Scientific Article
previous document  unige:10903  next document
add to browser collection

Transgenic mice expressing high levels of soluble TNF-R1 fusion protein are protected from lethal septic shock and cerebral malaria, and are highly sensitive to Listeria monocytogenes and Leishmania major infections

Miyazaki, Y.
Araki, Kimi
Araki, Masatake
Lucas, R.
Grau, G. E.
Milon, G.
Belkaid, Y.
show hidden authors show all authors [1 - 10]
Published in European Journal of Immunology. 1995, vol. 25, no. 8, p. 2401-2407
Abstract Mice bearing a transgene coding for a soluble tumor necrosis factor receptor type 1 (TNFR1)-FcIgG3 fusion protein and placed under the control of the alpha-1-antitrypsin gene promoter were generated. Depending on the mouse line, blood levels of the protein ranged from 25 ng/ml to over 100 micrograms/ml; this level of expression was most often transmitted to the transgene-bearing progeny as a relatively stable feature. High-expressor mice were completely resistant to lipopolysaccharide-induced shock and lethality, including after D-galactosamine sensitization, and mice expressing about 1 microgram of the fusion protein/ml were partially (60%) protected. In contrast, mice expressing less than 0.1 microgram of the protein/ml were more sensitive than controls with respect to incidence and time of death, even though the biological activity of serum tumor necrosis factor (TNF) was partially neutralized. High-expressor mice of the adequate genetic background were markedly, although not completely, protected from death by cerebral malaria after injection with Plasmodium berghei. They were highly susceptible to Listeria monocytogenes, dying from bacterial dissemination after sublethal infection, and to Leishmania major, displaying severe, non-healing lesions after local infection. Under the same conditions, mice expressing about 1 microgram protein/ml were only partially sensitive to these last agents, compared to non-transgenic littermate mice which were fully resistant. These transgenic mice represent a model of permanent, complete or partial, impairment of TNF use, which compares favorably, for ease of breeding and for the range of effects, to mice bearing gene disruptions.
Keywords AnimalsAntigens, CD/biosynthesis/*physiologyBase Sequence*Leishmania majorLeishmaniasis, Cutaneous/*immunologyListeria Infections/*immunologyMalaria, Cerebral/*prevention & controlMiceMice, TransgenicMolecular Sequence DataReceptors, Tumor Necrosis Factor/biosynthesis/*physiologyReceptors, Tumor Necrosis Factor, Type IRecombinant Fusion Proteins/biosynthesis/physiologyShock, Septic/*prevention & controlTumor Necrosis Factor-alpha/antagonists & inhibitors
Stable URL
Full text
PMID: 7664802

120 hits

0 download


Deposited on : 2010-08-26

Export document
Format :
Citation style :