1998
DOI: 10.1016/s0192-0561(98)00007-1
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Enhanced clearance of a multiple antibiotic resistant Staphylococcus aureus in rats treated with PGG-glucan is associated with increased leukocyte counts and increased neutrophil oxidative burst activity

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Cited by 125 publications
(88 citation statements)
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“…54 By binding to those receptors, b-glucan initiates a cascade of events that results in enhanced macrophage and neutrophil function and increased microbial clearance. 55,56 Our observation of an increase in WBCs seems consistent with the mechanisms described for b-glucan and with the previous reporting of increased blood natural killer lymphocytes in children receiving fungal b-glucan. 22,57 To our knowledge, this is the first study reporting a potential impact of oral intake of yeast b-glucan on immune markers in healthy children.…”
Section: Discussionsupporting
confidence: 91%
“…54 By binding to those receptors, b-glucan initiates a cascade of events that results in enhanced macrophage and neutrophil function and increased microbial clearance. 55,56 Our observation of an increase in WBCs seems consistent with the mechanisms described for b-glucan and with the previous reporting of increased blood natural killer lymphocytes in children receiving fungal b-glucan. 22,57 To our knowledge, this is the first study reporting a potential impact of oral intake of yeast b-glucan on immune markers in healthy children.…”
Section: Discussionsupporting
confidence: 91%
“…Augmentation of the host response by immunomodulators is an alternative to the use of antibiotics in the prevention and/or treatment of infections caused by antibiotic-resistant bacteria. For instance, glucan, which has been studied extensively because of its ability to enhance host innate immunity, decreased septic complications and improved survival in septic hosts [18][19][20].…”
Section: Discussionmentioning
confidence: 99%
“…The protective effect of β-glucans was shown in experimental infection with Leishmania major (Al Tuwaiji et al, 1987) and L. donovani (Cook and Holbrook, 1984), C. albicans (Bacon and Farmer, 1968), Toxoplasma gondii (Bousquet et al, 1988), Streptococcus suis (Dritz (Kumar and Ahmad, 1985), Staphylococcus aureus (Liang et al, 1998), Escherichia coli (Rasmussen and Seljelid, 1990), Mesocestoides corti (White et al, 1988), Trypanosoma cruzi (Williams et al, 1989), Eimeria vermiformis (Yun et al, 1998), and anthrax infection (Vetvicka et al, 2002).…”
Section: Glucan and Immunological Reactionsmentioning
confidence: 99%