Literature DB >> 3514477

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

T Y Ha, N D Reed, P K Crowle.   

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.

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Year:  1986        PMID: 3514477     DOI: 10.1159/000234031

Source DB:  PubMed          Journal:  Int Arch Allergy Appl Immunol        ISSN: 0020-5915


  26 in total

1.  MD41, a novel T helper 0 clone, mediates mast-cell dependent delayed-type hypersensitivity in mice.

Authors:  Ikuko Torii; Shigeru Morikawa; Takayuki Harada
Journal:  Immunology       Date:  2002-12       Impact factor: 7.397

2.  Susceptibility of mast cell-deficient W/Wv mice to Cryptosporidium parvum.

Authors:  J A Harp; H W Moon
Journal:  Infect Immun       Date:  1991-02       Impact factor: 3.441

3.  Role of mast cells in ion transport abnormalities associated with intestinal anaphylaxis. Correction of the diminished secretory response in genetically mast cell-deficient W/Wv mice by bone marrow transplantation.

Authors:  M H Perdue; S Masson; B K Wershil; S J Galli
Journal:  J Clin Invest       Date:  1991-02       Impact factor: 14.808

4.  Gastric inflammation during systemic anaphylaxis: neutrophil recruitment in stomach wall of mice does not require mast cell participation.

Authors:  G T Furuta; Z S Wang; B K Wershil
Journal:  Dig Dis Sci       Date:  1998-09       Impact factor: 3.199

5.  Role of mast cells in anaphylaxis. Evidence for the importance of mast cells in the cardiopulmonary alterations and death induced by anti-IgE in mice.

Authors:  T R Martin; S J Galli; I M Katona; J M Drazen
Journal:  J Clin Invest       Date:  1989-04       Impact factor: 14.808

Review 6.  Protective and pathological roles of mast cells and basophils.

Authors:  David Voehringer
Journal:  Nat Rev Immunol       Date:  2013-04-05       Impact factor: 53.106

Review 7.  Regulatory roles of mast cells in immune responses.

Authors:  Hideaki Morita; Hirohisa Saito; Kenji Matsumoto; Susumu Nakae
Journal:  Semin Immunopathol       Date:  2016-05-06       Impact factor: 9.623

8.  Susceptibility of W/WV mice to murine cytomegalovirus infection.

Authors:  T Ohashi; Y Nawa; Y Minamishima; M Owhashi
Journal:  Arch Virol       Date:  1988       Impact factor: 2.574

9.  Accumulation of platelets in the lung and liver and their degranulation following antigen-challenge in sensitized mice.

Authors:  Atsushi Yoshida; Mami Ohba; Xia Wu; Takashi Sasano; Masanori Nakamura; Yasuo Endo
Journal:  Br J Pharmacol       Date:  2002-09       Impact factor: 8.739

10.  Effects of chronic treatment with the c-kit ligand, stem cell factor, on immunoglobulin E-dependent anaphylaxis in mice. Genetically mast cell-deficient Sl/Sld mice acquire anaphylactic responsiveness, but the congenic normal mice do not exhibit augmented responses.

Authors:  A Ando; T R Martin; S J Galli
Journal:  J Clin Invest       Date:  1993-10       Impact factor: 14.808

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