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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
1995-5-11
pubmed:abstractText
In a previous analysis of HIV-1-specific CTLs in lymphoid organs from HIV-seropositive patients, we reported high frequencies of in vivo differentiated CTLs directed against two immunodominant regions in the central and in the C-terminal part of the HIV-1 Nef protein. The present study analyzes the epitopes recognized by CTLs in the carboxyl terminus of Nef (amino acids 182-205). In addition to several epitopes that are recognized in association with different HLA molecules (A1, A2, A25(10), B35, B52), we defined an optimal nonapeptide (190-198). This nonapeptide was recognized by CTLs down to nanomolar concentrations in the context of at least two HLA molecules, HLA-B52 and HLA-A2, including three HLA-A2 subtypes: HLA-A2.1, -A2.2, and -A2.4. We also determined the relative frequencies of effector CTLs directed against peptide 190-198 to be as high as 10(-4), as opposed to lower frequencies ranging between 5 x 10(-5) and 5 x 10(-6) observed for the other peptides recognized in the same region, thus confirming the optimal presentation of this nonapeptide in vivo. Molecular modeling of the interactions between HLA-A2.1 and Nef peptide 190-198 suggests the formation of a stable complex and allowed us to study sequence motifs that are important for the binding of the HIV-1 peptide in the pockets of the HLA-A2.1 molecule.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
154
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4174-86
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:7535824-Base Sequence, pubmed-meshheading:7535824-Computer Simulation, pubmed-meshheading:7535824-Cytotoxicity, Immunologic, pubmed-meshheading:7535824-Epitope Mapping, pubmed-meshheading:7535824-Epitopes, pubmed-meshheading:7535824-Gene Products, nef, pubmed-meshheading:7535824-HIV Antigens, pubmed-meshheading:7535824-HIV Seropositivity, pubmed-meshheading:7535824-HIV-1, pubmed-meshheading:7535824-HLA-A2 Antigen, pubmed-meshheading:7535824-HLA-B Antigens, pubmed-meshheading:7535824-HLA-B52 Antigen, pubmed-meshheading:7535824-Humans, pubmed-meshheading:7535824-Immunity, Cellular, pubmed-meshheading:7535824-Lymph Nodes, pubmed-meshheading:7535824-Models, Molecular, pubmed-meshheading:7535824-Molecular Sequence Data, pubmed-meshheading:7535824-Protein Binding, pubmed-meshheading:7535824-Spleen, pubmed-meshheading:7535824-T-Lymphocytes, Cytotoxic, pubmed-meshheading:7535824-nef Gene Products, Human Immunodeficiency Virus
pubmed:year
1995
pubmed:articleTitle
CTLs from lymphoid organs recognize an optimal HLA-A2-restricted and HLA-B52-restricted nonapeptide and several epitopes in the C-terminal region of HIV-1 Nef.
pubmed:affiliation
Laboratory for Cellular and Tissue Immunology, University Hospital Center Pitié-Salpétrière, Paris, France.
pubmed:publicationType
Journal Article, In Vitro, Research Support, Non-U.S. Gov't