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Pharmacology · Agents Regulating Immune Processes

Daclizumab

Daclizumabum

Daclizumab is a humanized monoclonal antibody that blocks interleukin-2 receptors and suppresses the cellular immune response. It is used in transplantology to prevent organ rejection.

Structure90% human and 10% murine antibodies
Receptor actionReceptor blockade persists for up to 120 days
Treatment courseA total of 5 intravenous doses
TargetIL-2 receptors on T-lymphocytes
2 min readFor medical studentsUpdated 09/24/2026
Material prepared by WhiteCoat Pro editorial team based on platform study guidesReviewed by medical editor: Aulov A. A., general practitioner · 09/24/2026

Structural features and classification

By its chemical structure, daclizumab (Daclizumabum) belongs to humanized monoclonal antibodies. This molecule combines a protein structure of 90% human origin, while the remaining 10% are murine components. This hybrid structure provides the required binding specificity.

Mechanism of pharmacological action

The main objective of the drug is to target specific links of the immune system:

  • The substance selectively binds to interleukin-2 (IL-2) receptors.
  • The targets are exclusively activated T-lymphocytes.
  • Effective blockade of the cellular immune response activation occurs, which is critically important during organ transplantation.
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Pharmacokinetics and dosing regimens

The drug is prescribed for parenteral administration and has a strict dosing schedule:

  1. Route of administration: intravenous only.
  2. The course therapy consists of 5 consecutive doses.
  3. The first dose is administered exactly 24 hours before the transplantation procedure.
  4. Subsequent doses are administered at a fixed interval of 14 days.
  5. Once administered, a single dose provides prolonged blockade of the corresponding receptors for up to 120 days.

Safety profile and adverse effects

In general, daclizumab is characterized as a relatively non-toxic medicinal product. However, various adverse reactions may develop during pharmacotherapy:

  • Gastrointestinal: primary disorders of the digestive system predominate.
  • Systemic manifestations: headache, elevated body temperature (fever), pronounced tremor, and sleep disorders (insomnia) may occur.
  • Cardiovascular effects: blood pressure fluctuations in the form of hypertension or hypotension, palpitations (tachycardia), as well as lower extremity and pulmonary edema.
  • Other reactions: risk of infectious complications, shortness of breath, elevated blood sugar levels (hyperglycemia), as well as muscle and joint pain (myalgia and arthralgia).

Briefly: answers to topical questions

What are the official International Nonproprietary Names (INN) of daclizumab analogs?

The provided materials indicate basiliximab as a drug with a mechanism of action analogous to daclizumab. The indications, mechanism of action, and side effects of basiliximab are completely identical to those of daclizumab.

CharacteristicDaclizumabBasiliximab
StructureHumanized monoclonal antibodies (90% human, 10% murine)Chimeric monoclonal antibodies (75% human, 25% murine)
Activity—10-fold superior to daclizumab
Mechanism of actionBlocks IL-2 receptors (CD25) on T-lymphocytesBlocks IL-2 receptors (CD25) on T-lymphocytes
How to memorize

Dac-"LIZ"-umab lyses the activity of activated T-lymphocytes by blocking IL-2 for exactly 120 days (5 doses on schedule).

Class and exam questions

What class of substances does daclizumab belong to?

The drug is a humanized monoclonal antibody consisting of 90% human and 10% murine protein structures.

What is the standard course of administration for the drug?

The therapeutic course includes 5 doses. The first dose is administered 24 hours before transplantation, and subsequent ones at two-week intervals.

Which cells and receptors are targeted by the mechanism of action?

Daclizumab binds to interleukin-2 (IL-2) receptors located on the surface of already activated T-lymphocytes, thereby blocking cellular immunity.

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What else to study on this topic

  • Comparative characteristics of humanized and chimeric monoclonal antibodies
  • Pathophysiology of cellular immune response in transplantation
  • Criteria for evaluating infectious complications against the background of immunosuppression
  • Features of blood pressure correction and edema syndrome
  • Pharmacoeconomics of course administration of monoclonal antibodies

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