An evidence is accumulating that the oxygen tension exerts significant effe
ct on the virus replication in vitro. When the in vitro oxygen tension is m
aintained at an in vivo physiological level, as a rule higher yields of hum
an viruses are seen than at conventional culturing with access of an unphys
iologically high oxygen concentration in ambient air. Although not fully un
derstood, possible explanation for this phenomenon may be provided by a low
ered interferon (IFN) output and increased cell replication which is often
optimal at physiological oxygen tension. Furthermore, an indirect evidence
suggests that the expression of some virus receptors is affected by oxygen
ten-cion. Also, the antiviral cell-mediated immunity is likely to be found
oxygen tension-dependent as both the NK and cytotoxic T cell activities tow
ards uninfected target cells are oxygen tension-sensitive. At present, the
in vitro work with viruses at physiological oxygen tensions is hampered by
the fact that cells adapt in the course of several weeks to the new oxygen
tension. Whether viruses may adapt to different oxygen tensions is not clea
r. Workbenches combining safety in manipulation with hazardous viruses and
the convenience of controlled gas atmosphere during both manipulation and l
ong-term incubation have been developed. It is suggested that the in vitro
virology should ensure that the physiological oxygen tension is better mimi
cked in the in vivo processes. Much work is to be done to determine the mol
ecular interactions between oxygen tension-sensitive elements of the cell a
nd infecting viruses. Of no lesser importance are the questions regarding t
he role of oxygen in virus tissue tropism, the cost-benefit of virus produc
tion at different oxygen tension levels, and the potential significance of
oxygen tension for delivering gene effects to the selected target tissues.