La. Cohn et al., Plasma granulocyte colony-stimulating factor concentrations in neutropenic, parvoviral enteritis-infected puppies, J VET INT M, 13(6), 1999, pp. 581-586
We evaluated the temporal relationship between neutrophil numbers and plasm
a granulocyte colony-stimulating factor (G-CSF) concentrations in dogs infe
cted with canine parvovirus, a common infectious cause of neutropenia. G-CS
F is produced in response to neutropenia, infection, or inflammation, and r
esults in the production and release of neutrophils from the bone marrow. A
dequate numbers of functional neutrophils are necessary for protection from
infection, and the timely production of G-CSF is a crucial response to cer
tain diseases. The relationship between peripheral neutrophil numbers and p
lasma G-CSF concentrations during the course of an infectious disease chara
cterized by neutropenia has not been described previously in dogs. Eight mi
xed-breed puppies were given an oronasal challenge with canine parvovirus,
and peripheral neutrophil numbers as well as plasma G-CSF concentrations we
re measured daily. G-CSF was not detectable in plasma of any dog before the
onset of neutropenia, but G-CSF became detectable just after the onset of
neutropenia in the 7 dogs that developed clinical illness. Neutropenia pers
isted or worsened for at least 2 days after plasma G-CSF became detectable
in all 7 dogs, Neutrophil nadir, the highest plasma G-CSF concentrations, a
nd the most severe clinical illness occurred concurrently in most dogs. Alt
hough 1 dog died while still neutropenic, plasma G CSF concentrations decli
ned before resolution of neutropenia in the other 6 dogs, and were again be
low the limits of detection in 5 of the 6 dogs at the time of resolution.