In this project we are studying the immunoregulatory potential of human T cells which are activated by self-MHC antigens present on B cells or macrophages (autoreactive T cells). In previous studies we established autoreactive T cell clones which are maintained in IL-2 enriched cultures by periodic stimulation with autologous non-T cells. One of these clones, termed MTC-4, was found to have dual immunoregulatory potential, providing help for resting B cells and suppression for pokeweed-mitogen (PWM)-activated B cells. In current studies we showed that MTC-4 helper function involves recognition of class II MHC antigens by the MTC-4 cells via its T3-associated T cell receptor. Further, we showed that the helper function is mediated by a BCGF-like factor which is distinct from IL-2 and which acts on both resting (small) and activated (large) B cells. Also incurrent studies we showed that MTC-4 T cell suppressor function is elicited when MTC-4 cells are co-cultured with non-T cells (B cells plus monocytes) that are pre-incubated with PWM for four hours, but not with non-T cells pre-incubated with PWM for 24 hours; this implies that induction of suppressor function depends on a transiently expressed MHC-associated surface molecule. In addition, we showed that pre-treatment of non-T cells with neuraminidase leads to non-T cells which do induce MTC-4 suppressor function. This suggests that the glycosylation status of non-T cells surface antigen determines whether non-T cells elicit helper or suppressor function from the autoreactive T cell population. Finally, we showed that the MTC-4 T cell suppressor function is MHC-specific in the effector phase in that only MHC matched cells are able to be suppressed. This indicates that MHC recognition is necessary in the effector cell-target cell interaction. In all, these studies establish that autoreactive T cells can be induced to provide either help or suppression depending on the type of B cell stimulus. This bifunctionality endows autoreactive cells with the potential for important homeostatic function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000357-04
Application #
3960570
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Niaid Extramural Activities
Department
Type
DUNS #
City
State
Country
United States
Zip Code