Following Dr. Theoharides INTENSE talk we got to take a break (which I think everyone’s brains needed).
Then up next was Dr. Joseph Butterfield from the Mayo Clinic. Â He talked about the Mayo Clinic program for the study of Mast Cell and Eosinophilic Disorders.
His first slide said
- Ok, I’ve got mastocytosis, why are they interested in both mast cells and this other cell (eosinophil)?
- Ok, I’ve got eosinophilia, why are they interested in both eosinophils and this other cell (mast cell)?
Which I thought was funny, because I’m guessing many of us with mast cell diseases and eosinophilia can’t eat peanut butter… or probably jelly. Â LOL
- Inflammatory cells that:
- Originate in the bone marrow
- Â Â - Circulate briefly in the blood
- Â Â Â Â Wind up in the tissue especially GI tract, lung, skin
- Eosin (acidic red dye) + -phil (having an attraction for)
- Normal numbers </= 500/mm³
- Greatly increased (>1500/mm³) in: over 80 disorders: parasitic and certain fungal infections, immune deficiency, allergic diseases, skin disorders, toxic reactions to ingested agents, connective tissue diseases, certain cancers and myeloproliferative disorders, “hypereosinophilic syndromes”
- Despite over 100 years of research there is still debate about the function of eosinophils.
- We can live without them.
- Pro-inflammatory/host defense functions: asthma, paracsitic disorders
- OR
- Modulation of Local Immunity And/or Remodeling/Repair the “LIAR” hypotesis
- Commonly increased in atopic disorders such as asthma, allergic rhinits, nasal polyps, atopic dermatis
- With eosinophil #’s > 1500/mm³ [hypereosinophilia] a different “universe” of problems is encountered.
Locations: [tissue dwelling] perivascular, connective tissues, mucosal surfaces- Actions:
     -Adaptive immunity-migration of dedritic cells: T cell responses
    -Autoimmune diseases
      Inflammatory arthritis; multiple sclerosis; bullous pemphigoid, glomerulonephritis
    -Innate immunity to bacterial and parasitic infections
    -Other:  wound healing, fibrosis, angiogenesis, atherosclerosis, ischemic tissue injury
    -Asthma
    -IgE-mediated allergic reactions
      Anaphylaxis
      Uticaria & Angioedema
- Mast cells and eosinophils co-localize in disorders such as allergic asthma, parasitic infections, eosinophilic esophagitis, chronic gastritis, GI neoplasms, inflammatory bowel disease
- MC & Eosinophils interact
 -Via soluble mediators
 -Via cell-to-cell contact
It was a very interesting talk, and I wish I understood the science better! Â It definitely makes sense that eosinophils and mast cells could interact and each could make the other worse. Â Definitely an interesting combination of cells to look at. Â
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