Soluble recombinant human metapneumovirus G protein is immunogenic but not protective

被引:35
作者
Ryder, Alex B. [1 ]
Tollefson, Sharon J. [2 ]
Podsiad, Amy B. [2 ]
Johnson, Joyce E. [3 ]
Williams, John V. [1 ,2 ,4 ]
机构
[1] Vanderbilt Univ, Med Ctr, Sch Med, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Pediat, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Dept Pathol, Nashville, TN 37232 USA
[4] Dept Microbiol & Immunol, Nashville, TN USA
基金
美国国家卫生研究院;
关键词
Paramyxovirus; Metapneumovirus; Vaccine; Glycoprotein; OBSTRUCTIVE PULMONARY-DISEASE; RESPIRATORY-TRACT INFECTIONS; FUSION PROTEIN; TRANSPLANT RECIPIENTS; G-GLYCOPROTEIN; COTTON RATS; CHILDREN; VACCINE; ADULTS; MICE;
D O I
10.1016/j.vaccine.2010.04.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:4145 / 4152
页数:8
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