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Chapter 17: Immunization – Principles and Applications

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Immunization: Principles and Historical Context

Overview of Immunization

Immunization is a critical strategy in microbiology and public health, designed to protect individuals and populations from infectious diseases. It involves the administration of antigens or antibodies to induce immunity, either actively or passively.

  • Active Immunization: Administration of antigens so the patient actively mounts an adaptive immune response.

  • Passive Immunotherapy: Transfer of antibodies formed by an immune individual or animal to provide immediate, short-term protection.

Brief History of Immunization

The practice of immunization has evolved over centuries, beginning with observations of disease resistance and culminating in modern vaccine technology.

  • Early observations in China: Children who recovered from smallpox did not contract the disease again. This led to variolation, the deliberate infection with material from smallpox scabs.

  • 1796: Edward Jenner developed the process of vaccination using cowpox to protect against smallpox.

  • 1879: Louis Pasteur developed a vaccine against Pasteurella multocida.

  • Discovery that vaccines protect through the action of antibodies led to the development of antibody transfer techniques.

Despite advances, some developing nations lack access to vaccines, and effective vaccines for certain pathogens remain unavailable. Concerns about vaccine safety can also hinder development and uptake.

Impact of Immunization on Disease Prevalence

Vaccination programs have dramatically reduced the incidence of many infectious diseases, as illustrated by the decline in polio and measles cases following vaccine introduction.

Graph showing reduction in polio and measles cases after vaccine introduction

  • Example: The introduction of polio and measles vaccines in the United States led to a rapid and sustained decrease in reported cases.

Types of Vaccines and Their Characteristics

Attenuated (Modified Live) Vaccines

Attenuated vaccines use pathogens with reduced virulence, a process known as attenuation. These vaccines can cause mild infections but generally stimulate strong, long-lasting immune responses and may provide contact immunity.

  • Risk: Modified microbes may retain enough residual virulence to cause disease in susceptible individuals.

Inactivated (Killed) Vaccines

Inactivated vaccines are safer than live vaccines and come in two forms:

  • Whole agent vaccines: Contain inactivated but whole microbes.

  • Subunit vaccines: Contain antigenic fragments of microbes.

These vaccines often require multiple doses and may include adjuvants—chemicals that enhance antigenicity.

Toxoid Vaccines

Toxoid vaccines use chemically or thermally modified toxins to stimulate active immunity, particularly for bacterial diseases. They primarily induce antibody-mediated immunity and require multiple doses due to limited antigenic determinants.

Combination and Recombinant Vaccines

  • Combination vaccines: Simultaneously administer antigens from several pathogens.

  • Recombinant gene technology: Utilizes recombinant DNA techniques to improve vaccine efficacy, safety, and cost-effectiveness.

Vaccine Manufacture and Administration

Production Methods

Vaccines are mass-produced by growing microbes in culture vessels. Viruses are often cultured in chicken eggs, which can be problematic for individuals with egg allergies.

CDC-Recommended Immunization Schedule

The Centers for Disease Control and Prevention (CDC) provides guidelines for vaccine administration across different age groups to maximize public health benefits.

CDC-recommended immunization schedule

Principal Vaccines to Prevent Human Diseases

The following table summarizes key vaccines, their target diseases, types, and methods of administration, as recommended by the CDC.

Vaccine

Disease Agent

Disease

Vaccine Type

Method of Administration

Hepatitis B

Hepatitis B virus

Hepatitis B

Inactive subunit (recombinant yeast)

Intramuscular

Rotavirus

Rotavirus

Gastroenteritis

Attenuated, recombinant

Oral

DTaP

Diphtheria toxin, Tetanus toxin, Bordetella pertussis

Diphtheria, Tetanus, Whooping cough

Toxoid, Toxoid, Inactivated subunit

Intramuscular

Hib

Haemophilus influenzae

Meningitis, pneumonia, epiglottitis

Inactivated subunit

Intramuscular

Pneumococcal (PCV)

Streptococcus pneumoniae

Pneumonia

Inactivated subunit

Intramuscular

Polio

Poliovirus

Poliomyelitis

Inactivated (attenuated also available)

Subcutaneous or intramuscular (attenuated: oral)

Influenza

Influenzaviruses

Flu

Inactivated subunit

Intramuscular or oral

MMR

Measles, Mumps, Rubella viruses

Measles, Mumps, Rubella

Attenuated

Subcutaneous

Varicella-zoster

Chickenpox virus

Chickenpox, shingles

Attenuated

Subcutaneous

Hepatitis A

Hepatitis A virus

Hepatitis A

Inactivated whole

Intramuscular

HPV

Human papillomaviruses

Genital warts, cervical cancer

Inactive recombinant

Intramuscular

Meningococcal

Neisseria meningitidis

Meningitis

Inactive

Subcutaneous or intramuscular

Vaccine Safety and Limitations

Potential Problems with Immunization

  • Mild toxicity (e.g., soreness at injection site, fever)

  • Risk of anaphylactic shock (severe allergic reaction)

  • Residual virulence from attenuated viruses

  • Unsubstantiated allegations linking vaccines to autism, diabetes, and asthma

Extensive research has not confirmed a causal relationship between vaccines and these chronic conditions.

Passive Immunotherapy

Principles and Applications

Passive immunotherapy involves the administration of antiserum containing preformed antibodies, providing immediate but temporary protection against infection or disease.

  • Limitations include the risk of allergic reactions (serum sickness), rapid degradation of antibodies, and lack of long-term protection.

  • Development of hybridomas (cells that produce monoclonal antibodies) has helped overcome some limitations.

Summary Table: Active vs. Passive Immunity

Characteristic

Active Immunization

Passive Immunotherapy

Source of Immunity

Antigen exposure (vaccine)

Preformed antibodies (antiserum)

Onset of Protection

Delayed (days to weeks)

Immediate

Duration of Protection

Long-term (memory cells)

Short-term (antibodies degrade)

Memory Response

Yes

No

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