发明名称 Cytocapacity test
摘要 The present invention relates to a method for determining the hematopoietic cytocapacity of a subject comprising the steps of: (a) determining the amount of leukocytes present in a blood sample obtained from a subject, wherein said subject has been subjected to administration of a single dose of G-CSF and has been maintained for a time sufficient to allow mobilization or release of the leukocytes from hematopoietic production and storage tissues and sites of margination into the blood; and (b) determining the hematopoietic cytocapacity by assessing the amount of leukocytes determined in step (a) with the amount of leukocytes which have been mobilized or released in a control subject wherein said control subject is selected from the group consisting of subjects having (i) a high risk for a disease, disorder or complication associated with high-dose cytotoxic chemotherapy and/or hematopoietic cell transplantation, (ii) an intermediate risk for a disease, disorder or complication associated with high-dose cytotoxic chemotherapy and/or hematopoietic cell transplantation or (iii) a low risk for a disease, disorder or complication associated with high-dose cytotoxic chemotherapy and/or hematopoietic cell transplantation.
申请公布号 AU2003221517(B2) 申请公布日期 2010.02.18
申请号 AU20030221517 申请日期 2003.03.24
申请人 LUDWIG MAXIMILIANS UNIVERSITAT 发明人 CHRISTIAN STRAKA
分类号 G01N33/49;A61K31/136;A61K31/198;A61K31/255;A61K31/282;A61K31/337;A61K31/4184;A61K31/4745;A61K31/475;A61K31/513;A61K31/519;A61K31/655;A61K31/675;A61K31/704;A61K31/7048;A61K31/7068;A61K31/7076;A61K33/24;A61K38/19;A61P1/04;A61P7/00;A61P11/00;A61P31/04;A61P31/10;A61P31/12;A61P33/02;A61P33/10;A61P35/00;A61P37/02;C12Q1/00;C12Q1/06;G01N33/15;G01N33/569;G01N33/574;G01N33/96 主分类号 G01N33/49
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