System And Method For Plasma Purification Prior To Mononuclear Cell Collection

Abstract

A method of collecting mononuclear cells includes separating whole blood into plasma and cellular components, purifying the plasma through a plasma adsorption column to create purified plasma, combining the cellular components with the purified plasma to form a first mixture, and separating the first mixture into mononuclear cells and at least one component. Alternatively, whole blood may be flowed through an adsorption column to create purified whole blood, with the purified whole blood then being separated into mononuclear cells and at least one component.

Claims

1-11. (canceled)

12. A method of collecting mononuclear cells, comprising: separating whole blood into plasma and cellular components; purifying the plasma through a plasma adsorption column to create purified plasma; combining the cellular components with the purified plasma to form a first mixture; and separating the first mixture into mononuclear cells and at least one component.

13. The method of claim 12, further comprising the step of performing extracorporeal photopheresis on the mononuclear cells, and wherein the purified plasma contains fewer proteins, lipids, and/or bilirubin than does the plasma.

14. The method of claim 12, wherein the step of separating whole blood into plasma and cellular components is performed by a centrifugal separator.

15. The method of claim 12, wherein step of separating whole blood into plasma and cellular components is performed by a spinning membrane separator.

16. The method of claim 12, wherein the mononuclear cells comprise at least one of lymphocytes, monocytes, and stem cells.

17. A method of collecting mononuclear cells, comprising: providing an adsorption column through which whole blood is flowed to create purified whole blood; and separating the purified whole blood into mononuclear cells and at least one component.

18. The method of claim 17, wherein the purified whole blood is separated by a centrifugal separator.

19. The method of claim 17, wherein the mononuclear cells comprise at least one of lymphocytes, monocytes, and stem cells.

20. The method of claim 17, wherein the purified whole blood contains fewer proteins, lipids, and/or bilirubin than does the whole blood.

21. A blood separation system comprising: a processing kit including an adsorption column, a first separation chamber, and a second separation chamber; and a separation component including a pump system and a controller, wherein the controller is configured to control the pump system to convey whole blood into the first separation chamber to separate the whole blood into plasma and cellular components, convey the plasma through the adsorption column to create purified plasma, combine the cellular components with the purified plasma to form a first mixture, and convey the first mixture into the second separation chamber to separate the first mixture into mononuclear cells and at least one component.

22. The blood separation system of claim 21, further comprising a photopheresis device configured to perform extracorporeal photopheresis on the mononuclear cells, wherein the purified plasma contains fewer proteins, lipids, and/or bilirubin than does the plasma.

23. The blood separation system of claim 21, wherein the first separation chamber is defined by a centrifugal separation container.

24. The blood separation system of claim 21, wherein the first separation chamber is defined by a spinning membrane separator.

25. The blood separation system of claim 21, wherein the mononuclear cells comprise at least one of lymphocytes, monocytes, and stem cells.

26. A blood separation system comprising: a processing kit including an adsorption column and a blood processing container; and a separation component including a pump system and a controller, wherein the controller is configured to control the pump system to convey whole blood through the adsorption column to create purified whole blood, and convey the purified whole blood into the blood processing container to separate the purified whole blood into mononuclear cells and at least one component.

27. The blood separation system of claim 26, wherein the blood processing container comprises a centrifugal separation container.

28. The blood separation system of claim 26, wherein the mononuclear cells comprise at least one of lymphocytes, monocytes, and stem cells.

29. The blood separation system of claim 26, wherein the purified whole blood contains fewer proteins, lipids, and/or bilirubin than does the whole blood.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0011] Features, aspects, and advantages of the present embodiments will become apparent from the following description, appended claims, and the accompanying exemplary embodiments shown in the drawings, which are briefly described below.

[0012] FIG. 1 is a diagrammatic depiction of a separation system useful in the separation and collection of mononuclear cells, according to an exemplary embodiment;

[0013] FIG. 2 is a perspective view of the front panel of a separation system with a disposable processing set for collecting mononuclear cells mounted on the device, according to an exemplary embodiment;

[0014] FIG. 3 is a diagram showing the disposable processing set of FIG. 2, according to an exemplary embodiment;

[0015] FIG. 4 is a flow diagram illustrating an improved method for obtaining mononuclear cells, according to an exemplary embodiment;

[0016] FIG. 5 is a flow diagram illustrating an improved method for obtaining mononuclear cells, according to another exemplary embodiment; and

[0017] FIG. 6 is a flow diagram illustrating an improved method for obtaining mononuclear cells, according to another exemplary embodiment.

DETAILED DESCRIPTION

[0018] There are several aspects of the present subject matter which may be embodied separately or together in the devices and systems described and claimed below. These aspects may be employed alone or in combination with other aspects of the subject matter described herein, and the description of these aspects together is not intended to preclude the use of these aspects separately or the claiming of such aspects separately or in different combinations as set forth in the claims appended hereto.

[0019] Some embodiments may provide for collecting MNCs with reduced plasma lipid interference during MNC harvest.

[0020] Some embodiments may provide for more accurate collection and harvest of MNCs by allowing for a clearer interface between blood component layers.

[0021] During harvest of MNCs, non-target substances may be present in the MNC product that can interfere with accurate harvesting of the target MNCs. Plasma proteins and lipids may interfere, for example, in the event that the donor/patient has certain disease states or medications, such as elevated bilirubin levels and drugs such as mycophenolate mofetil (MMF) and cyclosporine, which cause hyperlipidemia.

[0022] FIG. 1 is a diagrammatic depiction of a separation system 10 useful in the separation and collection of mononuclear cells, as described herein, and FIG. 2 shows an exemplary embodiment of the separation system 10, The system 10 may include a separation component 12 and a disposable processing kit 14 (FIG. 2) that is mounted thereon. Flow direction and rate may be controlled by a plurality of pumps 15 engaged with the processing kit 14, In one embodiment, the separation principle used by the separator 12 is based on centrifugation, but an automated separator based on a different separation principle (e.g., spinning membrane, etc.) may also be used.

[0023] A patient may be connected to the fluid circuit 14, which may provide a sterile closed pathway between the separation component 12 and the remainder of the processing kit 14, Whole blood that is withdrawn from the patient may be introduced into the separation component 12, where the whole blood may be separated to provide a target cell population, which in the context of the present disclosure may be mononuclear cells. Other components separated from the whole blood, such as red blood cells and platelets may be returned to the patient or collected in pre-attached containers of the blood processing set. The separated target cell population, e.g., mononuclear cells, may then be collected for future use or prepared for various therapies. One example of a therapy involving MNCs that may benefit from reducing plasma lipid interference during MNC harvest is extracorporeal photopheresis or “ECP”. ECP involves the extracorporeal exposure of MNCs combined with a photoactive compound, such as 8-methoxypsoralen or “8-MOP” which is then photoactivated by ultraviolet light, followed by re-infusion of the treated MNCs. Removal of plasma lipids, which absorb UV light during irradiation, may lead to generally more consistent and less variable irradiation procedures, thereby enhancing accuracy of irradiation dosing and shortening procedure time.

[0024] Apparatus useful in the collection of mononuclear cells, and providing the separation component 12 of FIG. 1, include for example the Amicus® Separator made and sold by Fenwal, Inc., of Lake Zurich, Ill. Mononuclear cell collections using a device such as the Amicus® are described in greater detail in U.S. Pat. No. 6,027,657, the contents of which are incorporated by reference herein in its entirety. The fluid circuit 14 (FIG. 3) may include a blood processing container 16 defining a separation chamber suitable for harvesting MNCs from whole blood.

[0025] As shown in FIG. 2, a disposable processing set or fluid circuit 14 (which includes container 16) may be mounted on the front panel of the separation component 12. The processing set (fluid circuit 14) may include a plurality of processing fluid flow cassettes 23L, 23M and 23R with tubing loops for association with peristaltic pumps 15 on the separation component 12. Fluid circuit 14 may also include a network of tubing and pre-connected containers for establishing flow communication with the patient and for processing and collecting fluids and blood and blood components, as shown in greater detail in FIG. 3.

[0026] As seen in FIG. 3, the disposable processing set 14 may include a container 60 for supplying anticoagulant, an in-process container 62, a container 64 for holding a crystalloid solution, such as saline, a container 66 for collecting plasma, and a container 68 for collecting the mononuclear cells.

[0027] With reference to FIG. 3, fluid circuit 14 may include inlet line 72, an anticoagulant (AC) line 74 for delivering AC from container 60, an RBC line 76 for conveying red blood cells from chamber 16 of set 14 to container 67, a platelet-poor plasma (PPP) line 78 for conveying PPP to container 66 and line 80 for conveying mononuclear cells to and from separation chamber 16 and collection container 68.

[0028] The blood processing set may also include one or more venipuncture needle(s) for accessing the circulatory system of the patient. As shown in FIG. 3, fluid circuit 14 may include inlet needle 70 and return needle 82. In an alternative embodiment, a single needle may serve as both the inlet and outlet needle.

[0029] Fluid flow through fluid circuit 14 may be driven, controlled and adjusted by a microprocessor-based controller in cooperation with the valves, pumps, weight scales and sensors of separation component 12 and fluid circuit 14, the details of which are described in the previously mentioned U.S. Pat. No. 6,027,657.

[0030] A separation chamber may be defined by the walls of the processing container 16. The processing container 16 may comprise two different compartments 16a and 16b (FIG. 3). Using both compartments 16a and 16b for separation in a procedure may enable multiple target products to be separated simultaneously and/or multiple steps to be completed simultaneously. If only one compartment is used for separation, the other compartment may optionally be used as an in-process, waste, or storage container. In operation, the separation device 12 may rotate the processing container 16 about an axis, creating a centrifugal field within the processing container 16. Details of the mechanism for rotating the processing container 16 are disclosed in U.S. Pat. No. 5,360,542 titled “Centrifuge with Separable Bowl and Spool Elements Providing Access to the Separation Chamber,” which is also incorporated herein by reference in its entirety.

[0031] In one embodiment, an apheresis device or system 10 may include a programmable controller that is pre-programmed with one or more selectable protocols. A user/operator may select a particular processing protocol to achieve a desired outcome or objective. The pre-programmed selectable protocol(s) may be based on one or more fixed and/or adjustable parameters. During a particular processing procedure, the pre-programmed controller may operate the separator 12 and processing chamber 16 associated therewith to separate blood into its various components, as well as operate one or more pumps to move blood, blood components and/or solutions through the various openable valves and tubing segments of a processing set, such as processing set 14 illustrated in FIG. 3. The various processing steps performed by the pre-programmed automated apheresis device may occur separately, in series, simultaneously or any combination of these.

[0032] An automated apheresis device may be used to perform MNC collection in a batch process in which MNCs continuously collect in the chamber 16 until the target cycle volume is reached. During the continuous collection of MNCs within the chamber 16, different blood components separate into layers that may be detected by an optical interface detector that monitors the location and presence of the interface between layers. Details of an exemplary mechanism for interface detection are disclosed in U.S. Pat. No. 6,027,657, the contents of which are incorporated by reference herein in its entirety. Before and during the transfer of the MNCs out of the chamber 16, MNCs and other blood components (e.g., plasma, etc.) may pass through an optical sensor 17, located downstream of the chamber 16, which detects the presence of cells in the tubing line to determine the start and end of the MNC harvest (i.e. when to open and close the valves leading to the product container). The term “downstream” describes an event proximal to post-separation, and the term “upstream” describes an event proximal to pre-separation. “Downstream” and “upstream” are relative terms, with the reference point being the time/location of separation. After MNC harvest is complete, the remaining cells in the line may be flushed into the product container with a predetermined volume of plasma known as the “plasma flush”.

[0033] The ability of the interface detector to accurately detect the interface between blood component layers may be facilitated by removal of non-target substances (e.g., plasma proteins and lipids) that may be present in the blood that can interfere with the separation procedure. Additionally, the removal of non-target substances may improve the ability of the optical sensor 17 to accurately detect the presence of cells in the tubing line to determine the start and end of the MNC harvest to facilitate precise harvesting of the target MNCs.

EXAMPLES

[0034] Without limiting any of the foregoing, the subject matter described herein may be found in one or more methods, systems and/or products. For example, in a first aspect of the present subject matter, an improved system and method for obtaining MNCs is set forth in FIG. 4. The inlet needle 70 of FIG. 3 attached to inlet line 72 may first be connected to a blood source 5 (e.g, donor, patient, blood bag, etc.). Whole blood may enter the separation chamber 16 of the separator 12, which separates the whole blood into plasma and cellular components. The plasma may be separated and directed into a plasma container 66, and the cellular components may be separated and directed into a different container 67. The separated cellular contents may be combined with a replacement fluid 69 that has minimal non-target content (e.g., plasma proteins and/or lipids) that may interfere with optical sensor readings. Examples of suitable replacement fluids include fresh frozen plasma, immunoglobulin solution, albumin, and/or other colloid solutions. The cellular components mixed with replacement fluid may then be returned to the separation chamber 16, where target MNCs may be collected. The target MNCs may be harvested into a designated container 68 to be processed for further treatment. Non-target components may be collected or returned to the patient/donor.

[0035] The process and steps of whole blood initially entering the separation chamber 16 and the cellular components and replacement fluid mix returning to the separation chamber 16 portrayed in FIG. 4 may take place substantially in series if only one compartment 16a or 16b is utilized. Alternatively, the process and steps of whole blood entering the separation chamber 16 and the fluid mix returning to the separation chamber 16 may take place substantially at the same time if both compartments 16a and 16b are utilized. In an embodiment in which the processes take place substantially in series, whole blood entering one of the compartments 16a or 16b may separate into plasma and cellular components, both of which may be directed to separate containers until separation of plasma and cellular components is complete. An optical sensor 17 may optionally be placed downstream of the separation chamber 16a and/or 16b at a tubing line leading to the MNC product container 68 and/or leading to the plasma container 66 to determine when plasma is clear enough and plasma diversion can stop. Subsequently, the cellular components may combine with the replacement fluid within one of the compartments 16a or 16b, and further separation into target MNCs and non-target components may take place.

[0036] In an embodiment in which the steps of whole blood entering the separation chamber 16 and the fluid mix returning to the separation chamber 16 take place substantially at the same time, whole blood entering a first compartment (e.g., 16a) may separate into plasma and cellular components, with the plasma being sent to an plasma container 62. Simultaneously, the cellular components may join the replacement fluid and together enter a second compartment (e.g., 16b) and there further separate into target MNCs and non-target components. An optical sensor 17 may optionally be placed downstream of the separation chamber 16a at a tubing line leading to the MNC product container 68 and/or leading to the plasma container 66 to determine when plasma is clear enough and plasma diversion can stop. As the replacement fluid continues to enter compartment 16b and the clarity of the plasma leaving compartment 16a improves sufficiently as determined by the optical sensor 17, the plasma diversion from compartment 16a into the plasma container 66 can be stopped, and any unseparated whole blood, including the contents of compartment 16a, may be directed to compartment 16b to continue MNC collection.

[0037] In another aspect of the present subject matter, an improved method for obtaining MNCs is set forth in FIG. 5. An inlet needle may first be connected to a blood source 5 (e.g, donor, patient, blood bag, etc.) at step 100 of FIG. 5. In step 200, whole blood enters a separator, which separates the whole blood into plasma (step 300a) and cellular components (step 300b). In the embodiment in FIG. 5, the separator of step 200 may be a centrifugal or spinning membrane separator. An exemplary spinning membrane and hardware is disclosed in greater detail in PCT Patent Application No. PCT/US2012/28492, which is incorporated herein by reference in its entirety, although any suitable membrane assembly may be used, Plasma separated in step 300a may be flowed through an adsorption column in step 400. An exemplary adsorption column is the MONET filter made and sold by Fresenius Medical Care. Another exemplary adsorption column is disclosed in greater detail in International Publication No, WO 2012/141697 and U.S. Pat. No. 6,569,112, each of which is hereby incorporated by reference herein in its entirety, although any suitable column may be used. In step 500, purified plasma from the adsorption column in step 400 may be combined with the cellular components of step 300b. The combined product of step 500 may then be separated in a separation chamber of a separator in step 600 to collect and harvest MNC target cells separated from non-target components.

[0038] In another aspect of the present subject matter, an improved method for obtaining MNCs is set forth in FIG. 6. An inlet needle may first be connected to a blood source 5 (e.g, donor, patient, blood bag, etc.) at step 101 of FIG. 6. In step 201, whole blood enters a whole blood adsorption column, which removes certain lipids, proteins, antibodies, and/or fatty acids in step 301. An exemplary whole blood adsorption column is the DALI® adsorber made and sold by Fresenius Medical Care, although any suitable whole blood adsorption column may be used. Purified whole blood exiting from the WB adsorption column of step 201 may then be separated in a separation chamber 16 of a separator in step 401 to collect and harvest MNC target cells separated from non-target components.

[0039] The embodiments disclosed herein are for the purpose of providing a description of the present subject matter, and it is understood that the subject matter may be embodied in various other forms and combinations not shown in detail. Therefore, specific embodiments and features disclosed herein are not to be interpreted as limiting the subject matter as defined in the accompanying claims.