A SIMULTANEOUS 3-COLOR T-CELL SUBSETS ANALYSIS WITH SINGLE LASER FLOW CYTOMETERS USING T-CELL GATING PROTOCOL - COMPARISON WITH CONVENTIONAL 2-COLOR IMMUNOPHENOTYPING METHOD

被引:50
作者
MANDY, FF
BERGERON, M
RECKTENWALD, D
IZAGUIRRE, CA
机构
[1] HLTH & WELF CANADA, BUR LABS & RES SERV, DIV INFECT IMMUNOL, OTTAWA K1A 0L2, ONTARIO, CANADA
[2] BECTON DICKINSON IMMUNOCYTOMETRY SYST, SAN JOSE, CA USA
关键词
AIDS; FLOW CYTOMETRY; PHENOTYPIC ANALYSIS; PERIDININ CHLOROPHYLL PROTEIN; IMMUNOPHENOTYPING; 3-COLOR IMMUNOFLUORESCENCE; T-GATING; FACSCAN; PROFILE-II; SIMULTANEOUS 3-COLOR METHOD; TANDEM FLUOROCHROMES; LINEAGE SPECIFIC GATING; CD4; SUBSET; CD8; T-CELL SUBSET;
D O I
10.1016/0022-1759(92)90021-K
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a method for simultaneous analysis of CD3, CD4, and CD8 positive cells from whole blood utilizing single laser flow cytometers. All three T cell values are attained from a single test tube. CD4 and CD8 positive cells are identified only if they are CD3 positive. Thus the values obtained by this method for T helper/inducer and T cytotoxic/suppressor cells can be reported directly as a percentage of T lymphocytes. Analysis for CD4 and CD8 positive cells is accomplished, by first gating on CD3 positive T lymphocytes, hence the approach is referred to as a T gating method. As the third dye, conjugated to anti-CD3 monoclonal antibodies (MAbs), we utilized peridinin chlorophyll protein (PerCP), a new red fluorochrome. The proposed method may prove to be practical for monitoring disease progression in AIDS, where longitudinal T helper/inducer and T cytotoxic/suppressor cell enumeration must be performed unambiguously by a simple, reproducible, and fast method.
引用
收藏
页码:151 / 162
页数:12
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