Introduction to the Immune System
Immunology is a branch of biology that covers the study of immune systems
in all organisms
Immunology deals with
physiological functioning of the immune system in states of both health and
diseases
malfunctions of the immune system in immunological disorders (such
as autoimmune diseases, hypersensitivities, immune deficiency,
and transplant rejection);
physical, chemical, and physiological characteristics of the components of the
immune system
Immunology has applications in numerous disciplines of medicine,
particularly in the fields of
organ transplantation
oncology
rheumatology
virology
bacteriology
parasitology
psychiatry
dermatology
Immune system
The immune system is a host defense system comprising many biological
structures and processes within an organism that protects against disease.
To function properly, an immune system must detect a wide variety of agents,
known as pathogens, from viruses to parasitic worms, and distinguish them
from the organism's own healthy tissue.
Immunity
Immunity is defined as resistance to disease, specifically infectious disease.
The collection of cells, tissues, and molecules that mediate resistance to
infections is called the immune system, and the coordinated reaction of these
cells and molecules to infectious microbes is the immune response.
Innate and adaptive immunity
Host defense mechanisms consist of innate immunity, which mediates the
initial protection against infections,
and adaptive immunity, which develops more slowly and provides more
specialized and effective defense against infections
Innate immunity
Also called natural immunity or native immunity,
present in healthy individuals, to block the entry of microbes and rapidly
eliminate microbes that do succeed in entering host tissues.
The first line of defense in innate immunity is provided by epithelial barriers
and by cells present in epithelia, all of which function to block the entry of
microbes.
If microbes do breach epithelia and enter the tissues or circulation, they are
attacked by phagocytes, specialized lymphocytes called natural killer cells,
and several plasma proteins, including the proteins of the complement system.
All these mechanisms of innate immunity specifically recognize and react
against microbes.
In addition to providing early defense against infections, innate immune
responses enhance adaptive immune responses against the infectious agents.
Adaptive immunity
Adaptive immunity is an immunity that occurs after exposure to an
antigen either from a pathogen or a vaccination.
This part of the immune system is activated when the
innate immune response is insufficient to control an infection
composed of specialized, systemic cells and processes that eliminates
pathogens by preventing their growth.
Functions
Recognition of specific "non-self" antigens in the presence of "self", during
the process of antigen presentation.
Generation of responses that are tailored to maximally eliminate specific
pathogens or pathogen-infected cells.
Development of immunological memory, in which pathogens are
"remembered" through memory B cells and memory T cells.
Also called specific immunity or acquired immunity,
Requires expansion and differentiation of lymphocytes in response to
microbes before it can provide effective defense
Defense against infectious microbes additionally requires adaptive immune
responses, especially with microbes that are pathogenic for humans and may
have evolved to resist innate immunity.
The adaptive immune system consists of lymphocytes and their products,
such as Antibodies.
Lymphocytes vs Phagocytes
Lymphocyte and phagocyte are two types of cells that mediate immune
responses in the body
Phagocytes are cells that protect the body by ingesting harmful foreign
particles, bacteria, and dead or dying cells.
Lymphocytes are white blood cells that are also one of the body's main types
of immune cells.
They are made in the bone marrow and found in the blood and lymph tissue.
The three types of lymphocytes are T cells, B cells, and natural killer cells.
Phagocytes can be either macrophages, neutrophils, monocytes, dendritic cells
or mast cells. They destroy pathogens by phagocytosis.
The job of B cells is to make antibodies, which are proteins produced by the
immune system to fight foreign substances known as antigens.
The job of T cells is to help the body kill cancer cells and control the immune
response to foreign substances. They do this by destroying cells in the body
that have been taken over by viruses or become cancerous.
A third type of lymphocyte, known as a natural killer or NK cell, comes from
the same place as B and T cells. NK cells respond quickly to several foreign
substances and are specialized in killing cancer cells and virus-infected cells.
The main difference between lymphocytes and phagocytes is that
lymphocytes generate specific immune responses against pathogens whereas
phagocytes generate the same response to any pathogen.
This means lymphocytes are the tools of the adaptive immunity whereas
phagocytes are the tools of innate immunity.
Types of adaptive immunity
The two types of adaptive immunity, humoral immunity and cell-
mediated immunity, are mediated by different cells and molecules
and provide defense against extracellular microbes and intracellular
microbes, respectively
Humoral immunity
Humoral immunity is mediated by proteins called antibodies, which are
produced by cells called B lymphocytes.
Antibodies are secreted into the circulation and mucosal fluids
They neutralize and eliminate microbes and microbial toxins that are present
outside of host cells, in the blood and in the lumens of mucosal organs, such
as the gastrointestinal and respiratory tracts.
One of the most important functions of antibodies is to stop microbes that
are present at mucosal surfaces and in the blood from gaining access to and
colonizing host cells and connective tissues.
In this way, antibodies prevent infections from ever being established.
Cell-mediated immunity
Antibodies cannot gain access to microbes that live and divide inside
infected cells.
Defense against such intracellular microbes is called cell-mediated immunity
because it is mediated by cells, which are called T lymphocytes.
Some T lymphocytes activate phagocytes to destroy microbes that have been
ingested by the phagocytes into intracellular vesicles.
Other T lymphocytes kill any type of host cells that are harboring infectious
microbes in the cytoplasm.
Thus, the antibodies produced by B lymphocytes recognize extracellular
microbial antigens, whereas T lymphocytes recognize antigens produced by
intracellular microbes.
Another important difference between B and T lymphocytes is that most T
cells recognize only protein antigens, whereas B cells and antibodies are
able to recognize many different types of molecules, including proteins,
carbohydrates, nucleic acids, and lipids.
Immunity may be induced in an individual by infection or vaccination (active
immunity) or conferred on an individual by transfer of antibodies or
lymphocytes from an actively immunized individual (passive immunity).
Active immunity
In active immunity, an individual exposed to the antigens of a microbe
mounts an active response to eradicate the infection and develops resistance
to later infection by that microbe.
Such an individual is said to be immune to that microbe, in contrast with a
naive individual, not previously exposed to that microbe’s antigens.
Passive immunity
In passive immunity, a naive individual receives antibodies or cells (e.g.,
lymphocytes, feasible only in genetically identical animals) from another
individual already immune to an infection; for the lifetime of the transferred
antibodies or cells, the recipient is able to combat the infection.
Passive immunity is therefore useful for rapidly conferring immunity even
before the individual is able to mount an active response, but it does not
induce long-lived resistance to the infection.
The only physiologic example of passive immunity is seen in newborns,
whose immune systems are not mature enough to respond to many pathogens
but who are protected against infections by acquiring antibodies from their
mothers through the placenta and breast milk.
Properties of adaptive immune responses
Several properties of adaptive immune responses are crucial for the
effectiveness of these responses in combating infections
Specificity
The adaptive immune system is capable of distinguishing among millions of
different antigens or portions of antigens.
Specificity is the ability to distinguish between many different antigens.
For example, immunization with inactivated poliovirus only protects against
poliomyelitis, not against viral influenza
Diversity
The diversity of the lymphocyte collection, which enables the immune system
to respond to a vast number and variety of antigens,
Memory
The immune system mounts larger and more effective responses to repeated
exposures to the same antigen.
The response to the first exposure to antigen, called the primary immune
response, is mediated by lymphocytes called naive lymphocytes that are
seeing antigen for the first time.
The term naive refers to these cells being immunologically inexperienced, not
having previously responded to antigens.
Subsequent encounters with the same antigen lead to responses called
secondary immune responses that usually are more rapid, larger, and better
able to eliminate the antigen than primary responses.
Secondary responses are the result of the activation of memory lymphocytes, which
are long-lived cells that were induced during the primary immune response.
Immunologic memory optimizes the ability of the immune system to combat
persistent and recurrent infections, because each encounter with a microbe generates
more memory cells and activates previously generated memory cells.
Memory also is one of the reasons why vaccines confer long-lasting protection
against infections.
Clonal expansion
Adaptive immune responses have other characteristics that are important for their functions.
When lymphocytes are activated by antigens, they undergo proliferation, generating many
thousands of clonal progeny cells, all with the same antigen specificity.
This process, called clonal expansion, rapidly increases the number of cells specific for the
antigen encountered, enabling few antigen-specific lymphocytes to serve their defensive
role
Nonreactivity to self
The immune system is able to react against an enormous number and variety
of microbes and other foreign antigens, but it normally does not react against
the host’s own potentially antigenic substances—so-called self antigens.
This unresponsiveness to self is called immunological tolerance, referring to
the ability of the immune system to coexist with (tolerate) potentially antigenic
self molecules, cells, and tissues.