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Related Concept Videos

Chronic Inflammation: Introduction01:12

Chronic Inflammation: Introduction

Chronic inflammation is a prolonged, dysregulated immune response that persists for weeks to years when the inciting stimulus is difficult to eradicate or when self‑antigens drive ongoing reactivity. Morphologically, it is defined by mononuclear cell infiltration, progressive tissue destruction, and concurrent attempts at healing via angiogenesis and fibrosis. Compared with acute inflammation, edema is less prominent while cellular infiltration predominates; triggers include persistent...
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Acute inflammation produces a coordinated set of local and systemic changes that limit injury, eliminate pathogens, and initiate repair. These responses arise within minutes of infection, trauma, or chemical insult and are driven by vascular alterations and leukocyte-derived mediators. When the stimulus resolves, the reaction typically abates within days.Local EffectsAt the site of injury, arteriolar vasodilation increases blood flow, resulting in redness and warmth. Simultaneously, increased...
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An inflammatory response is a localized, nonspecific immune reaction that occurs when a tissue is injured. It is characterized by redness, swelling, heat, and pain, which are commonly called the cardinal signs and symptoms of inflammation. Inflammation can sometimes result in a loss of function.
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Allergic Drug Reactions01:27

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Allergic reactions related to drugs are hypersensitivity responses driven by the immune system and bear no connection to the drug's therapeutic action. While drugs in isolation do not trigger an immune response, they can interact with endogenous proteins to form antigens. These antigens stimulate lymphocytes to produce antibodies. IgE-type antibodies attach themselves to mast cells. Upon subsequent exposure to the same stimulus, the antigen-antibody interaction is initiated, unleashing numerous...

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Related Experiment Video

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Intra-tracheal Administration of Haemophilus influenzae in Mouse Models to Study Airway Inflammation
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Mite-induced inflammation: More than allergy.

Mario Sánchez-Borges, Enrique Fernández-Caldas, Arnaldo Capriles-Hulett

    Allergy & Rhinology (Providence, R.I.)
    |August 2, 2012
    PubMed
    Summary

    Patients with atopic conditions and mite allergy often experience hypersensitivity reactions to nonsteroidal anti-inflammatory drugs (NSAIDs). This suggests a link between atopy, mite allergy, and NSAID intolerance, possibly involving leukotriene pathways.

    Keywords:
    AspirinDermatophagoidesNSAIDsacetylsalicylic acidangioedemacysteinyl-leukotrienesimmunoglobulin Eleukotriene C4 synthasemitesnonsteroidal anti-inflammatory drugs

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    Area of Science:

    • Immunology
    • Allergology
    • Pharmacology

    Background:

    • Clinical observations suggest a link between atopic conditions and hypersensitivity to nonsteroidal anti-inflammatory drugs (NSAIDs).
    • This association is particularly noted in patients with mite allergies.

    Purpose of the Study:

    • To review clinical and experimental evidence connecting atopy, mite allergy, and hypersensitivity to aspirin and NSAIDs.
    • To discuss potential mechanisms underlying this observed association.

    Main Methods:

    • A comprehensive review of the medical literature was conducted using PubMed and other relevant databases.
    • The review focused on studies examining the relationship between atopic diseases, mite hypersensitivity, and NSAID intolerance.

    Main Results:

    • NSAID-sensitive patients frequently exhibit atopy and mite allergy.
    • Patients with oral mite anaphylaxis (OMA) show a higher prevalence of NSAID hypersensitivity.
    • An interaction between atopic allergy and leukotriene synthesis/metabolism disorders is suggested.

    Conclusions:

    • The association between mite hypersensitivity and aspirin/NSAID intolerance is confirmed.
    • This finding offers insights into non-IgE-mediated pathways contributing to inflammation in atopic, mite-allergic individuals.
    • Further investigation into the clinical relevance of these findings is ongoing.