IMMUNOLOGY-AN
OVERVIEW
1 MARK QUESTIONS
1. Immunity
The power of a versatile
defence system that has evolved to protect animals from invading pathogenic
microorganisms and cancer is called immunity. It is able to generate an
enormous variety of cells and molecules capable of specifically recognizing and
eliminating an apparently limitless variety of foreign invaders like pathogens
or antigens
2. Innate immunity
Innate immunity is the less
specific component that provides the rapid, first line of defence against
infection. Most components of innate immunity are present before the onset of
infection. Phagocytic cells, such as macrophages and neutrophils, barriers such
as skin, and a variety of antimicrobial compounds synthesized by the host all
play important roles in innate immunity by recognizing and clearing frequently
encountered pathogens.
3. Acquired/adaptive immunity
Adaptive immunity is the quicker,
stronger and specific immunity against an antigen within five or six days after
the initial exposure to that antigen. Exposure to the same antigen sometimes in
the future results in a memory response. It is more effective in neutralizing
and clearing the pathogen by utilizing antibodies or cell mediated mechanisms.The
major agents of adaptive immunity are lymphocytes and the antibodies and other
molecules they produce.
4. Components of innate
immunity
Phagocytic cells
(macrophages, neutrophils, monocytes), NK cells, barriers (skin), Microbial
probionts, Surface
secretions (acids, sweat, sebum, mucus, proteolytic enzymes, lactoperoxidase in
milk), Mechanical action (Peristalsis, Washing effect of tears, saliva and
urine) etc.
5. Phagocytes
Phagocytes are some
specialized cells, such as blood monocytes, neutrophils, and tissue macrophages
which uptake materials from its environment. In phagocytosis, a cell’s plasma
membrane expands around the particulate material, (an antigen or whole
pathogenic microorganisms) to form large vesicles called phagosomes which are
later lysed by proteolytic secretions of the lysosomes in the cell.
6. NK cells
These are large granular
lymphocytes and one of the null cells thatlack surface antigens
(T-cell receptors or immunoglobulin incorporated in their plasma membranes).
These cells display cytotoxic activity against a wide range of tumour cells in
the absence of any previous immunization with the tumour. They
distinguish infected cells and tumours from normal and uninfected cells and
induce infected cells to undergo apoptosis (cell death) by releasing cytotoxic
granules.
7. Inflammation
Tissue damage caused by a
wound or by an invading pathogenic microorganism induces a complex sequence of
events collectively known as the inflammatory response for the clearance of the
invader. The sequence of events include vasodilation and increased blood supply
to the site of infection, increase in capillary permeability and an influx of
lymphocytes and serum proteins from the engorged capillaries into the tissue,
and the phagocytosis of antigens. Four cardinal signs of inflammation are rubor
(redness), tumor (swelling), calor (heat), and dolor (pain).
8. Pus
During inflammation, as
phagocytic cells (neutrophils and monocytes) accumulate at the site of
infection and begin to phagocytose antigens or pathogens, phagocytes release
lytic enzymes which can damage nearby healthy cells. The accumulation of dead
cells, digested material, and fluid forms a substance called pus.
9. Active immunity
Active immunity is the
form of immunity that is induced in an individual by exposure to a foreign
antigen either naturally or artificially. It is so called because the immunized
individual plays an active role in responding to the antigen by eliciting his
acquired immunity (proliferation of antigen-reactive T and B cells resulting in
the formation of memory cells).
e.g., Normal immune
response to an infection (natural) and immunity attained by vaccination
(artificial)
10. Passive immunity
The immunity against a
particular antigen/pathogen conferred on an individual by transferring serum or
lymphocytes from an immunized individual is called passive immunity. It is so
called because the individual does not play active role in attaining immunity
but he receives preformed antibody from another organism.
e.g., Immunity attained by
maternal antibodies obtained through breast milk (natural) and immunity
obtained by antivenom against snake bite (artificial).
11. Vaccines
Vaccines are either killed
or live attenuated pathogens or toxoids (inactive toxins). These are
administered to individual either orally or through injections. These vaccines
cannot actively infect cells or produce any harmful products but are soon
neutralized by the acquired immunity of the individual because vaccines are
killed or weakened pathogens or inactive toxins. During this immune response the
individual develops memory cells which will later identify the same pathogen up
on further exposure and neutralize it in a very short period of time.e.g.,
vaccines against typhoid, cholera, pertussis, plague, rabies, polio etc.
12. Humoral immunity
Immunity provided by
specific chemical substances called antibodies that are synthesised by plasma
cells derived from B lymphocytes is called humoralimmunity. It is so called
because the antibodies secreted circulate in the body fluids (humor) such as
blood plasma and lymph.
13. Cell-mediated immunity
Immunity provided by T
cells and their secretions like cytokines and lymphotoxins is called cell-mediated
immunity. Upon antigenic stimulation, effector T cells are generated. Both
activated TH cells and cytotoxic T lymphocytes (CTLs) serve as
effector cells in cell-mediated immune reactions. TH cells secretecytokines
which can activate various phagocytic cells, enabling them to phagocytose and
kill microorganisms more effectively. Cytokines also activate TC
cells to CTLs which kill altered self-cells (infected cells), virus infected
cells and tumour cells.
2/4 MARK QUESTIONS
1.
Explain various levels of innate immunity
i. Species
level-Immunity shown to a pathogen by all members of a species.
eg., 1. Salmonella, Vibrio
choleraeand Treponema pallidum are humanpathogens. But we are
resistant to Rinderpest, which is pathogenic to cattles.
ii. Racial level-Immunity
shared by most of the members of a genetically related population.
eg., 1. Algerian race sheep is resistant to anthrax. 2. Negroes in Central Africa
resistant to falciparum malaria
iii.
Individuallevel- Immunity shown to a pathogen by an individual within a
given race and not shared by most other members of the race or species.
eg., 1.
Homozygous twins show similar degree of resistance to leprosy or tuberculosis1. Briefly explain
inflammation
Tissue damage caused by a wound or by
an invading pathogenic microorganism induces a complex sequence of events
collectively known as the inflammatory response for the clearance of the
invader. The sequence of events include vasodilation and increased blood supply
to the site of infection, increase in capillary permeability and an influx of
lymphocytes and serum proteins from the engorged capillaries into the tissue
and phagocytosis of antigens.
Vasodilation and an increase in
capillary permeability facilitates an influx of fluid and cells from the
engorged capillaries into the tissue. An increase in the diameter of blood
vessels and accumulation of exudate contribute to tissue redness (erythema) and
tissue swelling (edema) and thereby an increase in tissue temperature. As phagocytes
influx(chemotaxis)from the capillaries into the tissues at the site of
infection and begin to phagocytose pathogens, they release lytic enzymes,which
can damage nearby healthy cells.The accumulation of dead cells,digested
material,and fluid forms a substance called pus.
2. Describe briefly Four
characteristic attributes of adaptive immunity
Adaptive
immunity displays four characteristic attributes:
1)
Antigenic specificity, 2) Diversity, 3) Immunologic memory and 4) Self/nonself
recognition.
The antigenic specificityof the
immune system permits it to distinguish subtle differences among antigens.
Antibodies can distinguish between two protein molecules that differ in only a
single amino acid. The immune system is capable of generating tremendous
diversityin its recognition molecules, allowing it to recognize billions of
unique structures on foreign antigens. Once the immune system has recognized
and responded to an antigen, it exhibits immunologic memory; that is, a second
encounter with the same antigen induces a heightened state of immune
reactivity. Because of this attribute,the immune system can confer life-long
immunity to many infectious agents after an initial encounter.Finally,the
immune system normally responds only to foreign antigens, indicating that it is
capable of self/non-self recognition. The ability of the immune system to
distinguish self from non-self and respond only to non-self molecules is
essential, for the outcome of an inappropriate response to self-molecules can
be fatal.
3.
Distinguish between innate immunity and adaptive
immunity.
Innate immunity is the
less specific component that provides the rapid, first line of defence against
infection by the components which are present in the body before the onset of
infection. Phagocytic cells, such as macrophages and neutrophils, barriers such
as skin, and a variety of antimicrobial compounds synthesized by the host all
play important roles in innate immunity by recognizing and clearing frequently
encountered pathogens.
Adaptive immunity is the
quicker, stronger and specific immunity against an antigen within five or six
days after the initial exposure to that antigen.Exposure to an antigen will
induce T cells to synthesize and secrete cytokines which in turn activates B
cells to secrete antibodies (humoral immunity) and Tc cells to secrete
lymphotoxins (cell mediated immunity). Antibodies bind neutralize antigens and
lymphotoxins destroys the infected cells. Exposure to the same antigen
sometimes in the future results in a memory response by retaining activated B
cells (Memory cells) during prior infection. Memory cells can identify the antigen
at once during later infections and bring about humoral immunity immediately
after the infection. Because of this attribute,the immune system can confer
life-long immunity to many infectious agents after an initial encounter.