Literature DB >> 2324526

Analysis of dose response of trinitrochlorobenzene contact hypersensitivity induction in mice: pretreatment with cyclophosphamide reveals an optimal sensitizing dose.

S Sullivan1, P R Bergstresser, J W Streilein.   

Abstract

A detailed dose-response curve has been established for induction of contact hypersensitivity (CH) in mice with trinitrochlorobenzene (TNCB). It was determined that in BALB/c, CBA/J, and C57BL/6 mice, the dose required to sensitize via epicutaneous application was between 1 and 10 micrograms TNCB. When doses of hapten of 200 micrograms or greater were painted on abdominal skin, CH responses were induced which were only marginally greater than responses induced by sensitizing doses of hapten in the 10-50-micrograms range, implying that no further dose-response relationship exists beyond 50 micrograms of hapten. However, in companion experiments, in which panels of mice were pretreated with cyclophosphamide, it was determined that sensitizing doses of hapten in excess of 50 micrograms induced both CH and concomitant induction of down-regulation of CH. Thus, at 200 micrograms or higher doses of TNCB, CH responses of cyclophosphamide pretreated mice were invariably more intense than in their untreated, hapten-painted cohorts. In the animals pretreated with cyclophosphamide, it was possible to see that a dose-response relationship continued to exist between the amount of epicutaneously applied hapten over a 200 micrograms to 14 mg range and the intensity of the CH induced. We conclude that the optimal dose for immunizing mice epicutaneously with TNCB is between 10 and 50 micrograms. This is considered optimal since animals sensitized in this manner display no evidence of concomitant down-regulation of their CH responses.

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Year:  1990        PMID: 2324526     DOI: 10.1111/1523-1747.ep12876288

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  6 in total

1.  Phenotype, functions and fate of adoptively transferred tumor draining lymphocytes activated ex vivo in mice with an aggressive weakly immunogenic mammary carcinoma.

Authors:  Catriona H T Miller; Laura Graham; Harry D Bear
Journal:  BMC Immunol       Date:  2010-11-04       Impact factor: 3.615

Review 2.  [Immunology of allergic contact dermatitis].

Authors:  A S Lonsdorf; A H Enk
Journal:  Hautarzt       Date:  2009-01       Impact factor: 0.751

3.  Sensitizing capacity of Langerhans' cells obtained from ultraviolet-B-exposed murine skin.

Authors:  R Dai; J W Streilein
Journal:  Immunology       Date:  1995-12       Impact factor: 7.397

4.  Delayed-type hypersensitivity responses regulate collagen deposition in the lung.

Authors:  R Kimura; H Hu; J Stein-Streilein
Journal:  Immunology       Date:  1992-12       Impact factor: 7.397

5.  A murine in vitro model of allergic contact dermatitis to sesquiterpene alpha-methylene-gamma-butyrolactones.

Authors:  N Alonso Blasi; R Fraginals; J P Lepoittevin; C Benezra
Journal:  Arch Dermatol Res       Date:  1992       Impact factor: 3.017

6.  Essential role of lymph nodes in contact hypersensitivity revealed in lymphotoxin-alpha-deficient mice.

Authors:  P D Rennert; P S Hochman; R A Flavell; D D Chaplin; S Jayaraman; J L Browning; Y X Fu
Journal:  J Exp Med       Date:  2001-06-04       Impact factor: 14.307

  6 in total

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