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CD4+ T-Cell Responses Against the VP1- Unique Region in Individuals with Recent and Persistent Parvovirus B19 Infection.

Authors :
Lindner, J.
Barabas, S.
Saar, K.
Altmann, D.
Pfister, A.
Fleck, M.
Deml, L.
Modrow, S.
Source :
Journal of Veterinary Medicine Series B; Sep2005, Vol. 52 Issue 7/8, p356-361, 6p, 1 Diagram, 1 Chart, 2 Graphs
Publication Year :
2005

Abstract

To date cellular immune responses against parvovirus B19 (B19) have not been studied extensively. The aim of this study was to examine the T-cell response against the VP1- unique region as the immunodominant part of the viral structural protein VP1 in individuals with different courses of B19 infection. Therefore, a group of 13 parvovirus-positive probands was separated into subgroups characterized for recent or acute, past or persistent infection by means of the presence of specific immunoglobulin (Ig)M and IgG isotypes and of viral DNA in blood and tissue. Transiently transfected B-cells expressing VP1- unique region were used in ELISpot assays to investigate T-cell responses directed against the VP1- unique region in peripheral blood mononuclear cells (PBMC) of individual donors. Significant numbers of interferon- γ (IFN- γ) secreting lymphocytes were detectable in PBMC of all individuals with recent, acute or persistent B19 infection, but not in PBMC of donors with past B19 infection and seronegative individuals. A more detailed analysis of IFN- γ producing cells by intracellular cytokine staining by flow cytometry revealed, that CD4<superscript>+</superscript> T cells but not CD8<superscript>+</superscript> cytotoxic lymphocytes (CTL) were the major subpopulation of IFN- γ producing cells. These data strongly suggest the need of virus protein production for the maintenance of VP1- unique region-specific CD4<superscript>+</superscript> T-helper cell responses in B19-infected individuals. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09311793
Volume :
52
Issue :
7/8
Database :
Complementary Index
Journal :
Journal of Veterinary Medicine Series B
Publication Type :
Academic Journal
Accession number :
18712168
Full Text :
https://doi.org/10.1111/j.1439-0450.2005.00860.x