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May 14, 2026
September 8, 2026
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Three DxTerity Abstracts Accepted for Presentation at ACR Convergence 2026
Clinical data supporting anifrolumab
Anifrolumab obtained FDA approval through results from TULIP-1 and TULIP-2 phase 3 clinical trials, demonstrating broad efficacy with improvements across multiple organ systems.
Studies examine the Type I interferon gene signature and a low-density granulocyte neutrophil signature as tools for identifying lupus patients with severe disease, inadequate response to standard of care, and signs of resistance to anifrolumab therapy
DxTerity today announced that three abstracts featuring the company’s RNA-based immune monitoring technology have been accepted for presentation at ACR Convergence 2026, the annual meeting of the American College of Rheumatology, taking place November 6–11, 2026 at the Orange County Convention Center in Orlando, Florida.
The three abstracts apply RNA gene signature measurement to systemic lupus erythematosus (SLE), a disease in which clinical presentation and treatment response vary widely between patients. Together they examine whether molecular signatures of immune activity can help identify which patients are likely to have severe disease, which are responding inadequately to standard of care, and which show signs of resistance to targeted interferon-blocking therapy.
Demonstrated in a cohort of 943 samples from 395 SLE patients that IFN-1 High patients were more 3 times more likely to have Immunologic (Positive for dsDNA and Low Complement) symptoms, and 2 times more likely to have renal symptoms and active lupus nephritis than IFN-1 low patients (p<0.0001).
Demonstrated in a cohort of 395 SLE patients, at time of initial enrollment in the study, patients that were LDG-Neutrophil high were 4 times more likely to have active lupus nephritis and 28 times less likely to be in the Prevalent cohort with well managed disease (p<0.0001).
Uses serial Type I Interferon gene signature measurements (IFN-1 testing) in a cohort of 17 patients being treated with the interferon receptor blocking drug anifrolumab, 2 patients showed loss of drug efficacy based on increasing IFN-1 score and return to IFN-1 high, while 1 patient is showing initialsigns of therapy resistance due to increasing IFN-1 score. Both IFN-1 high patients experienced disease flares.
Presentation Details
Meeting: ACR Convergence 2026, American College of Rheumatology
Venue: Orange County Convention Center, Orlando, Florida
Session: Poster Session C
Date: Tuesday, November 10, 2026
Time: 10:30 a.m. – 12:30 p.m. ET
said Bob Terbrueggen, CEO of DxTerity.
Full abstract text will be available through the ACR Convergence online program. DxTerity representatives will be available at the meeting to discuss the data and the company’s immune monitoring programs.
DxTerity’s patient-focused mission is to bring the power of at-home RNA-based genomic monitoring to improve the management of immune-mediated diseases and overall patient well-being. DxTerity’s Type 1 Interferon (IFN-1) and Modular Immune Profile tests are run in the company’s CAP-accredited, CLIA-certified laboratory in Torrance, California. DxTerity also holds ISO 13485 certification for its product
development services.
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DxTerity Receives New York Authorization for Type 1 Interferon (IFN-1) for Systemic Lupus Erythematosus
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May 14, 2026
Precision Medicine using Modular Genomics
A simple look at how RNA-based testing can help uncover patterns in immune system activity and support more informed care decisions.
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DxTerity Receives CE Mark for DxCollect® Fingerstick Blood RNA Stabilization Device
Learn how patient-friendly testing can reduce barriers, improve convenience, and help people stay more connected to their health journey.
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DxTerity’s patient-focused mission is to bring the power of at-home RNA-based genomic monitoring to improve the management of immune-mediated diseases and overall patient well-being.
← Back
Company
•
September 8, 2026
Three DxTerity Abstracts Accepted for Presentation at ACR Convergence 2026
Studies examine the Type I interferon gene signature and a low-density granulocyte neutrophil signature as tools for identifying lupus patients with severe disease, inadequate response to standard of care, and signs of resistance to anifrolumab therapy
DxTerity today announced that three abstracts featuring the company’s RNA-based immune monitoring technology have been accepted for presentation at ACR Convergence 2026, the annual meeting of the American College of Rheumatology, taking place November 6–11, 2026 at the Orange County Convention Center in Orlando, Florida.
The three abstracts apply RNA gene signature measurement to systemic lupus erythematosus (SLE), a disease in which clinical presentation and treatment response vary widely between patients. Together they examine whether molecular signatures of immune activity can help identify which patients are likely to have severe disease, which are responding inadequately to standard of care, and which show signs of resistance to targeted interferon-blocking therapy.
Demonstrated in a cohort of 943 samples from 395 SLE patients that IFN-1 High patients were more 3 times more likely to have Immunologic (Positive for dsDNA and Low Complement) symptoms, and 2 times more likely to have renal symptoms and active lupus nephritis than IFN-1 low patients (p<0.0001).
Demonstrated in a cohort of 395 SLE patients, at time of initial enrollment in the study, patients that were LDG-Neutrophil high were 4 times more likely to have active lupus nephritis and 28 times less likely to be in the Prevalent cohort with well managed disease (p<0.0001).
Uses serial Type I Interferon gene signature measurements (IFN-1 testing) in a cohort of 17 patients being treated with the interferon receptor blocking drug anifrolumab, 2 patients showed loss of drug efficacy based on increasing IFN-1 score and return to IFN-1 high, while 1 patient is showing initialsigns of therapy resistance due to increasing IFN-1 score. Both IFN-1 high patients experienced disease flares.
Presentation Details
Meeting: ACR Convergence 2026, American College of Rheumatology
Venue: Orange County Convention Center, Orlando, Florida
Session: Poster Session C
Date: Tuesday, November 10, 2026
Time: 10:30 a.m. – 12:30 p.m. ET
said Bob Terbrueggen, CEO of DxTerity.
Full abstract text will be available through the ACR Convergence online program. DxTerity representatives will be available at the meeting to discuss the data and the company’s immune monitoring programs.
DxTerity’s patient-focused mission is to bring the power of at-home RNA-based genomic monitoring to improve the management of immune-mediated diseases and overall patient well-being. DxTerity’s Type 1 Interferon (IFN-1) and Modular Immune Profile tests are run in the company’s CAP-accredited, CLIA-certified laboratory in Torrance, California. DxTerity also holds ISO 13485 certification for its product
development services.
Related articles
•
May 18, 2022
DxTerity Receives New York Authorization for Type 1 Interferon (IFN-1) for Systemic Lupus Erythematosus
IFN-1 gene signature testing represents the advancement of precision medicine beyond cancer in autoimmune disease
Research
•
May 14, 2026
Precision Medicine using Modular Genomics
A simple look at how RNA-based testing can help uncover patterns in immune system activity and support more informed care decisions.
Research
•
February 27, 2020
DxTerity Receives CE Mark for DxCollect® Fingerstick Blood RNA Stabilization Device
Learn how patient-friendly testing can reduce barriers, improve convenience, and help people stay more connected to their health journey.
Stay in the know.
Get the latest updates and news.
DxTerity’s patient-focused mission is to bring the power of at-home RNA-based genomic monitoring to improve the management of immune-mediated diseases and overall patient well-being.