Journal of Leukocyte Biology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Originally published online as doi:10.1189/jlb.1204701 on March 14, 2005

Published online before print March 14, 2005
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
jlb.1204701v1
77/6/923    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Balmelli, C.
Right arrow Articles by Summerfield, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Balmelli, C.
Right arrow Articles by Summerfield, A.
(Journal of Leukocyte Biology. 2005;77:923-933.)
© 2005 by Society for Leukocyte Biology

Fibrocytes are potent stimulators of anti-virus cytotoxic T cells

Carole Balmelli, Nicolas Ruggli, Kenneth McCullough and Artur Summerfield1

Institute of Virology and Immunoprophylaxis, Mittelhäusern, Switzerland

1Correspondence: Institute of Virology and Immunoprophylaxis, Sensemattstrasse 293, CH-3147 Mittelhäusern, Switzerland. E-mail: Artur.Summerfield{at}ivi.admin.ch

Fibrocytes (Fb) are a population of circulating leukocytes reported to be capable of presenting antigen to CD4+ T lymphocytes. In contrast, no information is available about their capacity to stimulate CD8+ cytolytic T lymphocyte (CTL) responses. To this end, Fb were isolated from porcine blood to investigate their ability to stimulate CTL responses using a classical swine fever virus model. The isolated Fb (referred to as primary Fb) displayed the phenotype previously reported for mouse and human Fb, particularly in terms of the surface proteins necessary for antigen presentation, major histocompatibility complex (MHC) classes I and II, and CD80/86. These primary Fb endocytosed and degraded antigen efficiently. In absence of exogenous stimuli, endocytosis and MHC II expression were lost when the Fb were passaged and cultured. Treatment of such secondary Fb with interferon-{gamma} (IFN-{gamma}) restored the MHC II expression. The primary and secondary Fb were capable of stimulating antigen-specific CD4+ T lymphocytes relating to previous reports. In addition, an efficient stimulation of virus-specific CD8+CTL was measured in terms of CD8+ T cell proliferation, IFN-{gamma} production, and cytotoxic activity. This was noted even at low Fb/T lymphocyte ratios, at which dendritic cells were less efficient. Although IFN-{gamma} pretreatment of Fb was not necessary for this function, it could enhance the Fb activity. These results demonstrate that Fb are efficient, accessory cells for the presentation of viral antigen to specific CD8+ CTL.

Key Words: antigen presentating cells • cellular activation • CD8+ T lymphocytes • swine




This article has been cited by other articles:


Home page
J. Leukoc. Biol.Home page
J. Wang, H. Jiao, T. L. Stewart, M. V. H. Lyons, H. A. Shankowsky, P. G. Scott, and E. E. Tredget
Accelerated wound healing in leukocyte-specific, protein 1-deficient mouse is associated with increased infiltration of leukocytes and fibrocytes
J. Leukoc. Biol., December 1, 2007; 82(6): 1554 - 1563.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
M. Ceppi, M. G. M. de Bruin, T. Seuberlich, C. Balmelli, S. Pascolo, N. Ruggli, D. Wienhold, J. D. Tratschin, K. C. McCullough, and A. Summerfield
Identification of classical swine fever virus protein E2 as a target for cytotoxic T cells by using mRNA-transfected antigen-presenting cells
J. Gen. Virol., September 1, 2005; 86(9): 2525 - 2534.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2005 by the Society for Leukocyte Biology.