Immunization with recombinant transferrin binding protein B enhances clearance of nontypeable Haemophilus influenzae from the rat lung

被引:29
|
作者
Webb, DC
Cripps, AW
机构
[1] Australian Natl Univ, John Curtin Sch Med Res, Leukocyte Signalling & Regulat Lab, Membrane Biochem Grp,Div Biochem & Mol Biol, Canberra, ACT 2601, Australia
[2] Univ Canberra, Gadi Res Ctr, Fac Sci Appl, Canberra, ACT 2601, Australia
关键词
D O I
10.1128/IAI.67.5.2138-2144.1999
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nontypeable Haemophilus influenzae (NTHI) is an opportunistic pathogen, and heterogeneity in the surface-exposed immunodominant domains of NTHI proteins is thought to be associated with the failure of an infection to stimulate an immune response that is cross protective against heterologous NTHI strains. The aim of this study was to assess the vaccine potential of a surface exposed component of the NTHI human transferrin receptor, TbpB, and to determine if the antibody response elicited was cross-reactive with heterologous strains of NTHI, The efficacy of immunization with a recombinant form of TbpB (rTbpB) was determined by assessing the pulmonary clearance of viable bacteria 4 h after a live challenge with NTHI, There was a significant reduction in the number of viable bacteria in both the bronchoalveolar lavage fluid (34% for the 20-mu g dose and 58% for the 40-mu g dose) and lung homogenates (26% for the 20-mu g dose and 60% for the 40-mu g dose) of rats immunized with rTbpB compared to the control animals. While rTbpB-specific antibodies from immunized rats were nonspecific in the recognition of TbpB from six heterologous NTHI strains on Western blots, these antibodies differed in their ability to block transferrin binding to heterologous strains and to cross-react in bactericidal assays, If bactericidal antibodies are key indicators of the efficacy of the immune response in eliminating NTHI, this data suggests that while immunization with rTbpB stimulates protective responses against the homologous isolate, variability in the recognition of TbpB from heterologous isolates may limit the potential of rTbpB as an NTHI vaccine component.
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收藏
页码:2138 / 2144
页数:7
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