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Interleukin 4 and interferon-gamma secretion by antigen and mitogen-stimulated mononuclear cells in the hyper-IgE syndrome: no TH-2 cytokine pattern.

AbstractBACKGROUND:
Enhanced production of TH-2 cytokines plays a key role in increased IgE production in allergic diseases. Reports about the cytokine profile secreted by peripheral blood mononuclear cells of patients with hyper-IgE syndrome, however, are controversial, suggesting alternative causes for increased IgE production in this syndrome.
OBJECTIVE:
We wished to determine whether mononuclear cells from patients with hyper-IgE syndrome have a pattern of interleukin-4 (IL-4) and interferon-gamma (IFN-gamma) production characteristic of a predominance of TH-2 cells and whether the cytokine production pattern is constant over time.
METHODS:
IL-4 and IFN-gamma secretion by peripheral blood mononuclear cells stimulated with phytohemagglutinin and D. pteronyssinus was measured by ELISA in culture supernatants. Patients with the hyper-IgE syndrome were evaluated 3 times at 4-week intervals and compared with asthmatic patients and normal subjects.
RESULTS:
In PHA-stimulated cultures, patients with hyper-IgE syndrome had an IL-4 and IFN-gamma secretion similar to that of controls, while asthmatic patients had increased IL-4 and decreased IFN-gamma production. Cultures stimulated with D. pteronyssinus showed a variable pattern of secretion for both cytokines.
CONCLUSIONS:
In allergic diseases, increased serum IgE level is the result of a TH-2 pattern of cytokine production, with high IL-4 and decreased IFN-gamma protein secretion. The increased serum IgE concentration typical of the hyper-IgE syndrome is likely the result of a different immunoregulatory process.
AuthorsM F Rodríguez, P J Patiño, F Montoya, C J Montoya, R U Sorensen, D García de Olarte
JournalAnnals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology (Ann Allergy Asthma Immunol) Vol. 81 Issue 5 Pg. 443-7 (Nov 1998) ISSN: 1081-1206 [Print] United States
PMID9860038 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens
  • Cytokines
  • Mitogens
  • Phytohemagglutinins
  • Interleukin-4
  • Interferon-gamma
Topics
  • Adolescent
  • Adult
  • Antigens (pharmacology)
  • Cytokines (analysis)
  • Female
  • Humans
  • Interferon-gamma (metabolism)
  • Interleukin-4 (metabolism)
  • Job Syndrome (blood, metabolism)
  • Leukocytes, Mononuclear (metabolism)
  • Male
  • Mitogens (pharmacology)
  • Phytohemagglutinins (pharmacology)
  • Th2 Cells (chemistry)

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