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Immune
cells are found circulating in the blood stream or patrolling in the
intercellular spaces of all body tissues. Immune networks are also
distributed in discrete organs of the lymphatic system which includes
lymph nodes, tonsils, liver and spleen. Bone marrow is the major
manufacturing area of immune cells.
The thymus is the organ which originates one of two populations of immune
cells, T-lymphocytes, at least in early life. In later life the thymus continues to
exert regulatory influences on the immune system. Immunity means that immune cells
remember the identity of an antigen challenge and initiate a successful defensive
response. Immunizing injections contain antigens which belong to the infecting organisms.
The first response to the injected antigen is the activation of antigen-specific
lymphocytes who proliferate into clones of antigen-specific cells. These immune clones can
later identify and attack the infecting organism. Several exposures to the vaccine
(antigen) boost immune memory to an effective level of vigilance against the infecting
organism.
We are really a community of cells in prodigious array. Lymphocytes are important
immune players and to get an idea of the size of immune populations, think of a young
tadpole as containing about one million lymphocytes. Human immune networks contain about
10 trillion cells.
Some of our cells stay in place and do more or less predictable things. Immune cells
tend to wander around and, like bees, forage in our various body parts looking for items
of interest. An appropriate image of immune networks would be the foraging and swarming of
ants, each moving about, with different job descriptions in the colony and a meta order
achieved by the collective behavior of many individuals. The overall activity of the hive
or colony decides how the society or system looks and acts. They have the property of
getting excited, recruiting their peers and attacking interlopers.
The Cells of Immune Networks
Immune cells circulating in the blood are collectively referred to as white blood
cells. White blood cells (WBC) are routinely counted and recognized on stained
blood smears, one the most common medical lab tests. WBC groups include lymphocytes,
neutrophils, eosinophils, basophils, and monocytes. These cells are made in the bone
marrow and the lymphatic tissues (lymph nodes, thymus, spleen, and gut-associated
lymphatic tissue).
Some cells identify the characteristic molecular shape of an antigen and respond
by proliferation. A virus, for example, will have protein identifiers stuck to its capsule
which mark it, much like an ID badge. Several cell populations will emerge when the
virus is present to identify and combat it. One cell group manufactures antibody, a
protein specific to one antigen. Molecules in the food supply, especially proteins, act as
antigens. Food additives and contaminants may increase the probability of allergic
reactions to food. Immune cells do not know the difference between viral, bacterial or
food antigens. We expect and regularly observe similar immune reactions to different
antigen sources.
A diverse population of cells present antigens to other immune cells, initiating immune
responses. These antigen-presenting cells are found, for example, on the surface of
blood vessels especially in the liver and spleen. These cells act as monitors and filters
of the blood stream. In tissues these cells are called
macrophages.
Lymphocytes are the cells which recognize antigens presented by macrophages,
proliferate after contact with antigens, attack antigen-labelled cells, and manufacture
antibodies. These cells belong to many different functional groups which interact in a
complex way, resembling a large military organization. Some T-Lymphocytes (Killer cells or
K-cells) act directly to attack cells identified by specific antigen and are responsible
for cell-mediated delayed immune-injury.
Other T-lymphocytes act as controllers of the antibody-producing cells, the
B-Lymphocytes. Controller T-cells fall into groups which remember how to respond (memory
cells) and other groups which enhance immune response (helper cells). Helper cells secrete
cytokines - activation and growth factors such as interleukins which stimulate other cells
to act and proliferate. B-lymphocytes are transformed to make antibodies to specific
antigens.
B-lymphocytes leave the bloodstream and enter tissues where they transform into
antibody producers, called plasma cells. Other immune cells directly attack foreign
cells or infecting organisms, removing them from the body space. Improperly labeled cells,
such as tissue transplanted into a body, will be rejected and destroyed. Transplant
surgery is made possible by matching donor and recipient as closely as possible for the
same cell labels, known as histocompatibility antigens.
Imagine (but do not do) an experiment: make a small incision in the skin of your
arm and place a few fibers of meat (eg.scraping from the surface of a
steak) in the incision; tape the incision closed and cover with a
protective dressing; observe at daily intervals. The meat fibers include
muscle cell components from an animal whose tissue is foreign to yours.
Many of these cell components will act as antigens. Immune cells will
swarm around the foreign cells and, within 48 hours, local inflammation
will set in. The small wound will swell and fester. The typical signs of
inflammation, redness, swelling, pain, heat will persist for many days,
leaving a scarred lump behind as a permanent reminder of the event. This
experiment would illustrate the transplant rejection reaction. Similar
zones of inflammation can be set up in your tissues by meat-fiber antigens
arriving via an internal route.
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