1 / 64

Duke University School of Medicine Immunology Quality Assessment Center

Learn the role, assessment process, and FAQs of the Immunology Quality Assessment Center for PBMC cryopreservation. Detailed guidelines on equipment, reagents, and procedures for successful cell storage. Stay informed to maintain high-quality lab standards.

christinecox
Download Presentation

Duke University School of Medicine Immunology Quality Assessment Center

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Duke University School of Medicine Immunology Quality Assessment Center Tania Garrelts / Raul Louzao ACTG Meeting June 23,2009

  2. OUTLINE • Role of IQA • Frequently Asked Questions • Reagents • Equipment • Cell counts • Site Visit Findings

  3. What is the role of the IQA? • To assess the ability of laboratories to process and store viable peripheral blood mononuclear cells (PBMC) for use in various immunology and virology based assays. • To provide assistance to faltering laboratories. • Currently there are 63 domestic and 21 international laboratories enrolled in the program.

  4. How is the assessment accomplished? • The assessment is accomplished by comparing the viability of PBMCs and the viable yield before freezing and after thawing. • Proper processing and freezing is a critical component of the process for storage of viable PBMCs.

  5. How often do participating sites should submit samples? • Every three months (March, June, September and December), frozen PBMCs must be shipped from the participating laboratory to the NIAID Immunology Quality Assessment Program (IQA) • Shipping schedule can be found at our website (iqa.center.duke.edu)

  6. What should the participating labs achieve? *Laboratories who serve both the ACTG and IMPAACT must conform to the more stringent criteria of the ACTG (80% viability and 80% viable cell recovery)

  7. Frequently Asked Questions AboutThe Cryopreservation Of Peripheral Blood Mononuclear Cells

  8. Are Ficoll–Hypaque and Histopaque-1077 the same?

  9. Are Ficoll–Hypaque and Histopaque-1077 the same? • IQA currently uses Histopaque-1077 by Sigma Aldrich because of the known density gradient, 1.077 ± 0.001 gram/ml which is between that of plasma and red blood cells. • One part of blood to one of part of buffer, equal part of density gradient.

  10. What is the difference between Ficoll Ovelayering and UndelayeringTechnique?

  11. Before and After Density Gradient

  12. Video of Overlaying Technique Manual Ficoll using Overlay and Underlay Methods Click on the link bellow http://youtu.be/-SqlIMLUfcI

  13. Video of Overlaying Technique Click on Link http://youtu.be/andvFWRzQ0c

  14. Insufficient amount of density gradient

  15. Buffy Coat Isolation

  16. Good versus Poor Mononuclear cell isolation

  17. Why do I have to remove the supernatant (HBSS-Plasma layer)? • Removing the PBMC band with the supernatant will promote contamination by platelets and plasma proteins. Leave Platelets + proteins= cell clumps

  18. Why I can’t remove all the density gradient? • Removing the excess amount of Ficoll with the mononuclear layer will increase a chance of granulocyte contamination. Granulocyte contamination = misleading cell counts

  19. How much supernatant should I leave before isolate the PBMC band? • Remove the plasma-HBSS fraction down to within approximately 1-2 cm of the PBMC band.

  20. Common used techniques to isolate theMononuclear Layers.

  21. Should I remove the cells stuck to the side of the test tube? • From previous experience the cells attached to the inner walls of the tubes are erythrocytes, cell debri and platelets. • The density gradient will separate the viable lymphocytes and monocytes.

  22. What should I do if I accidently mix the layered blood with ficoll? • Don’t Panic. • Finish Mixing the blood with ficoll. (New mixture) • Set up new ficoll tubes and overlay or underlay them with the new mixture.

  23. Why do we need to use a centrifuge with swinging -bucket rotor? • In swinging bucket rotors, the sample tubes are loaded into individual buckets that hang vertically while the rotor is at rest. When the rotor begins to rotate the buckets swing out to a horizontal position This rotor is particularly useful when samples are to be resolved in density.

  24. Can a vertical rotor be used with Ficoll? • In vertical rotors, sample tubes are held in vertical position during rotation. This type of rotor is not suitable for pelleting applications.

  25. Difference between Vertical versus Swinging-Bucket Rotor

  26. What temperature should I use during centrifugation? • During separation the centrifuge temperature should be control between 18-25 °C because the density components changes with temperature. For Example: Centrifugation at 4 °C may result in poor cell recovery due to cell clumping.

  27. What speed and time should I use in my centrifuge? • If using Sigma Ficoll centrifuge at 800 x g for 30 minutes. GE Ficoll centrifuge at 400 x g for 40 minutes. • If using Cell Separation tube with Frit Barrier (CSTFB) , centrifuge at 800 x g for 15 minutes or 1000 x g for 10 minutes. • No Brake, if brake is on it will disrupt the layers.

  28. What should I check if I do not get a PBMC layer? Check: • The centrifuge speed and time. • The centrifuge brake was off. • The centrifuge buckets are not sticking. • If the centrifuge buckets are balanced properly. • Maintenance record for last calibration.

  29. How much buffer do I need for my cell wash and why? • For the 1st cell wash, measure your isolated PBMC layer and the balanced salt solution volume should be add at least 3 times the volume of the harvest. Do not exceed 45 ml. • Centrifuge at 300 x g for 10 minutes. Low centrifugation + QS buffer= removes platelets and plasma contamination

  30. What is the total number of cell washes? • Minimum two cell washes, depending on the tech buffy coat isolation technique. • Decant or aspirate the medium solution. • Resuspend your pellet by gently pipetting them up and down, or finger flick. • Gently mix the solution by inverting the test tube.

  31. Video of incorrect pellet re-suspension Click on Link http://youtu.be/4wuSfHmPZ-k

  32. Video of gentle pellet re-suspension Click on Link http://youtu.be/4WObBqpJD0I

  33. How much buffer is left in my test tube after I decant the supernatant? • The amount of balanced buffer left over with the pellet after the HBSS is decanted is approximately 200 to 400uls. • You have enough buffer to gently finger flick your cells.

  34. What volume of buffer should I use to re-suspend my pellets? • If you have multiple tubes combine the pellets by adding 1ml of buffer on each tube. • Depending on the size of the cell pellet, the re-suspension volume would range from 10% to 50% of the usable whole blood. • For example: Starting volume of whole blood is 17 mls. IQA would re-suspend cells in 5 mls ~30%

  35. What type of pipettes and tips do I need to have?

  36. What is the Forward Pipetting Technique?

  37. What are the effects of how I pipette?

  38. What are some common pipetting technique errors? — Human Factor, working too quickly. — Removing the pipette tip before sample aspiration is complete. — Angle pipettes takes up too much liquid. Keep vertical. — Releasing the plunger too rapidly. — Not pre-wetting a new tip.

  39. What type of pipette aid should I use?

  40. What type of plasticware should I use? • Avoid using high binding plastics such as polystyrene to prevent monocyte adhesion. • Use Polypropylene

  41. Are powered gloves acceptable for processing PBMCS? • Powered gloves will contaminate the process by activating monocytes which will cause a lower percent recovery.

  42. What is the pH, solution storage requirement, and length of time that cells can stay in trypan blue? • pH: 7.0 – 7.4 • Storage requirement: 15-30 °C. Some of vendors recommend that it be protected from light and filter after prolonged storage. • Cells should be count within 3-10 minutes of mixing with trypan blue, longer incubation will result in cell death and low viability counts.

  43. What are some common problems with a Hemacytometer? • Dirty hemacytometer or cover slip, clean with 70% alcohol and lens paper. • The chamber may have been loaded incorrectly. • The cover slip may have been bumped. • Insufficient mixing of sample. • Using a wrong cover slip.

  44. Definition for Dilution • Dilutions are expressed as the ratio of the quantity of a desired solute (serum, urine, chemical solution, etc.) contained in a solvent (diluent). For example: A 1:10 dilution of serum was made by adding one part serum to nine parts diluent to make a total of ten parts. volume of serum/volume of solution = [1.0 mL serum ]/[1.0 ml serum + 9.0 mL H20]

  45. Video of Counting Cells Click on Link http://youtu.be/GTlAdxUX9mU

  46. How to perform an accurate count?

  47. Example: IQA re-suspend pellet in 5 mls • Mix cells with buffer by inverting the tube. • Take 20 uls of cellular solution and mix with 20 uls of trypan blue. (1:2 dilution) • Load in clean hematocytomer. Wait 10 seconds, for cells to settle and stain. • Count 4 quadrants. • Record Viable and Nonviable PBMCs.

  48. What are the formulas for cell counts?

More Related