Method of regenerating blood vessels

Abstract

A method for regenerating a blood vessel comprising introducing a cell-containing fluid containing vascular endothelial precursor cells and cells to be removed into a cell separator which allows at least the cells to be removed to substantially pass through but substantially captures the vascular endothelial precursor cells; recovering the vascular endothelial precursor cells once captured on said cell separator by introducing a fluid into the said cell separator;

Description

BACKGROUND OF THE INVENTION

[0002] (1) Field of the Invention

[0003] This invention relates to a method for separating and recovering only necessary cells from a fluid containing a mixture of various cells. The cells thus obtained can be used in providing therapy for various diseases, such as hematopoietic stem cell transplantation, and in fundamental sciences such as immunology and cell biology.

[0004] (2) Description of the Related Art

[0005] Japanese patent JP-A-54-119012 discloses a technique for recovering lymphocytes by capturing leukocytes on a filter from a body fluid such as blood containing leukocytes (granulocytes, monocytes and lymphocytes) and erythrocytes.

[0006] In the case of hematopoietic stem cell transplantation, cord blood stem cells are noted as a source of hematopoietic stem cells which does not cause any invasion to donors, and their clinical application is vigorously attempted, mainly in countries in Europe and America. Since cord blood stem cells are rarely transplanted to a patient immediately after being collected from a donor, unlike in other hematopoietic stem cell transfers, i.e., bone marrow transplantation and peripheral blood stem cell transplantation, they should be preserved for use after the collection. Such preservation is often needed, particularly in the case of unrelated setting. Before cryopreservation of cord blood, the separation of nucleated cells and the removal of erythrocytes is considered necessary in order to prevent side effects of erythrocytes lysis after thawing, and to reduce the volume during the cryopreservation. At present, cord blood is preserved after the separation, in most cases (“Peripheral Blood Stem Cell Transplantation” p. 173, NANKODO Ltd.). JP-B-8-69 discloses details of a protocol for separating cord blood by a Ficoll-Hypaque method, a centrifugation method using a liquid having an adjusted specific gravity, hereinafter referred to as “Ficoll method”. The Ficoll method, however, is disadvantageous in that it is only feasible on a laboratory level and requires very troublesome and time-consuming operations. International Publication No. WO 96/17514 discloses a bag system and method for separating erythrocytes in cord blood by agglutination and precipitation by the use of hydroxyethyl starch to obtain a concentrated nucleated cell suspension, and a cell suspension obtained by that method. This method is somewhat superior to the Ficoll method, a conventional method in that it involves fewer troublesome operations, but it also is time-consuming because two centrifugation runs are necessary.

[0007] Life style related diseases such as diabetes mellitus, hypertension, hyperlipidemia and obesity are risk factors for vascular lesion, and finally develop organ failures such as arteriosclerosis obliterans (ASO) or peripheral arterial occlusive disease (PAOD), myocardial infarction and renal failure. Large numbers of patients with the life-style related diseases are known, and it is no exaggeration to say that treatment of blood vessels is the most important subject in the modern medical care.

[0008] For example, in the arteriosclerosis obliterans which develops gangrene of the lower limb, there are not a few patients who are compelled to undergo below-knee amputation, as a result, quality of life (QOL) of patients decreases significantly [150,000 patients a year in the U.S. and 2,000 patients a year in Japan, Saishin Igaku, 56(8), 1748-1754 (2001)]. Therapeutic methods for such ischemic tissues and organs include the vasodilating operation using a balloon catheter, a stent and the surgical reconstruction of blood vessel by vein transplantation and the like, however none of these methods has not become an effective measure for severe patients.

[0009] Recently, therapeutic angiogenesis as a new therapeutic means is being performed. The therapeutic angiogenesis is roughly grouped into the gene therapy and the cell transplantation method.

[0010] U.S. Pat. No. 5,980,887 discloses a method for inducing neovascularization by transplanting human CD34 positive mononuclear blood cells isolated from peripheral blood into ischemic region of nude mice.

[0011] Further, a paper reports that when vascular endothelial precursor cells designated as attaching cells, which adhered to the culture dish, obtained from mononuclear cells from human-derived cord blood and peripheral blood, were transplanted to nude rats with ischemic limb, an effective improvement of the blood stream could be obtained as compared with the untreated control group (The Journal of Clinical Investigation, 105: 1527-1536, 2000).

[0012] In addition, in the cell transplantation method, an advantageous result has been obtained by introducing mononuclear cells derived from autologous bone marrow into a crus of patient with arteriosclerosis obliterans [Saishin Igaku 56(8), 1755-1764 (2001)].

[0013] On the other hand, in the gene therapy, an improvement of blood stream by introducing plasmid of vascular endothelial growth factor (VEGF) or hepatocyte growth factor (HGF) into the ischemic lesioned region has been reported (Circulation, 98; 2800-2804, 1998; Hypertension, 33:1379-1384, 1999).

[0014] Generally, in the cell transplantation method, in order to obtain an efficient vascularization of the vascular endothelial precursor cells at the ischemic region or in order to perform an efficient cell growth in vitro, erythrocytes, platelets, granulocytes and the like in the blood are removed and mononuclear cells including the vascular endothelial precursor cells are isolated and concentrated. Concentration method is mainly a gravity centrifugation using Ficoll (Pharmacia Inc.) and the like, but this method has a number of problems: i.e., complicated working operation due to prohibited waving of an interface; less reproducibility; a prolonged treatment time as long as 2 hours including a removal procedure for the remaining liquid having an adjusted specific gravity; and possible bacterial contamination caused by the operation under an open system. Consequently, a method for treating cells conforming to GMP (Good Manufacturing Practice) as well as suitable for a clinical application is desired. Further, since the centrifugal method is low in cell recovery rate, in order to obtain the vascular endothelial precursor cells necessary for transplantation, it is compelled to collect a large amount of raw blood considering cell loss, as a result, a blood donor (especially in case of an autologous blood donor) has to have a severe stress. In addition, since a large amount of blood collection is required due to the low recovery rate of cells, there is a problem of restriction for the frequent treatments resulting in a decreased treatment outcome.

[0015] In the separation of the vascular endothelial precursor cells in the prior art of the therapeutic angiogenesis described above, the gravity centrifugation and magnetic beads with immobilized antibody have been used, however, no description of a method using a filter is found.

[0016] On the other hand, some methods for separating hematopoietic stem cells have been reported as substitutes for the Ficoll method and the erythrocyte aggutination and removal. JP-A-8-104643 discloses a method for recovering hematopoietic stem cells by capturing them on a filter permeable to erythrocytes, and then causing a liquid flow in a direction opposite to the first liquid flow direction. This method, however, merely uses Hanks' Balanced Salt Solution (HBSS) as the liquid for the recovery.

[0017] Dextran is a polysaccharide composed of glucose units as monomer units mainly by α-1,6 linkages, and has been used since early times as an agent for separating leukocytes. The separation of leukocytes by the use of dextran, however, utilizes the effect of dextran as a hemagglutinating agent. After erythrocytes in a test tube are agglutinated and precipitated, centrifugation is carried out if necessary, and then leukocytes in the supernatant are recovered with a pipet (Shiro Miwa, Rinsho Kensa Gijutsu Zensho, Vol. 3, “Ketsueki Kensa” p. 425). Such an effect is not characteristic of only dextran, because hydroxyethyl starch and the like have the same hemagglutinating effect as that of dextran.

[0018] Next, systems for separating hematopoietic stem cells are described below. JP-A-7-184991 discloses an assembly for collecting cord blood, in particular, a filter for removing contaminants in cord blood, such as aggregates (e.g. micro-aggregates), tissue particles, bone particles, steatomas, etc., which is provided before a container for blood collection. This filter, however, is not for capturing cells which should be recovered, but for removing contaminants. Even if a material capable of capturing hematopoietic stem cells is used in the filter by chance, this reference does not describe the recovery of the captured hematopoietic stem cells at all.

[0019] JP-A-8-52206 discloses an apparatus comprising a membrane type plasma separator, as an apparatus for collecting cord blood which is used for separating hematopoietic stem cells from cord blood collected. This reference also discloses another separation method using an apparatus for density gradient separation, i.e., separation by the Ficoll method.

[0020] The present invention is intended to provide a method for separating cells which are desired to be recovered (hereinafter referred to as “cells to be recovered” or “necessary cells”) from a mixture of necessary cells and unnecessary cells (hereinafter referred to as “cells to be removed”) by a simple and rapid procedure. This procedure comprises a cell separation method which captures necessary cells by use of a capturing means such as filtering a fluid containing the cell mixture, and then recovering the captured cells with high recovery. The present invention also provides a line system obtained by embodiment of this method for practical clinical employment. The present invention also provides a recovering liquid used in said system, arid a cell-containing fluid obtained by using the method.

[0021] The present invention also provides a method of using the recovered cells for therapeutic vasculogenesis.

[0022] In order to solve the problems identified in the prior art, the present inventors noted properties of a liquid for recovering cells from a cell-capturing means, and earnestly investigated these properties to conclude that when cells are recovered by using a recovering liquid having a definite viscosity, a high recovery can be attained. As a result of earnest investigation on the compositions of various recovering liquids, the present inventors found such a striking effect that, when cells are recovered by using a physiological solution containing dextran, a very high recovery can be attained. Thus, the objectives of the present invention have been accomplished.

SUMMARY OF THE INVENTION

[0023] One aspect of the present invention is directed to a cell separation method comprising steps of introducing a cell-containing fluid containing cells to be recovered and cells to be removed into a cell-capturing means capable of substantially capturing the cells to be recovered and substantially permitting passage therethrough of the cells to be removed. Then, the resulting fluid containing the cells to be removed is taken from the cell-capturing means, and then a liquid with a viscosity of not more than 500 mPa.s and not less than 5 mPa.s is introduced into the cell-capturing means to recover therefrom the cells to be recovered which have been captured by the cell-capturing means.

[0024] Another aspect of the present invention is directed to a cell separation and preservation method comprising steps of introducing a cell-containing fluid containing cells to be recovered and cells to be removed, into a cell-capturing means capable of substantially capturing the cells to be recovered, and substantially permitting passage therethrough of the cells to be removed. The resulting fluid containing the cells to be removed is taken out of the cell-capturing means, and a liquid with a viscosity of not more than 500 mPa.s and not less than 5 mPa.s is introduced into the cell-capturing means to recover therefrom the cells to be recovered which have been captured by the cell-capturing means. The recovered cells are then preserved.

[0025] Another aspect of the present invention is directed to a cell separation and preservation method comprising steps of introducing a cell-containing fluid containing cells to be recovered and cells to be removed into a cell-capturing means capable of substantially capturing the cells to be recovered, and substantially-permitting passage of the cells to be removed. The resulting fluid containing the cells to be removed is taken from the cell-capturing means, and a liquid with a viscosity of not more than 500 mPa.s and not less than 5 mPa.s is introduced into the cell-capturing means to recover therefrom the cells to be recovered which have been captured by the cell-capturing means. The recovered cells are then subjected to cryopreservation and thawing.

[0026] Still another aspect of the present invention is directed to a cell separation system comprising a cell-capturing means which is capable of substantially capturing cells to be recovered and substantially permitting passage therethrough of cells to be removed, which has at least an inlet and an outlet. A line for introducing into the cell-capturing means a cell-containing fluid containing the cells to be recovered and the cells to be removed is connected upstream to the inlet of the cell-capturing means. A line for introducing a liquid into the cell-capturing means is connected downstream to the outlet of the cell-capturing means, and a line for cell recovery from the inlet side of the cell-capturing means is connected upstream to the inlet of the cell-capturing means.

[0027] Still another aspect of the present invention is directed to a cell separation method comprising steps of introducing a cell-containing fluid containing cells to be recovered and cells to be removed into a cell-capturing means capable of substantially capturing the cells to be recovered and substantially permitting passage therethrough of the cells to be removed, through a line connected upstream to the inlet of the cell-capturing means. The resulting fluid containing the cells to be removed is taken out through the outlet of the cell-capturing means, and then a liquid with a viscosity of not more than 500 mPa.s and not less than 5 mPa.s is introduced into the cell-capturing means through a line connected downstream to the outlet of the cell-capturing means to recover the cells to be recovered which have been captured by the cell-capturing means, through a line connected upstream to the inlet of the cell-capturing means.

[0028] Thus, the present invention relates to a method for regenerating a blood vessel comprising introducing a cell-containing fluid containing vascular endothelial precursor cells and cells to be removed into a cell-capturing means which allows at least the cells to be removed to substantially pass through but substantially captures the vascular endothelial precursor cells; recovering the vascular endothelial precursor cells once captured on said cell-capturing means by introducing a fluid into the said cell-capturing means; and using the recovered vascular endothelial precursor cells for regenerating a blood vessel. The present invention preferably comprises a step to substantially remove the cells to be removed remaining in the cell-capturing means by introducing a fluid into said cell-capturing means, after introducing the cell-containing fluid into the cell-capturing means.

[0029] Still another aspect of the present invention is directed to a liquid containing hematopoietic stem cells which is substantially free from erythrocytes and/or platelets and has a viscosity of not more than 500 mPa.s and not less than 5 mPa.s.

[0030] Still another aspect of the present invention is directed to a liquid containing cells to be recovered and substantially having no cells to be removed which is obtained by a cell separation method comprising steps of introducing a cell-containing fluid containing cells to be recovered and cells to be removed into a cell-capturing means capable of substantially capturing the cells to be recovered and substantially permitting passage therethrough of the cells to be removed. The resulting fluid containing the cells to be removed is taken out from the cell-capturing means, and then a liquid with a viscosity of not more than 500 mPa.s and not less than 5 mPa.s is introduced into the cell-capturing means to recover therefrom the cells to be recovered which have been captured by the cell-capturing means.

[0031] Still another aspect of the present invention is directed to a liquid for recovering captured cells from a cell-capturing means which has a viscosity of not more than 500 mPa.s and not less than 5 mPa.s.

BRIEF DESCRIPTION OF THE DRAWINGS

[0032] FIG. 1 is one embodiment of the cell separation system according to the present invention.

[0033] FIG. 2 is a schematic view of a cell separation system used in Example 1.

[0034] FIG. 3 is a schematic view of a cell separation system used in Example 4.

[0035] FIG. 4 is a schematic view of a cell separation system used in Example 6.

[0036] FIGS. 5-1 to 5-7 show optical microscopic photographs, fluorescent microscopic photographs and a PT-PCR analysis chart of the attaching cells obtained in Example 6.

[0037] FIGS. 6-1 to 6-6 are illustrative drawings of optical microscopic photographs and fluorescent microscopic photographs of the attaching cells obtained in Example 6.

[0038] FIG. 7 is a fluorescent microscopic photograph of the blood vessel regenerated in vitro in Example 6.

[0039] FIG. 8 is a drawing showing a recovery of the blood flow volume measured in a time-dependent manner by Laser Doppler Analysis equipment in an ischemic region of nude rat in Example 7.

PREFERRED EMBODIMENT Of THE INVENTION

[0040] In the present specification, the term “cells to be recovered” means cells used for some purpose after their separation and recovery. The term “cells to be removed” means cells unnecessary for the above purpose or cells which should be positively removed because they are, for example, pathogenic cells, so that contamination by them of cells to be recovered causes a problem.

[0041] The cell-containing fluid containing cells to be recovered and cells to be removed can be but is not limited to peripheral blood, bone marrow, cord blood (including not only that collected through a umbilical cord blood vessel but also that collected through a placenta blood vessel), lymph fluids, and those obtained by subjecting the above fluids to some treatment such as centrifugation, and suspensions obtained by resuspending cells extracted from any of various organs or tissues, in some liquid.

[0042] In the present invention, “a cell-containing fluid containing vascular endothelial precursor cells and cells to be removed” may be a cell-suspending fluid containing at least vascular endothelial precursor cells, and includes bone marrow, cord blood, placental blood, peripheral blood, lymph, cultured fluid thereof, a fluid treated by, for example, centrifugation, and a fluid in which cells extracted from various organs and tissues are resuspended in some liquid. Among them, bone marrow, cord blood, G-CSF (Granulocyte-Colony Stimulating Factor) mobilized peripheral blood and peripheral blood contain abundantly the vascular endothelial precursor cells, and these are the cell-suspending fluids preferably used in the present invention.

[0043] The term “nucleated cells” means cells having a nucleus therein. The nucleated cells include, for example, leukocytes, granulocytes, neutrophils, baso-phils, eosinophils, myelocytes, erythroblasts, lymphocytes, T lymphocytes, helper T lymphocytes, cytotoxic T lymphocytes, suppressor T lymphocytes, B lymphocytes, NK cells, NKT cells, monocytes, macrophages, dendritic cells, osteoclasts, osteoblasts, osteocytes, hematopoietic stem cells, fibroblasts and chondroblasts.

[0044] The term “mononuclear cell fraction containing hematopoietic stem cells” means a mononuclear cell population containing hematopoietic stem cells and/or hematopoietic progenitor cells (they are hereinafter given the general name “hematopoietic stem cells”). “Mononuclear cell” is a general term for cells having a nucleus therein, and specific examples thereof are lymphocytes (T cells, B cells and NK cells), monocytes, hematopoietic stem cells, myelocytes, blast cells, etc.

[0045] The content of hematopoietic stem cells in the mononuclear cell population is usually 0.01% to 99% and varies depending on the kind of a starting cell population, and whether cells are treated or not. The content of hematopoietic stem cells is usually, for example, about 0.01% in peripheral blood, 0.05 to 1.0% in cord blood and 0.5 to 2% in bone marrow in the case of a normal person. In peripheral blood having a granulocyte colony-stimulating factor (G-CSF) administered, the content of hematopoietic stem cells differs markedly among individuals, and is 0.1 to several per cent. When cell separation using a monoclonal antibody, in particular, cell separation by a flow cytometry method is carried out, the content of hematopoietic stem cells reaches 99% in some cases. In any case, the term “mononuclear cell fraction containing hematopoietic stem cells” does not concretely specify the content of hemato-poietic stem cells at all.

[0046] The cells having no nucleus which are referred to in the present specification include, for example, erythrocytes and platelets.

[0047] The expression “cells to be removed have a surface marker different from that of cells to be recovered” in the present specification means that the cells to be recovered and the cells to be removed are similarly nucleated cells, but are different in surface marker (the cells to be recovered and the cells to be removed belong different subgroups, respectively). For example, the cells to be recovered are helper T lymphocytes (having anti-CD4 antigen as a surface marker), and the cells to be removed are suppressor T lymphocytes (having anti-CDS antigen as a surface marker).

[0048] When cells to be recovered are nucleated cells, and cells to be removed are cells having no nucleus, examples of their combination and examples of use thereof are as follows, but the combination and use are not limited thereto.

[0049] 1. Cells to be recovered: leukocytes, cells to be removed: erythrocytes, use: interferon preparation.

[0050] 2. Cells to be recovered: lymphocytes, cells to be removed: erythrocytes and platelets, use: adoptive-immuno therapy.

[0051] 3. Cells to be recovered: a mononuclear cell traction containing hematopoietic stem cells, cells to be removed; erythrocytes and platelets, use: hematopoietic stem cell transplantation.

[0052] Cells to be recovered: endothelial precursor cells, cells to be removed; erythrocytes and platelets, use: therapeutic vasculogenesis.

[0053] The vascular endothelial precursor cells in the present invention mean cells existing in blood such as bone marrow, peripheral blood and cord blood and at least expressing KDR/Flk-1 on the cell surface and/or expressing it in RNA level. The KDR/Flk-1 expressed on the cell surface was analyzed by the flow cytometry using anti-KDR/Flk-1 antibody (Clone KDR-1; Sigma Inc.). Further, the KDR/Flk-1 expressed in RNA level was analyzed by the RT-PCR (reverse transcription—polymerase chain reaction). A sequence of the primer used was CAA CAA AGT CGG GAG AGG AG/ATG ACG ATG GAC AAG TAG CC. The attaching cells in the present invention mean cells existing in blood such as bone marrow, peripheral blood and cord blood and adhering on a surface when cells are cultivated on the surface coated with an extracellular matrix such as fibronectin, vitronectin, collagen, gelatin, and the like. Most of the attaching cells take a form of spindle. Further, the cells expressing KDR/Flk-1 are found to be about 30-70% of the total number of the attaching cells from an analysis of their surface markers, and therefore the vascular endothelial precursor cells are abundantly contained in the attaching cells.

[0054] When cells to be recovered are nucleated cells, and cells to be removed are nucleated cells having a surface marker different from that of the cells to be recovered, examples of their combination and examples of use thereof are as follows, but the combination and use are not limited thereto.

[0055] 1. Cells to be recovered: CD34-positive nucleated cells, cells to be removed: CD34-negative nucleated cells, Use: CD34-positive cell transplantation.

[0056] 2. Cells to be recovered: CD8-positive T lymphocytes, cells to be removed: CD8-negative T lymphocytes, use: adoptive-immuno therapy.

[0057] When cells to be recovered are nucleated cells and cells to be removed are cells having no nucleus and nucleated cells having a surface marker different from that of the cells to be recovered, examples of their combination and examples of use thereof are as follows, but the combination and use are not limited thereto.

[0058] 1. Cells to be recovered: CD34-positive nucleated cells, cells to be removed: erythrocytes, platelets and CD34-negative nucleated cells, use: CD34-positive cell transplantation. positive 2. Cells to be recovered: CD8-positive T lymphocytes, cells to be removed: erythrocytes, platelets and CD8-negative T lymphocytes, use: adoptive-immuno therapy.

[0059] In the present invention, the cell-capturing means capable of capturing at least cells to be recovered and substantially permitting passage therethrough of cells to be removed, may comprise a container having a liquid inlet and a liquid outlet which is packed with a material capable of capturing the cells to be recovered and substantially permitting passage therethrough of the cells to be removed, and a molded container having a cell-capturing surface on its inner surface. In the present invention, “cell-capturing means” may be called “cell separator”. The material capable of capturing the cells to be recovered and substantially permitting passage therethrough of the cells to be removed may be any conventional cell-capturing material so long as it can selectively capture the cells to be recovered. The following materials, for example, are preferable because of their excellent moldability, sterilizability, and low cytotoxicity: synthetic polymers such as polyethylenes, polypropylenes, polystyrenes, acrylic resins, nylons, polyesters, polycarbonates, polyacrylamides, polyurethanes, etc; natural polymers such as agarose, cellulose, cellulose acetate, chitin, chitosan, alginates, etc.; inorganic materials such as hydroxyapatite, glass, alumina, titania, etc.; and metals such as stainless steel, titanium, aluminum, etc.

[0060] These capturing materials may be used as they are, or after being subjected to surface modification necessary for selective passage or capture of cells, etc. For example, for improving the permeability to platelets, there is, for instance, the method comprising coating with a polymer having nonionic hydrophilic groups and basic nitrogen-containing functional groups which has been proposed in International Publication No. WO 87/05812. As a method for selective capture of cells, a method of immobilizing a ligand having affinity for specific cells, such as an amino acid, peptide, sugar or glycoprotein (including bio-ligands such as antibody and adhesion molecules) may be used, for example, by the haloaceamide method proposed in JP-A-2-261833.

[0061] The shape of the capturing material may be granular, a fiber mass, woven fabric, nonwoven fabric, a spongy structure, a flat plate, etc. The granules, fiber mass, woven fabric, nonwoven fabric and spongy structure are preferable because they have a large surface area per volume. From the viewpoint of ease of handling, porous structures such as the fiber mass, woven fabric, nonwoven fabric and spongy structure are more preferable. Among them, the nonwoven fabric and spongy structure are the most preferable from the viewpoint of the flowability of a cell suspension and productivity.

[0062] When the nonwoven fabric is used, its fiber diameter in the case of not immobilizing a so-called bio-ligand capable of specifically binding to specific cells, such as anti-CD34 monoclonal antibody on the fabric surface, is usually not more than 30 μm and not less than 1.0 μm, preferably not more than 20 μm and not less than 1.0 μm. more preferably not more than 10 μm and not less than 1.5 μm. When the fiber diameter is less than 1.0 μm. the cells to be recovered are undesirably liable to be tightly captured and become difficult to recover. When the fiber diameter is more than 30 μm. the cells to be recovered are very likely to pass through the nonwoven material without being captured by fiber. Both of such values are not desirable because they tend to decrease the recovery.

[0063] The term “fiber diameter” in the present specification means a value obtained by the following procedure.

[0064] Portions which are individually considered to be substantially uniform are sampled from a filter element which constitute a porous structure, and photographed at a magnification of 1,000 to 3,000 by using a scanning electron microscope and the like. The fiber diameter values are read from the photograph and averaged.

[0065] In the sampling, the effective filtration sectional area portion of the filter element is partitioned into sections 0.5 to 1 cm square, and of these sections, three or more sections, preferably five or more sections, are sampled at random. The random sampling is carried out, for example, by assigning a lot number to each of the above-mentioned sections and selecting sections in a necessary number or more by, for instance, a method using a table of random numbers. Then, three or more, preferably five or more portions of each sampled section are photographed, and the diameters of all photographed fibers are measured.

[0066] Here, the diameter of a fiber refers to the width of the fiber in a direction perpendicular to the fiber axis, and the average is calculated by dividing the sum of the diameters measured of all the fibers by the number of the fibers. However, data obtained in, for example; the following cases are omitted; the case where a plurality of fibers overlap one another and the width of any of them cannot be measured because the view of this fiber is obstructed by the other fibers; the case where a plurality of fibers form a thick fiber owing to their melting or the like; and the case where fibers widely different in diameter are present as a mixture.

[0067] The average of the fiber diameters is calculated from data obtained for 500 or more fibers, preferably 1,000 or more fibers by the method described above.

[0068] When the spongy structure is used, its pore size is usually not more than 25 μm and not less than 2.0 μm, preferably not more than 20 μm and not less than 3.0 μm, more preferably not more than 1.5 μm and not less than 4.0 μm. When the pore size is less than 2.0 μm, the flowability is very low, so that the passage of a fluid through the spongy structure tends to be difficult in itself. When the pore size is more than 25 μm, the capture rate of the cells to be recovered is undesirably decreased, resulting in a low recovery.

[0069] When the spongy structure is used, its pore size is usually not more than 25 μm and not less than 2.0 μm. preferably not more than 20 μm and not less than 3.0 μm, more preferably not more than 15 μm and not less than 4.0 μm. When the pore size is less than 2.0 μm, the flowability is very low, so that the passage of a fluid through the spongy structure tends to be difficult in itself. When the pore size is more than 25 μm, the capture rate of the cells to be recovered is undesirably decreased, resulting in a low recovery.

[0070] The term “pore size” in the present specification has the following meaning: a porous structure is cut perpendicularly to the direction of flow of blood, the area of each of pores dispersed in the whole section is measured, the diameter in terms of a circle of the pore is calculated from the area, the relationship between diameter and the number of pores is determined, and a diameter in terms of a circle at which the number of pores is largest is taken as the pore size.

[0071] That is, the term “pore size” used in the present specification has the following meaning: the diameter of each of pores dispersed in any section of the porous structure is converted to the diameter of a circle having the same area as that of the pore, a graph is obtained by plotting this diameter as abscissa at intervals of 0.1 μm, and plotting the number of pores in each interval (0.1 μm) as ordinate, and a diameter corresponding to the peak of the normal distribution curve obtained is taken as the pore size.

[0072] Specifically, the pore size is determined by photographing the surface of a capturing material by a scanning electron microscope, and visually measuring the diameters of 2,000 or more pores dispersed on the photographed surface, at random. Pores having a pore size large than the determined pore size are present in a smaller number, and the passage of particles with a diameter larger than the determined pore size through the capturing means is not always impossible.

[0073] When the measurement of the diameters of pores is difficult in determining the pore size of a porous structure, the pore size is determined as follows. A specimen with a certain thickness is obtained by cutting the porous structure at a distance of 0.5 mm or less from the surface of the porous structure in the direction of the thickness of the capturing means as perpendicularly as possible to the direction of flow of blood. The specimen is subjected to measurement by a mercury injection method (Pore Size 9320, Shimadzu Corp.). The amount of mercury injected is taken as 0% when no mercury has gotten into the pores of the porous structure. The amount of mercury injected is taken as 100% when mercury has gotten into all the pores of the porous structure. A pore size corresponding to an amount of mercury injected of 50% is taken as the pore size of the porous structure. In this case, the measurement is carried out in a pressure range of a mercury porosimeter of 1 to 1,000 psia.

[0074] In the case of a porous structure which is so flexible that when it is subjected to the measurement as it is, it is deformed during the measurement to make the detection of pores impossible, the above measurement is carried out by conducting a pretreatment such as fixation of the pores for preventing their deformation under pressure. The present invention includes such a porous structure.

[0075] The container packed with material capable of capturing the cells to be recovered and substantially permitting passage therethrough of the cells to be removed preferably uses, but is not limited to the following materials, for example, because of their excellent moldability, sterilizability, and low cytotoxicity: synthetic polymers such as polyethylenes, polypropylenes, polystyrenes, acrylic resins, nylons, polyesters, polycarbonates, polyacrylamides, polyurethanes, poly(vinyl chloride)s, etc.; inorganic materials such as hydroxyapatite, glass, alumina, titania, etc.; and metals such as stainless steel, titanium, aluminum, etc.

[0076] The molded container having a cell-capturing surface on its inner surface, i.e., an example of the cell-capturing means which is other than the container packed with the cell-capturing material, may be a flask, dish, conical tube, syringe, blood bag, etc.

[0077] In the present specification, the expression “substantially capturing cells to be recovered” means capturing 60% or more of cells to be recovered in a cell-containing fluid. The expression “substantially permitting passage therethrough of cells to be removed” means passing 60% or more of cells to be removed in the cell-containing fluid.

[0078] In the present invention, cells to be recovered which have been captured by the cell-capturing means are recovered by using a liquid with a specific viscosity (hereinafter referred to also as “recovering liquid” or “liquid for recovery”). The viscosity of this liquid should not be more than 500 mPa.s aid not less than 5 mPa.s, preferably not more than 100 mPa.s and not less than 5 mPa.s, more preferably not more than 50 mPa.s and not less than 7 mPa.s. When the viscosity is less than 5 mPa.s, the recovery is low. When the viscosity is more than 500 mPa.s, the passage of the liquid through the cell-capturing means is very difficult even if a pump is used, so that the work-efficiency is low. Moreover, a pressure increase is caused, so that leakage from a joint between tubes in a line tends to occur. Therefore, such viscosity values are not desirable. As a method for measuring the viscosity, use of a rotating viscometer is preferable because it is the simplest, and has a high precision.

[0079] Any liquid may be used as the recovering liquid, so long as it has little undesirable influence on cells. For example, solutions of synthetic polymers such as poly(ethylene glycol)s poly(vinylpyrrolidone)s, poly(vinyl alcohol)s etc.; solutions of natural polymers such as methyl cellulose, gelatin, hydroxyethyl starch, dextran, chitin derivatives, collagen, fibronectin, albumin, globulin, etc.; solutions of organic substances such as glucose, saccharose, maltose, trehalose, sorbitol, glycerol, dimethyl sulfoxide, silicone oil, etc.; and mixtures thereof may be used. Typical example of the plasma protein is HSA (human serum albumin) and that of the serum is human AB serum. From the viewpoint of safety such as protection of infection, a sample from the autologous blood is idealistic, however there is a problem for requiring great deal of time and labor for the preparation thereof. In addition, in view of the prion infection, use of blood derived from bovine is not recommendable. As a result of investigation by the present inventors, it was found that an especially high recovery can be attained by using dextran. Therefore, employment of dextran is explained below in detail.

[0080] The dextran referred to herein is a glucose polymer in which most of the glucose units are joined by α-1,6 linkages. The dextran includes its partial hydrolysis products and its derivatives such as sulfate esters. Although the dextran is not limited in molecular weight, its average molecular weight is preferably 1,000 to 10,000,000, more preferably 5,000 to 5,000,000, most preferably 10,000 to 1,000,000, in view of solubility, availability, etc. Since the viscosity varies depending on the molecular weight, even at the same concentration, the molecular weight of the concentration is properly adjusted so that the viscosity may be not more than 500 mPa.s and not less than 5 mPa.s. A sterilized dextran 40 injection (a 10 w/v % solution of dextran with a molecular weight of about 40,000 in physiological saline), approved as a medicine, is on the market and hence can be suitably used. In order to adjust the viscosity to not more than 500 mPa.s and not less than 5 mPa.s, the dextran may be used singly, or in admixture with other substances. Examples of the substances are synthetic polymers such as poly(ethylene glycol)s, poly(vinyl-pyrrolidone)s, poly(vinyl alcohol)s, etc.; natural polymers such as methyl cellulose, gelatin, hydroxyethyl starch, dextran, chitin derivatives, collagen, fibronectin, albumin, globulin, etc.; and organic substances such as glucose, saccharose, maltose, trehalose, sorbitol, glycerol, dimethyl sulfoxide, etc. Although a mechanism by which cells can be recovered with high recovery by using dextran is not known at present, the present inventors conjecture that the dextran has a property of reducing the adhesiveness of the cells to the capturing material.

[0081] The solvent used for dissolving a solute in the preparation of the liquid having a viscosity of not more than 500 mPa.s and not less than 5 mPa.s, may be physiological saline, buffer solutions such as Dulbecco phosphate buffer solution (D-PBS), Hank's Balanced Salt Solution (HBSS) and the like, and media such as RPMI1640 and the like. If necessary, dextran, hydroxyethyl starch, albumin, globulin, glucose, saccharose, trehalose, globulin, citrate-phosphate-dextrose (CPD), acid-citrate-dextrose (ACD), EDTA, heparin, etc. may be incorporated into the liquid for supply of a nutriment, protection of cell membrane, or impartment of anticoagulating effect, etc.

[0082] The liquid with a specific viscosity according to the present invention is preferably one which can be used for cryopreservation of cells to be recovered, or preservation of the cells in a liquid state. As described above, for hematopoietic stem cell transplanation, in particular, hematopoietic stem cell transplanation using cord blood, a cell population freed of erythrocytes by a Ficoll method or the like is washed (because a Ficoll solution is toxic), and a cryoprotectant and the like are added thereto to prepare a cell suspension, followed by cryopreservation in liquid nitrogen or a freezer until needed for practical use. In the present invention, a cell suspension to be preserved can be prepared without troublesome operations after cell separation by using a liquid suitable both for the preservation, in particular, cryopreservation, as well as for recovery, by having a specific viscosity. Specific examples of the liquid for recovery which is usable for cryopreservation and as a cryoprotectant are, a nutriment, or a cell membrane protecting component, etc. Cryoprotectants are classified into two categories, 1) extracellular cryoprotectants, and 2) intracellular cryoprotectants, according to the action mechanism. In the first category, water-soluble polymers such as hydroxyethyl starch, dextran, poly(vinylpyrrolidone)s, etc. are generally used. In the second category, low-molecular weight organic compounds such as dimethyl sulfoxide, glycerol, etc. are generally used. The nutriment includes sugars such as glucose and the like, and various media for cell culture. As the cell membrane protecting component, albumin is generally used. Plasma is used in some cases as a combination of the nutriment and the cell membrane protecting component. As described above, these components are preferably used singly, or in combination in the liquid for recovery having a specific viscosity of the present invention. The components described above may be added at the time of cryopreservation after cell recovery.

[0083] There are generally two freezing methods employed, i.e., a simple method using a deep-freezer at −80° C., or a method comprising slow cooling in a program freezer and preservation in liquid nitrogen. For thawing cells subjected to cryopreservation, rapid thawing in a warm bath at 37° C. is generally carried out.

[0084] As a method for introducing the cell-containing fluid referred to in the present specification into the cell-capturing means, there may be adopted either a method of connecting a bag or bottle containing the cell-containing fluid through a tube, and then introducing the fluid, for example, by utilizing its fall, a roller pump, causing a flow of the fluid by squeezing the bag, or by a method of connecting a syringe containing the cell-containing fluid, and introducing the fluid by pushing the piston of the syringe by hand or using a device such as a syringe pump. The pushing by hand is characterized by its simplicity, and the use of the device is characterized in that the control of the flow rate of the recovering liquid in its introduction is easy. Therefore, a suitable method is selected depending on the purpose.

[0085] When the cell-containing fluid is introduced into the cell-capturing means, the cells to be recovered are captured, and the cells to be removed flow out, but a minority thereof remain in the container in some cases. Therefore, the cell-capturing means is preferably rinsed in order to rinse away the slight amount of the remaining cells to be removed. Any rinse may be used, so long as it is a physiological solution. Several examples thereof are physiological saline, buffer solutions such as Dulbecco phosphate buffer solution (D-PBS), Hank's Balanced Salt Solution (HBSS) and the like, and media such as RPMI1640 and the like. If necessary, dextran, hydroxyethyl starch, albumin, globulin, glucose, saccharose, trehalose, globulin, citrate-phosphate-dextrose (CPD), acid-citrate-dextrose (ACD), EDTA, or heparin, etc. may be added to the physiological solutions mentioned above for supply of a nutriment, protection of cell membrane, and impartment of anticoagulating effect, etc.

[0086] There are two directions for introduction of the rinse, i.e., the same direction as the direction of introduction of the cell-containing fluid, and the direction opposite thereto. Of these, the same direction is preferable. In the case of the opposite direction, the cells to be recovered which have been captured are liable to leak out owing to the rinsing. The viscosity of the rinse is preferably less than 5 mPa.s. When the viscosity is 5 mPa.s or more, the cells to be recovered which have been captured are liable to leak out.

[0087] In the present invention, as a method for introducing the liquid with a viscosity of not more than 500 mPa.s and not less than 5 mPa.s into the above-mentioned cell-capturing means, there may be adopted either a method of connecting a bag or bottle containing the liquid to the cell-capturing means through a tube, and introducing the liquid by utilizing its fall, a roller pump, by squeezing the bag, or by a method of connecting a syringe containing the liquid, and introducing the liquid into the cell-capturing means by pushing the piston of the syringe by hand, or by using a device such as a syringe pump. In this case, as in the direction of introduction of the liquid, there are two directions, i.e., the same direction as the direction of introduction of the cell-containing fluid, and the direction opposite thereto. Of these, the latter is usually preferable because the cell recovery is higher. The flow rate of the recovering liquid is preferably rapid because the recovery tends to be increased. The linear speed obtained by dividing the flow rate by the filtration sectional area is usually 0.5 cm/min. or more, preferably 5 cm/min. or more, and more preferably 10 cm/min. or more.

[0088] It is also possible to recover a slight amount of cells (or their constituents) remaining in the cell-capturing means, by introducing another liquid after introducing the recovering liquid. By this recovery, the collection of a sample for HLA typing, which is indispensable, for example, in hematopoietic stem cell transplantation, can be carried but simultaneously with the cell separation procedure. A slight amount of the cells (or their constituents) remaining in the cell-capturing means are used for various purposes, other than HLA typing such as investigation of ex vivo expansion of hematopoietic stem cells, genetic diagnosis, or employment in cell transplantation in combination with the cells obtained by the first recovery. A brief supplementary explanation of HLA typing is given below.

[0089] HLA typing is carried out by using DNA present in the nuclei of nucleated cells. Therefore, recovering the DNA is preferable to recovering the cells themselves because it is laborsaving. Accordingly, a liquid capable of lysing or disrupting the cells is preferably used as a recovering liquid. The liquid includes, for example, hypotonic liquids such as solutions of surfactants (e.g. sodium dodecyl sulfate, lauryl sodium sulfate and Triton X-100), distilled water, ion-exchanged water, etc. The DNA recovered by the use of such a liquid is purified by a well-known phenol chloroform method or the like and subjected to HLA typing.

[0090] The phrase “use the recovered vascular endothelial precursor cells for regenerating a blood vessel” in the present invention means that the vascular endothelial precursor cells, which are once captured on the cell-capturing means and then recovered from the cell-capturing means, can be not only transplanted to the donor himself but also to another individual, or alternatively used for regenerating a blood vessel in vitro. Further, the vascular endothelial precursor cells obtained according to the present invention can be used as they are or, if necessary, after being subjected to further various treatments such as purification by isolation, culture, activation, differentiation-induction, amplification, gene transfer, cryopreservation and conjugation with artificial blood vessel, which has been proposed in the proceedings of 34th Japan Artificial Organ Association, S1-1, for treatment of vascular lesion and/or defect in various regions and for studies in the fundamental scientific fields.

[0091] The term “an ischemic damaged region” in the present invention means a functionally damaged or necrotized region caused by oxygen deficiency and malnutrition as a result of significantly decreased or terminated blood stream due to different diseases. Further, the term “a penumbral region thereof” means a region where the vascular endothelial precursor cells can arrive at the ischemic region by means of a blood stream or a migration. Examples of specific diseases include ASO (arteriosclerosis obliterans) or PAOD (peripheral arterial occlusive disease), Buerger's disease, ischemic heart disease, diabetic neuropathy, diabetic nephropathy, cerebral infarction and senile bedsore. For detection of the ischemic region, ultrasonography, myocardial scintigraphy, angiography and electrocardiography are used in the heart, and LDPI (Laser Doppler Perfusion Image) and angiography are used in the lower extremities and the superior limb.

[0092] The sentence “the vascular endothelial precursor cells are directly transplanted to a human ischemic damaged region and/or a penumbral region thereof” in the present invention has no specific limitation, so long as the transplantation is performed by a method other than the one via blood vessel. The simplest and preferable method is that the recovered vascular endothelial precursor cells or the attaching cells obtained by further cultivating them are filled in a syringe and introduced into the punctured tissues. In case of a broad region of the ischemic lesion, a transplantation of cells in plural regions is more preferable than a transplantation of a number of cells in a single region, since a rapid improvement of the blood stream can be obtained. The tissue to which the cells are transplanted is preferably muscle. In case of ischemic lower extremities, the vascular endothelial precursor cells in total amount of about 107 (in case of the mononuclear cells, about 108-109) are prepared in advance, and the cells are transplanted into the depth of 1-3 cm from the skin surface layer at 10-100 points on the crossing points of a grid having a space of about 3 cm. In case of myocardial ischemia, the vascular endothelial precursor cells in total amount of about 106 (in case of the mononuclear cells, about 107-108) is prepared in advance, and the cells are transplanted into the depth of about 3 mm from the surface of the heart at about 20 points randomly around the central part of the ischemic region. An amount of the fluid introduced in one point is preferably about 0.5-1 ml.

[0093] The “transvascular transplantation” in the present invention is the transplantation of the recovered vascular endothelial precursor cells or the attaching cells obtained by further cultivating them via blood vessel because of easy introduction to the patient. The blood vessel to which the cells are introduced through a needle Or a catheter is preferably the one in lower extremities or superior limb. The total amount of vascular endothelial precursor cells via blood vessel is preferably 2-10 times as much as those transplanted directly, since the efficiency to reach to the ischemic region is lower than that of direct transplantation.

[0094] The “physiological carrier” in the present invention is not limited specifically, so long as the fluid is a liquid in which the vascular endothelial precursor cells or the attaching cells obtained by further cultivating the cells can be suspended without damage. Examples thereof include physiological saline, medium for cell culture, autologous serum, autologous plasma, autologous blood and the like, alone or in combination thereof.

[0095] The components passing through the cell-capturing means, i.e. erythrocytes, platelets, plasma and the like, can be used for various tests and studies. Further specific use thereof is for collecting raw materials of pharmaceuticals, if donor is a healthy subject. In case of the autologous transplantation, the blood can be returned to the patient as the blood for transfusion. This is preferable from the viewpoint that a possibility of repeated treatments can be extended while anemia of the patient is avoided.

[0096] In the present invention, the phrase “recovering the attaching cells adhered on the extracellular matrix” means that after the cells recovered by the cell-capturing means are cultivated, the cultivated cells which are adhered to the substrate coated with the extracellular matrix are recovered. More specifically, it means that, for example, suspending the cells recovered by the cell-capturing means in the medium for cell culture; plating the cell suspension on the surface of the substrate, for example, a plastic dish for cell culture, coated with the extracellular matrix; removing the supernatant containing non-attaching cells such as erythrocytes, granulocytes and the like after several days of the cultivation; and detaching the adhered attaching cells by enzymatic treatment using trypsin-containing FDTA or suspending the cells by incubating with an addition of EDTA-containing PBS at 37° C.; to recover the cells, To recover the attaching cells from the cell-containing fluid containing the vascular endothelial precursor cells thus separated by the cell-capturing means is extremely preferable for regenerating a blood vessel, since the erythrocytes which inhibit the regeneration of a blood vessel and the granulocytes which cause inflammatory reaction can be removed efficiently. The medium for cell culture herein may be the medium wherein the attaching cells adhere to the substrate And the expression of surface markers of the vascular endothelial precursor cells is maintained, and the medium containing serum components, heparin, endothelial cell growth factor and the like is preferably used. The serum components are not limited specifically, and, for example, human AB serum and autoserum may be used.

[0097] In the present invention, “cocultivating the attaching cells with the human umbilical vein endothelial cells on the extracellular matrix” means; the cocultivation under the conditions of the plating cell concentration of 0.1-5×105/ml; the cell ratio of attaching cells/human umbilical vein endothelial cells=0.3-3.0 and the medium for cell culture as described hereinbefore. This method is suitable for confirming the function of the vascular endothelial precursor cells before transplantation, since a blood vessel-like network can be easily observed within 2-3 hours.

[0098] The extracellular matrix in the present invention means fibronectin, vitronectin, gelatin, collagen, laminin and the like, and may be used alone or admixed with collagen and laminin as in Matrigel (Beckton-Deckinson Inc.). Further, a commercially available plastic dish like BIO-COAT (Beckton-Deckinson Inc.), on which the extracellular matrix has been coated, may be used.

[0099] In the present invention, the recovered cells may be preserved until use. For the preservation, there are two methods, preservation in a liquid state, and cryopreservation. The cryopreservation is usually carried out because the preservation in a liquid state is limited in time to at most 2 to 3 days in the case of, for example, hematopoietic stem cells.

[0100] Next, the cell separation system of the present invention is explained below. The line referred to in the present specification, i.e., the line for introducing the cell-containing fluid into the cell-capturing means which is connected upstream to the inlet of the cell-capturing means is a line connectable to, for example, a container reserving the cell-containing fluid, or a line connectable to a living body tissue in which the cell-containing fluid is present. Specific examples of the former are as follows: a tube equipped with a spike or a tube equipped with a Luer adapter (male or female) is properly selected when the container reserving the cell-containing fluid is a blood bag, or a mere tube is properly selected when connection by a sterilized connector (hereinafter referred to as “SCD connection”) is made. In addition, a needlable tube having a septum is properly selected as the line when the container reserving the cell-containing fluid is a syringe equipped with a needle, or a Luer adapter (female) is properly selected as the line when the container is a syringe having a Luer opening but not a needle. Specific examples of the latter line are as follows, for example, when cord blood is used, the aforesaid living body tissue is umbilical cord and/or placenta, and a tube equipped with a metallic needle stickable into them is mentioned as the latter line. When a tube is used, it may be equipped between its ends with a clamp for opening or shutting the line, a roller clamp for adjusting the flow rate, a mesh chamber for removing aggregates, a syringe for giving the flow rate (including a flow path changing means), etc. When a syringe is used, it may be directly connected to the inlet of the cell-capturing means without a tube.

[0101] The other line referred to in the present specification, i.e., the line for introducing a liquid into the aforesaid cell-capturing means which is connected downstream to the outlet of the aforesaid cell-capturing means, includes lines which are classified as follows according to whether a container containing the liquid to be introduced into the cell-capturing means has been previously connected or is subsequently connectable, and according to the means used for introducing the liquid. That is, when the container containing the liquid to be introduced into the cell-capturing means is previously connected, the line includes, for example, a tube equipped with a bag, and a syringe. In the case of such a bag, a method for introducing the liquid into the cell-capturing means includes a method utilizing the fall of the liquid, a method of squeezing the bag, a method using a roller pump, etc. When the container containing the liquid to be introduced into the cell-capturing means is connected afterwards, the following tubes are selected. When a syringe is used, the line includes a needlable tube having a septum, a tube equipped with a Luer adapter (female), a tube equipped with a three-way stopcock, etc., to which the syringe can be connected. When a bag is used, a line connectable to the bag, i.e., a tube equipped with a spike, or a tube equipped with a Luer adapter (male or female) is properly selected as the aforesaid line. When SCD connection is made, a mere tube is properly selected as the aforesaid line. When a syringe is used, it may be directly connected to the outlet of the cell-capturing means without a tube.

[0102] The other line referred to in the present specification, i.e., the line for recovering cells from the inlet side of the aforesaid cell-capturing means which is connected upstream to the inlet of the aforesaid cell-capturing means, includes lines which are classified as follows according to a container for recovering cells which flow out of the cell-capturing means. That is, when the cells are recovered into a bag, a line connected or connectable to the bag, i.e., a tube equipped with a spike or a tube equipped with a Luer adapter (male or female) is properly selected as the aforesaid line. When SCD connection is made, a mere tube is properly selected as the aforesaid line. When the cells are collected into a conical tube, any open-ended line may be used. When the cells are collected by using a syringe having a Luer opening, a Luer adapter (female), a three-way stopcock and the like are used. When a syringe is used, it may be directly connected to the inlet of the cell-capturing means without a tube.

[0103] Instead of this other line, for example, a container for recovering the cells which flow out of the cell-capturing means is preferably able to withstand freezing and thawing, such as a freeze bag; because the transfer of the cells to a freeze bag can then be omitted. Examples of cryopreservation bags are freeze bags such as “Cryocyte” manufactured by Baxter, “Cell Freeze Bag” manufactured by Charter Med, “Hemo Freeze Bag” manufactured by NPBI, etc.

[0104] To the cell separation system according to the present invention, a line for introducing a liquid into the cell-capturing means may be added in order to rinse away a slight amount of cells to be removed which remain in the cell-capturing means, before recovering cells captured by the cell-capturing means. This line includes lines which are classified as follows according to whether a container containing the liquid is previously connected, or subsequently connectable, and according to the means for introducing the liquid. That is, when the container containing the liquid is previously connected, the line includes, for example, a tube equipped with a bag, and a syringe. When the container containing the liquid is connected afterwards, the following types of tubes are selected. When a syringe is used, the line includes a needlable tube having a septum, and a tube equipped with a Luer adapter (female), to which the syringe can be connected. When a bag is used, a line connectable to the bag, i.e., a tube equipped with a spike or a tube equipped with a Luer adapter (male or female) is properly selected as the line. When an SCD connection is made, a mere tube is properly selected as said line. When a syringe is used, it may be directly connected to the outlet of the cell-capturing means without a tube. Although the position of connecting said line to the cell-capturing means may be on either the inlet side or the outlet side, it is preferably on the inlet side from the viewpoint of ease of operation.

[0105] The present cell separation system, may have a line added for collecting cells (or their constituents) remaining in the cell-capturing means by further introducing a liquid after recovering cells to be recovered. In the case where cells different in purpose of use from the first recovered cells are recovered, for example, in the case where a solution capable of lysing or disrupting cells is used for collecting cells (or their constituents) remaining in the cell-capturing means for HLA typing, the line should comprise a means for changing the flow path, and a plurality of branches so that the cells (or their constituents) collected afterward will not be nixed with the first recovered cells. The flow path changing means may include clamps, spikes, etc.

[0106] The cell separation method using the above-mentioned line system comprises steps of introducing, through a line connected upstream, a cell-containing fluid containing cells to be recovered and cells to be removed into a cell-capturing means capable of substantially capturing the cells to be recovered and substantially permitting passage of the cells to be removed. The resulting fluid containing the cells to be removed is taken out through the outlet of the cell-capturing means, and then a liquid with a viscosity of not more than 500 mPa.s and not less than 5 mPa.s is introduced into the cell-capturing means through a line connected downstream from the outlet of the cell-capturing means in order to recover the cells. When the recovered cells are preserved, the line (e.g. a freeze bag) connected upstream to the inlet of the cell-capturing means and containing the cells recovered, is sealed up and separated. The sealing-up and separation are carried out, for example, as follows: the line is sealed up by heat fusion using a heat sealer or the like, and then cut off, or a tube connected through a Luer adapter is detached from the main body and then heat-fused by using a heat sealer or the like. In any case, the term “sealing-up and separation” does not specify the order of operations (e.g. sealing-up followed by separation) at all.

[0107] The present invention further provides a liquid which contains hematopoietic stem cells which is substantially free from erythrocytes and/or platelets, and has a viscosity of not more than 500 mPa.s and not less than 5 mPa.s. The expression “substantially free from” used here means that this cell-containing fluid is prepared by removing 60% or more of erythrocytes and/or platelets from a starting cell-containing fluid. Although cord blood contains erythrocytes in addition to hematopoietic stem cells, a hematopoietic stem cell suspension containing substantially no erythrocyte can be provided by employing the cell separation method of the present invention. Furthermore, the cell-containing fluid may contain a cryopreservative agent.

[0108] The present invention still further provides a liquid containing cells to be recovered and substantially no cells to be removed which is obtained by a cell separation method comprising steps of introducing a cell-containing fluid containing cells to be recovered and cells to be removed, into a cell-capturing means capable of substantially capturing said cells to be recovered and substantially permitting passage there-through of said cells to be removed. The resulting fluid containing the cells to be removed is taken out of the cell-capturing means, and then a liquid with a viscosity of not more than 500 mPa.s and not less than 5 mPa.s is introduced into the cell-capturing means to recover the cells which have been captured by the cell-capturing means. When the separation method of the present invention is applied to a suspension containing cells to be recovered and cells to be removed, it becomes possible to efficiently provide a suspension substantially comprising the cells to be recovered.

[0109] The present invention still further provides a liquid with a viscosity to not more than 500 mPa.s and not less than 5 mPa.s as a liquid for recovering captured cells from a cell-capturing means. This liquid is preferably one which can be used also as a preservative for cells. In the case of preservation in a liquid state, specific examples of the preservative are sugars (e.g. glucose), nutriments (e.g. various media for cell culture), cell membrane protecting components (e.g. albumin), and combinations of a nutrient and a cell membrane protecting component (e.g. plasma). In the case of cryopreservation, the preservative includes cryoprotectants, in addition to the above examples. The cryoprotectants are classified into two categories, 1) extracellular cryoprotectants, and 2) intracellular cryoprotectants, according to the action mechanism. In the first category, water-soluble polymers such as hydroxyethyl starch, dextran, and poly(vinylpyrrolidone)s, etc. are generally used. In the second category, low-molecular weight organic compounds such as dimethyl sulfoxide, and glycerol, etc. are generally used.

[0110] An embodiment of the cell separation system according to the present invention is explained below with reference to the drawings, which should not be construed as limiting the scope of the invention.

[0111] FIG. 1 shows one embodiment of the cell separation system according to the present invention. In this system, all of the following connections are made by the use of spikes; the connection of a starting-cell bag (containing a cell-containing fluid containing cells to be recovered and cells to be removed) to the main body of the system of the present invention; the connection of a bag for recovering a fluid which flows out through the outlet of a cell-capturing means, to the main body of the system of the present invention; and the connection of a bag for recovering cells from the outlet side of the cell-capturing means, to the main body of the system of the present invention. In the system, there is a three-way stopcock provided to which a syringe with a male Luer opening is connected for introducing a liquid into the cell-capturing means.

[0112] In FIG. 1, numeral 1 denotes the cell-capturing means capable of substantially capturing the cells to be recovered and substantially permitting passage there-through of the cells to be removed. Numeral 2 denotes a line for introducing the cell-containing fluid into the cell-capturing means from the starting-cell bag, which comprises a spike 2-1, a clamp 2-2 and a tube 2-3. Numeral 3 denotes a line for discharging the fluid which flows out through the outlet of the cell-capturing means 1, which comprises a spike 3-1 and a tube 3-2. Numeral 4 denotes a line for introducing the liquid into the cell-capturing means from the outlet side of the cell-capturing means 1, which shares the tube with the line 3 and has the three-way stopcock 4-1 to which the syringe is connected. Numeral 5 denotes a line for recovering cells from the inlet side of the cell-capturing means, which comprises a spike 5-1, clamp 5-2, a tube 5-3 and a part of the tube 2-3. This line shares the tube 2-3 with the line 2 from the inlet of the cell-capturing means 1 to the point at which the tube 5-3 diverges from the tube 2-3.

[0113] Next, a method for using the cell-capturing means is explained below. Initially, the clamp 2-2 is shut, the three-way stopcock 4-1 is closed only in the direction of syringe connection, and the clamp 5-2 is closed. Then, the spike 2-1 is stuck into the starting-cell bag and the spike 3-1 is stuck into an empty bag. When the clamp 2-2 is opened, the cell-containing fluid is supplied to the cell-capturing means 1 through the tube 2-3 of the line 2. The cells to be recovered are captured and the cells to be removed are taken out and then collected in the empty bag through the tube 3-2 of the line 3. After completion of the treatment of the cell-containing fluid, the clamp 2-2 is closed, and the spike 2-1 is pulled out of the starting-cell bag and stuck into a commercially available bottle of physiological saline. When the clamp 2-2 is opened, the physiological saline rinses the cell-capturing means 1 and is collected in the bag containing the collected cells to be removed, through the line 3. After completion of the rinsing, the clamp 2-2 and the tube 3-2 are closed. Subsequently, a syringe containing a liquid with a viscosity of not more than 500 mPa.s and not less than 5 mPa.s is connected to the three-way stopcock 4-1, and the spike 5-1 is stuck into a cell-recovering bag. The three-way stopcock is turned in such a direction that the syringe communicates only with the cell-capturing means 1. After the clamp 5-2 is opened, the piston of the syringe is pushed to introduce the liquid into the cell-capturing means 1 from its outlet side, whereby the cells captured by the cell-capturing means are recovered into the cell-recovering bag through the line 5.

[0114] The present invention is illustrated below in further detail with reference to examples, which should not be construed as limiting the scope of the invention.

EXAMPLE 1

[0115] This working example shows an example of cell separation in the case where a cell-containing fluid was cord blood, cells to be recovered are a mononuclear cell fraction containing hematopoietic stem cells, and cells to be removed are erythrocytes and platelets.

[0116] {circle over (1)} Cell Separator

[0117] A polycarbonate container with outside dimensions (length×width×thickness) of 41×41×18 mm having a liquid outlet and a liquid inlet on the diagonal was packed with 12 polyester nonwoven fabrics with an average fiber diameter of 2.3 μm on the inlet side and 25 polyester nonwoven fabrics with an average fiber diameter of 12 μm on the outlet side. The packing density was 0.24 g/cm3, the effective filtration area 9 cm2, and the effective filtration length 12.4 mm. In order to impart platelet permeability to the resulting filter, coating with a hydrophilic polymer was carried out. In detail, a 1% ethanolic solution of a hydroxyethyl methacrylate_dimethylaminoethyl methacrylate copolymer (molar ratio between hydroxyethyl methacrylate and dimethylaminoethyl methacrylate=97:3) was passed through the filter from the inlet side of the filter, after which the filter was dried by introducing nitrogen gas thereinto.

[0118] {circle over (2)} Preparation of a Recovering Liquid

[0119] A commercially available solution of dextran 40 in physiological saline (Dextran 40 Injection-Midori, a trade name, available from Green Cross Corp.) was incorporated with human serum albumin to prepare a liquid containing 4% human serum albumin as recovering liquid A. This recovering liquid A was diluted 1.2-fold or 1,3-fold with physiological saline to obtain recovering liquid B and recovering liquid C, respectively. The viscosities of the recovering liquids are as follows: recovering liquid A 10.5 mPA.s, recovering liquid B 8.0 mPA.s, recovering liquid C 5.3 mPA.s.

[0120] {circle over (3)} Cell Separation Procedure and Line System

[0121] 200 Milliliters of cord blood collected from a placenta and umbilical cord after delivery and containing 15 vol % CPD was divided into four portions, and an experiment was carried out at 4 recovering liquid viscosity values (including that in Comparative Example 1) by using the same blood divided.

[0122] As shown in FIG. 2, a blood bag was connected to the inlet side of the cell separator 6 produced in the above item {circle over (1)}, through a tube having between its ends a three-way stopcock 9 having a bag for cell recovery 10 connected thereto, a mesh chamber 8, and a diverging point to a tube equipped with a spike 13 to be connected to a bottle of physiological saline for rinsing. A drain bag 12 was connected to the outlet side of the cell separator 6 through a tube having between its ends a three-way stopcock 11 for connecting a syringe for recovery.

[0123] A fluid containing nucleated cells in the starting-blood bag 7 was introduced into the cell separator at a head of about 60 cm, and a fluid containing erythrocytes and platelets which had flowed out of the cell separator 6 was discharged into the drain bag 12. Then, the spike 13 was stuck into the bottle of physiological saline, and the clamp 14 was opened, whereby the inside of the filter was rinsed with about 20 ml of physiological saline to rinse away a slight amount of erythrocytes and platelets, which remained in the filter. Subsequently, a 30-ml disposable syringe containing 25 ml of each recovering liquid was connected to the three-way stopcock 11, and the three-way stopcock 11 was turned in such a direction that the syringe communicated only with the cell separator. The three-way stopcock 9 was turned in such a direction that the cell separator 6 communicated only with the bag for cell recovery 10. Then, the piston of the syringe was pushed to recover cells captured in the cell separator, into the bag for cell recovery 10.

[0124] {circle over (4)} Analysis

[0125] The number of nucleated cells, the number of mononuclear cells, the number of erythrocytes, and the number of platelets were determined with an automatic hemocytometer. The percentage of CD34-positive cells based on the total number of nucleated cells was measured by the use of FITC-labeled anti-CD34 antibody according to a flow cytometry method comprising display on SSC-FITC (Miyazaki et al. “Nichijo Shinryo to Ketsueki (Practical Hematology)” Vol. 5, No. 2, pp. 21-24, 1995).

[0126] The recovery and the removal rate were calculated by the following equations:

Recovery (%)=100×(number of recovered cells/number of cells in starting cell population)

Removal rate (%)=100−100×(number of recovered cells/number of cells in starting cell population)

[0127] {circle over (5)} Results

[0128] The time required for pushing the piston of the syringe completely was 3 seconds. The linear speed was calculated to be 55.6 cm/min. The results are summarized in Table 1. It can be seen that nucleated cells, mononuclear cells and CD34-positive cells could be recovered at high percentages in the cell suspension recovered, and that erythrocytes and platelets were removed at high percentages.

	TABLE 1
	Recovery (%)
Recovering			CD34-
liquid	Nucleated	Mononuclear	positive	Removal rate (%)
(mPa · s)	cell	cell	cell	Erythrocyte	Platelet
A (10.5)	75.2	90.2	97.0	99.0	88.0
B (8.0)	74.0	90.0	96.6	99.0	88.0
C (5.3)	73.0	89.6	95.5	99.0	88.0

[0129] The cells recovered by the use of the recovering liquid could be subjected to cryopreservation according to the protocol described in an instruction mannual for a cryopreservative agent “CP-1” manufactured by Kyokuto Pharmaceutical Industrial Co., Ltd. In detail, dimethyl sulfoxide was added to the recovered cell suspension to adjust its final concentration to 5%, and the resulting mixture was subjected to cryopreservation in a deep-freezer at −80° C. After 30 days of cryopreservation, the mixture was rapidly thawed in a warm bath at 37° C., and the cell viability was measured by a conventional trypan blue exclusion method and found to be maintained at a high value of 90.4%.

COMPARATIVE EXAMPLE 1

[0130] In this comparative example, results obtained by using a recovering liquid with a low viscosity containing no dextran were compared with those obtained in Example 1, though as in Example 1, a cell-containing fluid was cord blood, cells to be recovered are a mono-nuclear cell fraction containing hematopoietic stem cells, and cells to be removed are erythrocytes and platelets.

[0131] {circle over (1)} Cell Separator

[0132] The same cell separator as in Example 1 was used.

[0133] {circle over (2)} Cell Separation Procedure and Line System

[0134] One of the portions of the cord blood obtained in Example 1 was used as starting cord blood. The process of Example 1 was repeated except for using 25 ml of physiological saline as a recovering liquid. The same line system as in Example 1 was used. The viscosity of the recovering liquid was 1.0 mPa.s.

[0135] {circle over (3)} Analysis

[0136] The same analysis as in Example 1 was carried out.

[0137] {circle over (5)} Results

[0138] The time required for pushing the piston of the syringe completely was 3 seconds. The results are summarized in Table 2. The recoveries of nucleated cells, mononuclear cells and CD34-positive cells in the cell suspension recovered were lower than in Example 1.

	TABLE 2
	Recovery (%)
Recovering			CD34-
liquid	Nucleated	Mononuclear	positive	Removal rate (%)
(mPa · s)	cell	cell	cell	Erythrocyte	Platelet
Physio-	31.0	40.0	45.0	99.0	89.7
logical
saline
(1.0)

EXAMPLE 2

[0139] This working example shows an example of cell separation in the case where a cell-containing fluid was peripheral blood, cells to be recovered are leukocytes, and cells to be removed are erythrocytes and platelets.

[0140] {circle over (1)} Cell Separator

[0141] A polycarbonate container with outside dimensions (length×width×thickness) of 41×41×18 mm having a liquid outlet and a liquid inlet on the diagonal was packed with 25 polyester nonwoven fabrics with an average fiber diameter of 12 μm on the inlet side and 12 polyester nonwoven fabrics with an average fiber diameter of 2.3 μm on the outlet side. The packing density was 0.24 g/cm3, the effective filtration area 9 cm2, and the effective filtration length 12.4 mm. In order to impart platelet permeability to the resulting filter, coating with a hydrophilic polymer was carried out. A 1% ethanolic solution of a hydroxyethyl methacrylate dimethylaminoethyl methacrylate copolymer (molar ratio between hydroxyethyl methacrylate and dimethylaminoethyl methacrylate=97:3) was passed through the filter from the inlet side of the filter, after which the filter was dried by introducing nitrogen gas thereinto.

[0142] {circle over (2)} Cell Separation Procedure

[0143] Into the cell separator produced was introduced 50 ml of whole peripheral blood (containing 15 vol % CPD) of a healthy person through the liquid inlet by utilizing the head (about 60 cm; flow rate about 5 ml/min.). Thereafter, 30 ml of physiological saline was passed through the cell separator by means of head (about 60 cm) in order to rinse away erythrocytes and platelets, which remained in the cell separator. Then, 30 ml of a 3.5% solution of a poly(vinylpyrrolidone) (average molecular weight: 360,000) in physiological saline was introduced into the cell separator at a rate of 100 ml/min. through the liquid outlet by the use of a pump, and cells were recovered through the liquid inlet. The viscosity of this recovering liquid was 20.3 mPa.s.

[0144] {circle over (3)} Analysis

[0145] The number of leukocytes, the number of erythrocytes and the number of platelets were determined with an automatic hemocytometer.

[0146] {circle over (4)} Results

[0147] The results are summarized in Table 3. Leuko-cytes were recovered at a high percentage in the cell suspension recovered, and erythrocytes and platelets were removed at high percentages. The linear speed was calculated to be 11.1 cm/min.

TABLE 3
Recovery (%)	Removal rate (%)
Leucocyte	Erythrocyte	Platelet
75.0	99.1	90.3

EXAMPLE 3

[0148] This working example shows an example of cell separation in the case where a cell-containing fluid was cord blood, cells to be recovered are hematopoietic stem cells (CD34-positive cells), and cells to be removed are erythrocytes and platelets.

[0149] {circle over (1)} Cell Separator

[0150] A polycarbonate container with outside dimensions (length×width×thickness) of 41×41×18 mm having a liquid outlet and a liquid inlet on the diagonal was packed with 12 polyester nonwoven fabrics with an average fiber diameter of 12 μm on the inlet side and 25 polystyrene nonwoven fabrics with an average fiber diameter of 2.3 μm having anti-human CD34 monoclonal mouse antibody (clone name: Immu133, available from Coulter Corp.; hereinafter abbreviated as “CD34 antibody”) immobilized thereon, on the outlet side. The packing density of the resulting filter was 0.2 g/cm3. The immobilization of the anti-human CD34 monoclonal mouse antibody on-the polystyrene was carried out by the well-known haloacetamide method proposed in JP-A-2-261833. In detail, polystyrene nonwoven fabrics (previously cut to the above-mentioned dimensions) were immersed in a treating solution prepared by adding 3.6 g of hydroxy-methyliodoacetamide and 25 g of trifluoromethanesulfonic acid to 165 ml of sulfolane, at room temperature for 5 hours to be reacted, for the purpose of activating the polystyrene nonwoven fabrics. The nonwoven fabrics thus activated were washed with D-PBS, after which, in order to immobilize the antibody on them, they were immersed for 2 hours in 10 ml of a CD34 antibody solution having a concentration adjusted to 20 μg/ml with D-PBS, and they were washed with D-PBS and then freeze-dried, whereby the nonwoven fabrics having the antibody immobilized thereon were obtained.

[0151] {circle over (2)} Preparation of a Recovering Liquid

[0152] A commercially available solution of dextran 40 in physiological saline (Dextran 40 Injection-Midori, a trade name, available from Green Cross Corp.) was incorporated with human serum albumin to prepare a liquid containing 4% human serum albumin as a recovering liquid. The viscosity of the recovering liquid was 9.8 mPa.s.

[0153] {circle over (3)} Cell Separation Procedure

[0154] A blood bag containing 50 ml of fresh human cord blood (containing 15 vol % of an anticoagulant CPD) was connected to the inlet side of the cell separator produced in the above item {circle over (1)}, through a tube having between its ends, diverging points to a physiological saline bag and a bag for cell recovery, respectively. A blood bag for drain was connected to the outlet side of the cell separator through a tube having a three-way stopcock between the ends of the tube. Into the cell separator was introduced 50 ml of the fresh cord blood by utilizing its fall (about 60 cm), and an erythrocyte-containing fluid (also containing CD34-negative cells and platelets) which had flowed out of the filter was recovered into the drain bag. Then, 30 ml of physiological saline was passed through the filter in order to rinse away erythrocytes, platelets and CD34-negative cells, which remained in the filter.

[0155] Subsequently, a syringe containing 30 ml of the recovering liquid prepared in the above item {circle over (2)} was connected to the three-way stopcock of the tube on the outlet side of the cell separator, and the recovering liquid was introduced into the cell separator by pushing the piston of the syringe, to recover the captured cells into the bag connected to the inlet side.

[0156] {circle over (3)} Analysis

[0157] The same analysis as in Example 1 was carried out.

[0158] {circle over (4)} Results

[0159] The time required for pushing the piston of the syringe completely was 3 seconds. The linear speed was calculated to be 55.6 cm/min. The results are summarized in Table 4. It can be seen that CD34-positive cells could be recovered at a high percentage in the cell suspension recovered, and that erythrocytes, platelets and CD34-negative cells were removed at high percentages.

	TABLE 4
	Recovery (%)	Removal rate (%)
	CD34-positive			CD34-negative
	cell	Erythrocyte	Platelet	cell
	78	99.2	90.4	90

EXAMPLE 4

[0160] This working example shows an example of cell separation in the case where a cell-containing fluid was cord blood, cells to be recovered are a mononuclear cell fraction containing hematopoietic stem cells, cells to be removed are erythrocytes and platelets, and DNA for HLA typing was collected at the same time.

[0161] {circle over (1)} Cell Separator

[0162] The same cell separator as in Example 1 was used.

[0163] {circle over (2)} Preparation of Recovering Liquids

[0164] A commercially available solution of dextran 40 in physiological saline (Dextran 40 Injection-Midori, a trade name, available from Green Cross Corp.) was incorporated with human serum albumin to prepare a liquid containing 4% human serum albumin as a first recovering liquid (for cell recovery). Distilled water for injection, and a hypotonic liquid was used as an additional recovering liquid (for recovering cell constituents). The viscosity of the first recovering liquid was 10.5 mPa.s.

[0165] {circle over (3)} Line System

[0166] The cell separation system shown in FIG. 3 was obtained by incorporating the cell separator described in the above item {circle over (1)} into lines. In this system,, the connection of a cell-containing fluid bag to the main body of the system of the present invention, and the connection of a bag for recovering a fluid which flows out through the outlet of the cell separator 15, to the main body of the system of the present invention were made with spikes. A line for recovering cells from the inlet side of the cell-capturing means was equipped with a freeze bag for recovering cells for cell transfer, and a tube with a spike at the end for recovering DNA for HLA typing into a conical tube. In this line, the flow paths are changed by means of clamps.

[0167] {circle over (4)} Cell Separation Procedure

[0168] A cell separation procedure was carried out by using the line system shown in FIG. 3.

[0169] Initially, clamp 21 was shut, a three-way stopcock 25 was shut only in the direction of syringe connection, and clamps 27 and 28 were shut.

[0170] A spike 20 was stuck into a blood bag containing 50 ml of fresh human cord blood (containing 15 vol % of an anticoagulant CPD), and a spike 23 was stuck into an empty bag. When the clamp 21 was opened, the cell-containing fluid was supplied to the cell separator 15 through the tube 22 of a line 16, and a mononuclear cell fraction containing hematopoietic stem cells was captured, and erythrocytes and platelets were discharged into the empty bag through the tube 24 of a line 17.

[0171] After completion of the treatment of said cell-containing fluid, the clamp 21 was shut and the spike 20 was pulled out, and then stuck into a commercially available 100-ml bottle of physiological saline. When the clamp 21 was opened, the physiological saline rinsed away a slight amount of erythrocytes and platelets, which remained in the cell separator 15, and the physiological saline was discharged through the line 17. Then, the clamp 21 was shut. Next, a 30-ml syringe containing 25 ml of the recovering liquid prepared in the above item {circle over (2)} was connected to the three-way stopcock 25, after which the three-way stopcock 25 was turned in such a direction that the syringe communicated only with the cell-capturing means 15 through a line 18, and the clamp 27 was opened. The piston of the syringe was pushed to recover cells into a freeze bag 29 through a line 19. Subsequently, the syringe was detached from the three-way stopcock 25, and another syringe containing 25 ml of distilled water for injection was connected to the three-way stopcock 25. The clamp 27 was shut, and clamp 28 was opened, being attached to a tube 31 capable of communicating with the tube 32 of the line 19 through a Y-tube 26. A conical tube was placed under a spike 30, after which the distilled water for injection was introduced into the cell-capturing means by pushing the piston of the syringe, to disrupt the captured cells, and crude DNA in these cells was recovered in the conical tube. The crude DNA recovered was purified by a conventional method comprising deproteination using proteinase K and phenol chloroform method.

[0172] {circle over (5)} Analysis

[0173] The numbers of cells were determined by the same method as described in Example 1. The amount of the purified DNA was determined by a conventional method comprising measuring absorbance at 260 nm by means of a spectrophotometer (Nakayama et al., Cell Technology, extra issue “Bio-experiment Illustrated” {circle over (1)} Fundamentals of Molecular Biological Experiment, 1995).

[0174] {circle over (6)} Results

[0175] The time required for pushing the piston of the syringe completely was 3 seconds. The linear speed was calculated to be 55.6 cm/min. The results are summarized in Table 5. It can be: seen that eukaryotic cells, mononuclear cells and CD34-positive cells could be recovered at high percentages in the cell suspension recovered, and that erythrocytes and platelets were removed at high percentages. It can also be seen that the amount of the DNA obtained was about 10 μg, an amount sufficient for HLA typing.

TABLE 5
Recovery (%)		Amount
		CD34-		of
Nucleated	Mononuclear	positive	Removal rate (%)	purified
cell	cell	cell	Erythrocyte	Platelet	DNA (μg)
75.0	90.4	97.2	98.9	88.3	9.8

EXAMPLE 5

[0176] This working example shows an example of cell separation in the case where a cell-containing fluid was bone marrow, cells to be recovered are a mononuclear cell fraction containing hematopoietic stem cells, and cells to be removed are erythrocytes and platelets.

[0177] {circle over (1)} Cell Separator

[0178] The same cell separator as in Example 1 was used.

[0179] {circle over (2)} Preparation of a Recovering Liquid

[0180] A commercially available solution of dextran 40 in physiological saline (Dextran 40 Injection-Midori, a trade name, available from Green Cross Corp.) was incorporated with human serum albumin to prepare a liquid containing 4% human serum albumin as a recovering liquid. The viscosity of the recovering liquid was 101 mPa.s.

[0181] {circle over (3)} Cell Separation Procedure and Line System

[0182] As shown in FIG. 2, a blood bag containing 30 ml of bone marrow (containing 15 units/ml of an anticoagulant heparin) was connected to the inlet side of the cell separator 6 described in the item {circle over (1)}, through a tube having between its ends a three-way stopcock 9 having a bag for cell recovery 10 connected thereto, a mesh chamber 8, and a diverging point to a tube with a spike 13 to be connected to a bottle of physiological saline for rinsing. A drain bag 12 was connected to the outlet side of the cell separator 6 through a tube having between its ends a three-way stopcock 11 for connecting a syringe for recovery. The fluid containing nucleated cells in the starting-blood bag 7 was introduced into the cell separator at a fall of about 60 cm, and a fluid containing erythrocytes which had flowed out of the cell separator 6 was discharged into the drain bag 12. Then, the spike 13 was stuck into the bottle of physiological saline, and the clamp 14 was opened, whereby the inside of the filter was rinsed with about 20 ml of physiological saline to rinse away a slight amount of erythrocytes and platelets, which remained in the filter. Subsequently, a 30-ml disposable syringe containing 25 ml of the recovering liquid was connected to the three-way stopcock 11, and the three-way stopcock 11 was turned in such a direction that the syringe communicated only with the cell separator. The three-way stopcock 9 was turned in such a direction that the cell separator 6 communicated only with the bag for cell recovery 10. Then, the piston of the syringe was pushed to recover cells captured in the cell separator, into the bag for cell recovery 10.

[0183] {circle over (4)} Analysis

[0184] The number of nucleated cells, the number of mononuclear cells, the number of erythrocytes and the number of platelets were determined with an automatic hemocytometer. The percentage of CD34-positive cells based on the total number of nucleated cells was measured by the use of FITC-labeled anti-CD34 antibody according to a flow cytometry method comprising development on SSC-FITC (Miyazaki et al. “Nichijo Shinryo to Ketsueki (Routine Diagnosis and Treatment, and Blood)” Vol. 5, No. 2, pp. 21-24, 1995).

[0185] The recovery and the removal rate are calculated by the following equations:

Recovery (%)=100×(number of recovered cells/number of cells in starting cell population)

Removal rate (%)=100−100×(number of recovered cells/number of cells in starting cell population)

[0186] {circle over (5)} Results

[0187] The time required for pushing the piston of the syringe completely was 3 seconds. The linear speed was calculated to be 55.6 cm/min. The results are summarized in Table 6. It can be seen that nucleated cells, mononuclear cells and CD34-positive cells could be recovered at high percentages in the cell suspension recovered, and that erythrocytes and platelets were removed at high percentages.

TABLE 6
Recovery (%)
		CD34-
Nucleated	Mononuclear	positive	Removal rate (%)
cell	cell	cell	Erythrocyte	Platelet
74.3	91.2	97.6	99.0	88.0

EXAMPLE 6

[0188] In this working example, vascular endothelial precursor cells were separated from cord blood using a cell separator and blood vessels were regenarated in vitro from the precursor cells.

[0189] {circle over (1)} Cell Separator

[0190] Eighteen sheets of polyester nonwoven fabrics with an average fiber diameter of 2.3 μm (fiber weight; about 60 g/m2, thickness; about 0.3 mm) and 16 sheets of polyester nonwoven fabrics with an average fiber diameter of 12 μm (fiber weight: about 100 g/m2, thickness: about 0.47 mm) were put one on another and cut in 35×35 mm squire with a straw cutter to obtain a filter material. A polycarbonate container with outside dimensions (length×width×thickness) of 41×41×18 mm having a liquid outlet and a liquid inlet on the diagonal was packed with this filter material so that the polyester nonwoven fabrics with an average fiber diameter of 2.3 μm was at the side of the inlet and the polyester nonwoven fabrics with an average fiber diameter of 12 μm at the side of the outlet. Thus, a cell separator 40 was made. In order to make the nonwoven fabric hydrophilic, a 1% ethanolic solution of a hydroxyethyl methacrylate-dimethylaminoethyl methacrylate copolymer (molar ratio between hydroxyethyl methacrylate and dimethylaminoethyl methacrylate=97:3) was passed through the filter from the liquid outlet, after which an excessive amount of the polymer solution was removed by introducing nitrogen gas thereinto and the filter was dried at 60° C. for over 16 hours.

[0191] As shown in FIG. 4 a tube 34 equipped with a spike 33 at its end and having between its ends a three-way tube 36 having a bag for cell recovery 39 connected thereto was connected to the inlet side of the cell separator 40. A drain bag 44 was connected to the outlet side of the cell separator 40 through a tube 41 having between its ends an adapter 42 that is ordinarily closed with a cap but connectable to a syringe with the cap taken off. Thus, a cell separator was made.

[0192] {circle over (2)} Blood Material

[0193] Into an umbilical cord vein was inserted an injector which was connected to the end of the tube leading to a blood bag containing 28 ml of an anticoagulant (CPD). Cord blood was recovered by means of head, during which the blood bag was inclined at a horizontal state to sufficiently mix the cord blood with the anticoagulant (CPD) in order to prevent the blood from coagulation. The recovered cord blood was preserved at room temperature until it was filtrated and used within 48 hours. The total blood volume including the anticoagulant was 100 ml.

[0194] {circle over (3)} Cell Separation Procedure

[0195] A blood bag containing the cord blood of the above {circle over (2)} (hereinafter referred to as blood bag) was connected to the spike 33 of the cell separator produced in the above {circle over (1)}. Only the blood bag and the cell separator 40 were communicated to each other by closing clamp 37. Also, only the cell separator 40 and the drain bag 44 were communicated to each other by capping the adapter 42. The cord blood was passed through and filtrated with the cell separator 40 by means of head, thereby recovering a filtrate which flowed from the cell separator 40, into the drain bag 44. After introducing physiological saline into the empty bag, 40 ml of physiological saline was passed through the cell separator 40 in order to rinse away erythrocytes which remained in the cell separator 40. The rinse fluid was also recovered in the drain bag 44. Subsequently, a 30-ml injector (equipped with a lure lock) containing 16 ml of Dextran 40, 2 ml of human serum albumin (25% solution) and 19 ml of air was connected to the adapter 42. Only the injector and the cell separator 40 were communicated to each other by closing a clamp 43. Also, only the cell separator 40 and the bag for cell recovery 39 were communicated to each other by closing a clamp 35. Then, those cells captured in the cell separator 40 were recovered into the bag for cell recovery 39 by pushing the plunger of the injector by hands.

[0196] {circle over (4)} Regeneration and Analysis

[0197] The number of mononuclear cells recovered in the bag for recovery was 80% based on the mononuclear cells in the cord blood. The recovered mononuclear cells were suspended in a concentration of 3×107/10 ml in Medium 199 with 20% FBS, bovine pituitary extraction (Gibco) and heparin (10 units/ml) added thereto. The suspension was plated on a 100-mm plastic dish coated with gelatin and incubated in a 5% CO2 incubator at 37° C. The results are shown in FIGS. 5-1 to 5-7.

[0198] It is revealed from FIGS. 5-1 to 5-7 that a mass of cells was generated within 48 hours of the cultivation (FIG. 5-1) and spindle-shaped attaching cells appeared from the end of the mass of cells attached to the plastic dish at Day 3 (FIGS. 5-2 and 5-3). Seventy percents (70%) or more of these attaching cells had a capability of bonding to lectin and incorporation of acetyl LDL, which were the features of endothelial cells. FIG. 5-4 is a microscopic photograph of the attaching cells before fluorescent staining. FIGS. 5-5 and 5-6 are fluorescent microscopic photographs of the same cells after fluorescent staining to show the capability of bonding to lectin and incorporation of acetyl LDL. It is revealed from the analysis of RT-PCR as shown in FIG. 5-7 that these attaching cells expressed KDR/Flk-1, CD31, ecNOS, AC133, endothelin-1, LOX-1 and GAPDH, which were characteristic to endothelial cells. FIGS. 6-1 to 6-6 schematically illustrate the microscopic photographs of FIGS. 5-1 to 5-6, respectively.

[0199] The attaching cells obtained at Day 7 of the cultivation represented 10% of the plated mononuclear cells. The analysis of KDR positive cells by a flow cytometry method revealed that the vascular endothelial precursor cells represented 6% of the mononuclear cells in the blood material. The attaching cells cultivated for 7 days were incubated at 37° C. for 15 minutes with 1 ml of EDTA-containing PBS to allow the cells to suspend in the PBS, followed by fluorescent staining with PKH2-GL. The concentration of the attaching cells was then adjusted with the above-mentioned cell cultivation medium so as to have a total cell concentration of 1×105 cells/ml at a ratio of the attaching cells and PKH26-labelled HUVEC (human umbilical vain endothelial cells) being 1:1. Two milliliters of the mixed cells were plated onto a 35-mm plastic dish coated with MATRIGEL (Beckton-Deckinson Inc.) and co-cultivated in a 5%-CO2 incubator at 37° C. After 2-3 hours, observation through a fluorescent microscope revealed that a blood vessel-like network structure in which red HUVEC and green attaching cells were mixed together with one another was developed. Thus, a differentiation to blood vessils was confirmed (FIG. 7). The analysis in this Example was conducted according to the method disclosed in The Journal of Clinical Investigation, 105, 1527-1536 (2000).

EXAMPLE 7

[0200] In this working example, vascular endothelial precursor cells were separated from cord blood using a cell separator and blood vessels were regenerated in vivo from the precursor cells.

[0201] The same cell separator, blood material and cell separation procedure as in Example 6 were used in this example.

[0202] The left hind leg of a nude rat was made in an ischemic state. The attaching cells (3×105) obtained by the same separation procedure as in Example 6 were implanted in the ischemic region. Then, blood stream was examined on a laser Doppler rheometer (LDI, manufactured by Moor Instruments) to detect the flow rate of the blood stream. At Day 7 recovery of blood stream was acknowledged and at Day 21 the same blood stream as at the right hind leg, which was not made in an ischemic state, was confirmed at the left hind leg (FIG. 8).

COMPARATIVE EXAMPLE 2

[0203] In this experiment, vascular endothelial precursor cells were separated from cord blood by a gravity centrifugation method and the in vitro regeneration of blood vessels from the precursor cells was tried.

[0204] The same blood material as in Example 6 was used.

[0205] Five milliliters of Histopaque (Sigma) was put into a 15-ml conical tube. A blood dilution obtained by diluting 3 ml of cord blood with 6 ml of a phosphate buffer was put on the liquid surface of Histopaque taking care that the interface did not wave. After centrifugation at 475×g at room temperature for 45 minutes, the layer of mononuclear cells was recovered. One hundred milliliters of cord blood was all treated in this way.

[0206] The thus obtained mononuclear cells were put together and washed twice with a phosphate buffer. The recovery rate of the mononuclear cells was 25% based on the blood material. The recovered mononuclear cells were suspended in a concentration of 3×107/10 ml in Medium 199 with 20% FBS, bovine pituitary extraction (Gibco) and heparin (10 units/ml) added thereto. The suspension was plated on a 100-mm plastic dish coated with gelatin and incubated in a 5% CO2 incubator at 37° C. A mass of cells was generated within 48 hours of the cultivation and spindle-shaped attaching cells appeared from the end of the mass of cells attached to the plastic dish at Day 3. The attaching cells obtained at Day 7 of the cultivation represented 10% of the scattered mononuclear cells. The analysis of KDR/Flk-1 positive cells by a flow cytometry method revealed that the vascular endothelial precursor cells represented 1% of the mononuclear cells in the blood material. In this comparative example the analysis was conducted according to the method disclosed in The Journal of Clinical Investigation, 105, 1527-1536 (2000).

[0207] As described above, according to the present invention, useful cells such as hematopoietic stem cells can be recovered with high recovery by a simple and rapid procedure, and the thus obtained cell-containing fluid can be subjected to cryopreservation without a subsequent troublesome cell suspension preparation procedure, and hence can be utilized in a laborsaving cell processing in medical-care-related industries such as the field of hematopoietic stem cell transplatation, the field of adoptive-immuno therapy, etc.

[0208] Further, since very rare cells such as hematopoietic stem cells and vascular endothelial precursor cells can be recovered in high rate, the amount of blood sample to be collected required for treatment can be reduced, and the method can greatly contribute to reduction of the burden of blood donor and improvement in the treatment outcome by frequent treatments.

Claims

1. A method for regenerating a blood vessel comprising introducing a cell-containing fluid containing vascular endothelial precursor cells and cells to be removed into a cell-capturing means which allows at least the cells to be removed to substantially pass through but substantially captures the vascular endothelial precursor cells; recovering the vascular endothelial precursor cells once captured on said cell-capturing means by introducing a fluid into the said cell-capturing means; and using the recovered vascular endothelial precursor cells for regenerating a blood vessel.

2. The method for regenerating a blood vessel according to claim 1, wherein use of said recovered vascular endothelial precursor cells for regenerating a blood vessel comprises a direct transplantation of said vascular endothelial precursor cells into a human ischemic damaged region and/or a penumbral region thereof.

3. The method for regenerating a blood vessel according to claim 1, wherein use of said recovered vascular endothelial precursor cells for regenerating a blood vessel comprises a transvascular transplantation of said vascular endothelial precursor cells to a,human ischemic damaged region and/or a penumbral region thereof.

4. The method for regenerating a blood vessel according to any one of claims 1 to 3, comprising the steps of further introducing a fluid into said cell-capturing means to substantially remove the cells to be removed remaining in the cell-capturing means, after introducing the cell-containing fluid into the cell-capturing means.

5. The method for regenerating a blood vessel according to any one of claims 1 to 4, further comprising the steps of cultivating the vascular endothelial precursor cells recovered from the cell-capturing means on an extracellular matrix; then recovering the attaching cells adhered on the extracellular matrix.

6. The method for regenerating a blood vessel according to claim 4, further comprising cocultivating the attaching cells with the human umbilical vein endothelial cells on the extracellular matrix.

7. The method for regenerating a blood vessel according to any one of claims 1 to 5, wherein the cell-containing fluid containing vascular endothelial precursor cells and cells to be removed is any one of cord blood, bone marrow and peripheral blood.

8. A composition comprising vascular endothelial precursor cells, obtained by introducing a cell-containing fluid containing vascular endothelial precursor cells and cells to be removed into a cell-capturing means which allows at least the cells to be removed to substantially pass through but substantially captures the vascular endothelial precursor cells; and introducing a fluid into said cell-capturing means to recover the vascular endothelial precursor cells captured by said cell-capturing means, and a physiological carrier.

9. The composition according to claim 8, wherein the cell-containing fluid containing vascular endothelial precursor cells and cells to be removed is any one of cord blood, bone marrow and peripheral blood.

10. A composition comprising attaching cells, obtained by introducing a cell-containing fluid containing vascular endothelial precursor cells arid cells to be removed into a cell separator which allows at least the cells to be removed to substantially pass through but substantially captures the vascular endothelial precursor cells; and introducing a fluid into said cell-capturing means to recover the vascular endothelial precursor cells captured by said cell-capturing means; further cultivating the vascular endothelial precursor cells on an extracellular matrix; then recovering the attaching cells adhered on the extracellular matrix, and a physiological carrier.

11. The composition according to claim 10, wherein the cell-containing fluid containing vascular endothelial precursor cells and cells to be removed is any one of cord blood, bone marrow and peripheral blood.