Korean J Pathol.
2000 Jan;34(1):11-19.
The Effects of CD11c/CD18 and CD14 Blocking on Lipopolysaccharide-induced Endotoxemia
- Affiliations
-
- 1Department of Anatomic Pathology, Masan Samsung Hospital, Sungkyunkwan
University School of Medicine, Masan 630-522, Korea.
- 2Department of Pathology, College of Medicine, Kyungpook National University.
Abstract
-
We studied the morphologic changes and the expression of cytokines of major organs
by blocking CD14 and CD11c/CD18, which are known to be receptors of lipopolysaccharide
(LPS), in the LPS induced endotoxemic mice. In 2 and 8 hours after initial intraperitoneal
injection of 10 mg/kg of LPS into the mice, 500 microgram/kg of anti-CD14 antibody (Ab) and/or
the same dosage of the anti-CD11c/CD18 Ab were administered intravenously, respectively or
concomitantly. Under the light microscope, the LPS only and the LPS with the anti-CD14 Ab
injected groups (group 1 and 2) showed marked acute inflammation in the organs, especially
in the lung and liver, but the LPS with the anti-CD11c/CD18 Ab only or with both
anti-CD14 and anti-CD11c Abs injected groups (group 3 and 4) revealed only mild acute
inflammation. Under the electron microscope, there was marked inflammation in the group 1
and 2 such as marked infiltration of neutrophils, monocytes/ macrophages, lymphocytes,
aggregation of platelets, and marked edematous change of endothelial cells with separation
from the basement membrane. However in the group 3 and 4, there was only mild
inflammation such as mild infiltration of neutrophils in the tissue or aggregation of
neutrophils in the capillaries and sinusoids with mild endothelial swelling. The expressions of
tumor necrosis factor-alpha (TNF-alpha) and interleukin-1alpha (IL-1alpha), detected by RT-PCR method,
was remarkable in the group 2, but minimal in the group 3 and 4. We conclude that blocking
the CD11c/CD18 with anti-CD11C/CD18 Ab is effective for the prohibition of biologic
reactions and diminution of the inflammation induced by the LPS, even in the LPS induced
endotoxemia.