期刊
VACCINE
卷 28, 期 25, 页码 4145-4152出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2010.04.007
关键词
Paramyxovirus; Metapneumovirus; Vaccine; Glycoprotein
资金
- National Institute of Allergy and Infectious Diseases, National Institutes of Health [K08 AI-56170]
- Vanderbilt Department of Pediatrics Hazinski-Turner Award
- Infectious Diseases Society of America Summer Scholarship for Medical Students Award
Human metapneumovirus (HMPV) expresses the major surface glycoproteins F and G. We evaluated the protective efficacy of immunization with G. We generated a recombinant form of G ectodomain (G Delta TM) that was secreted from mammalian cells and purified by affinity chromatography. We tested the immunogenicity of G Delta TM in cotton rats. Animals were immunized with PBS, G Delta TM alone or adjuvanted, or were infected once with HMPV, and challenged with live HMPV at 28 days. Animals vaccinated with adjuvanted and non-adjuvanted G Delta TM developed high levels of serum antibodies to both recombinant and native G protein; however, vaccinated animals did not develop neutralizing antibodies and were not protected against virus challenge. Unlike the analogous non-fusion glycoproteins of other human paramyxoviruses, HMPV G does not appear to be a protective antigen. This represents an unusual feature of HMPV. (C) 2010 Elsevier Ltd. All rights reserved.
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