Immunology: Group Members
Immunology: Group Members
Immunology: Group Members
Group Members
Aaliya Blackman
Bibi Khan
Content
Definition of “immune response”
B-cells help fight against bacteria and viruses that enter the body. They are able to detect and bind to specific
foreign invaders (antigens) that enter the body. This triggers other immune cells to destroy the antigen. Naive B-
cells are B-cells that have not encountered an antigen yet. Once a B-cell has been exposed to an antigen, it is
called a plasma cell.
The first step of B cell maturation is an assessment of the functionality of their antigen-binding receptors. This
occurs through positive selection for B cells with normal functional receptors. A mechanism of negative selection
is then used to eliminate self-reacting B cells and minimize the risk of autoimmunity. Negative selection of self-
reacting B cells can involve elimination by apoptosis, editing or modification of the receptors so they are no
longer self-reactive, or induction of energy in the B cell. Immature B cells that pass the selection in the bone
marrow then travel to the spleen for their final stages of maturation. There they become naïve mature B cells, i.e.,
mature B cells that have not yet been activated.
T cell, also called T lymphocyte, type of leukocyte (white blood cell) that is an essential part of the immune
system. T cells are one of two primary types of lymphocytes—B cells being the second type—that determine
the specificity of immune response to antigens (foreign substances) in the body.
They are two main type of T cells: Helper T-cells and Killer T-cells
Helper T- cells stimulates B cells to make anti-bodies and help Killer cells develop
Killer T-cells directly kill cells that have already been infected by a foreign invader(antigen)
Maturation of T- Cells
T cells all originate from cells in the bone marrow that divide by mitosis. As a child grows and develops, these
immature T-cells move to the thymus gland in the neck, where they divide to form a large population of T-cells
As the T-cells mature, they begin to produce glycoproteins called CD4 and CD8.
These glycoproteins are placed in their plasma membranes, where they act as receptors. Each cell then stops
producing one of these types of glycoprotein, and becomes either a CD4 plus cell( producing CD4 only) or a
CD8 plus cell (producing CD8 only).
During their development in the thymus gland, only T cells that have a set of receptors enabling them to bind
to the proteins antigens on the body’s own cells ( called the MHC complex) are allowed to survive. Moreover,
any that interact with the MHC complex too strongly are also destroyed. This ensures that all of the T- cells that
remain in the body’s own cells, and will not initiate auto-immune reactions in which they attack and harm
them. Overall, only about 2% of all the T-cells that develop in the thymus gland pass these tests and survive.
Describe the mode of action of phagocytes
They are two of white blood cells (Phagocytes) known as:
Neutrophils
Macrophages
Neutrophils: are found in the blood, where they make up about
60% of the white blood cells
Macrophages: a large phagocytic cell found in stationary form in
the tissues or as a mobile white blood cell, especially at sites of
infection
Phagocytes: are known for their actin process, as they engulf the whole
foreign or harmful substances or cells. The plasma cells disappear after
the immune response work is over, but again the memory B-cells
remain active for a long time so that the invader may not be able to
attack the body and its immune system again as antibodies are already
present for them to fight and eradicate them.
Phagocytosis, process by which certain living cells called phagocytes ingest or engulf other
cells or particles. The phagocyte may be a free-living one-celled organism, such as an
amoeba, or one of the body cells, such as a white blood cell. In some forms of animal life, such
as amoebas and sponges, phagocytosis is a means of feeding. In higher animals phagocytosis
is chiefly a defensive reaction against infection and invasion of the body by foreign
substances (antigens).
Before phagocytosis is accomplished, the phagocyte and the particle must adhere to each
other, the possibility of which depends largely on the chemical nature of the surface of the
particle. In the case of bacteria, if the phagocyte cannot adhere directly, protein components
of the blood known as opsonins (e.g., complement and antibodies) form a surface film on
bacteria—a process known as opsonization. Phagocytes adhere to the opsonins, and
phagocytosis follows. Encapsulated bacteria are ingested with more difficulty. In the absence
of specific antibodies that recognize the bacteria, opsonization cannot occur, and the bacteria
repel phagocytes. The surfaces of such bacteria are coated with special antibodies only after
the body has mounted an immune response to the presence of that particular kind of
bacterium. Such antibodies are of great importance in establishing immunity to diseases.
The speed with which a phagocytic cell ingests a particle varies somewhat with the size of the
particle. Small particles, such as bacteria or minute grains of charcoal, are ingested almost
instantaneously. Larger objects, such as clumps of bacteria or tissue cells, are phagocytosed over
the course of a more-prolonged response. The cell flows around the object until it has been
completely engulfed. The engulfed object is thus enclosed within a membrane-bound vacuole
called a phagosome. The phagocyte digests the ingested particle with hydrolytic enzymes, which
are contained within membrane-enclosed sacs called lysosomes found within the cell. Phagocytic
enzymes are secreted into the vacuole in which digestion takes place. Small organic components of
the particle are used to build larger molecules needed by the cell.
Both systems are active immunities.
Both systems have immunological
memory present.
Similarities of the Both systems are ineffective in immune
Humoral and Cell deficient individuals.
Mediated Both systems are effective against a wide
Responses variety of microbial pathogen
Differences
Cell mediated Response Humoral (antibody) Response
It is mediated by T-cells. It is meditated by antibodies
Antibodies are not formed. (produced by B-cells).
Receptors are used to Antibodies are formed.
detect antigens. Antibodies are used to detect
T-cell receptors binds to antigens
the T-cells which binds to B-cells produce anti-bodies
the antigens them self. and the anti-bodies binds to
Protects against the antigens.
intracellular bacterial Protects against extracellular
pathogens (eg: viruses, bacterial and viral pathogens.
Roles of memory cells in long term immunity