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Department of Immunochemistry and Biochemical Microbiology, Research Center Borstel, 23845 Borstel, Germany
CD34+ hematopoietic stem cells, which circulate in peripheral blood with very low frequency, exert essential accessory function during lipopolysaccharide (LPS)-induced human T lymphocyte activation, resulting in interferon
production and proliferation. In contrast, stimulation of T cells by "conventional" recall antigens is not controlled by blood stem cells. These conclusions are based on the observation that depletion of CD34+ blood stem cells results in a loss of LPS-induced T cell stimulation as well as reduced expression of CD80 antigen on monocytes. The addition of CD34-enriched blood stem cells resulted in a recovery of reactivity of T cells and monocytes to LPS. Blood stem cells could be replaced by the hematopoietic stem cell line KG-1a. These findings may be of relevance for high risk patients treated with stem cells or stem cell recruiting compounds and for patients suffering from endotoxin-mediated diseases.
Key Words: antigen presentation immunity, cellular immunoreactivity immunocompetence lymphocyte cooperation
This work was financially supported by the Deutsche Forschungsgemeinschaft (SFB 367, project C5) and the Fond der Chemischen Industrie (to H.D. Flad and E.T. Rietschel).
Abbreviations used: GaM, goat anti–mouse; HS, human serum; PPD, purified protein derivative; TT, tetanus toxoid.
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