IN-VIVO PRODUCTION OF TUMOR-NECROSIS-FACTOR-ALPHA AND INTERLEUKIN-6 IN BALB C MICE INOCULATED INTRANASALLY WITH A HIGH-DOSE OF RESPIRATORY SYNCYTIAL VIRUS/
Pj. Hayes et al., IN-VIVO PRODUCTION OF TUMOR-NECROSIS-FACTOR-ALPHA AND INTERLEUKIN-6 IN BALB C MICE INOCULATED INTRANASALLY WITH A HIGH-DOSE OF RESPIRATORY SYNCYTIAL VIRUS/, Journal of medical virology, 42(4), 1994, pp. 323-329
Intranasal administration of an inoculum of 10(7) focus-forming units
(FFU) of respiratory syncytial (RS) virus induced disease in BALB/c mi
ce with signs of anorexia, cachexia, ruffled fur, and pneumonia. Mice
displayed mild signs of illness on day 1 postinoculation (PI), followe
d by a transient recovery phase of 3 days. Disease rapidly reappeared
on day 5 PI and worsened on subsequent days, with mortalities by day 7
PI. Mice inoculated with 5 x 10(6) FFU exhibited milder signs of dise
ase, while those inoculated with 2 x 10(6) FFU and control mice given
only Hep-2c cell suspension exhibited no noticeable signs of illness.
High levels of bioactive tumour necrosis factor-alpha (TNF-alpha) and
interleukin-6 (IL-6) were detected in both lungs and sera of mice inoc
ulated with 10(7) FFU of virus. Peak levels of both cytokines were det
ected at day 1 PI but remained detectable throughout the 7 day period
studied postinoculation. Cytokine levels were much lower or were undet
ectable in control mice. These results suggest that the macrophage is
stimulated in vivo to produce inflammatory cytokines in response to RS
virus infection. (C) 1994 Wiley-Liss, Inc.