I can expand a little bit on what Gandalf said:
The simplified model for cell-mediated immunity is that you have two major types of T cells: helper and cytotoxic T-cells. Scientists use the protein markers CD4 (helper) and CD8 (cytotoxic) to identify them, as these proteins are a key part of their interaction with MHCs. MHCI interacts with CD8 co-receptor, the T-cell receptor of cytotoxic T-cells, and the antigenic protein, while MHCII interacts with CD4, TCR of helper T-cells, and the antigenic protein. I remember this as MHCI, where "I" marks the primary function of the immune system (kill off the bug), and MHCII "II" as the secondary function of enhancing the attack through help.
In viral infections, for example, cytotoxic T-cells release granules containing perforin and granzyme B, which induce apoptosis of the virus-infected cell. Helper T-cells can activate B cells to send out antibodies against viral proteins that they recognize in their CD4-TCR-antigen complex. B cells then become plasma cells, which produce vast amounts of antibody specific for the antigen. These antibodies are then recognized by the complement system, and that is all gobbled up then by macrophages.
I will also just add that it's good to know that there is at least one further major type of T cell, the regulatory T cell (Treg), which acts to inhibit/tone down the response of lymphocytes (T, B cells) to antigen. Tregs are thought to prevent auto-immune responses and to prevent organ rejection for very well-matched MHC donor/recipients (suppression by Tregs is definitely not strong enough for a partial/full allogeneic mismatch).
I think this is sufficient for the MCAT, but let me know if you have any more questions about it.