Show simple item record

dc.contributor.authorLin, Meei-Yun
dc.contributor.authorSelin, Liisa K.
dc.contributor.authorWelsh, Raymond M.
dc.date2022-08-11T08:09:01.000
dc.date.accessioned2022-08-23T16:15:29Z
dc.date.available2022-08-23T16:15:29Z
dc.date.issued2000-09-01
dc.date.submitted2008-11-05
dc.identifier.citationMicrobes Infect. 2000 Jul;2(9):1025-39.
dc.identifier.issn1286-4579 (Print)
dc.identifier.pmid10967283
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34100
dc.description.abstractCD8 T cells exist in a dynamic network whose repertoire remains static in the absence of infection but changes in the presence of foreign antigens. Individuals each have unique T-cell repertoires that continually evolve in the presence of antigen and of cross-reactive heterologous antigens, and homeostatic forces drive deletions in T-cell memory pools to accommodate the entry of new memory cells into a finite immune system.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=10967283&dopt=Abstract">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/S1286-4579(00)01257-0
dc.subjectAnimals; Antigens, Viral; CD8-Positive T-Lymphocytes; Epstein-Barr Virus Infections; Flow Cytometry; Herpesvirus 4, Human; Interferon Type II; Lymphocytic Choriomeningitis; Lymphocytic choriomeningitis virus; Mice; Mice, Inbred C57BL; Mice, Knockout; Receptors, Antigen, T-Cell, alpha-beta; Spleen; T-Lymphocyte Subsets; Virus Latency
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleEvolution of the CD8 T-cell repertoire during infections
dc.typeJournal Article
dc.source.journaltitleMicrobes and infection / Institut Pasteur
dc.source.volume2
dc.source.issue9
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/764
dc.identifier.contextkey661873
html.description.abstract<p>CD8 T cells exist in a dynamic network whose repertoire remains static in the absence of infection but changes in the presence of foreign antigens. Individuals each have unique T-cell repertoires that continually evolve in the presence of antigen and of cross-reactive heterologous antigens, and homeostatic forces drive deletions in T-cell memory pools to accommodate the entry of new memory cells into a finite immune system.</p>
dc.identifier.submissionpathgsbs_sp/764
dc.contributor.departmentPathology
dc.source.pages1025-39


This item appears in the following Collection(s)

Show simple item record