Oncological Drugs

Subtopic:

Immunity

Immunity: Refers to the body’s ability to prevent the invasion of pathogens.

Pathogens: These are foreign disease-causing substances, such as bacteria and viruses, that people are exposed to every day.

Antigens: These are attached to the surface of pathogens and stimulate an immune response in the body.

Immune Response: This is the body’s defense system to fight against antigens and protect the body.

Types of Immunity

The body’s defense mechanisms are broadly classified into several types of immunity:

  1. Innate Immunity

  2. Acquired (Adaptive) Immunity

  3. Passive Immunity

1. Innate Immunity

This type of immunity represents the inherent protection a person is born with. It comprises general defenses, such as physical barriers, defense mechanisms, and generalized immune responses like inflammation. These are non-specific defense mechanisms, meaning they react rapidly to any pathogen without precise identification of the antigen.

Aspects of Innate Immunity

This type of immunity is functionally divided into:

  1. First Line of Defenses

  2. Second Line of Defenses

First Line of Defenses: External/Physical/Barrier Defenses

These are the initial obstacles that impede pathogen entry, functioning as the first type of protection:

  1. The stratum corneum of the epidermis, being a non-living layer, acts as an excellent barrier when unbroken, protecting against various pathogens.

  2. Fatty acids in sebum help to inhibit bacterial growth on the skin; living epidermal cells also produce antimicrobial defensins.

  3. Mucous membranes lining the respiratory, digestive, urinary, and reproductive tracts are living barriers, preventing entry.

  4. The ciliated epithelium of the upper respiratory tract is especially effective; dust and pathogens are trapped in mucus and then swept to the pharynx for disposal.

  5. Hydrochloric acid in gastric juice destroys most pathogens entering the stomach via mucus or through ingestion.

  6. Lysozyme, an enzyme present in saliva, perspiration, nasal secretions, and tissue fluids, limits bacterial growth in the oral cavity and on the eye’s surface.

  7. The unidirectional flow of urine through the urethra prevents the ascending of microorganisms.

  8. The lacrimal apparatus of the eyes produces and drains away tears in response to irritants.

  9. Blinking helps to spread tears across the eye surface, diluting microbes and preventing settling. Tears also contain lysozyme, which can degrade bacterial cell walls.

  10. Saliva washes microbes away from teeth and the mouth’s mucous membrane, reducing colonization similar to how tears act in the eyes.

  11. Defecation and vomiting expel microbes. For instance, some toxins cause vigorous smooth muscle contractions in the lower GI tract, resulting in diarrhea that rapidly eliminates microbes.

  12. The skin’s acidity (pH 3–5) is due in part to fatty and lactic acid secretion.

  13. Perspiration helps flush microbes from the surface of the skin.

  14. Gastric juice, which includes hydrochloric acid, enzymes, and mucus, has a high acidity (pH 1.2–3.0), destroying many bacteria and bacterial toxins.

  15. Acidic vaginal secretions prevent bacterial growth and, similarly, move microbes out of the body in females.

Second Line of Defenses: Internal Defenses

Once pathogens breach the initial barriers, they encounter internal defenses, representing another type of response, including:

  1. Internal Antimicrobial Substances:

    • Interferons: (alpha, beta, and gamma) Proteins produced by virus-infected cells or T cells; they inhibit viral reproduction.

    • Complement: A group of >20 plasma proteins that circulate until activated; they are involved in lysing cellular antigens, tagging non-cellular antigens, and stimulating histamine release.

    • Iron-binding proteins: Inhibit the growth of certain bacteria by limiting available iron. Examples include transferrin, lactoferrin, ferritin, and hemoglobin.

    • Antimicrobial proteins (AMPs): Short peptides with broad antimicrobial activity. Examples include dermicidin, defensins, cathelicidins, and thrombocidin.

  2. Defensive Cells:

    • Phagocytes: Such as macrophages (fixed and wandering), and dendritic cells (Langerhans cells) engulf foreign material through phagocytosis.

    • Neutrophils: Rapidly produced and deployed to injury or infection sites; they are phagocytes that attack foreign substances.

    • Eosinophils: Myelocytic leukocytes involved in allergic reactions and removing immune response components from the site of an allergic reaction

    • Basophils: Myelocytic leukocytes that release mediators (e.g., histamine, heparin) for initiating and sustaining immune or inflammatory responses.

    • Mast cells: Fixed basophils that release chemical mediators when stimulated by local irritation, found in the respiratory and GI tracts, as well as skin.

  3. Inflammation:

    A physiological response to tissue damage characterized by local changes, designed to isolate, inactivate, and remove causative agents and damaged tissue to facilitate healing.

    • Redness: Resulting from increased blood flow due to local vasodilation, initiated by chemical mediators.

    • Heat: Caused by an endogenous pyrogen (interleukin 1) that resets the hypothalamus thermostat at a higher level, leading to pyrexia. The increased temperature helps to inhibit microbial growth while promoting phagocyte activity.

    • Swelling: Occurs due to fluid leaving blood vessels and entering interstitial spaces. This increases tissue fluid osmotic pressure, drawing more fluid from the blood.

    • Pain: Caused by swelling that compresses sensory nerve endings, exacerbated by mediators such as bradykinin and prostaglandins. Although unpleasant, it encourages protection of the damaged area.

    4. Immunological surveillance; see IMMUNOLOGY for details

 

2. Acquired (Adaptive) Immunity

This type of immunity develops from immunological memory. The body, upon exposure to a specific antigen (typically attached to a pathogen), produces antibodies tailored to that particular antigen. This is also referred to as specific defense mechanisms or active immunity. Upon subsequent invasion by the same antigen, the body, having a memory of it, is already equipped with antibodies to combat it.

Acquired immunity can arise from exposure to an infection, where a person develops the disease and subsequently becomes immune, or through vaccination, where the vaccine mimics a particular disease, thus triggering an immune response without causing illness.

Types of Adaptive (Active) Immunity

There are two primary types of adaptive (active) immunity:

  1. Naturally Acquired (Active) Immunity

  2. Artificially Acquired (Active) Immunity

Naturally Acquired (Active) Immunity

This type of immunity arises when the body produces antibodies following natural exposure to an infection. A classic example is an individual encountering chickenpox for the first time without prior immunity. The body starts producing antibodies against the chickenpox virus. While the production of sufficient antibodies takes time, resulting in the initial expression of the disease, the body continues to produce antibodies during the infection. These antibodies, which circulate in the individual’s bloodstream for life, mobilize to destroy the chickenpox virus upon any future exposure.

Artificially Acquired (Active) Immunity

This type of immunity develops when an individual receives a killed or weakened antigen, which stimulates the production of antibodies against the antigen. While the antigen does not cause the disease itself, the individual’s body will produce specific antibodies against it. When a vaccine contains a live attenuated (weakened) antigen, the recipient may experience minor symptoms or a mild form of the disease, but these are typically much less severe and of shorter duration than the disease itself.

3. Passive Immunity

This type of immunity arises from the body’s capacity to resist pathogens by “borrowing” antibodies. Antibodies can be transferred from a mother to a baby through breast milk or by blood products containing antibodies, such as immunoglobulin, transferred from one person to another.

The most common form of passive immunity is the transfer of antibodies from mother to infant. During the last one to two months of pregnancy, antibodies are transported across the placenta, resulting in a full-term infant having similar antibodies to their mother. These maternal antibodies offer protection against certain diseases for up to a year, defending against specific antigens. While beneficial, this type of immunity is temporary, as the body does not produce these antibodies, and they eventually wane.

Types of Passive Immunity

There are two types of passive immunity:

  1. Passive Naturally Acquired Immunity: This type of immunity is acquired through the passage of maternal antibodies across the placenta to the fetus and to the baby through breast milk. The variety of antibodies depends on the mother’s active immunity. The baby’s lymphocytes are not stimulated, making this form of immunity short-lived.

  2. Passive Artificially Acquired Immunity: In this type of immunity, ready-made antibodies, derived from human or animal serum, are injected into the recipient. The source of the antibodies might be a recovered individual or artificially immunized animals (such as horses). Specific immunoglobulins (antiserum) can be administered prophylactically to prevent the development of disease in those exposed to an infection (e.g., rabies) or therapeutically after the disease has developed.