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Effects of Cryptococcus neoformans-specific suppressor T cells on the amplified anticryptococcal delayed-type
K L Buchanan1, P L Fidel, J W Murphy
1Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City 73190.
Infection and Immunity
|January 11, 1991
Summary
Newly identified Tamp cells amplify delayed-type hypersensitivity (DTH) responses against Cryptococcus neoformans. T suppressor (Ts) cells inhibit Tamp cell induction but not their function, suggesting Tamp cells may counteract Ts cell suppression.
Area of Science:
- Immunology
- Microbial Pathogenesis
Background:
- Cell-mediated immunity is crucial for controlling Cryptococcus neoformans infections.
- Antigen-specific T suppressor (Ts) cells down-regulate anticryptococcal delayed-type hypersensitivity (DTH) responses.
- A novel CD4 T cell population, termed Tamp cells, amplifies anticryptococcal DTH responses.
Purpose of the Study:
- To investigate the interaction between C. neoformans-specific Ts cells and Tamp cells.
- To determine how Ts cells affect Tamp cell induction and function.
- To elucidate the role of Tamp cells in modulating the anticryptococcal DTH response.
Main Methods:
- Adoptive transfer of T suppressor cells (Ts1 and Ts2) and Tamp cells in mice.
- Measurement of delayed-type hypersensitivity (DTH) responses.
- Analysis of Tamp cell induction and function in the presence of Ts cells.
Main Results:
- Ts1 cells inhibited Tamp cell induction when administered during immunization.
- Ts1 cells did not impair the function of established Tamp cells.
- Ts2 cells had no significant effect on the amplified DTH response mediated by Tamp cells.
- Tamp cells may protect anticryptococcal DTH cells from Ts cell-mediated suppression.
Conclusions:
- Tamp cells amplify anticryptococcal DTH responses and may possess contrasuppressor-like functions.
- The interaction between Tamp cells and Ts cells is complex, with Ts cells affecting Tamp cell generation but not their effector function.
- Anticryptococcal Tamp cells differ from contrasuppressor cells in other systems due to their lack of Viscia villosa lectin adherence.