pubmed-article:7685408 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:7685408 | lifeskim:mentions | umls-concept:C0020971 | lld:lifeskim |
pubmed-article:7685408 | lifeskim:mentions | umls-concept:C0042214 | lld:lifeskim |
pubmed-article:7685408 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:7685408 | lifeskim:mentions | umls-concept:C1332717 | lld:lifeskim |
pubmed-article:7685408 | lifeskim:mentions | umls-concept:C1706438 | lld:lifeskim |
pubmed-article:7685408 | lifeskim:mentions | umls-concept:C0039195 | lld:lifeskim |
pubmed-article:7685408 | lifeskim:mentions | umls-concept:C0085358 | lld:lifeskim |
pubmed-article:7685408 | lifeskim:mentions | umls-concept:C1413244 | lld:lifeskim |
pubmed-article:7685408 | lifeskim:mentions | umls-concept:C2698600 | lld:lifeskim |
pubmed-article:7685408 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
pubmed-article:7685408 | pubmed:issue | 7 | lld:pubmed |
pubmed-article:7685408 | pubmed:dateCreated | 1993-7-12 | lld:pubmed |
pubmed-article:7685408 | pubmed:abstractText | The M2 protein of respiratory syncytial virus (RSV) is a protective antigen in H-2d, but not H-2b or H-2k mice. None of the other RSV proteins, excluding the surface glycoproteins that induce neutralizing antibodies, is protective in mice bearing these haplotypes. Thus, the M2 protein stands alone as a nonglycoprotein-protective antigen of RSV. The M2 protein is a target for murine Kd-restricted cytotoxic T lymphocytes (CTLs), and the resistance induced by infection with a vaccinia virus-RSV M2 (vac-M2) recombinant is mediated by CD8+ CTLs. Since the nonameric consensus sequence for H-2 Kd-restricted T-cell epitopes and the amino acid sequence of the M2 protein of subgroup A and B strains of RSV are known, the present study sought to identify the specific epitope(s) on the M2 protein recognized by CD8+ CTLs. This was done by examining the ability of four predicted Kd-specific motif peptides present in the M2 amino acid sequence of an RSV subgroup A strain to sensitize target cells for lysis by pulmonary or splenic CTLs obtained from mice infected with RSV or vac-M2. The following observations were made. First, two of the four peptides sensitized target cells for lysis by pulmonary or splenic CTLs induced by infection with either vac-M2 or RSV. Second, one of the two peptides, namely the 82-90 (M2) peptide, sensitized targets at a very low peptide concentration (10(-10) to 10(-12) M). Third, cold-target competition experiments revealed that the predominant CTL population induced by infection with vac-M2 or RSV recognized the 82-90 (M2) peptide, and this CTL population appeared to recognize the 71-79 (M2) peptide in a cross-reactive manner. Fourth, CTL recognition of targets sensitized with either the 71-79 (M2) or the 82-90 (M2) peptide was Kd restricted. Fifth, CTLs induced by infection with RSV subgroup A or B strains recognized the two M2 peptides. The findings suggest that the M2 protein of RSV contains an immunodominant Kd-restricted CTL epitope consisting of amino acid residues 82 to 90 (SYIGSINNI), which are shared by subgroup A and B RSVs. | lld:pubmed |
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pubmed-article:7685408 | pubmed:language | eng | lld:pubmed |
pubmed-article:7685408 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7685408 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:7685408 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7685408 | pubmed:month | Jul | lld:pubmed |
pubmed-article:7685408 | pubmed:issn | 0022-538X | lld:pubmed |
pubmed-article:7685408 | pubmed:author | pubmed-author:MorseH CHC3rd | lld:pubmed |
pubmed-article:7685408 | pubmed:author | pubmed-author:BenninkJ RJR | lld:pubmed |
pubmed-article:7685408 | pubmed:author | pubmed-author:YewdellJ WJW | lld:pubmed |
pubmed-article:7685408 | pubmed:author | pubmed-author:MurphyB RBR | lld:pubmed |
pubmed-article:7685408 | pubmed:author | pubmed-author:KulkarniA BAB | lld:pubmed |
pubmed-article:7685408 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7685408 | pubmed:volume | 67 | lld:pubmed |
pubmed-article:7685408 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7685408 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:7685408 | pubmed:pagination | 4086-92 | lld:pubmed |
pubmed-article:7685408 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:7685408 | pubmed:year | 1993 | lld:pubmed |
pubmed-article:7685408 | pubmed:articleTitle | Immunization of mice with vaccinia virus-M2 recombinant induces epitope-specific and cross-reactive Kd-restricted CD8+ cytotoxic T cells. | lld:pubmed |
pubmed-article:7685408 | pubmed:affiliation | Respiratory Viruses Section, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892. | lld:pubmed |
pubmed-article:7685408 | pubmed:publicationType | Journal Article | lld:pubmed |
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