Class I major histocompatibility complex (MHC)-restricted CD8+ T cells have been demonstrated to be effective mediators of both acquired and adoptive immunity to the intracellular bacterium Listeria monocytogenes. We have recently determined that L. monocytogenes-infected H-2d mice recognize a nonamer peptide, residues 91-99, of the secreted protein listeriolysin O (LLO), in a H-2Kd-restricted fashion. In this report we have generated CD8+ T cell lines with specificity for LLO 91-99 in the context of H-2Kd by in vitro stimulation with P815 (H-2d) cells transfected with LLO. These CD8+ lines have been generated from immune donors after sublethal infection with L. monocytogenes, or after in vivo immunization with syngeneic spleen cells coated with synthetic LLO 91-99 peptide. LLO-specific CD8+ T cells derived from either protocol were capable of significant protection against L. monocytogenes infection. The in vivo protection by these CD8+ T cell lines has been shown to be solely due to recognition of LLO 91-99 in the context of H-2Kd. These studies demonstrate that CD8+ T cell immunity to a single, naturally produced peptide epitope has the potential for significant protection in a bacterial infection. Thus, the allele-specific motif approach to epitope prediction has identified a naturally produced bacterial epitope with biological relevance.
Skip Nav Destination
Article navigation
1 June 1992
Article|
June 01 1992
CD8+ T cells specific for a single nonamer epitope of Listeria monocytogenes are protective in vivo.
J T Harty
,
M J Bevan
Howard Hughes Medical Institute, University of Washington, Seattle 98195.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1992) 175 (6): 1531–1538.
Citation
J T Harty, M J Bevan; CD8+ T cells specific for a single nonamer epitope of Listeria monocytogenes are protective in vivo.. J Exp Med 1 June 1992; 175 (6): 1531–1538. doi: https://doi.org/10.1084/jem.175.6.1531
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionEmail alerts
Advertisement