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Single-cell Analysis of Immunophenotype and Cytokine Production in Peripheral Whole Blood via Mass Cytometry
Published on: June 26, 2018
Gene Expression Profiles from Disease Discordant Twins Suggest Shared Antiviral Pathways and Viral Exposures among
Lu Gan1, Terrance P O'Hanlon1, Zhennan Lai2
1Environmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.
Abstract:
Viral agents are of interest as possible autoimmune triggers due to prior reported associations and widely studied molecular mechanisms of antiviral immune responses in autoimmunity. Here we examined new viral candidates for the initiation and/or promotion of systemic autoimmune diseases (SAID), as well as possible related signaling pathways shared in the pathogenesis of those disorders. RNA isolated from peripheral blood samples from 33 twins discordant for SAID and 33 matched, unrelated healthy controls was analyzed using a custom viral-human gene microarray. Paired comparisons were made among three study groups-probands with SAID, their unaffected twins, and matched, unrelated healthy controls-using statistical and molecular pathway analyses. Probands and unaffected twins differed significantly in the expression of 537 human genes, and 107 of those were associated with viral infections. These 537 differentially expressed human genes participate in overlapping networks of several canonical, biologic pathways relating to antiviral responses and inflammation. Moreover, certain viral genes were expressed at higher levels in probands compared to either unaffected twins or unrelated, healthy controls. Interestingly, viral gene expression levels in unaffected twins appeared intermediate between those of probands and the matched, unrelated healthy controls. Of the viruses with overexpressed viral genes, herpes simplex virus-2 (HSV-2) was the only human viral pathogen identified using four distinct oligonucleotide probes corresponding to three HSV-2 genes associated with different stages of viral infection. Although the effects from immunosuppressive therapy on viral gene expression remain unclear, this exploratory study suggests a new approach to evaluate shared viral agents and antiviral immune responses that may be involved in the development of SAID.
Insights
This study explored viral triggers for systemic autoimmune diseases (SAID). Herpes simplex virus-2 (HSV-2) showed higher expression in patients, suggesting a potential role in SAID development and antiviral immune responses.
Area of Science:
- Immunology
- Virology
- Genetics
Background:
- Viral infections are implicated in autoimmune diseases.
- Understanding viral triggers and immune responses in systemic autoimmune diseases (SAID) is crucial.
Purpose of the Study:
- To identify novel viral candidates and shared signaling pathways in SAID pathogenesis.
- To investigate the role of viral gene expression in SAID development.
Main Methods:
- Analyzed RNA from peripheral blood of 33 SAID-discordant twins and 33 healthy controls using a custom viral-human gene microarray.
- Performed statistical and molecular pathway analyses comparing probands, unaffected twins, and controls.
- Identified differentially expressed human and viral genes, focusing on herpes simplex virus-2 (HSV-2).
Main Results:
- Significant differences in 537 human genes between probands and unaffected twins, with 107 linked to viral infections.
- Overexpressed viral genes found in probands, with intermediate levels in unaffected twins.
- Herpes simplex virus-2 (HSV-2) was identified as a potential viral agent involved in SAID.
Conclusions:
- Suggests a novel approach to evaluate viral agents and antiviral immune responses in SAID.
- Highlights the potential role of HSV-2 in the initiation or promotion of systemic autoimmune diseases.
- Further research is needed to clarify the impact of immunosuppressive therapy on viral gene expression in SAID.
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