CD4+TCRαβ+ T-cells developing after allogeneic bone marrow transplantation in patients with chronic myelogenous leukaemia. Dipyridamole inhibits functionally heterogeneous T-cell clones-Reference-Cited by-同舟云学术

CD4+TCRαβ+ T-cells developing after allogeneic bone marrow transplantation in patients with chronic myelogenous leukaemia. Dipyridamole inhibits functionally heterogeneous T-cell clones

Published:1991-01 Issue:8 Volume:13 Page:1127-1135
ISSN:0192-0561
Container-title:International Journal of Immunopharmacology
language:en
Short-container-title:International Journal of Immunopharmacology

Author:

Bruserud Øystein,Hamann Wilfried,Patel Sarita,Pawelec Graham

Publisher

Elsevier BV

Subject

Pharmacology,Immunology

Reference25 articles.

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4. Dipyridamol inhibits activation of human T lymphocytes in vitro;Bruserud;Clin. Immun. Immunopath.,1986

5. The additive effect of certain drugs on the Cyclosporine A inhibition of human T-cell proliferation;Bruserud;APMIS,1990

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. IL2- and IL4-dependent proliferation of T-cell clones derived early after allogeneic bone marrow transplantation: Studies of patients with chronic myelogenous leukaemia;European Journal of Haematology;2009-04-24

2. IFN-γ and TNF-α secretion by CD4+ and CD8+ TCRαβ+ T-cell clones derived early after allogeneic bone marrow transplantation;European Journal of Haematology;2009-04-24

3. Human T lymphocyte activation in the presence of acute myelogenous leukaemia blasts; studies of normal polyclonal T cells and T lymphocyte clones derived early after allogeneic bone marrow transplantation;Cancer Immunology, Immunotherapy;1996-05-08

4. Secretion of IL-2, IL-3, IL-4, IL-6 and GM-CSF by CD4+ and CD8+ TCRalphabeta+ T-Cell Clones derived early after Allogeneic Bone Marrow Transplantation;Scandinavian Journal of Immunology;1993-07

5. CD4+ TCRαβ+ T-cell clones derived shortly after allogeneic bone marrow transplantation: Theophyllamine and verapamil inhibit proliferation of functionally heterogeneous T-cells;International Journal of Immunopharmacology;1992-07