Literature DB >> 26802050

Impaired killing of Candida albicans by granulocytes mobilized for transfusion purposes: a role for granule components.

Roel P Gazendam1, Annemarie van de Geer2, John L van Hamme2, Anton T J Tool2, Dieke J van Rees2, Cathelijn E M Aarts2, Maartje van den Biggelaar2, Floris van Alphen2, Paul Verkuijlen2, Alexander B Meijer2, Hans Janssen3, Dirk Roos2, Timo K van den Berg2, Taco W Kuijpers4.   

Abstract

Granulocyte transfusions are used to treat neutropenic patients with life-threatening bacterial or fungal infections that do not respond to anti-microbial drugs. Donor neutrophils that have been mobilized with granulocyte-colony stimulating factor (G-CSF) and dexamethasone are functional in terms of antibacterial activity, but less is known about their fungal killing capacity. We investigated the neutrophil-mediated cytotoxic response against C. albicans and A. fumigatus in detail. Whereas G-CSF/dexamethasone-mobilized neutrophils appeared less mature as compared to neutrophils from untreated controls, these cells exhibited normal ROS production by the NADPH oxidase system and an unaltered granule mobilization capacity upon stimulation. G-CSF/dexamethasone-mobilized neutrophils efficiently inhibited A. fumigatus germination and killed Aspergillus and Candida hyphae, but the killing of C. albicans yeasts was distinctly impaired. Following normal Candida phagocytosis, analysis by mass spectrometry of purified phagosomes after fusion with granules demonstrated that major constituents of the antimicrobial granule components, including major basic protein (MBP), were reduced. Purified MBP showed candidacidal activity, and neutrophil-like Crisp-Cas9 NB4-KO-MBP differentiated into phagocytes were impaired in Candida killing. Together, these findings indicate that G-CSF/dexamethasone-mobilized neutrophils for transfusion purposes have a selectively impaired capacity to kill Candida yeasts, as a consequence of an altered neutrophil granular content. Copyright© Ferrata Storti Foundation.

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Year:  2016        PMID: 26802050      PMCID: PMC5004374          DOI: 10.3324/haematol.2015.136630

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  42 in total

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