Literature DB >> 321157

Drug-induced immunological unresponsiveness: selective inhibition of T-cell 'helper function' by cyclophosphamide in mice pretreated with phytohaemagglutinin.

G Schwarze.   

Abstract

Studies involving the combined use of phytohaemagglutinin (PHA) and cyclophosphamide (CY) indicate that both agents can act together to produce immunological unresponsiveness: following injection of PHA into mice, splenic DNA synthetic responses [14C]thymidine incorporation) and haemolysin plaque formation against sheep red blood cells were determined in daily intervals. Both immunosuppression and DNA synthetic activity were maximally developed 5 days after treatment with PHA. Administration of CY at this time resulted in immunological unresponsiveness lasting for about 18 days. Antibody production could be completely restored with antigen-activated T cells (but not with B cells), thus indicating a selective inhibition of T-cell 'helper function' in mice treated with PHA and CY. This observation is consistent with the general assumption that cells involved in the response to PHA are predominantly T cells. Apparently, these cells are highly sensitive to an inactivation by CY after stimulation with PHA.

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Year:  1977        PMID: 321157      PMCID: PMC1540908     

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


  26 in total

1.  Influence of cyclophosphamide on the delayed hypersensitivity of the mouse.

Authors:  J A Kerckhaert; G J Van den Berg; J M Willers
Journal:  Ann Immunol (Paris)       Date:  1974 Mar-Apr

2.  Cellular cooperation and stimulatory factors in antibody responses: limiting dilution analysis in vitro.

Authors:  D C Vann; C R Dotson
Journal:  J Immunol       Date:  1974-03       Impact factor: 5.422

Review 3.  Elicitation of selective T and B lymphocyte responses by cell surface binding ligands.

Authors:  M Greaves; G Janossy
Journal:  Transplant Rev       Date:  1972

4.  In vitro cooperation of cells of bone marrow and thymus origins in the generation of antibody-forming cells.

Authors:  D C Vann; J R Kettman
Journal:  J Immunol       Date:  1972-01       Impact factor: 5.422

5.  Drug-induced immunological tolerance to sheep red blood cells in mice: effective combination therapy with vincristine and cyclophosphamide.

Authors:  G Schwarze; P G Scheurlen
Journal:  Int Arch Allergy Appl Immunol       Date:  1974

6.  Phi-isoantigenic marker in phytohemagglutinin-responding mouse blood lymphocytes.

Authors:  L Andersson; P Häyry
Journal:  Experientia       Date:  1972-01-15

7.  Functional aspects of the selective depletion of lymphoid tissue by cyclophosphamide.

Authors:  J L Turk; D Parker; L W Poulter
Journal:  Immunology       Date:  1972-10       Impact factor: 7.397

Review 8.  Antigen binding cells in tolerance and immunity.

Authors:  G L Ada
Journal:  Transplant Rev       Date:  1970

Review 9.  Immunologic complementation between thymus and marrow cells--a model for the two-cell theory of immunocompetence.

Authors:  H N Claman; E A Chaperon
Journal:  Transplant Rev       Date:  1969

10.  Potentiation of T-cell-mediated immunity by selective suppression of antibody formation with cyclophosphamide.

Authors:  P H Lagrange; G B Mackaness; T E Miller
Journal:  J Exp Med       Date:  1974-06-01       Impact factor: 14.307

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  2 in total

1.  Delayed-type hypersensitivity responses in mice infected with St. Louis encephalitis virus: kinetics of the response and effects of immunoregulatory agents.

Authors:  B W Hudson; K Wolff; J C DeMartini
Journal:  Infect Immun       Date:  1979-04       Impact factor: 3.441

2.  Murine mercury-induced immune-complex disease: effect of cyclophosphamide treatment and importance of T-cells.

Authors:  P Hultman; S Eneström
Journal:  Br J Exp Pathol       Date:  1989-06
  2 in total

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