Immune System - AP Biology

Natural passive immunity is conveyed from mother to child in-utero or through colostrum in breast milk. Natural passive immunity provides temporary immunity to many diseases.

Natural active immunity occurs when an individual develops a disease as a result of being exposed to a live pathogen, and acquires immunity to that pathogen as a result.

Artificial active immunity is acquired as a result of intentional exposure to a pathogen, as in a vaccination.

Artificial passive immunity occurs when antibodies are transferred from one person to another. Immediate short-term protection may be conveyed to immune-compromised patients, such as chemotherapy recipients, by this mean.

Essentially, active immunity requires exposure to a live pathogen; passive immunity does not (only antibodies). Artificial immunity requires intervention in the form of a vaccine or medical care, while natural immunity occurs unintentionally through exposure.

Toll-like receptors (TLRs) are a family of receptors found within innate immune antigen-presenting cells such as dendritic cells, monocytes, and macrophages. These receptors recognize specific elements of various infectious agents such as lipopolysaccharides, DNA, and RNA. Binding and activation of these receptors stimulates inflammatory responses and CD4/CD8 T-cell responses to drive an effective immune response.

TLRs do not control B-cell clonal selection, the process by which B-cells replicate to amplify the production of a certain antibody.

Innate immunity is a generalized form of protection against pathogens in the body. The cells of innate immunity generally attack all types of invasive agents and do not interact with antibody production.

Neutrophils, eosinophils, and macrophages are all generalized leukocytes that are present in the body. Neutrophils, basophils, and eosinophils are the primary granulocytes, all of which are involved in innate immunity. Macrophages are differentiated monocytes, capable of phagocytosis against non-specific invaders.

Plasma cells are differentiated B-lymphocytes. They release antibodies into the bloodstream that are specific for a given pathogen. As a result, plasma cells are only present following a specific infection. They are a crucial part of the adaptive immune response, but are not involved in innate immunity.

The spleen plays a key role in the immune system as one of the blood filtration centers of the body. It is also involved as a lymphatic organ, allowing filtrates from the blood to be distributed to the body via lymph.

The lymphatic system is responsible for removing excess fluid from the interstitium and returning it to the bloodstream. The fluid will travel through lymph nodes, which monitor for the presence of microbes in the blood. If microbes are present, the lymph nodes will mount an immune response. The lymphatic system also reroutes fat digestates from the small intestine's capillaries and drains them into the veins of the neck. Lymphatic vessels do not assist in the transfer of oxygen to body tissues.

Some viruses evade the immune system using a mechanism known as latency. The virus essentially becomes dormant, usually in cells such as neurons that have few major histocompatibility (MHC) class I molecules. The combination of limited to no active viral replication combined with residence in cells with few MHC lass I molecules allows the virus to evade routine immune monitoring.

When conditions arise, such as fever due to infection caused by another pathogen or emotional stress, the virus can becomes reactivated and can result in an outbreak.

Red blood cells generally do not leave the circulatory system; thus there are very few opportunities for lymphatic vessels to pick up red blood cells in the extracellular space.

The lymphatic system plays a key role in transporting immune cells, such as lymphocytes, throughout the body. When fats are emulsified and digested in the small intestine, they are transported into the lymph rather than into the blood. When plasma and fluids leak out of capillaries, the lymphatic system is responsible for collecting and returning these fluids to circulation. A fault in this function of the lymphatic system results in edema.

T-cells generally serve to recognize antigens and escort them to B-cells to elicit a response (helper T-cells) or to recognize antibodies bound to infected cells (cytotoxic T-cells). B-cells, in contrast, will directly secrete antibodies against the antigen after binding of the antigen at the membrane.

Both types of cells have receptors that can bind to antigens, allowing for recognition and communication. Other commonalities include the presence of a transmembrane domain and the presence of a variable region, which will allow for specificity in antigen binding.

The similarities are mainly structural, and the receptors have many functional differences. T-cell receptors will only bind fragments of antigens, while B-cell receptors will bind full molecules. Only T-cell receptors will interact with major histocompatibility complexes (MHC). Though the structure of both receptors types is determined by peptide chains, B-cells use heavy and light chains, while T-cells use alpha and beta chains.

Macrophages and neutrophils are the major cells of the immune system responsible for phagocytosis. Phagocytosis means ingestion of material. Therefore these cells work as "garbage collectors" within the body. Cells destined for destruction are tagged for phagocytosis by special molecules.

B-cells produce antibodies (a subset of adaptive immunity called humoral immunity). The usual sequence involves B-cell activation via interleukins from helper T-lymphocytes, which cause the B-cell to undergo mitosis, creating numerous clones that will differentiate into plasma cells (rapid antibody producers) or memory B-cells.

Antibodies (or immunoglobulins) are produced by B-leukocytes and plasma cells, and are a key part of humoral (having to do with bodily fluids) immunity. As such, they can be found in several of the fluids circulating or exiting the body. Some types of immunoglobulins can even cross the placenta or be secreted in breast milk to pass immunity from a mother to her child.

All of the given answer options describe mechanisms for immunoglobulin function.

Neutralization occurs when the antibodies simply cover the biologically active portion of the pathogen, rendering it harmless. Complement fixation refers to the antibodies binding to the pathogen and facilitating the activation of the complement system (a series of plasma proteins that activate other immune processes). Precipitation is when antibodies link the antigens on many pathogens together, creating an insoluble clump ready for removal.

B-cells produce antibodies (a subset of adaptive immunity called humoral immunity). The usual sequence involves B-cell activation via interleukins from helper T-lymphocytes, which cause the B-cell to undergo mitosis, creating numerous clones that will differentiate into plasma cells (rapid antibody producers) or memory B-cells.

Antibodies (or immunoglobulins) are produced by B-leukocytes and plasma cells, and are a key part of humoral (having to do with bodily fluids) immunity. As such, they can be found in several of the fluids circulating or exiting the body. Some types of immunoglobulins can even cross the placenta or be secreted in breast milk to pass immunity from a mother to her child.

All of the given answer options describe mechanisms for immunoglobulin function.

Neutralization occurs when the antibodies simply cover the biologically active portion of the pathogen, rendering it harmless. Complement fixation refers to the antibodies binding to the pathogen and facilitating the activation of the complement system (a series of plasma proteins that activate other immune processes). Precipitation is when antibodies link the antigens on many pathogens together, creating an insoluble clump ready for removal.

The ability to form any of the three germ layers is known as pluripotency. Totipotent cells, such as the zygote, are able to form an entire organism, multipotent cells are able to form any cell within the same germ layer lineage, and progenitor cells are cells closer to differentiation, often found in adult organisms.

Humoral, or B-cell, immunity is associated with the formation of antibodies. Plasma cells are B-lymphocytes that have been differentiated with the help of a helper T-cell. They release antibodies, which are created to respond to a specific pathogen in the body.

Cytotoxic T-cells are also activates by help T-cells, but are involved in cell-mediated immunity rather than humoral immunity. They target infected cells based on antibody tagging. Monocytes are a part of the innate immune response and are not involved in antibody interactions. They primarily differentiate into macrophages, which engage in phagocytosis of pathogens.

Basophils are the least common leukocyte found in the body, but play a key role in the inflammatory response. They contain histamine, which is a potent vasodilator. Upon release, histamine will increase blood flow to infected areas. Mast cells are another immune cell that is involved in histamine release, but are generally localized to various regions of the body rather than found in circulation.

Basophils, mast cells, eosinophils, and neutrophils are all considered granulocytes and are essential cells in the innate immune response. Plasma cells are differentiated B-lymphocytes that are responsible for mass-producing antibodies to a specific antigen.

The granulocytes are responsible for numerous functions of innate immunity, from secreting histamine, to phagocytosis, to anti-inflammatory processes. These cells are the basophils, neutrophils, eosinophils, macrophages (monocytes), and mast cells.

Eosinophils have a more limited role in innate defense than the other granulocytes. They possess only low phagocytic activity, however, they are more specialized to respond to multi-cellular pathogens, such as parasitic worms. Rather than phagocytosing an invading organism, eosinophils function by releasing an arsenal of destructive enzymes and free radicals to ward off the organism. The other granulocytes are specialized for phagocytosis of bacteria, viruses, and cellular debris.