In my last article I wrote about
“The Healing Properties of Our Body. Is
Prevention Better than Cure?”
here:
https://scientificlogic.blogspot.com/2024/05/the-healing-properties-of-our-body-is.html
I mentioned about injuries such as bleeding,
wounds, and fractures. It is not always we are injured and traumatised. But
what we are facing every second, every minute in our lives are pathogenic
organisms from the environment. These are far more threatening to our existence
than occasional injuries such as cuts, bruises, and fractures from accidents. I
thought it is only fair I should give priority to discuss a little bit how our
body defend itself against invading pathogenic organisms from outside and
within our bodies. This is “Our Wonderful
Immune System”. Later, perhaps I may deal with an internal threat from our own
cells - cancer. But let me deal with infection first.
The human body has a highly
sophisticated and multi-layered defence system to protect itself against
infections caused by pathogens such as bacteria, viruses, fungi, and parasites.
This defence system can be broadly categorized into innate (nonspecific) and
adaptive (specific) immunity. We shall briefly outline how each component
works:
First, we have this innate immunity
which can be classified as physical and chemical barriers. The skin for
instance acts as a physical barrier preventing the entry of pathogens. It also
produces antimicrobial proteins and peptides. Mucous membranes line the
respiratory, gastrointestinal, and genitourinary tracts, trapping pathogens in
mucus.
Secretions such as saliva, tears, and
mucus contain enzymes like lysozyme that break down bacterial cell walls. Then
there is this stomach acid where the acidic environment (low pH) destroys many
ingested pathogens. Cilia which are tiny hair-like structures in the
respiratory tract that move mucus and trapped pathogens out of the lungs.
Secondly, the body is also equipped
with cellular defences that are the phagocytes, the white blood cells such as
neutrophils and macrophages that engulf and digest pathogens. These phagocytes
are made up of neutrophils which are the most abundant white blood cells that
respond quickly to infections, the macrophages found in tissues and organs.
They ingest pathogens and dead or dying cells.
Comes next the natural killer (NK)
cells that destroy infected or cancerous cells by releasing cytotoxic granules
that induce apoptosis (cell death). The blood also has the dendritic cells.
These cells act as antigen-presenting cells that capture antigens and present
them to T cells, initiating the adaptive immune response.
That’s not all. We have the
inflammatory response that initiates inflammation, a process that isolates and
limits tissue damage and infection. It involves vasodilation, an increased
blood flow to the affected area, causing redness and heat. Increased permeability
in the area allows immune cells and proteins to enter tissues, causing
swelling. Like an army, there is also phagocyte recruitment that attracts
immune cells to the site of infection to eliminate pathogens.
Then other components that come into
action are the antimicrobial proteins which are a complement system where a
group of proteins enhance the ability of antibodies and phagocytic cells to
clear pathogens. Added to that are the opsonization which means coating
pathogens to make them more recognizable to phagocytes. That’s not all. There
is this thing called Membrane Attack Complex (MAC). These form pores in the
membranes of pathogens, leading to their lysis. Comes next the interferons
which are proteins produced by virus-infected cells that help protect
neighbouring cells from viral infection.
Next in line we have the adaptive
immunity that involves specificity and memory. Here lymphocytes, the primary
cells are involved in adaptive immunity, involving B cells that produce
antibodies that bind to specific antigens. Upon activation, they differentiate
into plasma cells that produce large quantities of antibodies which we shall
classify them shortly.
The immunological system is also armed
with memory B cells. These cells have memories that provide long-lasting
immunity by remembering past infections. Comes another type or army – the T
cells. They are involved in cell-mediated immunity. There are two main types,
the helper T Cells (CD4+) where they activate B cells and other immune cells by
releasing cytokines. The immune system has yet another type of army we call
them as cytotoxic T Cells (CD8+). They directly kill infected or cancerous
cells.
Having said all that, next comes the
antigen presentation that is made of a major histocompatibility complex (MHC).
These are molecules that present antigens on the surface of cells.
Immunologists group them as MHC Class I, found on all nucleated cells, present
antigens to cytotoxic T cells. MHC Class II are found on antigen-presenting
cells (APCs) like dendritic cells, macrophages, and B cells, present antigens
to helper T cells.
That’s not all. The immunological
system also has the Clonal Selection and Expansion. When a lymphocyte
recognizes its specific antigen, it undergoes clonal expansion, producing many
identical cells that can respond to the pathogen. They have the effector cells
that actively respond to the infection. The memory cells then provide a rapid
and robust response if the pathogen is encountered again.
Having explained all that, comes the
antibodies most people have heard of.
Antibodies have a structure that
consists of variable regions that bind specific antigens and constant regions
that determine the class of the antibody. Their functions are:
Neutralization that blocks pathogens or
toxins from interacting with host cells. Opsonization that marks pathogens for
phagocytosis. Complement Activation that triggers the complement system leading
to pathogen destruction.
Agglutination then clumps pathogens
together for easier removal. There are many types of antibodies. Antibodies,
also known as immunoglobulins (Ig), play a crucial role in the immune defence
against pathogens and abnormal cells. There are five main classes of
antibodies, each with specific functions and characteristics:
Classes of Antibodies are:
IgG (Immunoglobulin G). They are the
most abundant antibodies in the blood and extracellular fluid. They provide
long-term protection and memory. They are capable of crossing the placenta to
provide passive immunity to the foetus.
Involved in opsonization,
neutralization of toxins and viruses, and activation of the complement system.
IgA (Immunoglobulin A):
Functions:
IgA are found in mucous membranes
lining the respiratory and gastrointestinal tracts, as well as in saliva,
tears, and breast milk. They protect the mucosal surfaces by preventing the
attachment and entry of pathogens. They play a role in mucosal immunity.
IgM (Immunoglobulin M):
Functions:
IgM is the first antibody produced in
response to an infection.
It is found in the blood and lymphatic
fluid. It is effective at forming antigen-antibody complexes and activating the
complement system. It plays a crucial role in the primary immune response.
IgE (Immunoglobulin E):
Functions:
IgE is involved in allergic reactions
and responses to parasitic infections. It binds to allergens and triggers
histamine release from mast cells and basophils. It mediates immediate
hypersensitivity reactions.
IgD (Immunoglobulin D):
Functions:
IgD presents in small amounts in the
blood and on the surface of B cells. It is involved in the activation and
regulation of B cells during the immune response. Its precise role is less well
understood compared to other antibody classes.
Antibody Subclasses. Some antibody
classes have further subclasses that provide more specialized functions. For
example, IgG Subclasses are:
IgG1: Most abundant subclass, effective
in opsonization and complement activation.
IgG2: Involved in responses to
bacterial polysaccharides.
IgG3: Highly effective in complement
activation.
IgG4: Involved in responses to
allergens and chronic infections, and less effective in complement activation.
IgA Subclasses:
IgA1: Found primarily in serum.
IgA2: Found primarily in secretions at
mucosal surfaces.
Specific Antibodies:
In addition to the general classes and
subclasses, there are specific antibodies used in clinical and therapeutic
contexts. These are often monoclonal antibodies, designed to target specific
antigens associated with diseases. Some notable examples include:
Rituximab (anti-CD20): Used to treat
certain autoimmune diseases and cancers, particularly B-cell non-Hodgkin
lymphomas.
Trastuzumab (Herceptin, anti-HER2/neu):
Used to treat HER2-positive breast cancer.
Pembrolizumab (Keytruda, anti-PD-1):
Used in cancer immunotherapy to block the PD-1 pathway and enhance the immune
response against tumours.
Infliximab (Remicade, anti-TNF-alpha):
Used to treat autoimmune diseases such as rheumatoid arthritis and Crohn’s
disease.
Omalizumab (Xolair, anti-IgE): Used to
treat allergic asthma and chronic spontaneous urticaria.
These monoclonal antibodies are
specifically engineered to target particular molecules involved in disease
processes, and they represent an important application of antibody technology
in modern medicine.
Integration of Innate and Adaptive
Immunity:
·
Cytokines and Chemokines: Small proteins released by cells
that mediate and regulate immunity, inflammation, and haematopoiesis. They help
in the communication between innate and adaptive immune responses.
·
Antigen-Presenting Cells (APCs): Such as dendritic cells and
macrophages, bridge the innate and adaptive immune systems by presenting
antigens to T cells.
The coordination and interplay between
these various mechanisms ensure that the body can effectively detect, respond
to, and remember pathogens, providing both immediate and long-term protection
against infections.
We can see how wonderful our
Immunological System works for us. In fact, all their components and
subcomponents are active all the time, every second, every minute in our entire
life defending us silently against infection without us knowing it.
And yet, doctors unnecessarily
prescribe all those antibiotics for us for every infection, causing an abuse in
antibiotics resulting in a lot of antibiotic strains of bacteria that have
developed resistance to antibiotics. This resistance can be to a single
antibiotic or multiple antibiotics, making infections caused by these bacteria
more difficult to treat when in truth the body by itself can easily handle most
of the infections.
We shall talk about this in another
article.
“A True Doctor is One Who Teaches, The
Best Healer is Your Own Body” (Motto of my blog)
Lim ju boo
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