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1.
Cytotherapy ; 17(9): 1302-13, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-26038175

RESUMO

BACKGROUND AIMS: The Pall Celeris system is a filtration-based point-of-care device designed to obtain a high concentrate of peripheral blood total nucleated cells (PB-TNCs). We have characterized the Pall Celeris-derived TNCs for their in vitro and in vivo angiogenic potency. METHODS: PB-TNCs isolated from healthy donors were characterized through the use of flow cytometry and functional assays, aiming to assess migratory capacity, ability to form capillary-like structures, endothelial trans-differentiation and paracrine factor secretion. In a hind limb ischemia mouse model, we evaluated perfusion immediately and 7 days after surgery, along with capillary, arteriole and regenerative fiber density and local bio-distribution. RESULTS: Human PB-TNCs isolated by use of the Pall Celeris filtration system were shown to secrete a panel of angiogenic factors and migrate in response to vascular endothelial growth factor and stromal-derived factor-1 stimuli. Moreover, after injection in a mouse model of hind limb ischemia, PB-TNCs induced neovascularization by increasing capillary, arteriole and regenerative fiber numbers, with human cells detected in murine tissue up to 7 days after ischemia. CONCLUSIONS: The Pall Celeris system may represent a novel, effective and reliable point-of-care device to obtain a PB-derived cell product with adequate potency for therapeutic angiogenesis.


Assuntos
Isquemia/terapia , Neovascularização Fisiológica , Doença Arterial Periférica/terapia , Sistemas Automatizados de Assistência Junto ao Leito , Animais , Remoção de Componentes Sanguíneos , Diferenciação Celular , Movimento Celular , Separação Celular/métodos , Quimiocina CXCL12/metabolismo , Modelos Animais de Doenças , Células Endoteliais/citologia , Filtração , Citometria de Fluxo , Membro Posterior/irrigação sanguínea , Humanos , Leucócitos/imunologia , Camundongos , Reperfusão , Fator A de Crescimento do Endotélio Vascular/metabolismo
2.
Haematologica ; 91(7): 983-5, 2006 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16757413

RESUMO

We observed a significant increase of Pseudomonas aeruginosa bacteremias during 2002. Eighty-five microbiological samples were taken from different potential sources of infection. Twenty-nine out of 46 specimens obtained from water taps, shower heads and siphons tested positive for Pseudomonas aeruginosa. Weekly pharyngeal and rectal swabs in high risk patients, use of tap water after running the tap for at least 5 minutes and use of weekly disposable sterile filters in all taps and showers resulted in a significant decrease in Pseudomonas aeruginosa bacteremias. Moreover, we observed a significant reduction in Pseudomonas aeruginosa-positive surveillance cultures after implementation of these measures.


Assuntos
Surtos de Doenças , Infecções por Pseudomonas/epidemiologia , Pseudomonas aeruginosa , Purificação da Água/métodos , Infecção Hospitalar , Filtração , Unidades Hospitalares , Humanos
3.
Transfus Apher Sci ; 26(3): 167-74, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12126201

RESUMO

Lymphocyte subsets were determined in 20 packed red blood cell units (PRC) before and after filtration (FPRC) with the Pall Leukotrap RC inline filter system; 10 units were prepared by low spin and platelet rich plasma (PRP) removal (Group A) and 10 with high spin, plasma and buffy-coat (BC) removal (Group B). Flow cytometry was employed for white blood cell (WBC) enumeration and phenotype analysis. Median WBCs in prefiltered units was 2.08 x 10(9) (Group A) vs. 0.8 x 10(9) (Group B) (p < 0.0001). Five Group A and three Group B filtered units had WBC counts above the limit of detection (LD), median values being 25.59 and 3.08 x 10(3), respectively. Whereas CD3+, CD3+CD4+ and CD3+CD8+ lymphocyte subsets were assessable in 20-40% of Group A units, inline filtration of Group B units lowered lymphocytes below the LD of the present study. Post-filtration CD19+ lymphocytes were below the LD in all the 20 units.


Assuntos
Separação Celular/métodos , Separação Celular/normas , Eritrócitos/citologia , Subpopulações de Linfócitos/citologia , Antígenos CD/análise , Coleta de Amostras Sanguíneas , Centrifugação/métodos , Transfusão de Eritrócitos/normas , Filtração/métodos , Citometria de Fluxo , Humanos , Imunofenotipagem , Contagem de Leucócitos/instrumentação , Contagem de Leucócitos/métodos
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