Bangert, Mathieu, Wright, Adam, Rylance, J., Kelly, M. J., Wright, Angela, Carlone, G. M., Sampson, J. S., Rajam, G., Ades, E. W., Kadioglu, A. and Gordon, Stephen ORCID: https://orcid.org/0000-0001-6576-1116 (2013) 'Immunoactivating Peptide P4 Augments Alveolar Macrophage Phagocytosis in Two Diverse Human Populations'. Antimicrobial Agents and Chemotherapy, Vol 57, Issue 9, pp. 4566-4569.
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Abstract
New treatment strategies are urgently needed to overcome early mortality in acute bacterial infections. Previous studies have shown that administration of a novel immunoactivating peptide (P4) alongside passive immunotherapy prevents the onset of septicemia and rescues mice from lethal invasive disease models of pneumococcal pneumonia and sepsis. In this study, using two diverse populations of adult volunteers, we determined whether P4 treatment of human alveolar macrophages would upregulate phagocytic killing of Streptococcus pneumoniae ex vivo. We also measured macrophage intracellular oxidation, cytokine secretion, and surface marker expression following stimulation. Peptide treatment showed enhanced bacterial killing in the absence of nonspecific inflammation, consistent with therapeutic potential. This is the first demonstration of P4 efficacy on ex vivo-derived human lung cells.
Item Type: | Article |
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Subjects: | QU Biochemistry > Proteins. Amino Acids. Peptides > QU 68 Peptides QW Microbiology and Immunology > Immunotherapy and Hypersensitivity > QW 800 Biological products producing immunity WC Communicable Diseases > Infection. Bacterial Infections > Bacterial Infections > WC 200 Bacterial infections (General or not elsewhere classified) |
Faculty: Department: | Clinical Sciences & International Health > Clinical Sciences Department |
Digital Object Identifer (DOI): | https://doi.org/10.1128/AAC.00742-13 |
Depositing User: | Lynn Roberts-Maloney |
Date Deposited: | 11 Nov 2014 10:04 |
Last Modified: | 07 Jun 2022 11:09 |
URI: | https://archive.lstmed.ac.uk/id/eprint/4564 |
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