Hostname: page-component-848d4c4894-75dct Total loading time: 0 Render date: 2024-06-08T09:38:36.436Z Has data issue: false hasContentIssue false

MCP-1 and MIP-2 levels during Echinococcus granulosus infections in mice

Published online by Cambridge University Press:  07 February 2017

Y. Theodorides
Affiliation:
Laboratory of Parasitology, Aristotle University of Thessaloniki, 54006 Thessaloniki, Greece
S. Frydas*
Affiliation:
Laboratory of Parasitology, Aristotle University of Thessaloniki, 54006 Thessaloniki, Greece
T. Rallis
Affiliation:
Department of Clinical Studies, Aristotle University of Thessaloniki, 54006 Thessaloniki, Greece
K. Adamama-Moraitou
Affiliation:
Department of Clinical Studies, Aristotle University of Thessaloniki, 54006 Thessaloniki, Greece
R. Papazahariadou
Affiliation:
Laboratory of Parasitology, Aristotle University of Thessaloniki, 54006 Thessaloniki, Greece
C. Batzios
Affiliation:
Laboratory of Economics of Animal Production, Faculty of Veterinary Medicine, Aristotle University of Thessaloniki, 54006 Thessaloniki, Greece
P. Conti
Affiliation:
Immunology Division, School of Medicine, University of Chieti, Italy
*
*Author for correspondence Fax: +30 31 999947 E-mail: trallis@vet.auth.gr

Abstract

Ten BALB/c mice were infected with the cestode Echinococcus granulosus. After the infection, serum was collected at different periods of time and monocyte chemotactic protein-1 (MCP-1) and macrophage inflammatory protein-2 (MIP-2) were determined. The level of MCP-1 increased from 290±12 pg ml-1 (mean±SD) at day 20 post infection (p.i.), to a maximum of 820±23 pg ml-1 on day 60 p.i., then decreased to 460±12.6 pg ml-1 on day 130 p.i. A second peak was observed at day 150 p.i. In addition, MIP-2 was detectable in serum as late as day 100 p.i. The highest level (100±11 pg ml-1) was observed on day 130 p.i., and decreased thereafter. Serum from noninfected animals (controls) contained no detectable levels of either MCP-1 or MIP-2. However, MCP-1 and MIP-2 appear to be implicated in E. granulosus infections, but their exact role during the disease is under determination.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2001

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)