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TH1/TH2 Cytokine Ratios by Flow Cytometry with Prednisolone

Principle

The TH1:TH2 cytokine ratio in the cytoplasm of CD3⁺CD4⁺ lymphocytes is determined by flow cytometry. Mononuclear cells are stimulated with phorbol myristate acetate (PMA) and ionomycin in the presence of GolgiPlug (brefeldin A), a Golgi transport inhibitor, and prednisolone, a corticosteroid that inhibits inflammatory cell activation, for 18 hours.

Following stimulation, cells are harvested, permeabilized, and stained with phycoerythrin-conjugated antibodies to TNF-α, IFN-γ, or IL-10. Four-color flow cytometry is used to identify intracellular cytokine expression within CD3⁺CD4⁺ lymphocytes.

Because stimulation causes down-regulation of CD4 surface expression, CD3⁺CD4⁺ cells are identified using negative gating with ECD-anti-CD3 and FITC-anti-CD8. Lymphocytes that do not bind CD8 (CD3⁺CD8⁻) represent the CD3⁺CD4⁺ subset. The percentage of cytokine-positive CD3⁺CD8⁻ cells is determined for each cytokine, and ratios are calculated for TNF-α:IL-10 and IFN-γ:IL-10.

Results from this assay are compared to those from the TH1:TH2 Intracellular Cytokine Ratio test performed without prednisolone to assess corticosteroid-mediated inhibition of CD3⁺CD4⁺ lymphocyte activation.

Specimen Requirements

Specimen

Whole blood

Collection

Green-top tubes (sodium heparin). Mix well immediately after collection to prevent clotting.

Storage and Transport

Send at room temperature. Do not refrigerate.

Minimum Volume

30–40 mL

Unacceptable Specimens

  • Cold samples (due to refrigeration or shipment on ice)
  • Extensive clotting
  • Hemolyzed samples
  • Specimens >48 hours old

If a specimen is >48 hours old, lymphocytes will be isolated and viability assessed.

  • If viability ≥80%, the assay will be performed.
  • If viability <80%, the specimen will be rejected.

Stability

Deliver to the laboratory within 24 hours.

Method

Flow Cytometry

Note

The TH1:TH2 Intracellular Cytokine Ratio with Prednisolone may only be performed in conjunction with the TH1:TH2 Intracellular Cytokine Ratio test.

References

  • Ng SC, Thaker P, Gilman-Sachs A, Beaman KD, Beer AE, Kwak-Kim JYH. Expression of Intracellular Th1 and Th2 cytokines in women with recurrent spontaneous abortion, implantation failures after IVF/ET or normal pregnancy. Am J Reprod Immunol 48:77-86; 2002.
  • Sacks GP, Clover LM, Bainbridge DR, Redman CW, Sargent IL, Flow cytometric measurement of intracellular Th1 and Th2 cytokine production by human villous and extravillous cytotrophoblast. Placenta 22:550-9; 2001.
  • Prussin C, Metcalfe DD. Detection of intracytoplasmic cytokine using flow cytometry and directly conjugated anti-cytokine antibodies. J Immunol Method. 188:117-28; 1995.
  • determination of interleukin-1 beta., interleukin-6, and tumor necrosis factor-alpha in monocytes. Cytometry 46:172-176-2001.

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