Systemic sclerosis & Raynaud's

Adeno‐Associated Virus Type 5 Infection via PDGFRα Is Associated With Interstitial Lung Disease in Systemic Sclerosis and Generates Composite Peptides and Epitopes Recognized by the Agonistic Immunoglobulins Present in Patients With Systemic Sclerosis

Arthritis RheumatolPublished Mechanistic study

Authors' conclusion

These data link AVV5 with the immune reactivity to endogenous antigens in SSc and provide a novel element in the pathogenesis of SSc.

Study context

Population
Patients with systemic sclerosis (SSc) with ILD and controls; SSc lung tissue, bronchoalveolar lavage (BAL) fluid and sera
Participants
66 vs 66
Comparison
AAV5 detection in BAL fluid of SSc patients with ILD vs controls
  • SSc WITH ILDn = 66
  • CONTROLSn = 66reference
Outcome
AAV5 detection in BAL fluid
Methodological detailsin silico molecular docking, surface plasmon resonance, in situ hybridisation, immunohistochemistry, confocal microscopy
  • In silico molecular docking
  • Surface plasmon resonance
  • In situ hybridisation, immunohistochemistry, confocal microscopy

Main finding

As reported in the abstract

AAV5 detected in BAL fluid

P < 0.001

Further findings

AAV5 localisation in SSc lungs

AAV5 localised in type II pneumocytes and in interstitial cells

AAV5 capsid–PDGFRα molecular complex

Molecular complex of spatially contiguous epitopes of the AAV5 capsid and of PDGFRα identified and characterised

Binding of composite epitopes to agonistic anti-PDGFRα antibodies

Spatially contiguous epitopes derived from PDGFRα and AAV5 interacted with SSc agonistic antibodies to PDGFRα

Binding of peptides to total IgG

Peptides bound total IgG isolated from patients with SSc, not from healthy controls

Original publication

Adeno‐Associated Virus Type 5 Infection via PDGFRα Is Associated With Interstitial Lung Disease in Systemic Sclerosis and Generates Composite Peptides and Epitopes Recognized by the Agonistic Immunoglobulins Present in Patients With Systemic Sclerosis. Arthritis Rheumatol. Published 15 February 2024. doi:10.1002/art.42746

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.