed viral particles are formed and that the resulting viruses stimulate the innate immune system, thereby initiating the autoimmune response.",
keywords = "Journal Article, Research Support, Non-U.S. Gov't",
author = "Nex{\o}, {Bj{\o}rn A} and Palle Villesen and Nissen, {Kari K} and Lindegaard, {Hanne M} and Peter Rossing and Thor Petersen and Lise Tarnow and Bettina Hansen and Tove Lorenzen and Kim H{\o}rslev-Petersen and Jensen, {Sara B} and Shervin Bahrami and Maria Lajer and Schmidt, {Kathrine L M} and Hans-Henrik Parving and Peter Junker and Laska, {Magdalena J}",
year = "2016",
month = feb,
doi = "10.1007/s12026-015-8671-z",
language = "English",
volume = "64",
pages = "55--63",
journal = "Immunologic Research",
issn = "0257-277X",
publisher = "Humana Press",
number = "1",

}

RIS

TY - JOUR

T1 - Are human endogenous retroviruses triggers of autoimmune diseases? Unveiling associations of three diseases and viral loci

AU - Nexø, Bjørn A

AU - Villesen, Palle

AU - Nissen, Kari K

AU - Lindegaard, Hanne M

AU - Rossing, Peter

AU - Petersen, Thor

AU - Tarnow, Lise

AU - Hansen, Bettina

AU - Lorenzen, Tove

AU - Hørslev-Petersen, Kim

AU - Jensen, Sara B

AU - Bahrami, Shervin

AU - Lajer, Maria

AU - Schmidt, Kathrine L M

AU - Parving, Hans-Henrik

AU - Junker, Peter

AU - Laska, Magdalena J

PY - 2016/2

Y1 - 2016/2

N2 - Autoimmune diseases encompass a plethora of conditions in which the immune system attacks its own tissue, identifying them as foreign. Multiple factors are thought to contribute to the development of immune response to self, including differences in genotypes, hormonal milieu, and environmental factors. Viruses including human endogenous retroviruses have long been linked to the occurrence of autoimmunity, but never proven to be causative factors. Endogenous viruses are retroviral sequences embedded in the host germline DNA and transmitted vertically through successive generations in a Mendelian manner. In this study by means of genetic epidemiology, we have searched for the involvement of endogenous retroviruses in three selected autoimmune diseases: multiple sclerosis, type 1 diabetes mellitus, and rheumatoid arthritis. We found that at least one human endogenous retroviral locus was associated with each of the three diseases. Although there was a significant overlap, most loci only occurred in one of the studied disease. Remarkably, within each disease, there was a statistical interaction (synergy) between two loci. Additional synergy between retroviral loci and human lymphocyte antigens is reported for multiple sclerosis. We speculate the possibility that recombinants or mixed viral particles are formed and that the resulting viruses stimulate the innate immune system, thereby initiating the autoimmune response.

AB - Autoimmune diseases encompass a plethora of conditions in which the immune system attacks its own tissue, identifying them as foreign. Multiple factors are thought to contribute to the development of immune response to self, including differences in genotypes, hormonal milieu, and environmental factors. Viruses including human endogenous retroviruses have long been linked to the occurrence of autoimmunity, but never proven to be causative factors. Endogenous viruses are retroviral sequences embedded in the host germline DNA and transmitted vertically through successive generations in a Mendelian manner. In this study by means of genetic epidemiology, we have searched for the involvement of endogenous retroviruses in three selected autoimmune diseases: multiple sclerosis, type 1 diabetes mellitus, and rheumatoid arthritis. We found that at least one human endogenous retroviral locus was associated with each of the three diseases. Although there was a significant overlap, most loci only occurred in one of the studied disease. Remarkably, within each disease, there was a statistical interaction (synergy) between two loci. Additional synergy between retroviral loci and human lymphocyte antigens is reported for multiple sclerosis. We speculate the possibility that recombinants or mixed viral particles are formed and that the resulting viruses stimulate the innate immune system, thereby initiating the autoimmune response.

KW - Journal Article

KW - Research Support, Non-U.S. Gov't

U2 - 10.1007/s12026-015-8671-z

DO - 10.1007/s12026-015-8671-z

M3 - Journal article

C2 - 26091722

VL - 64

SP - 55

EP - 63

JO - Immunologic Research

JF - Immunologic Research

SN - 0257-277X

IS - 1

ER -

ID: 165939869