跳至主要内容

Flow Cytometer Performance Characterization, Standardization and Calibration against CD4 on T Lymphocytes Enables Quantification of Biomarker Expressions for Immunological Applications

Read full paper at:
http://www.scirp.org/journal/PaperInformation.aspx?PaperID=48151#.VEXyOVfHRK0

There is an urgent need for developing a procedure for biomarker standardization and relative quantificationin clinical laboratories. Measuring the expression levels of cell antigens is critical for the diagnosis of many diseases, e.g. leukemia, lymphoma and immunodeficiency diseases. One of the most significant challenges in flow cytometry is obtaining inter-laboratory and intra-laboratory consistent and reproducible results across multiple cytometer platforms and locations longitudinally over time. To obtain measurement consistency, the target flow cytometer voltages should be optimized to segregate the negative population from the electronic noise, and to keep the brightest positive population within the dynamic range of each detector. Then target values should be determined and transferred to selected cytometers. In this study, we optimized a procedure for instrument standardization across three different flow cytometer platforms from the same vendor and in two different locations. The biomarker quantification was implemented on standardized instruments using CD4 expression on T lymphocytes with a known amount of antibody bound per cell as a quantification standard. Our results on blood cell subset typing and CD19 quantification demonstrated that consistent and reliable results could be accomplished between instruments using the developed procedure. Quantitating the expression levels of certain cell biomarkers relative to a known reference marker before, during, and after therapy would provide important information for monitoring antibody-based therapy and could be potentially used to adjust dosing. Presently, we are implementing this protocol to quantify critical disease biomarkers, and making necessary modifications to the procedure to include instruments from different instrument manufacturers.
Cite this paper
Degheidy, H. , Bauer, S. , Marti, G. and Wang, L. (2014) Flow Cytometer Performance Characterization, Standardization and Calibration against CD4 on T Lymphocytes Enables Quantification of Biomarker Expressions for Immunological Applications. Journal of Biomedical Science and Engineering, 7, 756-768. doi: 10.4236/jbise.2014.79074
 

[1] Van de Loosdrecht, A.A., Alhan, C., Bene, M.C., Della Porta, M.G., Drager, A.M., Feuillard, J., et al. (2009) Standardization of Flow Cytometry in Myelodysplastic Syndromes: Report from the First European Leukemia Net Working Conference on Flow Cytometry Inmyelodysplastic Syndromes. Haematologica, 94, 1124-1134.
http://dx.doi.org/10.3324/haematol.2009.005801
[2] Bjorklund, E., Matinlauri, I., Tierens, A., Axelsson, S., Forestier, E., Jacobsson, S. et al. (2009) Quality Control of Flow Cytometry Data Analysis for Evaluation of Minimal Residual Disease in Bone Marrow from Acute Leukemia Patients during Treatment. Journal of Pediatric Hematology/Oncology, 31, 406-415.
http://dx.doi.org/10.1097/MPH.0b013e3181a1c0e8
[3] Dworzak, M.N., Gaipa, G., Ratei, R., Veltroni, M., Schumich, A., Maglia, O., et al. (2008) Standardization of Flow Cytometric Minimal Residual Disease Evaluation in Acute Lymphoblastic Leukemia: Multicentric Assessment Is Feasible. Cytometry Part B: Clinical Cytometry, 74, 331-340.
http://dx.doi.org/10.1002/cyto.b.20430
[4] Irving, J., Jesson, J., Virgo, P., Case, M., Minto, L., Eyre, L., et al. (2009) Establishment and Validation of a Standard Protocol for the Detection of Minimal Residual Disease in B Lineage Childhood Acute Lymphoblastic Leukemia by Flow Cytometry in a Multicenter Setting. Haematologica, 94, 870-874.
http://dx.doi.org/10.3324/haematol.2008.000414
[5] Letestu, R., Rawstron, A., Ghia, P., Villamor, N., Leuven, N.B., Boettcher, S., Buhl, A.M., Duerig, J., Ibbotson, R., Kroeber, A., Langerak, A., Le Garff-Tavernier, M. and Mockridge, I. (2006) Evaluation of ZAP-70 Expression by Flow Cytometry in Chronic Lymphocytic Leukemia: AMulticentric International Harmonization Process. Cytometry Part B (Clinical Cytometry), 70B, 309-314.
[6] Kraan, J., Gratama, J.W., Keeney, M., D’Hautcourt, J.L. (2003) Setting up and Calibration of a Flow Cytometer for Multicolor Immunophenotyping. Journal of Biological Regulators Homeostatic Agents, 17, 223-233.
[7] Shankey, T.V., Forman, M., Scibelli, P., Cobb, J., Smith, C.M., Mills, R., et al. (2006) An Optimized Whole Blood Method for Flow Cytometric Measurement of ZAP-70 Protein Expression in Chronic Lymphocytic Leukemia. Cytometry Part B: Clinical Cytometry, 70, 259-269.
http://dx.doi.org/10.1002/cyto.b.20135
[8] Kalina, T., Flores-Montero, J., van der Velden, V.H.J., Martin-Ayuso, M., Bottcher, S., Ritgen, M., Almeida, J., Lhermitte, L., Asnafi, V., Mendonca, A., de Tute, R., Cullen, M., Sedek, L., Vidriales, M.B., Perez, J.J., teMarvelde, J.G., Mejstrikova, E., Hrusak, O., Szczepanski, T., van Dongen, J.J.M. and Orfao, A. (2012) On Behalf of the EuroFlow Consortium. EuroFlow Standardization of Flow Cytometer Instrument Settings and Immunophenotyping Protocols. Leukemia, 26, 1986-2010.
http://dx.doi.org/10.1038/leu.2012.122
[9] Hultin, L.E., Matud, J.L. and Giorgi, J.V. (1998) Quantitation of CD38 Activation Antigen Expression on CD8+ T cells in HIV-1 Infection Using CD4 Expression on CD4+ T Lymphocytes as a Biological Calibrator. Cytometry, 33, 123-132.
http://dx.doi.org/10.1002/(SICI)1097-0320(19981001)33:2<123::AID-CYTO6>3.0.CO;2-K
[10] Wang, L., Gaigalas, A.K., Marti, G.E., Abbasi, F. and Hoffman, R.A. (2008) Toward Quantitative Fluorescence Measurements with Multicolor Flow Cytometry. Cytometry Part A, 73A, 279-288.
http://dx.doi.org/10.1002/cyto.a.20507
[11] Wang, L., Gaigalas, A.K. and Yan, M. (2011) Quantitative Fluorescence Measurements with Multicolor Flow Cytometry. Flow Cytometry Protocols, 3rd Edition, Humana Press/Springer, New York, 53-65.
[12] Poncelet, P., Poinas, G., Corbeau, P., Devaux, C., Tubiana, N., Muloko, N., Tamalet, C., Chermann, J.C., Kourilsky, F., and Sampol, J. (1991) Surface CD4 Density Remains Constant on Lymphocytes of HIV-Infected Patients in the Progression of Disease. Research in Immunology, 142, 291-298.
http://dx.doi.org/10.1016/0923-2494(91)90078-W
[13] Davis, K.A., Abrams, B., Iyer, S.B., Hoffman, R.A. and Bishop, J.E. (1998) Determination of CD4 Antigen Density on Cells: Role of Antibody Valency, Avidity, Clones, and Conjugation. Cytometry, 33, 197-205.
http://dx.doi.org/10.1002/(SICI)1097-0320(19981001)33:2<197::AID-CYTO14>3.0.CO;2-P
[14] Wang L., Abbasi F., Ornatsky O., Cole K.D., Misakian M., Gaigalas A.K., He, H.-J., Marti, G.E., Tanner, S. and Stebbings, R. (2012) Human CD4+ Lymphocytes for Antigen Quantification: Characterization Using Conventional Flow Cytometry and Mass Cytometry. Cytometry Part A, 81A, 567-575.
http://dx.doi.org/10.1002/cyto.a.22060
[15] Technical Bulletin of BD Biosciences: BD_FACSDiva_Stndrd_App_Setup_TechBulletin.pdf
[16] Wang, L., Abbasi, F., Gaigalas, A.K., Vogt, R.F. and Marti, G.E. (2006) Comparison of Fluorescein and Phycoerythrin Conjugates for Quantifying CD20 Expression on Normal and Leukemic B-Cells. Cytometry Part B: Clinical Cytometry, 70B, 410-415.
http://dx.doi.org/10.1002/cyto.b.20140                     eww141021lx

评论

此博客中的热门博文

A Comparison of Methods Used to Determine the Oleic/Linoleic Acid Ratio in Cultivated Peanut (Arachis hypogaea L.)

Cultivated peanut ( Arachis hypogaea L.) is an important oil and food crop. It is also a cheap source of protein, a good source of essential vitamins and minerals, and a component of many food products. The fatty acid composition of peanuts has become increasingly important with the realization that oleic acid content significantly affects the development of rancidity. And oil content of peanuts significantly affects flavor and shelf-life. Early generation screening of breeding lines for high oleic acid content greatly increases the efficiency of developing new peanut varieties. The objective of this study was to compare the accuracy of methods used to classify individual peanut seed as high oleic or not high oleic. Three hundred and seventy-four (374) seeds, spanning twenty-three (23) genotypes varying in oil composition (i.e. high oleic (H) or normal/not high oleic (NH) inclusive of all four peanut market-types (runner, Spanish, Valencia and Virginia), were individually tested ...

Location Optimization of a Coal Power Plant to Balance Costs against Plant’s Emission Exposure

Fuel and its delivery cost comprise the biggest expense in coal power plant operations. Delivery of electricity from generation to consumers requires investment in power lines and transmission grids. Placing a coal power plant or multiple power plants near dense population centers can lower transmission costs. If a coalmine is nearby, transportation costs can also be reduced. However, emissions from coal plants play a key role in worsening health crises in many countries. And coal upon combustion produces CO 2 , SO 2 , NO x , CO, Metallic and Particle Matter (PM10 & PM2.5). The presence of these chemical compounds in the atmosphere in close vicinity to humans, livestock, and agriculture carries detrimental health consequences. The goal of the research was to develop a methodology to minimize the public’s exposure to harmful emissions from coal power plants while maintaining minimal operational costs related to electric distribution losses and coal logistics. The objective was...

Evaluation of the Safety and Efficacy of Continuous Use of a Home-Use High-Frequency Facial Treatment Appliance

At present, many home-use beauty devices are available in the market. In particular, many products developed for facial treatment use light, e.g., a flash lamp or a light-emitting diode (LED). In this study, the safety of 4 weeks’ continuous use of NEWA TM , a high-frequency facial treatment appliance, every alternate day at home was verified, and its efficacy was evaluated in Japanese individuals with healthy skin aged 30 years or older who complained of sagging of the facial skin.  Transepidermal water loss (TEWL), melanin levels, erythema levels, sebum secretion levels, skin color changes and wrinkle improvement in the facial skin were measured before the appliance began to be used (study baseline), at 2 and 4 weeks after it had begun to be used, and at 2 weeks after completion of the 4-week treatment period (6 weeks from the study baseline). In addition, data obtained by subjective evaluation by the subjects themselves on a visual analog scale (VAS) were also analyzed. Fur...