1/10
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai | Chat |
|---|
No analytics yet
Send a link to your students to track their progress
Two distinguishing features of adaptive immunity
Specificity - the ability to recognise and target specific antigens
Immunological memory - the ability to remember antigens and mount a larger, faster response when encountering the same antigen again
Antibody
Proteins called immunoglobulins that are produced in response to specific antigens
Functions of antibodies (PIANO)
Precipitation - antibodies bind to soluble antigens and cause them to precipitate out of solution
Inflammation - antibodies trigger a release of histamine
Agglutination - antibodies bind to antigens and form antigen-antibody complexes that clump together to be phagocytosed
Neutralisation of pathogens - antibodies bind to antigens which are required for pathogens to enter host cells, thus preventing the pathogen from invading
Neutralisation of bacterial toxins - antibodies bind to toxins and block their action
Opsonisation - antigen-antibody complexes are formed and tag the pathogen for destruction
Structure of antibodies
Y shaped molecule made up of 4 polypeptide chains - 2 identical heavy chains and 2 identical light chains
The variable regions acts as receptors for antigens
Steps of the humoral immune response (5)
Clonal selection - An antigen or APC reaches the lymph nodes and binds to a specific B cell that recognises the antigen
Helper T cells bind to the antigen and release cytokines that activate B cells and stimulate them to divide
Clonal expansion - B cells differentiate and divide into plasma B cells and memory B cells
Plasma B cells produce and secrete antibodies that bind to antigens, forming antigen-antibody complexes that are phagocytosed
Memory B cells remain in the body after the infection to enable a stronger, faster immune response if the antigen is encountered again
Antigen presenting cells in the humoral immune response
Dendritic cells and macrophages are APCs that engulf and digest antigens
These antigens are presented on MHC-II makers, which are recognised by B cells to initiate the humoral immune response
Naive B cells in the humoral immune response
If the antigen has never been encountered before, a naive B cell will phagocytose the antigen
The naive B cell edits its DNA so that it becomes a specific B cell to the antigen that it engulfed, allowing it to carry out clonal selection and initiate the humoral immune response
T helper cells (include 3 functions)
Control the activity of other immune cells
T helper cells are activated when they bind to antigens presented on APCs
1. Release cytokines to stimulate B cells and cytotoxic T cells to divide
2. Activate cytotoxic T cells
3. Enhance the action of phagocytes
Cytotoxic T cells
Destroy body cells infected with viruses by releasing cytotoxins such as perforin which punches holes in the cell membrane to induce apoptosis
Target specific antigens presented on MHC-I markers
Can also target abnormal cells such as cancer cells or organ transplants
Steps in the cell-mediated adaptive response (5)
APCs displaying foreign antigens on MHC-II markers bind to specific helper T cells (usually in lymph nodes)
Helper T cells secrete cytokines that stimulate clonal selection and expansion to produce more helper T cells and memory T cells
Helper T cells secrete cytokines that activate cytotoxic T cells
Cytotoxic T cells bind to body cells presenting abnormal MHC-I markers and release perforin to induce apoptosis
Memory T helper cells and memory T cytotoxic cells remain in the body to provide future immunity
Naive cytotoxic T cells in the cell-mediated response
Naive cytotoxic T cells bind to abnormal MHC-I markers on body cells or MHC-II markers on APCs
Helper T cells release cytokines that stimulate cytotoxic T cells to proliferate, producing activated cytotoxic T cells and memory T cells through clonal selection and expansion