Deficient expression of bactericidal/permeability-increasing protein in immunocompromised hosts: Translational potential of replacement therapy

Christine D. Palmer, Eva C. Guinan, Ofer Levy*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

BPI (bactericidal/permeability-increasing protein) is a 55 kDa anti-infective molecule expressed in neutrophil and eosinophil granules and on some epithelial cells. BPI's high affinity for the lipid A region of endotoxin targets its opsonizing, microbicidal and endotoxin-neutralizing activities towards Gram-negative bacteria. Several immunocompromised patient populations demonstrate BPI deficiency, including newborns, those with anti-neutrophil cytoplasmic antibodies (as in cystic fibrosis and HIV infection) and those exposed to radiochemotherapy. BPI may be replenished by administering agents that induce its expression or by administration of recombinant BPI congeners, potentially shielding BPI-deficient individuals against Gramnegative bacterial infection, endotoxemia and its toxic sequelae.

Original languageEnglish
Pages (from-to)994-999
Number of pages6
JournalBiochemical Society Transactions
Volume39
Issue number4
DOIs
StatePublished - Aug 2011
Externally publishedYes

Funding

FundersFunder number
National Institute of Allergy and Infectious DiseasesR01AI067353

    Keywords

    • Antibody (Ab)
    • Bactericidal/permeability-increasing protein (BPI)
    • Cystic fibrosis (CF)
    • Host defence
    • Lipoxin (LX)

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