Cargando…

Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help

Class I–restricted presentation is usually associated with cytoplasmic degradation of cellular proteins and is often considered inaccessible to exogenous antigens. Nonetheless, certain exogenous elements can gain entry into this so-called endogenous pathway by a mechanism termed cross-presentation....

Descripción completa

Detalles Bibliográficos
Autores principales: Bennett, Sally R.M., Carbone, Francis R., Karamalis, Freda, Miller, Jacques F.A.P., Heath, William R.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2198964/
https://www.ncbi.nlm.nih.gov/pubmed/9206998
_version_ 1782148102369574912
author Bennett, Sally R.M.
Carbone, Francis R.
Karamalis, Freda
Miller, Jacques F.A.P.
Heath, William R.
author_facet Bennett, Sally R.M.
Carbone, Francis R.
Karamalis, Freda
Miller, Jacques F.A.P.
Heath, William R.
author_sort Bennett, Sally R.M.
collection PubMed
description Class I–restricted presentation is usually associated with cytoplasmic degradation of cellular proteins and is often considered inaccessible to exogenous antigens. Nonetheless, certain exogenous elements can gain entry into this so-called endogenous pathway by a mechanism termed cross-presentation. This is known to be effective for class I–restricted cytotoxic T lymphocyte (CTL) cross-priming directed against a variety of exogenous tumor, viral, and minor transplantation antigens. The related effect of cross-tolerance can also effectively eliminate responses to selected self components. In both cases, this presentation appears to require the active involvement of a bone marrow–derived antigen presenting cell (APC). Here, we show that CTL induction by cross-priming with cell-associated ovalbumin requires the active involvement of CD4(+) helper T cells. Importantly, this CD4(+) population is only effective when both the helper and CTL determinants are recognized on the same APC. Moreover, we would argue that the cognitive nature of this event suggests that the CD4(+) T cell actively modifies the APC, converting it into an effective stimulator for the successful priming of the CTL precursor.
format Text
id pubmed-2198964
institution National Center for Biotechnology Information
language English
publishDate 1997
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21989642008-04-16 Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help Bennett, Sally R.M. Carbone, Francis R. Karamalis, Freda Miller, Jacques F.A.P. Heath, William R. J Exp Med Article Class I–restricted presentation is usually associated with cytoplasmic degradation of cellular proteins and is often considered inaccessible to exogenous antigens. Nonetheless, certain exogenous elements can gain entry into this so-called endogenous pathway by a mechanism termed cross-presentation. This is known to be effective for class I–restricted cytotoxic T lymphocyte (CTL) cross-priming directed against a variety of exogenous tumor, viral, and minor transplantation antigens. The related effect of cross-tolerance can also effectively eliminate responses to selected self components. In both cases, this presentation appears to require the active involvement of a bone marrow–derived antigen presenting cell (APC). Here, we show that CTL induction by cross-priming with cell-associated ovalbumin requires the active involvement of CD4(+) helper T cells. Importantly, this CD4(+) population is only effective when both the helper and CTL determinants are recognized on the same APC. Moreover, we would argue that the cognitive nature of this event suggests that the CD4(+) T cell actively modifies the APC, converting it into an effective stimulator for the successful priming of the CTL precursor. The Rockefeller University Press 1997-07-07 /pmc/articles/PMC2198964/ /pubmed/9206998 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Bennett, Sally R.M.
Carbone, Francis R.
Karamalis, Freda
Miller, Jacques F.A.P.
Heath, William R.
Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help
title Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help
title_full Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help
title_fullStr Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help
title_full_unstemmed Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help
title_short Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help
title_sort induction of a cd8(+) cytotoxic t lymphocyte response by cross-priming requires cognate cd4(+) t cell help
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2198964/
https://www.ncbi.nlm.nih.gov/pubmed/9206998
work_keys_str_mv AT bennettsallyrm inductionofacd8cytotoxictlymphocyteresponsebycrossprimingrequirescognatecd4tcellhelp
AT carbonefrancisr inductionofacd8cytotoxictlymphocyteresponsebycrossprimingrequirescognatecd4tcellhelp
AT karamalisfreda inductionofacd8cytotoxictlymphocyteresponsebycrossprimingrequirescognatecd4tcellhelp
AT millerjacquesfap inductionofacd8cytotoxictlymphocyteresponsebycrossprimingrequirescognatecd4tcellhelp
AT heathwilliamr inductionofacd8cytotoxictlymphocyteresponsebycrossprimingrequirescognatecd4tcellhelp