Final answer:
Centrocytes and centroblasts must compete for antigen on FDCs, hence the answer is d. A & B. TCRs of CD4+ helper T cells bind to antigens presented with MHC II, while CD8+ cytotoxic T cells bind to antigens presented with MHC I on APCs.
Step-by-step explanation:
The immune cells that must compete with each other to gain access to antigen on a Follicular Dendritic Cell (FDC) are both centrocytes and centroblasts. However, TFH cells, also known as T Follicular Helper cells, do not compete for antigen on FDCs in the same way.
To address some background knowledge, CD8+ T cells, also known as cytotoxic T lymphocytes (CTLs), bind to MHC I molecules on Antigen-Presenting Cells (APCs) via their CD8 coreceptors. MHC I molecules are found on virtually all nucleated cells, enabling these cells to present endogenous antigens to cytotoxic T cells. On the other hand, MHC II molecules are present on professional APCs such as dendritic cells, macrophages, and B cells, and are used for presenting exogenous antigens to CD4+ helper T cells.
Regarding T cell properties, it is false that MHC II is found on most body cells, as it is primarily on professional APCs. T cell receptors (TCRs) are found on both CD4+ and CD8+ T cells, which bind to MHC II and MHC I respectively. While helper T cells (CD4+) release cytokines and assist other immune cells, cytotoxic T cells (CD8+) directly kill infected or cancerous cells.