Introduction
In 1796, a
British physician named Edward Jenner discovered a ground-breaking
concept of preventing a disease. Jenner, curious and determined, decided to
test his hypothesis by injecting fluid from cowpox pustules into a young boy. Why
cowpox, you ask? Jenner suspected it might prevent the boy from catching
the much more severe chickenpox.
To his amazement, Jenner's experiment worked—the boy didn't develop chickenpox. However, Jenner didn't fully understand the mechanism behind this newfound protection. It wasn't until later, when another scientist Louis Pasteur recognized the significance of Jenner's discovery. He coined the term "Vaccine" from the Latin word "Vacca" meaning "cow" in homage to Jenner's discovery. So, through related experimentation the foundation of vaccination as we know it today was laid.
What are
Vaccines?
Vaccines are
biological preparations of pathogens or their antigens made up of:
· Inactivated (killed) disease-causing organism
(virus or bacteria) or
· Attenuated organisms (lost the ability to
cause disease) or
· Proteins/toxins/polysaccharides of those
organisms.
A particular vaccine
mimics an infection upon its injection into the human body. This stimulates and
strengthens the immune system against that particular infection (antigen). Vaccines, thus
train the immune system to recognize and remember the pathogen, allowing the
body to act faster upon its encounter with real pathogen later on. This process
involves the activation and development of immune cells, including B cells and
T cells, which generate antibodies and initiate cellular immunity,
respectively.
Vaccine Types and Their Mechanism of Action
Different types
of vaccines are designed to stimulate an immune response against specific
pathogens. Here are some common types:
1. Whole organism vaccines: These
are of two types
A. Inactivated (killed) vaccines:
The targeted pathogen (disease causing
organism) is isolated and cultured in laboratory conditions.
The cultured pathogen has to be killed
using different methods such as Heat, Chemicals (e.g. Formaldehyde) or Radiations.
During this process, structure and properties
of antigens should not get altered. Heat is the least preferred method as it may
denature or spoil the structure of the antigens hence might not be unable to
activate the immune system.
Polio vaccines is prepared by using chemical
method (formaldehyde)
Inactivated polio virus are injected,
intramuscularly or subcutaneously. Immune system recognizes the antigens present
on the surface of inactivated pathogen and generates an immune response
characterized by the production of antibodies and activation of immune cells (B
cells and T cells).
Because the pathogen is not live, these
vaccines usually require multiple doses or booster shots to provide
sufficient immunity. Examples include the Influenza (flu) vaccine, Hepatitis
A vaccine, Rabies vaccine, Polio vaccine etc.
B. Attenuated Vaccines:
Attenuated vaccines contain live
organisms that have been modified to reduce their virulence
(disease causing ability) but their antigenic properties remain preserved to
stimulate an immune response.
It is mostly done by growing the pathogen in
abnormal conditions (e.g. high bile salt concentrations) for prolonged period
of time. This causes genetic mutations in the organism.
The selection of mutant involves
rigorous testing ensuring reduced virulence, confirmation of their antigenic
stability, immunogenicity, and safety profile. This ensure that the attenuated
strain is sufficiently weakened not to cause disease but still capable of
inducing a strong immune response.
These vaccines provide long-lasting immunity.
Examples include the Measles (virus induced rashes in children), mumps
(virus causing swelling of salivary glands), Bacillus Calmette-Guerin (BCG)
for Tuberculosis and the oral Polio vaccine.
2. Purified Macromolecule as Vaccine
These vaccines include purified and specific
parts of the virus or bacteria, such as Proteins, Polysaccharides,
or Toxoids (A bacterial toxin weakened until it is no longer
toxic) to stimulate an immune response.
Proteins based antigens are more immunogenic
due to their structural complexity, diversity of antigenic epitope, better
presentation by antigen presenting cells (APC) through MHC to T-cells and
effective inducers of immunological memory. Examples include Hepatitis B
vaccine and Human papillomavirus (HPV) vaccine.
Toxoid
vaccines include inactivated exotoxin of Corynebacterium diphtheriae
to prevent disease called Diphtheria involving formation of false
membrane in throat causing difficulty in breathing. Tetanus Toxoid
vaccine to prevent lockjaw caused by toxins of Clostridium tetani.
Polysaccharide vaccines Certain pathogenic bacteria have capsule
composed of polysaccharides such as Pneumonia causing Pneumococcal bacteria. Pneumococcal
conjugate Vaccine contains 13 or 23 antigenically different capsular
polysaccharides activating B-cells to produce IgM. Examples include vaccines
for Hemophilus influenza, Streptococcus pneumoniae.
These vaccines do not contain the pathogens
itself, hence are safer for certain populations, such as people with weak
immune systems.
3. Viral Vector Vaccines:
These vaccines use a harmless virus
(the vector) such as Vaccinia virus (cowpox virus) or Adenovirus. Chosen based
on their safety profile, capacity for genetic manipulation, and ability to
infect target cells.
The genes encoding “specific antigens”
from a pathogenic virus or bacteria are incorporated into the genetic material
of the Vector. The vector vaccine containing this modified virus is injected
into the human body's cells. The human cells then produce encoded proteins or
other components (antigens) of the pathogen, in its natural form without any
denaturation or modification triggering an immune response. Examples include
the COVID-19 vaccines developed by AstraZeneca (using a chimpanzee adenovirus
vector) and Johnson & Johnson (using a human adenovirus vector) incorporated
genes encoding spike proteins of the COVID-19 virus.
4. Nucleic acid vaccines:
These vaccines use genetic material, such as
DNA or RNA, from the pathogen to stimulate an immune response.
The antigenic
genes are cloned into the plasmid (a circular DNA molecule capable of
replication and gene expression in host cells). The delivery system mostly
includes lipid nanoparticles or viral vectors to protect the genetic material
from degradation and facilitate its uptake by host cells.
The genetic material is typically injected either
intramuscularly, subcutaneously, or intradermally taken up by cells in
the body. Cells then produce proteins (antigens) similar to those of the
pathogen, prompting an immune response. mRNA vaccines, like the Pfizer-BioNTech
and Moderna encoding the spike proteins of COVID-19 are examples of
nucleic acid vaccines.
Vaccination
schedule
The general
outline of the recommended vaccine schedule for children is based on guidance
from the Centre for Disease Control (CDC):
· Hepatitis B (Hep B) vaccine: First dose at birth, Second dose at 1-2
months, and Third dose at 6-18 months.
· Influenza vaccine: Two doses in first year (at 6th
month and 7th month) then Annually single dose up to 8 years.
Following
Vaccines should be given with First dose at 2nd months, Second dose
at 4th month and Third dose at 6th month
· DTaP
(Diphtheria, Tetanus, Pertussis) vaccine: Fourth dose after 15 months
and Last dose after 4 years
· Hib
(Haemophilus influenzae type b) vaccine: Last dose after 12
months
· IPV
(Inactivated Poliovirus) vaccine: Last dose after 4 years
· PCV13
(Pneumococcal conjugate) vaccine: Last dose after 12 months
· Rotavirus
vaccine
· MMR
(Measles, Mumps, Rubella) vaccine: Second dose after 4 years
· Varicella (Chickenpox) vaccine: Second
dose after 4 years
· Hep A
(Hepatitis A) vaccine: Second dose Six months after the first dose
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