Zusammenfassung der Ressource
Humoral Immunity - Antibody Response II - B-cell response
- Primary Antibody Response
- 1. Clonal Selection
- antigen enters + localized in secondary lymphoid tissue
- here: attaches to specific B cell antigen receptors
- T-independent (polysaccharide) antigens directly activate B cells to make IgM antibodies
- T-dependent protein antigens only activate B cells with help of Th cells
- to activate Th cells , antigen is processed by APCs and presented to Th cells on MHCII
- Hence Clonal selection - antigen selects specific B cells to take part in antibody response
- selected B cells do rapid clonal proliferation = increase no. antigen-specific cells to deal w. pathogen
- some become memory cells
- many become plasma cells
- Time taken for process
- I) Lag period before detectable antibody levels
- cellular events take time
- ii) Log phase
- increasing antibody amounts
- as more cells divide = more plasma cells
- iii) Plateau phase
- bound antigen is removed
- lymphocytes no longer stimulated
- antibody decline in serum
- most plasma cells die after completing function
- Affinity Maturation
- Germinal centres
- made after B cell activation
- in secondary lymphoid tissue
- where B cells undergo
- class switching
- clonal expansion
- somatic hypermutation of variable region genes
- espec. Complementary Determining Regions (part that makes contact with antigen)
- random mutations = occasional cells produced with higher affinity receptor
- rescued through recognition of antigen that are on the immune complex on FDC
- these B cells proliferates
- some become memory cellos
- o/ become plasma cell precursors
- leave germinal centres
- become plasma cells in lymph nodes' medulla or spleen's red pulp
- others bind less well and can't stimulate b cells
- these die by apoptosis in germinal centre
- removed by phagocytic macrophages
- selection of high affinity clones leading to affinity maturation of antibody response
- Class Switching
- 1st antibodies made in 1ary response - IgM
- as IgM B cells stimulated to divide = plasma cells secreting IgM
- Cytokines - from Th cells
- influence some B cells
- to switch to IgG, IgA or IgE during proliferation
- some develop into memory cells
- e.g. cytokin IL-4: cause switch to make IgE
- driving proliferation + plasma cell differentiation
- Polyclonal
- bc microbe has many diff. antigens
- each w/ several epitopes
- Immunoloical Memory
- adapative immune response
- many memory cells remain after primary response
- can respond to same antigen
- so secondary immune response = bigger and faster
- none/little w/out Th cells