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Infection and Immunity, April 2000, p. 1840-1848, Vol. 68, No. 4
Department of Infectious and Tropical
Diseases, London School of Hygiene and Tropical Medicine, London,
United Kingdom
Received 15 October 1999/Returned for modification 22 November
1999/Accepted 4 January 2000
In this study, we have analyzed hematopoietic activity in the
spleen, bone marrow, and blood of BALB/c and scid mice
infected with Leishmania donovani. Our analysis
demonstrates that infection induces a rapid but transient mobilization
of progenitor cells into the circulation, associated with elevated
levels of granulocyte/macrophage colony-stimulating factor (GM-CSF) and
MIP-1
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Enhanced Hematopoietic Activity Accompanies
Parasite Expansion in the Spleen and Bone Marrow of Mice Infected
with Leishmania donovani
. From 14 to 28 days postinfection, when parasite expansion
begins in the spleen and bone marrow, both the frequency and cell cycle
activity of hematopoietic progenitors, particulary CFU-granulocyte,
monocyte, are dramatically increased in these organs. This is
associated with increased accumulation of mRNA for GM-CSF, M-CSF, and
G-CSF, but not interleukin-3. Our data also illustrate that
hematopoietic activity, as assessed by changes in the frequency of
progenitor cell populations and their levels of cell cycle activity,
can be regulated in both a T-cell-independent and T-cell-dependent, as
well as in an organ-specific, manner. Collectively, these data add to
our knowledge of the long-term changes which occur in organs in which
L. donovani is able to persist.
*
Corresponding author. Mailing address: Department of
Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT United Kingdom. Phone: 44 171 927 2390. Fax: 44 171 323 5687. E-mail:
paul.kaye{at}lshtm.ac.uk.
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