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PMID: 2965302 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A prospective study of platelets and plasma proteolytic systems during the early stages of Rocky Mountain spotted fever.

The New England journal of medicine ·Vol. 318 ·No. 16 ·1988-04-21 ·Pages 1021-8

Rao AK, Schapira M, Clements ML, Niewiarowski S, Budzynski AZ, Schmaier AH, Harpel PC, Blackwelder WC, Scherrer JR, Sobel E

Abstract

We prospectively examined early changes in platelets and plasma proteolytic systems in 12 vaccinated and 6 unvaccinated volunteers in whom Rocky Mountain spotted fever developed after challenge with Rickettsia rickettsii. The platelet counts declined while the plasma concentration of beta-thromboglobulin and the ratio of beta-thromboglobulin to platelet factor 4 increased, indicating in vivo activation of platelets. Plasma levels of antithrombin III decreased and levels of fibrinopeptide A increased, indicating in vivo activation of the coagulation system. Plasma fibrinogen levels peaked at 24 hours and gradually declined; this is consistent with the behavior of fibrinogen as an acute-phase reactant. Prolongation of the prothrombin time and a decrease in plasma levels of factor VII in the absence of evidence of liver injury suggested possible activation of the extrinsic pathway of coagulation. A decline in plasma prekallikrein levels with an increase in plasma C1-inhibitor-kallikrein complexes suggested activation of kallikrein, probably through the intrinsic coagulation system. Elevations in levels of plasma fibrin-degradation products and alpha 2-antiplasmin-plasmin complexes with declines in plasminogen and alpha 2-antiplasmin levels provided evidence of activation of the fibrinolytic system. Elevated plasma levels of tissue plasminogen activator and von Willebrand factor reflected endothelial stimulation. Thus, even early in the course of Rocky Mountain spotted fever that is treated promptly, there is activation of platelets, coagulation pathways, and the fibrinolytic system. These changes may be related to endothelial perturbation, a major pathogenetic mechanism in the disorder.

MeSH Terms
Antithrombin III/analysis Blood Coagulation Factor VII/analysis Fibrin Fibrinogen Degradation Products/analysis Fibrinogen/analysis Fibrinolysis Fibrinopeptide A/analysis Humans Platelet Count Platelet Factor 4/analysis Prekallikrein/analysis Prospective Studies Prothrombin Time Rocky Mountain Spotted Fever/blood,immunology Vaccination beta-Thromboglobulin/analysis von Willebrand Factor/analysis
Chemicals
Fibrin Fibrinogen Degradation Products beta-Thromboglobulin von Willebrand Factor Fibrinopeptide A Platelet Factor 4 Antithrombin III Factor VII Fibrinogen Prekallikrein
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Rao A K
Thrombosis Research Center, Temple University School of Medicine, Philadelphia, PA 19140.
Schapira M
Clements M L
Niewiarowski S
Budzynski A Z
Schmaier A H
Harpel P C
Blackwelder W C
Scherrer J R
Sobel E
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
0028-4793
Published
1988-04-21
Pages
1021-8
Language
English
Region
United States
NLM ID
0255562
Subset
IM
Grants
NHLBI NIH HHS · HL-14217 · United States
NHLBI NIH HHS · HL-33337 · United States
NIAID NIH HHS · N0IAI 12666 · United States
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