Related Experiment Video
Updated: Jul 4, 2026

12:59
Isolation and Th17 Differentiation of Naïve CD4 T Lymphocytes
Published on: September 26, 2013
Amelioration of delayed-type hypersensitivity responses by IL-27 administration
Yoshiyuki Miyazaki1, Yohei Shimanoe, Seng Wang
1Department of Biomolecular Sciences, Division of Molecular and Cellular Immunoscience, Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga 849-8501, Japan.
Biochemical and Biophysical Research Communications
|June 24, 2008
Summary
Interleukin 27 (IL-27) suppresses immune responses in vivo, specifically reducing delayed-type hypersensitivity (DTH) by acting on the effector phase. This finding highlights IL-27
Area of Science:
- Immunology
- Cytokine Biology
- Inflammation Research
Background:
- Interleukin 27 (IL-27) is part of the IL-12 cytokine family.
- Previous studies suggested immunosuppressive functions of IL-27, but its in vivo role and therapeutic potential were unclear.
- WSX-1 (IL-27 receptor alpha chain) deficient mice and in vitro data hinted at IL-27's immunosuppressive capacity.
Purpose of the Study:
- To investigate the in vivo effect of Interleukin 27 (IL-27) administration on delayed-type hypersensitivity (DTH).
- To elucidate the therapeutic potential of IL-27 in immune-mediated conditions.
Main Methods:
- Utilized WSX-1 deficient mice to assess DTH responses.
- Administered recombinant IL-27 to experimental models.
- Measured footpad swelling as an indicator of DTH.
- Analyzed the activation status of draining lymph node cells.
Main Results:
- WSX-1 deficient mice exhibited heightened DTH responses, indicated by increased footpad swelling.
- Administration of IL-27 significantly reduced footpad swelling in the DTH model.
- IL-27 deficiency did not alter the activation status of lymph node cells, suggesting an effect on the effector phase.
Conclusions:
- Interleukin 27 (IL-27) demonstrates a suppressive effect on activated T cells in vivo.
- IL-27 ameliorates delayed-type hypersensitivity responses.
- IL-27 holds therapeutic potential for diseases driven by immune dysregulation.
Related Concept Videos
Hypersensitivity Reactions: Delayed Hypersensitivity Reactions
Delayed-Type Hypersensitivity (DTH), or Type IV hypersensitivity, is a cell-mediated immune response. It occurs when T cells, rather than antibodies, mediate a reaction to specific antigens. It is characterized by a delayed onset (1-2 days) and involves the recruitment of macrophages to the inflammation site.The initiation of a DTH response begins with the sensitization of T cells. During this phase, which lasts at least 1-2 weeks, antigen-specific T cells are activated, clonally expanded, and...
T Cell Types and Functions
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Hypersensitivities
Hypersensitivity, also known as a hypersensitivity reaction or allergic reaction, is a condition where the body's immune system reacts abnormally to a foreign substance. Such substances, that cause hypersensitivity are referred to as an allergen, could be something typically harmless to most people, like pollen or certain foods.
Types of Hypersensitivities
Hypersensitivity reactions are categorized into four types: Type 1, Type 2, Type 3, and Type 4. Each type has a distinct mechanism...
Types of Hypersensitivities
Hypersensitivity reactions are categorized into four types: Type 1, Type 2, Type 3, and Type 4. Each type has a distinct mechanism...
Allergic Drug Reactions
Allergic reactions related to drugs are hypersensitivity responses driven by the immune system and bear no connection to the drug's therapeutic action. While drugs in isolation do not trigger an immune response, they can interact with endogenous proteins to form antigens. These antigens stimulate lymphocytes to produce antibodies. IgE-type antibodies attach themselves to mast cells. Upon subsequent exposure to the same stimulus, the antigen-antibody interaction is initiated, unleashing numerous...

