cell mediated immunity and lymph ontogeny Flashcards
CD8 T cell clonal activation
- peptide antigen presented on class 1 HLA
- downstream proliferation & differentiation to cytotoxic T and memory cells
killing mechanism of cytotoxic T cells
- release cytoplasmic granules when they bind, which punch holes in the membrane, called perforin
- release enzymes which travel through the holes and get inside the cell
- release cytokines (TNF) inducing apoptosis
antigen specific
lymphocyte ontogeny
- T cell precursors from marrow and thymus
- after maturation in thymus, export T cells to secondary typhoid organs
B cell lineage
- haematopoietic stem cells -> pre-B cell
- immature B cell (with surface IgM)
- mature B cell (with surface IgM and IgD)
immunoglobulin genes
- heavy chains defined by constant regions
- multiple V, D, J axons recombine giving V- region variability
- recombination occurs independently of antigen
exposure - 1 gene set codes for heavy chain, 2x sets for light chains
central tolerance
before leaving bone marrow, immature B cells are deleted if receptors have high affinity for self-antigens expressed in the marrow
(prevents self-reactivity)
describe monoclonal
- Immortalised antibodies that can be engineered to be specific for particular target.
- Therapies used in chemotherapies
- Target specific cells not just everything dividing
antibody class switching
- B cells able to switch antibody classes while maintain the same variable regions (antigen specificity)
- B cells can switch from one class to another by chopping out intervening sequences but still maintaining the same J, D or V meaning they retain the same antigen specificity (helper cells trigger deletion of genes)
initial make IgM –> IgG
what gives the variable region its diversity
multiple V, D, and J axons that recombine
independent of antigen
difference between B cell and T cell repertoire
B cell constantly being produced throughout life
Thymus shrinks with age and therefore fewer T cells later in life
T cell ontogeny and T cell receptor genes
- development in the thymus
- multiple V, D and J axons recombine => V-region
- recombination independent of antigen
- T cells become committed to one Va and one Vb
- positive selection for HLA class 1 or 2 recognition (requires CD8 or CD4)
- negative selection process to rule out self-reactivity