Reacciones alérgicas inmediatas y selectivas a AINES.Nuevos fenotipos

  1. PEREZ ALZATE, DIANA VICTORIA
Dirigida por:
  1. Maria Gabriela Canto Diez Director/a
  2. Luis Antonio Álvarez-Sala Walther Director
  3. Natalia Blanca-López Director/a

Universidad de defensa: Universidad Complutense de Madrid

Fecha de defensa: 12 de julio de 2022

Tribunal:
  1. Luis Puente Maestu Presidente
  2. Elpidio Calvo Manuel Secretario
  3. José Augusto García-Agúndez Pérez-Coca Vocal
  4. Miguel Ángel Tejedor Alonso Vocal
  5. M. Elena Seoane Reula Vocal

Tipo: Tesis

Resumen

Nonsteroidal anti-inflammatory drugs (NSAIDs) are the most commonly used drugs and widely prescribed for treating pain and inflammatory conditions. Hypersensitivity drug reactions (HDRs) are classified as a type B reaction, or not predictable, which are triggered by the release of anti-inflammatory mediators eliciting a variety of clinical entities ranging from urticaria and angioedema to anaphylactic shock and bronchial asthma. Recent data shows that NSAIDs are the most frequent triggers of hypersensitivity drug reactions (HDR), which may be induced by both specific immunological mechanisms mediated by IgE antibodies or T cells (allergic or selective reactions SR) and mechanisms not based on immunological recognition related to the inhibition of the cyclooxygenase (COX)-1 enzyme and subsequent release of inflammatory mediators from arachidonic acid pathway (cross-hypersensitivity reactions [CRs]). Currently, CRs mediated clinical entities are the best studied models. However, SR are also play a fundamental role in HDRs to NSAIDs, being the main trigger of drug-induced anaphylaxis and it has recently been reported that in some countries they represent the most frequent type of NSAID hypersensitivity.