TY - JOUR
T1 - Evidence that α-fetoprotein suppresses the immunological function in transgenic mice
AU - Yamashita, Tadashi
AU - Nakane, Akio
AU - Watanabe, Tomomasa
AU - Miyoshi, Ichiro
AU - Kasai, Noriyuki
PY - 1994/6/30
Y1 - 1994/6/30
N2 - We examined the in vivo immunosuppressive effect of alpha-fetoprotein (AFP) by infection experiments with Listeria monocytogenes, a facultative intracellular pathogen, using transgenic mice that express and produce human AFP. The transgenic mice showed diminished ability to eliminate bacteria in the early stage of infection. In addition, the transgenic mice had significantly reduced production of IFN-γ in their livers and sera and TNF in their spleens. These data indicate that AFP suppresses the production of the cytokines, IFN-γ and TNF in NK cells and macrophages so that the mice could not eliminate the bacteria. This is the first report that AFP has an in vivo immunosuppressive effect on cytokine production related to the early host defense against infection by microorganisms.
AB - We examined the in vivo immunosuppressive effect of alpha-fetoprotein (AFP) by infection experiments with Listeria monocytogenes, a facultative intracellular pathogen, using transgenic mice that express and produce human AFP. The transgenic mice showed diminished ability to eliminate bacteria in the early stage of infection. In addition, the transgenic mice had significantly reduced production of IFN-γ in their livers and sera and TNF in their spleens. These data indicate that AFP suppresses the production of the cytokines, IFN-γ and TNF in NK cells and macrophages so that the mice could not eliminate the bacteria. This is the first report that AFP has an in vivo immunosuppressive effect on cytokine production related to the early host defense against infection by microorganisms.
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U2 - 10.1006/bbrc.1994.1826
DO - 10.1006/bbrc.1994.1826
M3 - Article
C2 - 7517667
AN - SCOPUS:0028168746
SN - 0006-291X
VL - 201
SP - 1154
EP - 1159
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -