Schlüter D, Bertsch D, Frei K, Hübers S B, Wiestler O D, Hof H, Fontana A, Deckert-Schlüter M
Institut für Med. Mikrobiologie und Hygiene, Klinikum Mannheim, Fakultät für Klinische Medizin der Universität Heidelberg, Germany.
J Neuroimmunol. 1998 Jan;81(1-2):38-48. doi: 10.1016/s0165-5728(97)00156-2.
The in vivo modulating activity of recombinant transforming growth factor (TGF)-beta2 on acute toxoplasmosis was evaluated in both Toxoplasma gondii susceptible C57BL/6 and resistant BALB/c mice. TGF-beta2 lethally exacerbated Toxoplasma encephalitis in C57BL/6, but not in BALB/c mice. In C57BL/6 mice, TGF-beta2 induced a profound dose-dependent increase of the intracerebral parasitic load as well as a reduction of IFN-gamma levels in serum and cerebrospinal fluid with a coincident decrease of MHC class II antigen expression of macrophages, microglial cells, and B cells. Furthermore, TGF-beta2-treated C57BL/6 mice showed a reduced activation of CD4+ and CD8+ T cells and a diminished recruitment of immune cells to the brain. The TGF-beta2-mediated development of lethal toxoplasmosis in C57BL/6 mice was abolished by treatment with recombinant interferon (IFN)-gamma.