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Immune response potential of mast cell-deficient W/Wv mice.

Abstract
Immune responses of mast cell-deficient WBB6F1-W/Wv mice and their mast cell-sufficient littermates (LM: WBB6F1-W/+, Wv/+ and +/+) were compared. After a single intravenous injection of sheep erythrocytes (SE), polyvinylpyrrolidone or bacterial lipopolysaccharide, the antigen-specific IgM plaque-forming cell (PFC) response of W/Wv mice was similar to or greater than the response of LM mice. When both primary and secondary injections of SE or chicken gamma-globulin were given to mice and antigen-specific IgG PFC responses quantified, the response of W/Wv again was similar to or greater than that of LM mice. Serum titers of antigen-specific IgE were higher in W/Wv than in LM mice after injections of ovalbumin in alum or infections of Nippostrongylus brasiliensis. Ovalbumin-sensitized W/Wv and LM mice developed active systemic anaphylaxis after ovalbumin challenge. The ability of W/Wv mice to be sensitized for and elicit contact sensitivity (CS) reactions was studied using picryl chloride or dinitrofluorobenzene as sensitizing and challenge agents and quantifying 24-hour reactions by change in ear thickness. SE or methylated bovine serum albumin was used to sensitize and challenge mice for delayed-type hypersensitivity (DTH) reactions which were quantified at 24 h by change in foot pad or ear thickness. CS and DTH reactions of W/Wv and LM mice were similar. No evidence of immune deficiency of W/Wv mice was found.
AuthorsT Y Ha, N D Reed, P K Crowle
JournalInternational archives of allergy and applied immunology (Int Arch Allergy Appl Immunol) Vol. 80 Issue 1 Pg. 85-94 ( 1986) ISSN: 0020-5915 [Print] Switzerland
PMID3514477 (Publication Type: Comparative Study, Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antigens
Topics
  • Anaphylaxis (etiology)
  • Animals
  • Antigens (administration & dosage)
  • Bone Marrow Transplantation
  • Female
  • Hemolytic Plaque Technique
  • Hypersensitivity, Delayed (immunology)
  • Injections, Intravenous
  • Male
  • Mast Cells (immunology)
  • Mice
  • Mice, Mutant Strains (immunology)

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