MHC class i-restricted cytotoxic lymphocyte responses induced by enterotoxin-based mucosal adjuvants

<p style="text-align:justify;">The ability of enterotoxin-based mucosal adjuvants to induce CD8+ MHC class I-restricted CTL responses to a codelivered bystander Ag was examined. Escherichia coli heat-labile toxin (LT), or derivatives of LT carrying mutations in the A subunit (LTR72,...

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Κύριοι συγγραφείς: Simmons, C, Mastroeni, P, Fowler, R, Ghaem-Maghami, M, Lycke, N, Pizza, M, Rappuoli, R, Dougan, G
Μορφή: Journal article
Γλώσσα:English
Έκδοση: American Association of Immunologists 1999
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author Simmons, C
Mastroeni, P
Fowler, R
Ghaem-Maghami, M
Lycke, N
Pizza, M
Rappuoli, R
Dougan, G
author_facet Simmons, C
Mastroeni, P
Fowler, R
Ghaem-Maghami, M
Lycke, N
Pizza, M
Rappuoli, R
Dougan, G
author_sort Simmons, C
collection OXFORD
description <p style="text-align:justify;">The ability of enterotoxin-based mucosal adjuvants to induce CD8+ MHC class I-restricted CTL responses to a codelivered bystander Ag was examined. Escherichia coli heat-labile toxin (LT), or derivatives of LT carrying mutations in the A subunit (LTR72, LTK63), were tested in parallel with cholera toxin (CT) or a fusion protein consisting of the A1 subunit of CT fused to the Ig binding domain of Staphylococcus aureus protein A (called CTA1-DD). Intranasal (i.n.) immunization of C57BL/6 mice with CT, CTA1-DD, LT, LTR72, LTK63, but not rLT-B, elicited MHC class I-restricted CD8+ T cell responses to coadministered OVA or the OVA CTL peptide SIINFEKL (OVA257–264). CT, LT, and LTR72 also induced CTL responses to OVA after s.c. or oral coimmunization whereas LTK63 only activated responses after s.c. coimmunization. rLT-B was unable to adjuvant CTL responses to OVA or OVA257–264 administered by any route. Mice treated with an anti-CD4 mAb to deplete CD4+ T cells mounted significant OVA-specific CTL responses after i.n. coadministration of LT with OVA or OVA257–264. Both 51Cr release assays and IFN-γ enzyme-linked immunospot assays indicated that IFN-γ−/− and IL-12 p40−/− gene knockout mice developed CTL responses equivalent to those detected in normal C57BL/6 mice. The results highlight the versatility of toxin-based adjuvants and suggest that LT potentiates CTL responses independently of IL-12 and IFN-γ and probably by a mechanism unrelated to cross-priming. </p>
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spelling oxford-uuid:de943f35-444b-4ba5-a3c0-ffaa353ff27f2022-03-27T09:33:12ZMHC class i-restricted cytotoxic lymphocyte responses induced by enterotoxin-based mucosal adjuvantsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:de943f35-444b-4ba5-a3c0-ffaa353ff27fEnglishSymplectic Elements at OxfordAmerican Association of Immunologists1999Simmons, CMastroeni, PFowler, RGhaem-Maghami, MLycke, NPizza, MRappuoli, RDougan, G <p style="text-align:justify;">The ability of enterotoxin-based mucosal adjuvants to induce CD8+ MHC class I-restricted CTL responses to a codelivered bystander Ag was examined. Escherichia coli heat-labile toxin (LT), or derivatives of LT carrying mutations in the A subunit (LTR72, LTK63), were tested in parallel with cholera toxin (CT) or a fusion protein consisting of the A1 subunit of CT fused to the Ig binding domain of Staphylococcus aureus protein A (called CTA1-DD). Intranasal (i.n.) immunization of C57BL/6 mice with CT, CTA1-DD, LT, LTR72, LTK63, but not rLT-B, elicited MHC class I-restricted CD8+ T cell responses to coadministered OVA or the OVA CTL peptide SIINFEKL (OVA257–264). CT, LT, and LTR72 also induced CTL responses to OVA after s.c. or oral coimmunization whereas LTK63 only activated responses after s.c. coimmunization. rLT-B was unable to adjuvant CTL responses to OVA or OVA257–264 administered by any route. Mice treated with an anti-CD4 mAb to deplete CD4+ T cells mounted significant OVA-specific CTL responses after i.n. coadministration of LT with OVA or OVA257–264. Both 51Cr release assays and IFN-γ enzyme-linked immunospot assays indicated that IFN-γ−/− and IL-12 p40−/− gene knockout mice developed CTL responses equivalent to those detected in normal C57BL/6 mice. The results highlight the versatility of toxin-based adjuvants and suggest that LT potentiates CTL responses independently of IL-12 and IFN-γ and probably by a mechanism unrelated to cross-priming. </p>
spellingShingle Simmons, C
Mastroeni, P
Fowler, R
Ghaem-Maghami, M
Lycke, N
Pizza, M
Rappuoli, R
Dougan, G
MHC class i-restricted cytotoxic lymphocyte responses induced by enterotoxin-based mucosal adjuvants
title MHC class i-restricted cytotoxic lymphocyte responses induced by enterotoxin-based mucosal adjuvants
title_full MHC class i-restricted cytotoxic lymphocyte responses induced by enterotoxin-based mucosal adjuvants
title_fullStr MHC class i-restricted cytotoxic lymphocyte responses induced by enterotoxin-based mucosal adjuvants
title_full_unstemmed MHC class i-restricted cytotoxic lymphocyte responses induced by enterotoxin-based mucosal adjuvants
title_short MHC class i-restricted cytotoxic lymphocyte responses induced by enterotoxin-based mucosal adjuvants
title_sort mhc class i restricted cytotoxic lymphocyte responses induced by enterotoxin based mucosal adjuvants
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