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Isolation and Th17 Differentiation of Naïve CD4 T Lymphocytes
Published on: September 27, 2013
Not only Th2 cells but also Th1 and Th0 cells express CD30 after activation
A Bengtsson1, C Johansson, M T Linder
1Department of Laboratory Medicine, Karolinska Hospital, Stockholm, Sweden.
Insights
CD30 molecule expression was studied in T helper cell subtypes. Activated Th2 cells showed sustained CD30 expression, unlike Th1 and Th0 cells, suggesting a distinct characteristic.
Area of Science:
- Immunology
- Cell Biology
Background:
- The CD30 molecule is expressed on a subset of T and B lymphocytes.
- T helper (Th) cells are crucial immune regulators with distinct subtypes (Th1, Th0, Th2).
Purpose of the Study:
- To determine if CD30 expression defines a specific subtype of T helper cells.
- To analyze CD30 expression kinetics in different T helper cell clones.
Main Methods:
- Pityrosporum orbiculare-specific CD4+ T cell clones were generated and classified as Th1, Th0, or Th2 based on cytokine mRNA profiles via RT-PCR.
- CD30 expression was assessed using flow cytometry, immunocytochemistry, and RT-PCR following anti-CD3 (OKT3) stimulation.
Main Results:
- OKT3 activation induced high CD30 expression in Th1, Th0, and Th2 clones within 1-3 days.
- Th2 clones maintained high CD30 expression beyond day 3, while Th1 and Th0 expression declined.
- CD30 is expressed on activated CD4+ T cells across all three subtypes.
Conclusions:
- CD30 is not exclusive to a single T helper subtype but is broadly expressed upon activation.
- Sustained CD30 expression is a characteristic feature distinguishing Th2 cells from Th1 and Th0 cells.
Abstract:
To investigate whether the CD30 molecule, expressed only by a minority of T and B cells, defines a subtype of T helper cells, Pityrosporum orbiculare-specific CD4+ T cell clones were assessed for CD30 protein and gene expression. The clones were defined as Th1, Th0, and Th2 according to their cytokine mRNA profile detected by reverse transcription PCR (RT-PCR). The kinetics of CD30 expression after OKT3 (anti-CD3) stimulation was analyzed by flow cytometry, immunocytochemistry, and RT-PCR. OKT3 activation induced a high expression of CD30 in cells of both Th1 and Th0 as well as Th2 type after 1-3 days. A difference between the clones was noted in that the Th2 clones remained highly positive in CD30 expression, whereas expression in the other clones started to decline from day 3. These data indicate that CD30 is expressed in activated CD4+ T cells of all three subtypes, and that the expression is sustained in Th2 cells.
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