Immune System - AP Biology

According to the passage, after the MHC II molecules are fully synthesized in the endoplasmic reticulum, they are transported to the endosome. Foreign molecules are transported into the cell where they are degraded in the endosome as well. From there, the degraded pathogen interact with the MHC II molecule.

According to the passage, MHC I and cytotoxic t-cells are responsible for identifying the body's own protein. During organ transplant, foreign MHC I molecules are presented into the body. The host's cytotoxic T-cells will recognize these as foreign and will attack.

White blood cells is the correct answer here. After pathogen has entered the body, the antibodies to combat it are created by B cells that are a part of the white blood cells in the human body.

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.

The adaptive immune system primarily relies on the function of B-cells and T-cells. T-cells help recognize antigens to which the body has been previously exposed and stimulate B-cell to release antibodies to combat that specific antigen.

Upon initial antigen exposure, all other cell types listed (which help comprise the innate immune system) kick in.

Mast cells contains secretory granules, rich in histamine and other hormonal mediators, that promote inflammation and other allergy symptoms in response to antigen exposure.

The humoral response refers to the antiquated term "humors", meaning body fluids, as used in ancient and medieval medicine. In response to antigen exposure, B-cells release antibodies into the extracellular fluid and throughout the body, thus eliciting a "humoral response."

Although helper T-cells are responsible for activating B-cells, the humoral response is limited to B-cells because they are the ones releasing products into the body fluids.

Metastasis is the proliferation of cancer cells into new tissues. Cancer usually metastasizes through the circulatory or lymphatic systems, and the cancerous cells take residence in other, seemingly unrelated parts of the body.

Memory B cells circulate the body and are ready to respond to subsequent infections while plasma cells generate many antibodies to a current infect. "Immunoglobulins" refers to both the B cell receptor and to the excreted form of these proteins (known as antibodies). IgG is a class of immunoglobulins (along with IgA, IgE, IgD, and IgM). Finally, macrophages are cells that engulf non-self (and often antibody-bound) cells and communicate with T cells to promote B cell proliferation.

Red blood cells are made in the bone marrow, and live for about 3-4 months. They are enucleated (lacking a nucleus), which makes more space available for hemoglobin molecules, which function to carry oxygen to the tissues. HIV infects T-helper cells, which are white blood cells, not red blood cells. Thus, the name makes sense since the virus infects cells of the immune system (white blood cells) and causes immunodeficiency. The liver and spleen play roles in recycling the red blood cells once they have carried out their function for about 120 days.

Keratinocytes are not immune cells. Rather, they secrete a protein called keratin which is a large proportion of the extracellular matrix and makes up hair, nails, skin, and other parts of the body. All other cells are immune cells.

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 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.

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.