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Published on: January 9, 2013
Candida albicans mannan-specific, delayed hypersensitivity down-regulatory CD8+ cells are genetically restricted
1Department of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, La., USA.
Insights
This study reveals that CD4+ and I-A+ cells are crucial for inducing CD8+ effector cells in a Candida albicans mannan-specific system. Genetic compatibility is also essential for the effector activity of these CD8+ cells.
Area of Science:
- Immunology
- Cellular Immunology
- Immunoregulation
Background:
- Down-regulatory cells play a role in immune system modulation.
- The precise mechanisms for inducing and activating these cells remain controversial.
- Previous work identified CD8+ cells as mediators of down-regulation in a Candida albicans mannan (MAN)-specific system.
Purpose of the Study:
- To investigate the requirements for CD4+ and I-A+ cells during the induction of CD8+ effector cells.
- To determine the role of genetic compatibility in the effector activity of CD8+ down-regulatory cells.
- To elucidate the cellular cooperation involved in down-regulating MAN-specific delayed hypersensitivity (DH).
Main Methods:
- Mice were treated with monoclonal antibodies against CD4 and I-A at various times relative to MAN administration.
- The ability of splenocytes from MAN-treated mice to suppress DH was assessed in recipient mice.
- Cell transfers were performed between genetically incompatible mouse strains (CBA/J and BALB/cByJ) to evaluate effector cell activity.
Main Results:
- Administration of anti-CD4 or anti-I-A antibodies up to 30 hours post-MAN treatment abrogated the development of CD8+ down-regulatory cells.
- Genetic incompatibility between donor and recipient mice restricted the effector activity of CD8+ down-regulatory cells.
- These findings indicate that CD4+ and I-A+ cells are necessary for the inductive phase, and genetically compatible cells are required for the effector phase.
Conclusions:
- Both the induction and effector stages of MAN-specific DH down-regulation require genetically compatible cells.
- CD4+ cells are essential for the development pathway of CD8+ effector cells.
- Cell-cell cooperation is critical for both inductive and effector phases of immune down-regulation.
Abstract:
There is considerable controversy over the induction and activity of down-regulatory cells active in various antigen-specific and antigen-nonspecific systems. We have been studying the nature of such cells in a Candida albicans mannan (MAN)-specific system for some time and report here the requirements for CD4+ and I-A+ cells during the inductive phase for the development of CD8+ effector cells, as well as the requirement for genetic compatibility for effector activity of CD8+ cells. Since we have shown previously that CD8+ down-regulatory cells were present in spleens of MAN-treated mice 4 days following the administration of MAN to naive mice, as determined by their ability to suppress delayed hypersensitivity (DH) when transferred to immunized recipients, we treated mice with monoclonal antibodies specific for CD4 and I-A at various times before, with or after the administration of MAN to assess the role of CD4+ and I-A+ cells in the development of the CD8+ effector cell. Both anti-CD4 and anti-I-A given before or up to 30 h after the administration of MAN abrogated the ability of splenocytes from MAN-treated mice to down-regulate MAN-specific DH in immunized recipients. Moreover, transfers of down-regulatory cells between H-2-incompatible strains of mice, specifically CBA/J and BALB/cByJ, provided evidence that the effector cell for the down-regulatory activity was also restricted genetically in its activity. Taken together, the data presented indicate that genetically compatible cells are required for both the inductive and effector stages of down-regulation of MAN-specific DH, suggesting that cell-cell cooperation is required for both stages and that CD4+ cells are required in a pathway leading to the development of the CD8+ effector cell.
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