Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
14
pubmed:dateCreated
1995-3-16
pubmed:abstractText
Influenza A/PR/8/34-derived chimeric (D) protein (SK&F 106160) composed of the first 81 amino acids (aa) of NS1 fused to the conserved 157 C-terminal aa of HA2 (NS1 1-81-HA2 65-222) was previously shown to induce H-2d-restricted protective cytotoxic T-lymphocyte (CTL) immunity in inbred mice. However, D protein, like other small peptides, exhibited haplotype dependence and was not immunogenic in H-2b and H-2K mice. A potential use of this antigen in humans and the role of T cells in any protection were evaluated in outbred Swiss and inbred CBF6F1 (H-2d/b) mice. Mice immunized with D protein and challenged by small-particle aerosol with a lethal dose of influenza virus were significantly protected against mortality from influenza A/H1N1 and A/H2N2 (p < 0.05-< 0.0000001), but not from A/H3N2 and influenza B viruses when compared with control mice. D protein did not induce serum virus-neutralizing antibody but caused virus to be cleared faster in immunized mice. Protection was long-lasting. In vivo depletion of either Lyt2 (CD8+) or L3T4 (CD4+) T cells with monoclonal antibodies led to abrogation of in vitro-generated CTL activity in CF6F1 mice and significant reduction in the protective efficacy of D protein against virus challenge in both Swiss and CF6F1 mice. These results suggest that protection was mediated by CD8+ and/or CD4+ cells and not antibody. Thus D protein, via a conserved sequence on the HA2 polypeptide, has the potential to induce partially cross-reactive CTL that may protect against influenza virus disease in humans.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0264-410X
pubmed:author
pubmed:issnType
Print
pubmed:volume
12
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1340-8
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:7856302-Aerosols, pubmed-meshheading:7856302-Animals, pubmed-meshheading:7856302-CD4-Positive T-Lymphocytes, pubmed-meshheading:7856302-CD8-Positive T-Lymphocytes, pubmed-meshheading:7856302-Cross Reactions, pubmed-meshheading:7856302-Cytotoxicity Tests, Immunologic, pubmed-meshheading:7856302-Female, pubmed-meshheading:7856302-Flow Cytometry, pubmed-meshheading:7856302-Influenza A virus, pubmed-meshheading:7856302-Influenza Vaccines, pubmed-meshheading:7856302-Mice, pubmed-meshheading:7856302-Mice, Inbred BALB C, pubmed-meshheading:7856302-Mice, Inbred C57BL, pubmed-meshheading:7856302-Neutralization Tests, pubmed-meshheading:7856302-Orthomyxoviridae Infections, pubmed-meshheading:7856302-Recombinant Proteins, pubmed-meshheading:7856302-Vaccines, Synthetic, pubmed-meshheading:7856302-Viral Proteins, pubmed-meshheading:7856302-Virus Replication
pubmed:year
1994
pubmed:articleTitle
Influenza A subtype cross-protection after immunization of outbred mice with a purified chimeric NS1/HA2 influenza virus protein.
pubmed:affiliation
Department of Microbiology and Immunology, Baylor College of Medicine, Houston, TX 77030-3498.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.