A P5 peptide that is homologous to peptide 10 of OprF from Pseudomonas aeruginosa enhances clearance of nontypeable Haemophilus influenzae from acutely infected rat lung in the absence of detectable peptide-specific antibody
被引:13
作者:
Webb, DC
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机构:Australian Natl Univ, John Curtin Sch Med Res, Leukocyte Signaling & Regulat Lab, Membrane Biochem Grp,Div Biochem & Mol Biol, Canberra, ACT 2601, Australia
Webb, DC
Cripps, AW
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机构:Australian Natl Univ, John Curtin Sch Med Res, Leukocyte Signaling & Regulat Lab, Membrane Biochem Grp,Div Biochem & Mol Biol, Canberra, ACT 2601, Australia
Cripps, AW
机构:
[1] Australian Natl Univ, John Curtin Sch Med Res, Leukocyte Signaling & Regulat Lab, Membrane Biochem Grp,Div Biochem & Mol Biol, Canberra, ACT 2601, Australia
[2] Univ Canberra, Gadi Res Ctr, Fac Appl Sci & Design, Canberra, ACT 2601, Australia
Nontypeable Haemophilus influenzae (NTHi) is an opportunistic pathogen associated with otitis media and the exacerbation of chronic bronchitis. This study reports the vaccine potential of three peptides representing conserved regions of the NTHi P5 outer membrane protein which have been fused to a promiscuous measles virus F protein T-cell eptitope (MVF). The peptides correspond to a region in surface loop one (MVF/L1A), the central region of loop four (MVF/L4), and a C-terminal region homologous to peptide 10 of OprF from Pseudomonas aeruginosa (MVF/H3). Immunization of rats with MVF/H3 was the most efficacious in significantly reducing the number of viable NTHi in both the broncho-alveolar lavage fluid (74%) and lung homogenates (70%), compared to control rats. Importantly, despite significantly increased rates of clearance, immunization with MVF/H3 elicited poor antibody responses, suggesting that cell-mediated rather than humoral responses play an important role in the enhanced clearance of NTHi in this model.
机构:
LOUISIANA STATE UNIV, MED CTR, SCH MED, DEPT MICROBIOL & IMMUNOL, SHREVEPORT, LA 71130 USALOUISIANA STATE UNIV, MED CTR, SCH MED, DEPT MICROBIOL & IMMUNOL, SHREVEPORT, LA 71130 USA
Hughes, EE
;
Gilleland, HE
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机构:
LOUISIANA STATE UNIV, MED CTR, SCH MED, DEPT MICROBIOL & IMMUNOL, SHREVEPORT, LA 71130 USALOUISIANA STATE UNIV, MED CTR, SCH MED, DEPT MICROBIOL & IMMUNOL, SHREVEPORT, LA 71130 USA
机构:
LOUISIANA STATE UNIV, MED CTR, SCH MED, DEPT MICROBIOL & IMMUNOL, SHREVEPORT, LA 71130 USALOUISIANA STATE UNIV, MED CTR, SCH MED, DEPT MICROBIOL & IMMUNOL, SHREVEPORT, LA 71130 USA
Hughes, EE
;
Gilleland, HE
论文数: 0引用数: 0
h-index: 0
机构:
LOUISIANA STATE UNIV, MED CTR, SCH MED, DEPT MICROBIOL & IMMUNOL, SHREVEPORT, LA 71130 USALOUISIANA STATE UNIV, MED CTR, SCH MED, DEPT MICROBIOL & IMMUNOL, SHREVEPORT, LA 71130 USA