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Prepublished online as a Blood First Edition Paper on May 24, 2002; DOI 10.1182/blood-2002-04-1017.
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Blood, 15 September 2002, Vol. 100, No. 6, pp. 2203-2207
PHAGOCYTES
Hydrocortisone reduced in vivo, inflammation-induced slow rolling
of leukocytes and their extravasation into human conjunctiva
Juha Kirveskari,
Maaret Helintö,
Jukka A. O. Moilanen,
Timo Paavonen,
Timo M. T. Tervo, and
Risto Renkonen
From the Rational Drug Design Program, Biomedicum
Helsinki; the Department of Bacteriology and Immunology and the
Department of Pathology, Haartman Institute, University of Helsinki;
Helsinki University Central Hospital (HUCS) Laboratory Diagnostics; and
the Department of Ophthalmology, Helsinki University Central Hospital,
Helsinki, Finland.
Hydrocortisone reduces the number of inflammatory leukocytes within
tissues, but thus far the site of action on the multistep adhesion
cascade leading to leukocyte extravasation has not been identified. We
have recently developed a noninvasive in vivo reflected-light confocal
microscopy technique to study this at sites of inflammation in human
patients. In the present study, we evaluated the effect of preoperative
intravenous hydrocortisone treatment on leukocyte trafficking after
conjunctival inflammation induced by cataract surgery in human subjects
in vivo. The surgery generated leukocyte rolling along the endothelial
lining of conjunctival vessels. While preoperative hydrocortisone did
not reduce the number of rolling cells, it significantly raised the
velocity of individual rolling leukocytes and concomitantly reduced
leukocyte emigration into conjunctival tissue. Immunohistology of
conjunctival biopsies excised from the individuals studied provided
circumstantial evidence that endothelial P-selectin might play a role
in the surgery-induced up-regulation of the leukocyte rolling.
Furthermore, hydrocortisone reduced surgery-induced P-selectin
induction, suggesting a role for this selectin in the regulation of
local leukocyte traffic into sites of inflammation in human
conjunctiva. Taken together, these results suggest that control of the
rolling velocity might be an effective way to adjust leukocyte traffic
in vivo in human subjects.

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