Positive (1→3)-β-d-glucan in blood components and release of (1→3)-β-d-glucan from depth-type membrane filters for blood processing

BACKGROUND : The false‐positive elevation of plasma (1→3)‐β‐ d ‐glucan level, a serodiagnostic test for deep‐seated mycosis, is suspected in patients administered with blood components. STUDY DESIGN AND METHODS : (1→3)‐β‐ d ‐Glucan and endotoxin levels in blood components consisting of 12 albumins,...

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Veröffentlicht in:Transfusion (Philadelphia, Pa.) Pa.), 2002-09, Vol.42 (9), p.1189-1195
Hauptverfasser: Usami, Makoto, Ohata, Atsushi, Horiuchi, Takeshi, Nagasawa, Koichi, Wakabayashi, Toshio, Tanaka, Shigenori
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container_end_page 1195
container_issue 9
container_start_page 1189
container_title Transfusion (Philadelphia, Pa.)
container_volume 42
creator Usami, Makoto
Ohata, Atsushi
Horiuchi, Takeshi
Nagasawa, Koichi
Wakabayashi, Toshio
Tanaka, Shigenori
description BACKGROUND : The false‐positive elevation of plasma (1→3)‐β‐ d ‐glucan level, a serodiagnostic test for deep‐seated mycosis, is suspected in patients administered with blood components. STUDY DESIGN AND METHODS : (1→3)‐β‐ d ‐Glucan and endotoxin levels in blood components consisting of 12 albumins, 8 immunoglobulins, and 3 blood coagulation factors were measured by fungal infection tests (Fungitec G‐test, Seikagaku Co.; the Wako WB003 test, Wako Pure Chemical Industries; and the Endospec ES test, Seikagaku Co.). In vitro release of (1→3)‐β‐ d ‐glucan from the depth‐type filters made by cellulose membrane to process blood components was analyzed through an in vitro filtration process as a source of (1→3)‐β‐ d ‐glucan in blood components. RESULTS : The amounts of (1→3)‐β‐ d ‐glucan in blood components ranged from 0 to 7510 pg per mL in the Fungitec G‐test, with wide variations among brands. The positive rates over 20 pg per mL were 75 percent in albumin solutions, 40 percent in blood coagulation factors, and 63 percent in immunoglobulin solutions. (1→3)‐β‐ d ‐Glucan levels released from the five depth filters ranged from 5 to 2516 pg per mL. The (1→3)‐β‐ d ‐glucan level in filtration fluid was decreased by rinsing with distilled water, but rebounded again during the albumin filtration process. CONCLUSION : Depth filters are considered the source of (1→3)‐β‐ d ‐glucan content in some blood components.
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STUDY DESIGN AND METHODS : (1→3)‐β‐ d ‐Glucan and endotoxin levels in blood components consisting of 12 albumins, 8 immunoglobulins, and 3 blood coagulation factors were measured by fungal infection tests (Fungitec G‐test, Seikagaku Co.; the Wako WB003 test, Wako Pure Chemical Industries; and the Endospec ES test, Seikagaku Co.). In vitro release of (1→3)‐β‐ d ‐glucan from the depth‐type filters made by cellulose membrane to process blood components was analyzed through an in vitro filtration process as a source of (1→3)‐β‐ d ‐glucan in blood components. RESULTS : The amounts of (1→3)‐β‐ d ‐glucan in blood components ranged from 0 to 7510 pg per mL in the Fungitec G‐test, with wide variations among brands. The positive rates over 20 pg per mL were 75 percent in albumin solutions, 40 percent in blood coagulation factors, and 63 percent in immunoglobulin solutions. (1→3)‐β‐ d ‐Glucan levels released from the five depth filters ranged from 5 to 2516 pg per mL. The (1→3)‐β‐ d ‐glucan level in filtration fluid was decreased by rinsing with distilled water, but rebounded again during the albumin filtration process. CONCLUSION : Depth filters are considered the source of (1→3)‐β‐ d ‐glucan content in some blood components.</description><identifier>ISSN: 0041-1132</identifier><identifier>EISSN: 1537-2995</identifier><identifier>DOI: 10.1046/j.1537-2995.2002.00162.x</identifier><identifier>PMID: 12430677</identifier><identifier>CODEN: TRANAT</identifier><language>eng</language><publisher>Boston, MA, USA: Blackwell Science Inc</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Bacterial Proteins - metabolism ; beta-Glucans ; Biological and medical sciences ; Biomarkers - blood ; Blood Coagulation Factors ; Blood Component Transfusion ; Blood Proteins ; Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis ; Cell Wall - chemistry ; Cellulose - chemistry ; Endotoxins - blood ; False Positive Reactions ; Filtration ; Fungi - chemistry ; Glucans - blood ; Glucans - chemistry ; Glycoside Hydrolases - metabolism ; Humans ; Immunoglobulins ; Medical sciences ; Membranes, Artificial ; Mycoses - blood ; Reagent Kits, Diagnostic ; Serum Albumin ; Solubility ; Solutions ; Transfusions. Complications. Transfusion reactions. 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STUDY DESIGN AND METHODS : (1→3)‐β‐ d ‐Glucan and endotoxin levels in blood components consisting of 12 albumins, 8 immunoglobulins, and 3 blood coagulation factors were measured by fungal infection tests (Fungitec G‐test, Seikagaku Co.; the Wako WB003 test, Wako Pure Chemical Industries; and the Endospec ES test, Seikagaku Co.). In vitro release of (1→3)‐β‐ d ‐glucan from the depth‐type filters made by cellulose membrane to process blood components was analyzed through an in vitro filtration process as a source of (1→3)‐β‐ d ‐glucan in blood components. RESULTS : The amounts of (1→3)‐β‐ d ‐glucan in blood components ranged from 0 to 7510 pg per mL in the Fungitec G‐test, with wide variations among brands. The positive rates over 20 pg per mL were 75 percent in albumin solutions, 40 percent in blood coagulation factors, and 63 percent in immunoglobulin solutions. (1→3)‐β‐ d ‐Glucan levels released from the five depth filters ranged from 5 to 2516 pg per mL. The (1→3)‐β‐ d ‐glucan level in filtration fluid was decreased by rinsing with distilled water, but rebounded again during the albumin filtration process. CONCLUSION : Depth filters are considered the source of (1→3)‐β‐ d ‐glucan content in some blood components.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Bacterial Proteins - metabolism</subject><subject>beta-Glucans</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Blood Coagulation Factors</subject><subject>Blood Component Transfusion</subject><subject>Blood Proteins</subject><subject>Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis</subject><subject>Cell Wall - chemistry</subject><subject>Cellulose - chemistry</subject><subject>Endotoxins - blood</subject><subject>False Positive Reactions</subject><subject>Filtration</subject><subject>Fungi - chemistry</subject><subject>Glucans - blood</subject><subject>Glucans - chemistry</subject><subject>Glycoside Hydrolases - metabolism</subject><subject>Humans</subject><subject>Immunoglobulins</subject><subject>Medical sciences</subject><subject>Membranes, Artificial</subject><subject>Mycoses - blood</subject><subject>Reagent Kits, Diagnostic</subject><subject>Serum Albumin</subject><subject>Solubility</subject><subject>Solutions</subject><subject>Transfusions. Complications. Transfusion reactions. 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Apheresis</topic><topic>Cell Wall - chemistry</topic><topic>Cellulose - chemistry</topic><topic>Endotoxins - blood</topic><topic>False Positive Reactions</topic><topic>Filtration</topic><topic>Fungi - chemistry</topic><topic>Glucans - blood</topic><topic>Glucans - chemistry</topic><topic>Glycoside Hydrolases - metabolism</topic><topic>Humans</topic><topic>Immunoglobulins</topic><topic>Medical sciences</topic><topic>Membranes, Artificial</topic><topic>Mycoses - blood</topic><topic>Reagent Kits, Diagnostic</topic><topic>Serum Albumin</topic><topic>Solubility</topic><topic>Solutions</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Usami, Makoto</creatorcontrib><creatorcontrib>Ohata, Atsushi</creatorcontrib><creatorcontrib>Horiuchi, Takeshi</creatorcontrib><creatorcontrib>Nagasawa, Koichi</creatorcontrib><creatorcontrib>Wakabayashi, Toshio</creatorcontrib><creatorcontrib>Tanaka, Shigenori</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transfusion (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Usami, Makoto</au><au>Ohata, Atsushi</au><au>Horiuchi, Takeshi</au><au>Nagasawa, Koichi</au><au>Wakabayashi, Toshio</au><au>Tanaka, Shigenori</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Positive (1→3)-β-d-glucan in blood components and release of (1→3)-β-d-glucan from depth-type membrane filters for blood processing</atitle><jtitle>Transfusion (Philadelphia, Pa.)</jtitle><addtitle>Transfusion</addtitle><date>2002-09</date><risdate>2002</risdate><volume>42</volume><issue>9</issue><spage>1189</spage><epage>1195</epage><pages>1189-1195</pages><issn>0041-1132</issn><eissn>1537-2995</eissn><coden>TRANAT</coden><abstract>BACKGROUND : The false‐positive elevation of plasma (1→3)‐β‐ d ‐glucan level, a serodiagnostic test for deep‐seated mycosis, is suspected in patients administered with blood components. STUDY DESIGN AND METHODS : (1→3)‐β‐ d ‐Glucan and endotoxin levels in blood components consisting of 12 albumins, 8 immunoglobulins, and 3 blood coagulation factors were measured by fungal infection tests (Fungitec G‐test, Seikagaku Co.; the Wako WB003 test, Wako Pure Chemical Industries; and the Endospec ES test, Seikagaku Co.). In vitro release of (1→3)‐β‐ d ‐glucan from the depth‐type filters made by cellulose membrane to process blood components was analyzed through an in vitro filtration process as a source of (1→3)‐β‐ d ‐glucan in blood components. RESULTS : The amounts of (1→3)‐β‐ d ‐glucan in blood components ranged from 0 to 7510 pg per mL in the Fungitec G‐test, with wide variations among brands. The positive rates over 20 pg per mL were 75 percent in albumin solutions, 40 percent in blood coagulation factors, and 63 percent in immunoglobulin solutions. (1→3)‐β‐ d ‐Glucan levels released from the five depth filters ranged from 5 to 2516 pg per mL. The (1→3)‐β‐ d ‐glucan level in filtration fluid was decreased by rinsing with distilled water, but rebounded again during the albumin filtration process. CONCLUSION : Depth filters are considered the source of (1→3)‐β‐ d ‐glucan content in some blood components.</abstract><cop>Boston, MA, USA</cop><pub>Blackwell Science Inc</pub><pmid>12430677</pmid><doi>10.1046/j.1537-2995.2002.00162.x</doi><tpages>7</tpages></addata></record>
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subjects Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Bacterial Proteins - metabolism
beta-Glucans
Biological and medical sciences
Biomarkers - blood
Blood Coagulation Factors
Blood Component Transfusion
Blood Proteins
Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis
Cell Wall - chemistry
Cellulose - chemistry
Endotoxins - blood
False Positive Reactions
Filtration
Fungi - chemistry
Glucans - blood
Glucans - chemistry
Glycoside Hydrolases - metabolism
Humans
Immunoglobulins
Medical sciences
Membranes, Artificial
Mycoses - blood
Reagent Kits, Diagnostic
Serum Albumin
Solubility
Solutions
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
title Positive (1→3)-β-d-glucan in blood components and release of (1→3)-β-d-glucan from depth-type membrane filters for blood processing
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