4.8 Article

Desmoglein-1-specific T lymphocytes from patients with endemic pemphigus foliaceus (fogo selvagem)

Journal

JOURNAL OF CLINICAL INVESTIGATION
Volume 105, Issue 2, Pages 207-213

Publisher

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI8075

Keywords

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Funding

  1. NHLBI NIH HHS [R01-HL47145] Funding Source: Medline
  2. NIAID NIH HHS [UO1-AI34621] Funding Source: Medline
  3. NIAMS NIH HHS [R01 AR032081, R01 AR032599, R01 AR040410, R01-AR40410] Funding Source: Medline
  4. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL047145] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [U01AI034621] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [R01AR040410] Funding Source: NIH RePORTER

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Pogo selvagem (FS), the endemic form of pemphigus foliaceus, is a cutaneous autoimmune disease characterized by subcorneal blistering of the epidermis and the production of autoantibodies against the desmosomal antigen desmoglein-1 (Dsg1). Previously, we showed that mice injected with autoantibodies from FS patients develop a skin disease that reproduces the clinical, histological, and immunological features of FS, indicating that autoantibodies play an essential role in the development of this disease. The purpose of this study was to characterize the autoimmune T-cell response associated with FS. We provide here the first evidence, to our knowledge, that the great majority of FS patients have circulating T lymphocytes that specifically proliferate in response to the extracellular domain of Dsg1. Long-term T cells developed from these patients also responded to Ds,ol, and this antigen-specific response was shown to be restricted to HLA-DR molecules. These Dsg1-reactive FS T cells exhibited a CD4-positive memory T-cell phenotype and produced a T helper 2-like cytokine profile. These findings represent the initial steps in defining the role of T cells in FS autoimmunity.

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