EPITOPE SPECIFICITY OF H-2K(B)-RESTRICTED, HSV-1-CROSS-REACTIVE, AND HSV-2-CROSS-REACTIVE CYTOTOXIC T-LYMPHOCYTE CLONES

被引:87
作者
BONNEAU, RH
SALVUCCI, LA
JOHNSON, DC
TEVETHIA, SS
机构
[1] PENN STATE UNIV, MILTON S HERSHEY MED CTR, COLL MED, DEPT MICROBIOL & IMMUNOL, HERSHEY, PA 17033 USA
[2] MCMASTER UNIV, DEPT PATHOL, MOLEC VIROL & IMMUNOL PROGRAM, HAMILTON L8N 3Z5, ONTARIO, CANADA
关键词
D O I
10.1006/viro.1993.1346
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
HSV-1-specific and HSV-1/HSV-2-cross-reactive H-2Kb-restricted cytotoxic T lymphocyte (CTL) clones were derived from a pool of splenic memory CTL (CTLm) obtained from HSV-l-infected C57BL/6 mice. Two of the HSV-1/HSV-2-cross-reactive CTL clones recognized HSV gB since H-2b cells infected with a recombinant adenovirus vector expressing HSV glycoprotein B (gB) provided a target for these CTL clones. The CTL recognition epitope was precisely defined as HSV-1 gB residues 498-505 using synthetic peptides and conforms to a predicted H-2Kb-binding motif. Immunization of C57BL/6 mice with the free synthetic peptide corresponding to this predicted minimal epitope (HSV-1 gB498-505) resulted in the generation of HSV-gB epitope-specific CD8+ CTL in the popliteal lymph nodes. The peptide-induced CTL recognize and lyse HSV-1 infected H-2b cells or cells pulsed with the synthetic peptide, gB498-505. The availability of CTL clones directed to this predicted minimal HSV CTL epitope should be helpful in understanding processing of HSV glycoprotein B and presentation of this CTL recognition epitope. © 1993 Academic Press. All rights reserved.
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页码:62 / 70
页数:9
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