Video: Who Am I?| Webinar: ACR/CHEST ILD Guidelines in Practice

An official publication of the ACR and the ARP serving rheumatologists and rheumatology professionals

  • Conditions
    • Axial Spondyloarthritis
    • Gout and Crystalline Arthritis
    • Myositis
    • Osteoarthritis and Bone Disorders
    • Pain Syndromes
    • Pediatric Conditions
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Sjögren’s Disease
    • Systemic Lupus Erythematosus
    • Systemic Sclerosis
    • Vasculitis
    • Other Rheumatic Conditions
  • FocusRheum
    • ANCA-Associated Vasculitis
    • Axial Spondyloarthritis
    • Gout
    • Lupus Nephritis
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Sjögren’s Disease
    • Systemic Lupus Erythematosus
  • Guidance
    • Clinical Criteria/Guidelines
    • Ethics
    • Legal Updates
    • Legislation & Advocacy
    • Meeting Reports
      • ACR Convergence
      • Other ACR meetings
      • EULAR/Other
    • Research Rheum
  • Drug Updates
    • Analgesics
    • Biologics/DMARDs
  • Practice Support
    • Billing/Coding
    • EMRs
    • Facility
    • Insurance
    • Technology
      • Information Technology
      • Apps
    • QA/QI
    • Workforce
  • Opinion
    • Patient Perspective
    • Profiles
    • Rheuminations
      • Video
    • Speak Out Rheum
  • Career
    • ACR ExamRheum
    • Awards
    • Career Development
      • Education & Training
    • Certification
  • ACR
    • ACR Home
    • ACR Convergence
    • ACR Guidelines
    • Journals
      • ACR Open Rheumatology
      • Arthritis & Rheumatology
      • Arthritis Care & Research
    • From the College
    • Events/CME
    • President’s Perspective
  • Search

Emerging Therapies for Antiphospholipid Syndrome, an Antibody-Mediated Disease

Katie Robinson  |  Issue: August 2025  |  August 6, 2025

At discharge, the patient received prescriptions for a prednisone taper and warfarin, while she continued taking hydroxychloroquine. After discharge, the patient’s creatinine stabilized to approximately 2.0 mg/dL.

At age 37, the patient reported shortness of breath and groundglass pul­monary infiltrates were found. Despite completing several courses of anti­biotics over a few months, the dyspnea and infiltrates persisted. When hospitalized during an acute exacerbation of dyspnea, she presented with reduced hemoglobin and diffuse alveolar hemorrhage, confirmed as bronchoalveolar lavage. The patient’s breathing improved with glucocorticoids and plasmapheresis, and she received a prescription for a prednisone taper at discharge.

ad goes here:advert-1
ADVERTISEMENT
SCROLL TO CONTINUE

On referral to your clinic for further management, you added a rituximab course to her prednisone taper followed by a second round of rituximab after six months, while she continued taking warfarin and hydroxychloroquine. The patient experienced no further pulmonary hemorrhage flares, despite unchanged aPL antibody levels, but her kidney function deteriorated over the next two years. The patient is under consideration for a living-donor kidney transplant.

Key Takeaways

“IgG isotype antibodies recognizing the plasma protein beta-2 glycoprotein I are clearly pathogenic, activating a variety of effector cells to create the prothrombotic state inherent to APS,” Dr. Knight says.

ad goes here:advert-2
ADVERTISEMENT
SCROLL TO CONTINUE

“The microvascular manifestations of APS often progress despite treatment with anticoagulation, highlighting a subgroup of patients who are especially in need of new approaches to therapy.

“Rheumatologists (and patients) should feel optimistic that we are closer than we have ever been to trialing new therapeutic strategies that endeavor to impact APS closer to its antibody-mediated source,” Dr. Knight concludes.


Katie Robinson is a medical writer in New York.

Disclosures

Dr. Knight has received consulting fees from ArgenX, BioCryst, Jazz Pharma, Ouro Medicines, Roche, Roivant Sciences and Visterra/Otsuka, along with grant funding from Jazz Pharma and Visterra/Otsuka.

References

  1. Bucala R, Solomon DH. Immunology for the rheumatologist: Arthritis & Rheumatology introduces a new problem-based immunology review series with great educational potential. Arthritis Rheumatol. 2024 Jan;76(1):9–10.
  2. Newman TG, Knight JS. Antiphospholipid syndrome: An antibody-mediated disease with emerging therapeutic opportunities. Arthritis Rheumatol. 2025 May 19. Epub ahead of print.

Page: 1 2 3 | Single Page
Share: 

Filed under:Biologics/DMARDsConditionsDrug UpdatesGuidanceOther Rheumatic ConditionsResearch Rheum Tagged with:AntibodiesanticoagulantAntiphospholipid syndromeautoantibodiesB cellsCAR-T cell therapyHYDROXYCHLOROQUINEImmunology Insightslupus anticoagulantPathogenesisrituximabthrombosiswarfarin

Related Articles

    APS: What Rheumatologists Should Know about Hughes Syndrome

    February 17, 2016

    The problem that dogs the work of all of those treating patients with antiphospholipid syndrome (APS) is the apparent lack of knowledge of the syndrome, both by the general public, as well as by swaths of the medical fraternity. Perhaps it was ever thus—a syndrome less than 40 years old could be described as new,…

    Antiphospholipid Antibody Testing Update

    January 13, 2012

    Successes, challenges, and controversies of diagnostic methods for APS

    What Rheumatologists Need to Know About Antiphospholipid Syndrome

    June 8, 2024

    Antiphospholipid syndrome (APS) is an acquired thromboinflammatory disease that can have severe, sometimes catastrophic, effects on patients and their families. Our modern understanding of APS began to emerge in the early 1980s. At that point, it was defined as a condition characterized by thrombotic episodes and/or pregnancy complications in the presence of antiphospholipid antibodies (aPL).1…

    Put Hughes Syndrome on Your Radar

    April 1, 2007

    Diagnosis of antiphospholipid syndrome is increasing. Here’s how to recognize and treat it

  • About Us
  • Meet the Editors
  • Issue Archives
  • Contribute
  • Advertise
  • Contact Us
  • Copyright © 2025 by John Wiley & Sons, Inc. All rights reserved, including rights for text and data mining and training of artificial technologies or similar technologies. ISSN 1931-3268 (print). ISSN 1931-3209 (online).
  • DEI Statement
  • Privacy Policy
  • Terms of Use
  • Cookie Preferences