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Enhanced expression of LAG-3 on lymphocyte subpopulations from persistently lymphocytotic cattle infected with bovine leukemia virus.

Authors :
Konnai S
Suzuki S
Shirai T
Ikebuchi R
Okagawa T
Sunden Y
Mingala CN
Onuma M
Murata S
Ohashi K
Source :
Comparative immunology, microbiology and infectious diseases [Comp Immunol Microbiol Infect Dis] 2013 Jan; Vol. 36 (1), pp. 63-9. Date of Electronic Publication: 2012 Nov 10.
Publication Year :
2013

Abstract

An immunoinhibitory receptor, lymphocyte activation gene-3 (LAG-3), which is mainly expressed in T-cells, is involved in the immune evasion of several pathogens causing chronic infections and tumors. However, unlike human or mouse LAG-3, no functional analysis of LAG-3 has been reported in domestic animals. Thus, in this study, bovine LAG-3 expression was analyzed in bovine leukemia virus (BLV)-infected cattle. In persistent lymphocytotic (PL) cattle, the numbers of LAG-3(+)CD4(+) cells and LAG-3(+)CD8(+) cells were conserved whilst the number of MHC class II(+) cells was remarkably higher than in the control animals. In contrast, the mean fluorescence intensity (MFI) for LAG-3 on PBMCs from PL cattle was significantly increased compared to control and asymptomatic (AL) cattle. Specifically, the LAG-3 expression level was significantly increased in both CD4(+) and CD8(+) T cells from PL cattle. LAG-3 expression correlated positively with increased numbers of lymphocytes and MHC class II(+) cells in infected animals. Preliminary results from PD-L1 and LAG-3 blockade assay revealed that IFN-γ and IL-2 expressions were significantly up-regulated by addition of anti- PD-L1 and LAG-3 antibodies in PBMCs from PL cattle. These findings suggest that LAG-3 might be involved in the inhibition of T-cell function through its binding and signaling on MHC class II molecule during BLV infection.<br /> (Copyright © 2012 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1878-1667
Volume :
36
Issue :
1
Database :
MEDLINE
Journal :
Comparative immunology, microbiology and infectious diseases
Publication Type :
Academic Journal
Accession number :
23146685
Full Text :
https://doi.org/10.1016/j.cimid.2012.09.005