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Decreased suppressor cell activity in disseminated granulomatous infections.

Abstract
The effect of granulomatous infections upon the activity of a T lymphocyte subclass in human peripheral blood that can be induced by concanavalin A (Con A) to function in a suppressor mode was studied. Peripheral blood lymphocytes (PBL) from eleven patients with disseminated mycotic or mycobacterial infections or from controls were preincubated with and without Con A, washed and cultured with allogeneic PBL freshly drawn from healthy donors sensitive to histoplasmin. DNA synthesis was then measured in co-cultures stimulated by Con A, histoplasmin, or by the mixed lymphocyte culture (MLC) reaction alone. As compared with cells preincubated without Con A, the Con A-pretreated cells were significantly less effective in suppressing the responses of normal PBL to histoplasmin (P < 0.01), and in a one-way MLC reaction (P < 0.05). The Con A-induced suppressor activity of PBL from nine patients with localized granulomatous infections did not differ significantly from that exerted by PBL of normal controls in two of the three co-culture systems employed. These studies suggest that either dysfunction or a reduction of the Con A-inducible T-suppressor cell subpopulation in peripheral blood is frequent among patients was disseminated granulomatous infections.
AuthorsR P Artz, R R Jacobson, W E Bullock
JournalClinical and experimental immunology (Clin Exp Immunol) Vol. 41 Issue 2 Pg. 343-52 (Aug 1980) ISSN: 0009-9104 [Print] England
PMID6449336 (Publication Type: Journal Article)
Chemical References
  • Concanavalin A
  • Histoplasmin
Topics
  • Adolescent
  • Adult
  • Aged
  • Blastomycosis (immunology)
  • Concanavalin A (pharmacology)
  • Histoplasmin (pharmacology)
  • Histoplasmosis (immunology)
  • Humans
  • Hypersensitivity, Delayed
  • Leprosy (immunology)
  • Leukocyte Count
  • Lymphocyte Activation
  • Lymphocyte Culture Test, Mixed
  • Male
  • Middle Aged
  • Skin Tests
  • T-Lymphocytes, Regulatory (immunology)
  • Tuberculosis (immunology)

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