Journal of Infectious Diseases and Treatment Open Access

  • ISSN: 2472-1093
  • Journal h-index: 7
  • Journal CiteScore: 1.06
  • Journal Impact Factor: 0.77
  • Average acceptance to publication time (5-7 days)
  • Average article processing time (30-45 days) Less than 5 volumes 30 days
    8 - 9 volumes 40 days
    10 and more volumes 45 days

Abstract

Inflammatory Mechanisms in soft tissue disease: Dissecting immune mechanisms in Dupuytren�??s Disease

Kristyn A. Carter

Dupuytren’s disease (DD) is a fibroproliferative disease that is the result of the palmar tissue thickening, causing the fingers to curl inward. Dupuytren’s disease is commonly presented by men, of European descent, that are 65 years or older. In the United states, there are 3 cases per 10,000 and in the United Kingdom, there are 3 cases per 100,000. This disease is usually not reported as many people don’t know they have the disease or do not care to undergo treatment because post-operative results have shown the disease recurs during the individual’s lifetime. Early stage DD presents as a nodule and progresses into a thickened cord causing the fourth and pinky finger to curl inwards. The etiology of the disease has not been sourced to a single factor; however, it has been suggested that labor intensive professions, diabetes, smoking, and drinking lead to higher chances of developing DD. Dupuytren’s disease tissue, characterized by thickened palmar tissue and the formation of nodules and a cord, is a model of tissue fibrosis and chronic inflammation. The development of the symptoms-nodules and cord- are the result of excess production of extracellular matrix (ECM) components. This study will assess the presence of stromal activation markers, identified by previous literature, in Dupuytren’s tissue. Additionally, we aim to characterize the immune cell population within Dupuytren’s. We hypothesize that Dupuytren’s disease tissue will express stromal activation markers and demonstrate an excess of immune cell phenotype-both of which contribute to the persistence of the disease.