Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2001-2-22
pubmed:abstractText
Cytotoxic T lymphocytes (CTLs) are an important defense against human immunodeficiency virus (HIV) type 1 but ultimately fail to control infection. To determine whether more efficient sustained immunity is induced by suppressing replication, the evolution of T cell phenotypes and HIV-specific CD8+ lymphocytes was prospectively investigated in 41 patients initiating combination therapy. Suppression of viremia to <200 copies/mL was associated with increases in naive cells (CD45RA+62L+) and declines in activated T cells (CD95+ cell counts and CD38+ HLA-DR+). HIV-specific tetramer-staining CD8+ T cells were detected in 6 of 10 HLA-A*0201-positive persons, which declined in 5 with treatment. CTL precursor frequencies were markedly consistent before and after treatment. Eight (72%) of 11 recognized > or =1 immunodominant epitope, representing either a new or an increased CTL response after treatment. Thus, activated CD8+ T cells, including those recognizing immunodominant epitopes, decline with combination therapy. However, the overall level of antigen-specific cells that are capable of differentiating into effectors remains stable, and the recognition of new epitopes may occur.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0022-1899
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
183
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
722-9
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:11181148-Anti-HIV Agents, pubmed-meshheading:11181148-Antigens, CD45, pubmed-meshheading:11181148-CD4 Lymphocyte Count, pubmed-meshheading:11181148-CD8-Positive T-Lymphocytes, pubmed-meshheading:11181148-Dose-Response Relationship, Immunologic, pubmed-meshheading:11181148-Drug Therapy, Combination, pubmed-meshheading:11181148-Epitopes, T-Lymphocyte, pubmed-meshheading:11181148-Flow Cytometry, pubmed-meshheading:11181148-HIV Infections, pubmed-meshheading:11181148-HIV-1, pubmed-meshheading:11181148-HLA-DR Antigens, pubmed-meshheading:11181148-Humans, pubmed-meshheading:11181148-Immunodominant Epitopes, pubmed-meshheading:11181148-Immunohistochemistry, pubmed-meshheading:11181148-Immunophenotyping, pubmed-meshheading:11181148-Indinavir, pubmed-meshheading:11181148-Lamivudine, pubmed-meshheading:11181148-Prospective Studies, pubmed-meshheading:11181148-Protein Tyrosine Phosphatase, Non-Receptor Type 1, pubmed-meshheading:11181148-T-Lymphocytes, Cytotoxic, pubmed-meshheading:11181148-Viral Load, pubmed-meshheading:11181148-Zidovudine
pubmed:year
2001
pubmed:articleTitle
Alterations in T cell phenotype and human immunodeficiency virus type 1-specific cytotoxicity after potent antiretroviral therapy.
pubmed:affiliation
Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
pubmed:publicationType
Journal Article, Clinical Trial, Research Support, U.S. Gov't, P.H.S.