Literature DB >> 3015783

Two phenotypically distinct T cells (Ly1+2- and Ly1-2+) are involved in ultraviolet-B light-induced suppression of the efferent DTH response to HSV-1 in vivo.

S E Howie, M Norval, J Maingay, J A Ross.   

Abstract

We have previously demonstrated that the delayed-type hypersensitivity (DTH) response to herpes simplex virus type 1 induced by subcutaneous injection with live virus was suppressed by irradiating mice with a low dose (96 mJ/cm2) of ultraviolet-B (UV-B) light 3 days before sensitization. In order to determine the nature of the suppression, cells from mice irradiated with UV-B before immunization with live virus were transferred to syngeneic animals that had been sensitized with live virus without prior UV-B exposure. Efferent suppression of DTH to HSV-1 was shown to be due to T lymphocytes, and two phenotypically distinct T cells were involved: an Ly1+2- subset and an Ly1-2+ subset.

Entities:  

Mesh:

Year:  1986        PMID: 3015783      PMCID: PMC1453103     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  13 in total

1.  Pathogenesis of recurrent herpes simplex infections.

Authors:  C E Wheeler
Journal:  J Invest Dermatol       Date:  1975-10       Impact factor: 8.551

2.  Cell-mediated immunity in herpes simplex virus-infected mice: induction, characterization and antiviral effects of delayed type hypersensitivity.

Authors:  A A Nash; H J Field; R Quartey-Papafio
Journal:  J Gen Virol       Date:  1980-06       Impact factor: 3.891

Review 3.  Tolerance and suppression in virus diseases.

Authors:  A A Nash
Journal:  Br Med Bull       Date:  1985-01       Impact factor: 4.291

4.  A rapid method for the isolation of functional thymus-derived murine lymphocytes.

Authors:  M H Julius; E Simpson; L A Herzenberg
Journal:  Eur J Immunol       Date:  1973-10       Impact factor: 5.532

5.  Type-specific delayed hypersensitivity and protective immunity induced by isolated herpes simplex virus glycoprotein.

Authors:  R D Schrier; L I Pizer; J W Moorhead
Journal:  J Immunol       Date:  1983-03       Impact factor: 5.422

6.  Membrane phenotype of murine effector and suppressor T cells involved in delayed hypersensitivity and protective immunity to herpes simplex virus.

Authors:  A A Nash; P G Gell
Journal:  Cell Immunol       Date:  1983-02-01       Impact factor: 4.868

7.  Cell-mediated immunity in herpes simplex virus-infected mice: H-2 mapping of the delayed-type hypersensitivity response and the antiviral T cell response.

Authors:  A A Nash; J Phelan; P Wildy
Journal:  J Immunol       Date:  1981-04       Impact factor: 5.422

8.  Exposure to low-dose ultraviolet radiation suppresses delayed-type hypersensitivity to herpes simplex virus in mice.

Authors:  S Howie; M Norval; J Maingay
Journal:  J Invest Dermatol       Date:  1986-02       Impact factor: 8.551

9.  Mechanism of systemic immune suppression by UV irradiation in vivo. II. The UV effects on number and morphology of epidermal Langerhans cells and the UV-induced suppression of contact hypersensitivity have different wavelength dependencies.

Authors:  F P Noonan; C Bucana; D N Sauder; E C De Fabo
Journal:  J Immunol       Date:  1984-05       Impact factor: 5.422

10.  Systemic suppression of contact hypersensitivity by UVB radiation is unrelated to the UVB-induced alterations in the morphology and number of Langerhans cells.

Authors:  W L Morison; C Bucana; M L Kripke
Journal:  Immunology       Date:  1984-06       Impact factor: 7.397

View more
  2 in total

1.  Suppression of delayed-type hypersensitivity to histocompatibility antigens by ultraviolet radiation.

Authors:  A Molendijk; R J van Gurp; I G Donselaar; R Benner
Journal:  Immunology       Date:  1987-10       Impact factor: 7.397

2.  The role of antigen presentation in the ontogeny of immune responses to herpes simplex virus.

Authors:  S E Howie; M Norval; J P Maingay; J A Ross; W A Neill
Journal:  Clin Exp Immunol       Date:  1988-05       Impact factor: 4.330

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.