z-logo
open-access-imgOpen Access
Expression of Granzyme B during Primary Cytomegalovirus Infection after Renal Transplantation
Author(s) -
Peter C. Wever,
L.H.A Spaeny,
Hans van Vliet,
Rob J. Rentenaar,
Angela M. Wolbink,
Janto Surachno,
P Wertheim,
P T Schellekens,
C. Erik Hack,
Ineke J. M. ten Berge
Publication year - 1999
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/314629
Subject(s) - granzyme b , lymphocytosis , immunology , cd8 , transplantation , cytomegalovirus , betaherpesvirinae , granzyme , immune system , cytotoxic t cell , medicine , biology , virus , herpesviridae , perforin , viral disease , biochemistry , in vitro
CD8+ T cells employ granzyme B (GrB) to induce apoptosis in target cells. Increased expression of GrB has been put forward as a diagnostic marker in transplant rejection and viral infection. Three-color flow cytometric analysis revealed that peripheral blood CD8+ T lymphocytosis during primary cytomegalovirus infection after renal transplantation resulted from expansion of a CD8+GrB+CD62L+ T cell subset that was almost absent during stable transplant function or acute rejection. This expansion coincided with a temporary increase in systemic soluble GrB (sGrB) levels. No such increase was observed during stable transplant function or acute rejection. Thus, the primary immune response to cytomegalovirus infection is accompanied by appearance of CD8+GrB+CD62L+ T cells and increased sGrB levels in the peripheral blood compartment. Determination of the latter may provide a novel approach for monitoring viral infections.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom