Source:http://linkedlifedata.com/resource/pubmed/id/19005468
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7226
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pubmed:dateCreated |
2009-1-8
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pubmed:abstractText |
Memory CD8 T cells, generated by natural pathogen exposure or intentional vaccination, protect the host against specific viral infections. It has long been proposed that the number of memory CD8 T cells in the host is inflexible, and that individual cells are constantly competing for limited space. Consequently, vaccines that introduce over-abundant quantities of memory CD8 T cells specific for an agent of interest could have catastrophic consequences for the host by displacing memory CD8 T cells specific for all previous infections. To test this paradigm, we developed a vaccination regimen in mice that introduced as many new long-lived memory CD8 T cells specific for a single vaccine antigen as there were memory CD8 T cells in the host before vaccination. Here we show that, in contrast to expectations, the size of the memory CD8 T-cell compartment doubled to accommodate these new cells, a change due solely to the addition of effector memory CD8 T cells. This increase did not affect the number of CD4 T cells, B cells or naive CD8 T cells, and pre-existing memory CD8 T cells specific for a previously encountered infection were largely preserved. Thus, the number of effector memory CD8 T cells in the mammalian host adapts according to immunological experience. Developing vaccines that abundantly introduce new memory CD8 T cells should not necessarily ablate pre-existing immunity to other infections.
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pubmed:grant | |
pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD44,
http://linkedlifedata.com/resource/pubmed/chemical/Cd44 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Immunodominant Epitopes,
http://linkedlifedata.com/resource/pubmed/chemical/L-Selectin,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Vaccines
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1476-4687
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
8
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pubmed:volume |
457
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
196-9
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pubmed:dateRevised |
2009-6-4
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pubmed:meshHeading |
pubmed-meshheading:19005468-Animals,
pubmed-meshheading:19005468-Antigens, CD44,
pubmed-meshheading:19005468-B-Lymphocytes,
pubmed-meshheading:19005468-CD4-Positive T-Lymphocytes,
pubmed-meshheading:19005468-CD8-Positive T-Lymphocytes,
pubmed-meshheading:19005468-Cells, Cultured,
pubmed-meshheading:19005468-Immunodominant Epitopes,
pubmed-meshheading:19005468-Immunologic Memory,
pubmed-meshheading:19005468-L-Selectin,
pubmed-meshheading:19005468-Lymphocyte Count,
pubmed-meshheading:19005468-Lymphocytic choriomeningitis virus,
pubmed-meshheading:19005468-Mice,
pubmed-meshheading:19005468-Mice, Inbred C57BL,
pubmed-meshheading:19005468-Vaccination,
pubmed-meshheading:19005468-Viral Vaccines
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pubmed:year |
2009
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pubmed:articleTitle |
Memory CD8 T-cell compartment grows in size with immunological experience.
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pubmed:affiliation |
Department of Microbiology and Center for Immunology, University of Minnesota, Minneapolis, Minnesota 55455, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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