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  • 1
    In: Vox Sanguinis, Wiley, Vol. 117, No. 4 ( 2022-04), p. 488-494
    Abstract: This study aimed to describe motives as well as donation experiences and the intention to return for further donations of German whole blood donors who donated at the beginning of the COVID‐19 pandemic. Materials and Methods To describe motives and donor experiences, a retrospective survey was conducted among whole blood donors that had a donation appointment at the German Red Cross Blood Donation Service in the first 4 weeks of the pandemic. A donor questionnaire including 17 retrospective questions was sent to 7500 donors. Donor motivation and donor experiences were compared for different donor groups using chi‐square statistics. Finally, in an ordinal logistic regression model predictors for the intention to return were identified. Results More than half of the participating donors (56.9%) wanted to contribute to the fight against the pandemic by donating blood. Most of the donors were satisfied with their last donation experience and felt safe during the blood donor appointment. However, some donors would have liked more information on how to deal with the pandemic (20.3%). Intention to return for further donations was strongly associated with overall satisfaction (OR: 1.67, CI: 1.47–1.90) and the feeling of being safe during blood donation (OR: 1.33, CI: 1.05–1.68). Conclusion Donor satisfaction with the last donation was high and the vast majority of donors felt very safe. However, those donors who felt unsafe expressed a low intention to return and blood donation services should therefore carefully monitor donor satisfaction.
    Type of Medium: Online Resource
    ISSN: 0042-9007 , 1423-0410
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 1483587-3
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  • 2
    Online Resource
    Online Resource
    Wiley ; 1998
    In:  Vox Sanguinis Vol. 75, No. 1 ( 1998-09), p. 12-17
    In: Vox Sanguinis, Wiley, Vol. 75, No. 1 ( 1998-09), p. 12-17
    Abstract: Background and Objectives: Peripheral blood mononuclear cells (PBMC) and cytokines accumulating in platelet concentrates (PC) during storage have been implicated in causing non‐hemolytic transfusion reactions, in particular after prolonged PC storage. We investigated the impact of major storage parameters, such as storage time, anticoagulation and temperature, on the capability of PBMC to secrete cytokines. Materials and Methods: In a first study, PBMC from whole blood donations (n = 16) were exposed to standard PC storage conditions: 22°C, citrate phosphate dextrose (CPD) anticoagulation. Secretion of the cytokines interleukin‐1β (IL‐1β), IL‐2, IL‐6 and interferon‐γ (IFN‐γ) on mitogenic stimulation was measured directly after blood donation and after 1, 3 and 5 days of storage. In a second study, paired whole blood samples (n = 24) were investigated for the mitogenic induction of IL‐2, IL‐6, IFN‐γ and IFN‐α. Cytokine values were compared with respect to incubation temperature (22 vs. 37°C) and anticoagulant (CPD vs. lithium‐heparin). Results: PBMC stored at 22°C with CPD anticoagulation showed an altered cytokine secretion pattern in comparison to freshly donated cells. After storage for 3 days, IL‐2 release was decreased (p 〈 0.05) and after 5 days secretion of all cytokines was significantly decreased, though still detectable (p 〈 0.01). In the second study, CPD anticoagulation resulted in a significantly impaired cytokine secretion compared with lithium‐heparin. Cytokine secretion at 22°C were significantly lower (p 〈 0.001) compared with 37°C for both anticoagulants. Conclusion: Storage of PBMC at 22°C with CPD leads to an impaired cytokine response, but PBMC are still capable of secreting cytokines after 5 days of storage. PBMC remain a potential source of cytokines even after 5 days of storage in CPD at 22°C.
    Type of Medium: Online Resource
    ISSN: 0042-9007 , 1423-0410
    Language: English
    Publisher: Wiley
    Publication Date: 1998
    detail.hit.zdb_id: 1483587-3
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  • 3
    In: Vox Sanguinis, Wiley, Vol. 78, No. 4 ( 2000-06), p. 242-249
    Abstract: Background and Objectives: Optimal mobilization and harvest of hematopoietic progenitors are essential for peripheral blood stem cell transplantation after myeloablative high‐dose chemotherapy. Conflicting data have been published concerning the most useful, cost‐effective collection strategy which is also convenient for patients. Materials and Methods: A total of 66 leukaphereses in 20 patients were retrospectively evaluated. We assessed the predictive value of the number of white blood cells, mononuclear cells (MNCs) and CD34+ cells in peripheral blood for the yield of CD34+ cells in leukapheresis products. The concentrations of MNCs and CD34+ cells were quantified simultaneously by a flow cytometric procedure using fluorescent microparticles. Their collection efficiencies were calculated based on a newly developed formula. Results: The collected hematopoietic progenitor concentration could be predicted only by the number of peripheral blood CD34+ cells prior to apheresis (r = 0.902; p 〈 0.01). Furthermore, the mobilization of at least 30 CD34+ cells/μl peripheral blood was a good predictor that a single leukapheresis would yield a minimum of 2.0 × 10 6 CD34+ cells/kg body weight. The collection efficiencies calculated by the new formula were 55.2±10.7% and 57.7±11.2% for MNCs and CD34+ cells, respectively. Conclusion: The precise quantification of MNCs and CD34+ cells by a direct flow cytometric assay, as well as the new formula to determine the collection efficiencies, has an impact on optimizing high‐quality stem cell products.
    Type of Medium: Online Resource
    ISSN: 0042-9007 , 1423-0410
    Language: English
    Publisher: Wiley
    Publication Date: 2000
    detail.hit.zdb_id: 1483587-3
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  • 4
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2013
    In:  AIDS Research and Therapy Vol. 10, No. 1 ( 2013), p. 26-
    In: AIDS Research and Therapy, Springer Science and Business Media LLC, Vol. 10, No. 1 ( 2013), p. 26-
    Type of Medium: Online Resource
    ISSN: 1742-6405
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2013
    detail.hit.zdb_id: 2173450-1
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  • 5
    In: International Journal of Molecular Sciences, MDPI AG, Vol. 23, No. 3 ( 2022-01-26), p. 1385-
    Abstract: Hyperglycemia, a hallmark of diabetes, can induce inflammatory programming of macrophages. The macrophage scavenger receptor CD163 internalizes and degrades hemoglobin-haptoglobin (Hb-Hp) complexes built due to intravascular hemolysis. Clinical studies have demonstrated a correlation between impaired scavenging of Hb-Hp complexes via CD163 and diabetic vascular complications. Our aim was to identify whether hyperglycemia is able to amplify inflammation via Hb-Hp complex interactions with the immune system. M(IFNγ), M(IL-4), and control M0 macrophages were differentiated out of primary human monocytes in normo- (5 mM) and hyperglycemic (25 mM) conditions. CD163 gene expression was decreased 5.53 times in M(IFNγ) with a further decrease of 1.99 times in hyperglycemia. Hyperglycemia suppressed CD163 surface expression in M(IFNγ) (1.43 times). Flow cytometry demonstrated no impairment of Hb-Hp uptake in hyperglycemia. However, hyperglycemia induced an inflammatory response of M(IFNγ) to Hb-Hp1-1 and Hb-Hp2-2 uptake with different dynamics. Hb-Hp1-1 uptake stimulated IL-6 release (3.03 times) after 6 h but suppressed secretion (5.78 times) after 24 h. Contrarily, Hb-Hp2-2 uptake did not affect IL-6 release after 6h but increased secretion after 24 h (3.06 times). Our data show that hyperglycemia induces an inflammatory response of innate immune cells to Hb-Hp1-1 and Hb-Hp2-2 uptake, converting the silent Hb-Hp complex clearance that prevents vascular damage into an inflammatory process, hereby increasing the susceptibility of diabetic patients to vascular complications.
    Type of Medium: Online Resource
    ISSN: 1422-0067
    Language: English
    Publisher: MDPI AG
    Publication Date: 2022
    detail.hit.zdb_id: 2019364-6
    SSG: 12
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  • 6
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2003
    In:  Stem Cells Vol. 21, No. 2 ( 2003-03-01), p. 208-216
    In: Stem Cells, Oxford University Press (OUP), Vol. 21, No. 2 ( 2003-03-01), p. 208-216
    Abstract: Umbilical cord blood (UCB) preparation needs to be optimized in order to develop more simplified procedures for volume reduction, as well as to reduce the amount of contaminating cells within the final stem cell transplant. We evaluated a novel filter device (StemQuick™E) and compared it with our routine buffy coat (BC) preparation procedure for the enrichment of hematopoietic progenitor cells (HPCs). Two groups of single or pooled UCB units were filtered (each n = 6), or equally divided in two halves and processed by filtration and BC preparation in parallel (n = 10). The engraftment capacity of UCB samples processed by whole blood (WB) preparation was compared with paired samples processed by filtration in the nonobese diabetic/severe combined immunodeficient (NOD/SCID) mouse animal model. Filtration of UCB units in the two groups with a mean volume of 87.8 and 120.7 ml, respectively, and nucleated cell (NC) content of 9.7 and 23.8 × 108 resulted in a sufficient mean cell recovery for mononucleated cells ([MNCs] 74.2%-77.5%), CD34+ cells (76.3%-79.0%), and colony-forming cells (64.1%-86.3%). Moreover, we detected a relevant depletion of the transplants for RBCs (89.2%-90.0%) and platelets ([PLTs] 77.5%-86.1%). In contrast, the mean depletion rate using BC processing proved to be significantly different for PLTs (10%, p = 0.03) and RBCs (39.6%, p & lt; 0.01). The NC composition showed a highly significant increase in MNCs and a decrease in granulocytes after filtration (p & lt; 0.01), compared with a less significant MNC increase in the BC group (p & lt; 0.05). For mice transplanted with WB-derived progenitors, we observed a mean of 15.3% ± 15.5% of human CD45+ cells within the BM compared with 19.9% ± 16.8% for mice transplanted with filter samples (p = 0.03). The mean percentage of human CD34+ cells was 4.2% ± 3.1% for WB samples and 4.5% ± 3.2% for filter samples (p = 0.68). As the data of NOD/SCID mice transplantation demonstrated a significant engraftment capacity of HPCs processed by filtration, no negative effect on the engraftment potential of filtered UCB cells versus non-volume-reduced cells from WB transplants was found. The StemQuick™E filter devices proved to be a useful tool for Good Manufacturing Practices conform enrichment of HPCs and MNCs out of UCB. Filtration enables a quick and standardized preparation of a volume-reduced UCB transplant, including a partial depletion of granulocytes, RBCs, and PLTs without the need for centrifugation. Therefore, it seems very probable that filter-processed UCB transplants will also result in sufficient hematopoietic reconstitution in humans.
    Type of Medium: Online Resource
    ISSN: 1066-5099 , 1549-4918
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2003
    detail.hit.zdb_id: 2030643-X
    detail.hit.zdb_id: 1143556-2
    detail.hit.zdb_id: 605570-9
    SSG: 12
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  • 7
    In: Stem Cells, Oxford University Press (OUP), Vol. 27, No. 9 ( 2009-09-01), p. 2331-2341
    Abstract: Mesenchymal stromal cells (MSCs) are promising candidates for novel cell therapeutic applications. For clinical scale manufacturing, human factors from serum or platelets have been suggested as alternatives to fetal bovine serum (FBS). We have previously shown that pooled human serum (HS) and thrombin-activated platelet releasate in plasma (tPRP) support the expansion of adipose tissue-derived MSCs. Contradictory results with bone marrow (BM)-derived MSCs have initiated a comprehensive comparison of HS, tPRP, and pooled human platelet lysate (pHPL) and FBS in terms of their impact on MSC isolation, expansion, differentiation, and immunomodulatory activity. In addition to conventional Ficoll density gradient centrifugation, depletion of lineage marker expressing cells (RosetteSep) and CD271+ sorting were used for BM-MSC enrichment. Cells were cultured in medium containing either 10% FBS, HS, tPRP, or pHPL. Colony-forming units and cumulative population doublings were determined, and MSCs were maximally expanded. Although both HS and tPRP comparable to FBS supported isolation and expansion, pHPL significantly accelerated BM-MSC proliferation to yield clinically relevant numbers within the first two passages. MSC quality and functionality including cell surface marker expression, adipogenic and osteogenic differentiation, and immunosuppressive action were similar in MSCs from all culture conditions. Importantly, spontaneous cell transformation was not observed in any of the culture conditions. Telomerase activity was not detected in any of the cultures at any passage. In contrast to previous data from adipose tissue-derived MSCs, pHPL was found to be the most suitable FBS substitute in clinical scale BM-MSC expansion. Disclosure of potential conflicts of interest is found at the end of this article.
    Type of Medium: Online Resource
    ISSN: 1066-5099 , 1549-4918
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2009
    detail.hit.zdb_id: 2030643-X
    detail.hit.zdb_id: 1143556-2
    detail.hit.zdb_id: 605570-9
    SSG: 12
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  • 8
    In: Immunobiology, Elsevier BV, Vol. 222, No. 10 ( 2017-10), p. 952-959
    Type of Medium: Online Resource
    ISSN: 0171-2985
    RVK:
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2017
    detail.hit.zdb_id: 2060227-3
    SSG: 12
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  • 9
    Online Resource
    Online Resource
    Georg Thieme Verlag KG ; 2014
    In:  Der Klinikarzt Vol. 43, No. 01 ( 2014-2-5), p. 9-9
    In: Der Klinikarzt, Georg Thieme Verlag KG, Vol. 43, No. 01 ( 2014-2-5), p. 9-9
    Type of Medium: Online Resource
    ISSN: 0341-2350 , 1439-3859
    URL: Issue
    RVK:
    Language: German
    Publisher: Georg Thieme Verlag KG
    Publication Date: 2014
    detail.hit.zdb_id: 2106610-3
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  • 10
    Online Resource
    Online Resource
    Georg Thieme Verlag KG ; 2014
    In:  Der Klinikarzt Vol. 43, No. 01 ( 2014-2-5), p. 42-47
    In: Der Klinikarzt, Georg Thieme Verlag KG, Vol. 43, No. 01 ( 2014-2-5), p. 42-47
    Type of Medium: Online Resource
    ISSN: 0341-2350 , 1439-3859
    URL: Issue
    RVK:
    Language: German
    Publisher: Georg Thieme Verlag KG
    Publication Date: 2014
    detail.hit.zdb_id: 2106610-3
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