Progress made towards the development of a CMV peptide vaccine
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Paston, SJ
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UCL Royal Free & Univ Coll Med Sch, Anthony Nolan Res Inst, London NW3 2QG, EnglandUCL Royal Free & Univ Coll Med Sch, Anthony Nolan Res Inst, London NW3 2QG, England
Paston, SJ
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Dodi, .A
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UCL Royal Free & Univ Coll Med Sch, Anthony Nolan Res Inst, London NW3 2QG, EnglandUCL Royal Free & Univ Coll Med Sch, Anthony Nolan Res Inst, London NW3 2QG, England
Dodi, .A
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Madrigal, JA
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UCL Royal Free & Univ Coll Med Sch, Anthony Nolan Res Inst, London NW3 2QG, EnglandUCL Royal Free & Univ Coll Med Sch, Anthony Nolan Res Inst, London NW3 2QG, England
Madrigal, JA
[1
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[1] UCL Royal Free & Univ Coll Med Sch, Anthony Nolan Res Inst, London NW3 2QG, England
Cytomegalovirus disease still remains a major cause of morbidity and mortality in hematopoietic stem cell transplantation recipients. The cell-mediated immune response is essential in the maintenance of latency and the resolution of primary infections. The identification of immunodominant cytomegalovirus antigens has enabled researchers to determine the best candidate antigens to be included in a cytomegalovirus vaccine. Such a vaccine would have to stimulate both a cell-mediated and humoral immune response. Recent advances have enabled the rapid identification of minimal cytotoxic epitopes required to trigger such responses. Epitope mapping to date has mainly focused on the pp65 antigen but other antigens such as IE1 are starting to be mapped. A human leukocyte antigen allele hierarchy is starting to emerge that is dependent on the alleles present in an individual; this is relevant when considering what peptides should be included in a vaccine. This review looks at the current methods available for epitope mapping and the progress that has been made to date. Human Immunology 65, 544-549 (2004). (C) American Society for Histocompatibility and Immunogenetics, 2004. Published by Elsevier Inc.
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Univ Oxford, Hosp Trop Dis, Wellcome Trust Major Overseas Programme, Clin Res Unit, Ho Chi Minh City, VietnamJohn Radcliffe Hosp, Dept Infect Dis & Microbiol, Oxford OX3 9DU, England
Farrar, Jeremy
Rowland-Jones, Sarah
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Univ Oxford, Human Immunol Unit, Weatherall Inst Mol Med, Oxford, EnglandJohn Radcliffe Hosp, Dept Infect Dis & Microbiol, Oxford OX3 9DU, England
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Duke Univ, Sch Med, Human Vaccine Inst, Durham, NC USADuke Univ, Sch Med, Human Vaccine Inst, Durham, NC USA
Bialas, Kristy M.
Permar, Sallie R.
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Duke Univ, Sch Med, Human Vaccine Inst, Durham, NC USA
Duke Univ, Dept Pediat, Sch Med, Durham, NC 27706 USADuke Univ, Sch Med, Human Vaccine Inst, Durham, NC USA
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PO Royal Brisbane Hosp, Queensland Inst Med Res, Australian Ctr Vaccine Dev, Brisbane, Qld 4029, AustraliaPO Royal Brisbane Hosp, Queensland Inst Med Res, Australian Ctr Vaccine Dev, Brisbane, Qld 4029, Australia
Batzloff, Michael R.
McMillan, David
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PO Royal Brisbane Hosp, Queensland Inst Med Res, Australian Ctr Vaccine Dev, Brisbane, Qld 4029, AustraliaPO Royal Brisbane Hosp, Queensland Inst Med Res, Australian Ctr Vaccine Dev, Brisbane, Qld 4029, Australia
McMillan, David
Pandey, Manisha
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PO Royal Brisbane Hosp, Queensland Inst Med Res, Australian Ctr Vaccine Dev, Brisbane, Qld 4029, AustraliaPO Royal Brisbane Hosp, Queensland Inst Med Res, Australian Ctr Vaccine Dev, Brisbane, Qld 4029, Australia