Literature DB >> 1085308

Cutaneous basophil hypersensitivity uncovered in the cell transfer of classical tuberculin hypersensitivity.

P W Askenase.   

Abstract

Cellular transfer of cutaneous basophil hypersensitivity (CBH) was studied. Guinea pigs immunized for CBH with incomplete Freund's adjuvant (IFA) provided cells which could transfer delayed and basophil-rich reactions in skin tests of recipients. Guinea pigs immunized with complete classical tuberculin-type delayed hypersensitivity reactions (DH), which are characteristically devoid of basophils. However, recipients of cells from donors with DH, surprisingly, were found to have delayed skin reactions containing large basophil infiltrates which were lacking in the donors. Thus, recipients of classical cell transfers of tuberculin-type DH had delayed reactions which resembled CBH. Control experiments verified that the cell transfer of CBH from donors with DH was due to passive transfer with live cells and not transfer of contaminating humoral factors or active sensitization of recipients. It was concluded that cutaneous basophil responses were suppressed in CFA-immunized donors and expressed in cell transfer recipients. Cells from donors immunized with CFA were enriched for nonadherent and nonimmunoglobulin-bearing lymphocytes by passage through nylon wool columns, and these cells transferred conjugate specific CBH reactions. It was concluded that cells mediating these transfers were probably T cells. The finding of basophils in cell transfers of DH and a variety of other findings suggesting complex regulation of basophil numbers in tissue lead to the conclusion that the term CBH be used to simply describe a basophil-containing skin reaction.

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Year:  1976        PMID: 1085308

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  14 in total

1.  Relationship between the tuberculin-type and Jones-Mote-type hypersensitivities: suppression of basophil infiltration by mycobacterial adjuvant.

Authors:  S Nakamura; H Sanui; K Nomoto
Journal:  Immunology       Date:  1986-07       Impact factor: 7.397

2.  Inhibition of guinea-pig lymphocyte activation by histamine and histamine analogues.

Authors:  J L Beets; M M Dale
Journal:  Br J Pharmacol       Date:  1979-07       Impact factor: 8.739

3.  Delayed hypersensitivity in mice induced by intravenous sensitization with sheep erythrocytes: evidence for tuberculin type delayed hypersensitivity of the reaction.

Authors:  A Mitsuoka; T Teramatsu; M Baba; S Morikawa; K Yasuhira
Journal:  Immunology       Date:  1978-03       Impact factor: 7.397

4.  Suppression of antibody-mediated accumulation of eosinophils in chronic inflammatory lesions by concomitant delayed hypersensitivity reactions.

Authors:  W B van den Berg; T C Haasakker; J Bax; R J Scheper
Journal:  Immunology       Date:  1980-12       Impact factor: 7.397

5.  Comparative migration of T- and B-lymphocyte subpopulations into skin inflammatory sites.

Authors:  A C van Dinther-Janssen; A C van Maarsseveen; J de Groot; R J Scheper
Journal:  Immunology       Date:  1983-03       Impact factor: 7.397

6.  Cutaneous basophil anaphylaxis. Immediate vasopermeability increases and anaphylactic degranulation of basophils at delayed hypersensitivity reactions challenged with additional antigen.

Authors:  P W Askenase; R Debernardo; D Tauben; M Kashgarian
Journal:  Immunology       Date:  1978-11       Impact factor: 7.397

7.  A new method for obtaining viable cells from dermal infiltrates. A study on 2,4 dinitrochlorobenzene induced contact dermatitis.

Authors:  L Molnár; J M Baló-Banga; J Leibinger; K Király
Journal:  Arch Dermatol Res       Date:  1979-03-31       Impact factor: 3.017

Review 8.  Basophils in human disease.

Authors:  E B Mitchell; P W Askenase
Journal:  Clin Rev Allergy       Date:  1983-09

9.  Basophils in tuberculin and "Jones-Mote" delayed reactions of humans.

Authors:  P W Askenase; J E Atwood
Journal:  J Clin Invest       Date:  1976-11       Impact factor: 14.808

10.  Cutaneous basophil-associated resistance to ectoparasites (ticks). I. Transfer with immune serum or immune cells.

Authors:  P W Askenase; B G Bagnall; M J Worms
Journal:  Immunology       Date:  1982-03       Impact factor: 7.397

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