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Updated: Jun 10, 2026

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Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells
Published on: April 16, 2012
CD25 appears non essential for human peripheral T(reg) maintenance in vivo
Marie-Ghislaine de Goër de Herve1, Emmanuel Gonzales, Houria Hendel-Chavez
1Unité d'Immunologie Biologique, CHU Bicêtre, Le Kremlin-Bicêtre, France.
Plos One
|August 7, 2010
Summary
Basiliximab, an anti-CD25 antibody, did not deplete regulatory T cells (Tregs) in pediatric liver transplant patients. However, altered Treg function was suggested by increased food allergies post-transplant.
Area of Science:
- Immunology
- Transplantation immunology
Background:
- Interleukin-2 (IL-2) is crucial for regulatory T cell (Treg) survival in mice.
- Basiliximab, an anti-CD25 antibody, is used therapeutically in organ transplantation.
Purpose of the Study:
- To investigate the effect of basiliximab on Treg maintenance and function in pediatric liver transplant recipients.
- To determine if CD25 blockade impacts peripheral Treg survival in humans.
Main Methods:
- Flow cytometry was used to analyze FoxP3+ CD4 T cells before and after liver transplantation.
- Patients received basiliximab, and Treg markers (CD25, FoxP3, IL-2Rbeta, IL-2Rgamma) were assessed.
Main Results:
- Basiliximab treatment did not deplete Tregs; FoxP3+ cell proportion and expression remained unchanged.
- IL-2Rbeta expression increased on Tregs post-basiliximab, while other IL-2 receptor subunits showed no significant change.
- Despite stable Treg numbers, recipients treated with basiliximab experienced earlier onset of food allergies.
Conclusions:
- CD25 is not essential for the peripheral maintenance of human Tregs in vivo.
- Therapeutic targeting of CD25 may affect Treg functionality, warranting further investigation.
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