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Immunobiological Preparations

For medical students2 min readUpdated 2026-10-10

Immunobiological preparations are agents designed for the specific prophylaxis, diagnosis, and treatment of infectious and non-infectious diseases. They function by activating, suppressing, or normalizing immune system functions, establishing active or passive immunity.

OriginMay contain microbes, antibodies, cytokines, and plant extracts
GoalInduction of resistance to pathogens or immune modulation
TherapyCornerstone of treatment for toxemic infections (e.g., tetanus, botulism)
DiagnosticsUsed to detect antigens and antibodies in clinical practice

Main Areas of Application

Immunobiological preparations are used in two key areas that constitute the core of immunology:

Strategically, these methods execute three scenarios: activation (immune stimulation), suppression (downregulation of hyperactivity), and correction (normalization during imbalance).

Classification of Preparations

According to standard pharmacological classification, there are five main groups:

  1. Microbial-derived preparations. Include live or killed bacteria, viruses, fungi, and their metabolic products (toxoids). This group includes vaccines, bacteriophages, and probiotics.
  2. Antibody-based preparations. Derived from specific antibodies. These include immunoglobulins, immune sera, immunotoxins, catalytic antibodies (abzymes), as well as receptor-based and minibodies.
  3. Immunomodulators. Used to correct immunity during infections and immunodeficiencies. They are divided into exogenous (adjuvants, hormones, antimetabolites, interferon inducers) and endogenous (cytokines, thymic peptides, myelopeptides).
  4. Adaptogens. Substances of natural origin (e.g., ginseng and eleuthero extracts) exhibiting broad biological activity.
  5. Diagnostic preparations. Agents for detecting antigens, antibodies, enzymes, and foreign cells.

Production of Monoclonal Antibodies

Under physiological conditions (in vivo), exposure to an antigen activates multiple B-lymphocyte clones, resulting in a heterogeneous mixture known as polyclonal antibodies.

For laboratory and medical applications, monoclonal antibodies—identical molecules synthesized by a single cell clone—are required. However, normal B-lymphocytes cannot proliferate indefinitely in vitro. This limitation is overcome using the hybridoma technology developed by Köhler and Milstein.

The method involves fusing an immune B-lymphocyte (providing specificity) with a myeloma tumor cell (providing immortal proliferation capacity). The resulting hybridoma actively replicates and produces the desired antibodies. To prevent human anti-mouse antibody (HAMA) rejection responses, humanized (chimeric) antibodies are created, featuring a human constant region and a murine variable region.

Clinical Significance

Immunobiological preparations are often the primary or sole treatment modality for severe conditions.

Mnemonic

To remember the 3 immune modulation scenarios, use the ASC acronym: Activation, Suppression, Correction.

Frequently asked questions

What is the difference between active and passive immunity in immunoprophylaxis?

Active immunity develops when the host's immune system generates antibodies in response to an introduced antigen (e.g., vaccination). Passive immunity is conferred immediately through the administration of preformed donor antibodies (e.g., immune sera).

What is the purpose of hybridomas?

Hybridomas are used for the industrial production of monoclonal antibodies. They combine the capacity of a B-lymphocyte to synthesize a specific antibody with the immortality of a myeloma cell in artificial culture media.

What are humanized antibodies?

They are engineered chimeric antibodies in which the antigen-binding variable regions are derived from a mouse, while the structural constant regions are human. This significantly reduces the risk of immune rejection by the patient.

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