1982
DOI: 10.1016/0090-1229(82)90030-7
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Studies on T-cell subsets in atopic dermatitis: Human T-cell subpopulations defined by specific monoclonal antibodies

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Cited by 25 publications
(11 citation statements)
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“…The total number of T lymphocytes was estimated both by the standard E-rosette technique [14] and by OKTII and OKT3 monoclonal antibodies (Ortho Pharmaceutical Corp., Raritan, N.J.) which recog nize the E-rosette forming cells and the whole T-cell, population [15,16], respectively. In addition, OKT4 OKT6 and OK.T8 monoclonal antibodies (Ortho Pharmaceutical Corp., Raritan, N.J.) were used to re cognize T-cell subsets in which helper T cells, com mon thymocytes and cytotoxic-suppressor T cells are thought to be included [15], Indirect immunofluores- cence was used to assess binding of monoclonal an tibodies [15], and fluorescent cells were counted on a Leitz Orthoplan microscope (E. Leitz, Wetzlar, FRG) and compared to the total number of cells.…”
Section: T-cell Subsetsmentioning
confidence: 99%
See 1 more Smart Citation
“…The total number of T lymphocytes was estimated both by the standard E-rosette technique [14] and by OKTII and OKT3 monoclonal antibodies (Ortho Pharmaceutical Corp., Raritan, N.J.) which recog nize the E-rosette forming cells and the whole T-cell, population [15,16], respectively. In addition, OKT4 OKT6 and OK.T8 monoclonal antibodies (Ortho Pharmaceutical Corp., Raritan, N.J.) were used to re cognize T-cell subsets in which helper T cells, com mon thymocytes and cytotoxic-suppressor T cells are thought to be included [15], Indirect immunofluores- cence was used to assess binding of monoclonal an tibodies [15], and fluorescent cells were counted on a Leitz Orthoplan microscope (E. Leitz, Wetzlar, FRG) and compared to the total number of cells.…”
Section: T-cell Subsetsmentioning
confidence: 99%
“…In addition, OKT4 OKT6 and OK.T8 monoclonal antibodies (Ortho Pharmaceutical Corp., Raritan, N.J.) were used to re cognize T-cell subsets in which helper T cells, com mon thymocytes and cytotoxic-suppressor T cells are thought to be included [15], Indirect immunofluores- cence was used to assess binding of monoclonal an tibodies [15], and fluorescent cells were counted on a Leitz Orthoplan microscope (E. Leitz, Wetzlar, FRG) and compared to the total number of cells. Ab solute numbers of T-cell subsets were obtained by white cell and differential counts performed on ED-TA-treated peripheral blood.…”
Section: T-cell Subsetsmentioning
confidence: 99%
“…In fact, a reduced percentage of T cells or of positive T8 lymphocytes was found in patients with atopic dermatitis and in those with E-hypergammaglobulin emia [Romagnani et al, 1978;Canonica et al, 1979;Faure et al, 1982;Leung et al, 1983;Chandra and Baker, 1983], A de pressed lymphoproliférative response to T-cell mitogens was also demonstrated [Grove et al, 1975;Rivlin et al, 1981;Romagnani et al, 1985].…”
Section: Discussionmentioning
confidence: 99%
“…Deficiency in T cells was more pronounced in certain subsets of T lym phocytes. In fact, no significant modifica tion of helper responsiveness has been found, while many data suggest the pres ence of a relative, selective suppressor Tcell deficiency in atopic patients with high serum levels of immunoglobulin E [Canonica et al, 1979;Bruno et al, 1983;Faure et al, 1982;Chandra and Baker, 1983;Kesarwala et al, 1984], Moreover, a signi ficant reduction in NK-cell activity has been shown in patients with atopic derma titis [Lever et al, 1984], Obviously, defects in the host defense system may predispose to greater than normal susceptibility to bacterial, viral and mycotic infections [Rosen et al, 1984], Conflicting results have been reported about the susceptibility of atopic patients to infections. It is well known that patients with severe atopic dermatitis [Jones et al, 1973;Hanifin and Lobitz, 1977;Minor et al, 1974] and atopic children less than 1 year of age frequently suffer from serious and recurrent infections.…”
Section: Introductionmentioning
confidence: 99%
“…(e) Patients with atopic dermatitis and those with E-hypergammaglobulinemia have in creased percentages of T4+ and reduced percentages of T8+ lymphocytes [16,17]. (f) The defect of T-cell subsets precedes clinical atopic disease and seems to be of primary pathogenetic importance, as well as of predictive value [18].…”
Section: Impairment O F Ige-specific Regulatory Tcells In Atopic Subjmentioning
confidence: 99%