作者: Kaiming Zhang , Xinhua Li , Guohua Yin , Yufeng Liu , Xuyuan Tang
DOI: 10.1111/J.1600-0625.2009.01016.X
关键词: Cytotoxic T cell 、 Bone marrow 、 Interleukin 3 、 Immunology 、 Interleukin 12 、 CD40 、 CD34 、 Biology 、 Haematopoiesis 、 Interleukin 21
摘要: Please cite this paper as: Functional characterization of T cells differentiated in vitro from bone marrow-derived CD34+ psoriatic patients with family history. Experimental Dermatology 2010; 19: e128–e135. Abstract Background: The strong but complex genetic background suggests that inherent and intrinsic rather than exogenous factors have a key role immunopathogenesis psoriasis. It is reasonable to speculate the dysfunctional activity may partly originate abnormal haematopoietic cells. Objectives: To test if originated progenitor psoriasis display functional alternations similar previously reported abnormalities circulating cells. Methods: Bone marrow were isolated history healthy subjects, into thymic stromal co-culture system. These further subjected comparisons such as proliferation, secretion cytokines IL-4, IL-8 IFN–γ, inducing production C-myc, Bcl-xL, Ki67 proteins human keratinocytes. Results: While both volunteers developed mature within weeks environment vitro, showed higher proliferation stronger capacity secret TH1 response streptococcal superantigen. patients, not normal controls, induced overexpression C-myc Ki67, Bcl-XL, keratinocytes. Conclusions: are functionally cells, suggesting can be traced back early development cells.