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Updated: Aug 8, 2026

Rapid Quantification of Mitogen-induced Blastogenesis in T Lymphocytes for Identifying Immunomodulatory Drugs
Published on: December 27, 2016
Thalidomide and its metabolites have no effect on human lymphocyte proliferation
T Santos-Mendoza1, L Favila-Castillo, A Oltra
1Department of Immunology, National School of Biological Sciences IPN, Mexico City, D.F., Mexico.
Insights
Thalidomide does not impact immune cell proliferation. This study found no direct effects of thalidomide or its metabolites on human mononuclear cells
Area of Science:
- Immunology
- Pharmacology
Background:
- Thalidomide is used for diseases with an immunological component.
- Its effects on immune functions are not fully understood.
Purpose of the Study:
- To investigate thalidomide's impact on human mononuclear cell proliferation.
- To determine if thalidomide or its metabolites affect immune responses.
Main Methods:
- Assessed proliferation of human mononuclear cells stimulated by purified protein derivative (PPD) and concanavalin A (Con-A).
- Evaluated cells from subjects post-thalidomide ingestion and plasma from humans and rabbits treated with thalidomide.
Main Results:
- Thalidomide up to 50 micrograms/ml showed no direct effect on cell cultures.
- Cells from subjects 6 hours after 200 mg thalidomide ingestion proliferated similarly to pre-administration cells.
- Plasma from thalidomide-treated subjects or rabbits did not inhibit human mononuclear cell proliferation.
Conclusions:
- Thalidomide and its metabolites do not affect the proliferative capacity of human mononuclear cells.
- The drug's impact on immune cell proliferation is negligible at tested concentrations and conditions.
Abstract:
Thalidomide is a drug that is being used in several diseases with an immunological component, but the effects on the different immune functions have only been studied partially. Therefore, we studied the effect of thalidomide on PPD-or Con-A-induced proliferation of human mononuclear cells. We found no direct effect of thalidomide at up to 50 micrograms/ml on the cultures. Cells taken from subjects 6 h after ingestion of 200 mg of thalidomide proliferated equally well to PPD and Con-A than cells taken prior to drug administration. Plasma taken from subjects that ingested 200 mg of thalidomide 6 h before did not affect the proliferative response of their own cells when added to the cultures. Plasma from rabbits that were injected with doses 5 or 15 times higher than the dose given to humans did not diminish the proliferative response of human mononuclear cells to PPD. We conclude that neither thalidomide nor its metabolites affect the proliferative response of human mononuclear cells.
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