Nonradioactive techniques for measurement of in vitro T-cell proliferation: alternatives to the [(3)H]thymidine incorporation assay

  • T Messele
  • , M T Roos
  • , D Hamann
  • , M Koot
  • , A L Fontanet
  • , F Miedema
  • , P T Schellekens
  • , T F Rinke de Wit

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

T-cell proliferation is an important in vitro parameter of in vivo immune function and has been used as a prognostic marker of human immunodeficiency virus type 1 (HIV-1) disease progression. The proliferative capacity of T cells in response to various stimuli is commonly determined by a radioactive assay based on incorporation of [(3)H]thymidine ([(3)H]TdR) into newly generated DNA. In order to assess techniques for application in laboratories where radioactive facilities are not present, two alternative methods were tested and compared to the [(3)H]TdR assay as a "gold standard." As an alternative, T-cell proliferation was measured by flow cytometric assessment of CD38 expression on T cells and by an enzyme-linked immunosorbent assay (ELISA) based on bromo-2'-deoxyuridine (BrdU) incorporation. Peripheral blood mononuclear cells (PBMCs), either in whole blood or Ficoll-Isopaque separated, from a total of 26 HIV-1-positive and 18 HIV-1-negative Dutch individuals were stimulated with CD3 monoclonal antibody (MAb) alone, a combination of CD3 and CD28 MAbs, or phytohemagglutinin. BrdU incorporation after 3 days of stimulation with a combination of CD3 and CD28 MAbs correlated excellently with the [(3)H]TdR incorporation in both study groups (HIV-1 positives, r = 0.96; HIV-1 negatives, r = 0.83). A significant correlation of absolute numbers of T cells expressing CD38 with [(3)H]TdR incorporation, both in HIV-1-positive (r = 0.96) and HIV-1-negative (r = 0.84) individuals, was also observed under these conditions. The results of this study indicate that determination of both the number of CD38-positive T cells and BrdU incorporation can be used as alternative techniques to measure the in vitro T-cell proliferative capacity. The measurement of CD38 expression on T cells provides the additional possibility to further characterize the proliferating T-cell subsets for expression of other surface markers.

Original languageEnglish
Pages (from-to)687-92
Number of pages6
JournalClinical and Diagnostic Laboratory Immunology
Volume7
Issue number4
DOIs
Publication statusPublished - Jul 2000
Externally publishedYes

Keywords

  • ADP-ribosyl Cyclase
  • ADP-ribosyl Cyclase 1
  • Acquired Immunodeficiency Syndrome/immunology
  • Antigens, CD
  • Antigens, Differentiation
  • Cell Division
  • Flow Cytometry/methods
  • HIV-1
  • Humans
  • Lymphocyte Activation
  • Membrane Glycoproteins
  • NAD+ Nucleosidase
  • Predictive Value of Tests
  • Prognosis
  • T-Lymphocytes/immunology

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