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 Gram-negative bacterial infection, endotoxemia and its toxic sequelae.
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August 2011
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Conference Article|
July 20 2011
Deficient expression of bactericidal/permeability-increasing protein in immunocompromised hosts: translational potential of replacement therapy Available to Purchase
Christine D. Palmer;
Christine D. Palmer
*Children's Hospital Boston, 300 Longwood Avenue, Boston, MA 02115, U.S.A.
†Harvard Medical School, Boston, MA 02115, U.S.A.
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Eva C. Guinan;
Eva C. Guinan
*Children's Hospital Boston, 300 Longwood Avenue, Boston, MA 02115, U.S.A.
†Harvard Medical School, Boston, MA 02115, U.S.A.
‡Dana Farber Cancer Institute, Boston, MA 02115, U.S.A.
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Ofer Levy
Ofer Levy
1
*Children's Hospital Boston, 300 Longwood Avenue, Boston, MA 02115, U.S.A.
†Harvard Medical School, Boston, MA 02115, U.S.A.
1To whom correspondence should be addressed (email [email protected]).
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Publisher: Portland Press Ltd
Received:
January 13 2011
Online ISSN: 1470-8752
Print ISSN: 0300-5127
© The Authors Journal compilation © 2011 Biochemical Society
2011
Biochem Soc Trans (2011) 39 (4): 994–999.
Article history
Received:
January 13 2011
Citation
Christine D. Palmer, Eva C. Guinan, Ofer Levy; Deficient expression of bactericidal/permeability-increasing protein in immunocompromised hosts: translational potential of replacement therapy. Biochem Soc Trans 1 August 2011; 39 (4): 994–999. doi: https://doi.org/10.1042/BST0390994
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