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PMID: 11859143 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, P.H.S.

Depletion of dendritic cells, but not macrophages, in patients with sepsis.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 168 ·No. 5 ·2002-03-01 ·Pages 2493-500

Hotchkiss RS, Tinsley KW, Swanson PE, Grayson MH, Osborne DF, Wagner TH, Cobb JP, Coopersmith C, Karl IE

Abstract

Dendritic cells (DCs) are a group of APCs that have an extraordinary capacity to interact with T and B cells and modulate their responses to invading pathogens. Although a number of defects in the immune system have been identified in sepsis, few studies have examined the effect of sepsis on DCs, which is the purpose of this study. In addition, this study investigated the effect of sepsis on macrophages, which are reported to undergo apoptosis, and MHC II expression, which has been noted to be decreased in sepsis. Spleens from 26 septic patients and 20 trauma patients were evaluated by immunohistochemical staining. Although sepsis did not decrease the number of macrophages, sepsis did cause a dramatic reduction in the percentage area of spleen occupied by FDCs, i.e., 2.9 +/- 0.4 vs 0.7 +/- 0.2% in trauma and septic patients, respectively. The number of MHC II-expressing cells, including interdigitating DCs, was decreased in septic, compared with trauma, patients. However, sepsis did not appear to induce a loss of MHC II expression in those B cells, macrophages, or DCs that were still present. The dramatic loss of DCs in sepsis may significantly impair B and T cell function and contribute to the immune suppression that is a hallmark of the disorder.

MeSH Terms
Adolescent Adult Aged Antigens, CD/analysis,immunology Antigens, Differentiation, Myelomonocytic/analysis,immunology Apoptosis Dendritic Cells/immunology Female Histocompatibility Antigens Class II/analysis,immunology Humans Immunohistochemistry Lipopolysaccharide Receptors/analysis,immunology Macrophages/immunology Male Middle Aged Receptors, Complement 3d/analysis,immunology Sepsis/diagnosis,immunology Spleen/immunology
Chemicals
Antigens, CD Antigens, Differentiation, Myelomonocytic CD68 antigen, human Histocompatibility Antigens Class II Lipopolysaccharide Receptors Receptors, Complement 3d
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Hotchkiss Richard S
Department of Anesthesiology, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, USA. hotch@morpheus.wustl.edu
Tinsley Kevin W
Swanson Paul E
Grayson Mitchell H
Osborne Dale F
Wagner Tracey H
Cobb J Perren
Coopersmith Craig
Karl Irene E
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
2002-03-01
Pages
2493-500
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIGMS NIH HHS · GM 44118 · United States
NIGMS NIH HHS · GM 55194 · United States
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