Complement as an endogenous adjuvant for dendritic cell-mediated induction of retrovirus-specific CTLs.
Previous studies have demonstrated the involvement of complement (C) in induction of efficient CTL responses against different viral infections, but the exact role of complement in this process has not been determined. We now show that C opsonization of retroviral particles enhances the ability of d...
Main Authors: | , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2010-04-01
|
Series: | PLoS Pathogens |
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20442876/pdf/?tool=EBI |
id |
doaj-cc9f407cf1f7471bba414ce1478bfaa0 |
---|---|
record_format |
Article |
spelling |
doaj-cc9f407cf1f7471bba414ce1478bfaa02021-04-21T17:34:48ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742010-04-0164e100089110.1371/journal.ppat.1000891Complement as an endogenous adjuvant for dendritic cell-mediated induction of retrovirus-specific CTLs.Zoltán BánkiWilfried PoschAsim EjazVerena OberhauserSuzanne WilleyChristoph GassnerHeribert StoiberUlf DittmerManfred P DierichKim J HasenkrugDoris WilflingsederPrevious studies have demonstrated the involvement of complement (C) in induction of efficient CTL responses against different viral infections, but the exact role of complement in this process has not been determined. We now show that C opsonization of retroviral particles enhances the ability of dendritic cells (DCs) to induce CTL responses both in vitro and in vivo. DCs exposed to C-opsonized HIV in vitro were able to stimulate CTLs to elicit antiviral activity significantly better than non-opsonized HIV. Furthermore, experiments using the Friend virus (FV) mouse model illustrated that the enhancing role of complement on DC-mediated CTL induction also occurred in vivo. Our results indicate that complement serves as natural adjuvant for DC-induced expansion and differentiation of specific CTLs against retroviruses.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20442876/pdf/?tool=EBI |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zoltán Bánki Wilfried Posch Asim Ejaz Verena Oberhauser Suzanne Willey Christoph Gassner Heribert Stoiber Ulf Dittmer Manfred P Dierich Kim J Hasenkrug Doris Wilflingseder |
spellingShingle |
Zoltán Bánki Wilfried Posch Asim Ejaz Verena Oberhauser Suzanne Willey Christoph Gassner Heribert Stoiber Ulf Dittmer Manfred P Dierich Kim J Hasenkrug Doris Wilflingseder Complement as an endogenous adjuvant for dendritic cell-mediated induction of retrovirus-specific CTLs. PLoS Pathogens |
author_facet |
Zoltán Bánki Wilfried Posch Asim Ejaz Verena Oberhauser Suzanne Willey Christoph Gassner Heribert Stoiber Ulf Dittmer Manfred P Dierich Kim J Hasenkrug Doris Wilflingseder |
author_sort |
Zoltán Bánki |
title |
Complement as an endogenous adjuvant for dendritic cell-mediated induction of retrovirus-specific CTLs. |
title_short |
Complement as an endogenous adjuvant for dendritic cell-mediated induction of retrovirus-specific CTLs. |
title_full |
Complement as an endogenous adjuvant for dendritic cell-mediated induction of retrovirus-specific CTLs. |
title_fullStr |
Complement as an endogenous adjuvant for dendritic cell-mediated induction of retrovirus-specific CTLs. |
title_full_unstemmed |
Complement as an endogenous adjuvant for dendritic cell-mediated induction of retrovirus-specific CTLs. |
title_sort |
complement as an endogenous adjuvant for dendritic cell-mediated induction of retrovirus-specific ctls. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Pathogens |
issn |
1553-7366 1553-7374 |
publishDate |
2010-04-01 |
description |
Previous studies have demonstrated the involvement of complement (C) in induction of efficient CTL responses against different viral infections, but the exact role of complement in this process has not been determined. We now show that C opsonization of retroviral particles enhances the ability of dendritic cells (DCs) to induce CTL responses both in vitro and in vivo. DCs exposed to C-opsonized HIV in vitro were able to stimulate CTLs to elicit antiviral activity significantly better than non-opsonized HIV. Furthermore, experiments using the Friend virus (FV) mouse model illustrated that the enhancing role of complement on DC-mediated CTL induction also occurred in vivo. Our results indicate that complement serves as natural adjuvant for DC-induced expansion and differentiation of specific CTLs against retroviruses. |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20442876/pdf/?tool=EBI |
work_keys_str_mv |
AT zoltanbanki complementasanendogenousadjuvantfordendriticcellmediatedinductionofretrovirusspecificctls AT wilfriedposch complementasanendogenousadjuvantfordendriticcellmediatedinductionofretrovirusspecificctls AT asimejaz complementasanendogenousadjuvantfordendriticcellmediatedinductionofretrovirusspecificctls AT verenaoberhauser complementasanendogenousadjuvantfordendriticcellmediatedinductionofretrovirusspecificctls AT suzannewilley complementasanendogenousadjuvantfordendriticcellmediatedinductionofretrovirusspecificctls AT christophgassner complementasanendogenousadjuvantfordendriticcellmediatedinductionofretrovirusspecificctls AT heribertstoiber complementasanendogenousadjuvantfordendriticcellmediatedinductionofretrovirusspecificctls AT ulfdittmer complementasanendogenousadjuvantfordendriticcellmediatedinductionofretrovirusspecificctls AT manfredpdierich complementasanendogenousadjuvantfordendriticcellmediatedinductionofretrovirusspecificctls AT kimjhasenkrug complementasanendogenousadjuvantfordendriticcellmediatedinductionofretrovirusspecificctls AT doriswilflingseder complementasanendogenousadjuvantfordendriticcellmediatedinductionofretrovirusspecificctls |
_version_ |
1714665970702745600 |