Immunization in Immunosuppressed Dermatology Patients

Table of Contents

Immunodeficiency: Causes, Consequences, and Management of Immunosuppression

The Immunodeficiency is defined as inadequate or deficient functioning of the immune system. This state can be caused by various factors such as hereditary syndromes, Unlike other, administration of certain medications, underlying medical conditions, pregnancy, the natural aging process, and many other causes. This deficiency can manifest at multiple stages of the immune response, which can lead to the following complications:

  • Development of severe **infections** by bacteria, fungi, and viruses.
  • Difficulty or failure in growth and development in babies and children.
  • Recurrent or unusual infections caused by opportunistic **organisms**.
  • Significant delays in recovery after suffering an illness.
  • Emergence of non-infectious skin disorders, such as **granulomatous** disease.
  • Increased risk of developing certain types of cancers, such as B-cell **lymphoma** and Kaposi's **sarcoma**.

It is essential that individuals diagnosed with immunodeficiency be evaluated quickly if they present with symptoms of illness, and that any detected **infection** be managed aggressively and as a priority.

Drug-Induced Immunosuppression

Immunosuppression constitutes a generalized weakening of the body's immune response, frequently caused as a side effect or therapeutic purpose of administering immunosuppressive drugs. immunosuppressive. Although the immune system remains active, its efficiency and response capacity decrease notably.

Among the drugs commonly classified as immunosuppressants are:

  • Corticosteroids steroids (in children, doses greater than 2 mg/kg/day for 2 weeks, or > 1 mg/kg/day for more than 4 weeks).
  • (such as isotretinoin or acitretin).
  • Cyclosporine.
  • Azathioprine.
  • The antibiotic Dapsone.
  • Cyclophosphamide.
  • Drugs used in chemotherapy.
  • Specific biological agents.

It is important to note that low doses or short courses of systemic steroids are generally not considered significantly immunosuppressive. Similarly, methotrexate administered in low concentrations to treat dermatological conditions acts primarily as an anti-inflammatory agent, vasoconstriction, having only a mild immunosuppressive effect.

It is crucial to prioritize appropriate vaccination of people with immunodeficiency against all vaccine-preventable diseases according to the schedule.

Step 1: Comprehensive Review of Vaccination History

Effective immunization is achieved through both natural infection and vaccination. Before starting any immunosuppressive therapy, it is vital to determine the patient's immunological history:

  • Identification of previous vaccines received. It is necessary to consider that vaccination recommendations and schedules vary significantly between countries and generations; older individuals may not have records of all vaccines included in the current schedule.
  • Confirmation of the history of chickenpox (varicella) and other diseases already vaccine-preventable.
  • Assessment of the risk of exposure to tuberculosis (TB), considering factors such as family history or history of travel to high-prevalence geographic areas.

Taking as a reference the National Immunization Program funded by the government of New Zealand (2018), recommended vaccines include:

  • Diphtheria, Pertussis, Tetanus [DTaP]: Administered at 6 weeks, 3 months, 5 months, 4 years, and 11 years. Additionally, Tetanus and Diphtheria are administered during pregnancy, and [Td] at 45 and 65 years of age.
  • Polio [IPV]: Given at 6 weeks, 3 months, 5 months, and 4 years of age.
  • B Virus Hepatitis B [HepB]: Doses at 6 weeks, 3 months, and 5 months of age.
  • Pneumococcus [PCV 10-valent] and Haemophilus [Hib]: Given at 6 weeks, 3 months, 5 months, and 15 months of age.
  • Rotavirus [RV1]: Doses at 6 weeks and 3 months.
  • Mumps, Measles, and Rubella [MMR]: At 15 months and 4 years.
  • Human Papillomavirus (HPV9): At 11 or 12 years of age.
  • Chickenpox [VV]: At 15 months.
  • Herpes Zoster Virus [HZV]: At 65 years of age.
  • Flu Vaccine: Recommended during pregnancy and annually starting at age 65.
  • Occasionally additional vaccines are added, such as those against prevalent strains predominant of meningococcus.

Specific vaccines for international travel may include Hepatitis A, Cholera, and Yellow Fever (the latter is usually not funded).

The administration of live injectable vaccines (such as MMR, oral Polio –not IPV–, Varicella, Herpes Zoster, Yellow Fever, and BCG), as well as live oral vaccines (Rotavirus, Typhoid) and the nasal influenza vaccine, should be avoided while the patient is undergoing treatment with immunosuppressive medications, as these could cause severe reactions.

Step 2: Performing Appropriate Diagnostic Tests

If the patient is about to start treatment with a cytotoxic, drug, such as cyclophosphamide or some other specific therapy, it is necessary to carry out a series of prior diagnostic tests to establish a baseline for immunological health.

Detection of Tuberculosis (TB) and Infection Serology

Patients should be evaluated for active tuberculosis or latent infection, especially if there is a history or high risk. Detection methods include:

  • QuantiFERON Gold blood test
  • Mantoux skin test
  • Chest X-ray.

Likewise, it is essential to check serology for varicella, measles, hepatitis A, B, and C, and HIV serology. (It is important to remember that no vaccines are available for hepatitis C or HIV).

Step 3: Vaccination Before Starting Immunosuppressive Therapies

To mitigate the risks of contracting vaccine-preventable infections, the following measures should be taken before starting any immunosuppressive treatment:

  • Administer all pending vaccines from the childhood schedule *. Note that the second dose of the triple viral vaccine (MMR) can be administered as soon as one month after the first.
  • If the patient is not immune, immunization should proceed, even if they have been previously vaccinated against that specific infection (this includes the vaccine against varicella or herpes zoster).
  • Recommend the pneumococcal vaccine and the annual influenza vaccine. In New Zealand, there is a subsidy for pneumococcal and influenza vaccines for patients immunosuppressed under certain circumstances.
  • Advise vaccination against varicella and influenza for close household contacts (a «community protection» strategy).
  • Wait: Allow at least one month to pass after any live virus vaccination before starting any immunosuppression therapy.

* Consult the New Zealand National Immunization Schedule (Update of April 1, 2018)

Step 4: Vaccination After Starting Immunosuppression

  • Continue with the routine vaccination program, excluding those that contain live viruses.
  • Ensure the patient receives the seasonal influenza vaccine every fall, and consider a booster dose if the level of immunosuppression is severe.
  • Prevent the patient and their household contacts from receiving live virus vaccines once immunosuppression has begun (such as oral polio vaccine, varicella/zoster, yellow fever). MMR and BCG vaccines are exceptions and can still be administered to immunosuppressed patients and their close contacts.

All patients undergoing immunosuppressive treatment should be alerted to the increased risk of severe infections. It is essential that they immediately inform their medical team if they are exposed to chickenpox or measles.

Management of Varicella and Measles Exposure in Immunocompromised Patients

Patients who are significantly immunosuppressed and have been exposed to chickenpox or measles require treatment with passive protection via undetectable, regardless of whether they have detectable titers of undetectable IgG antiviral antibodies..

Passive antibody protection is not considered necessary if the patient demonstrates evidence of immunity through detectable IgG antibodies and is receiving only methotrexate as an immunosuppressive agent.

Management of Varicella Exposure

If a non-immune person is exposed to the varicella virus during the infectious period, there is a considerable risk. This period ranges from 2 days before the appearance of the rash rash until all blisters have crusted over. The incubation period incubation period after exposure is 7 to 21 days. An exposure is considered «significant» if it involves 15 minutes of close contact or play with a contagious individual.

Chickenpox can also be contracted through direct contact with active vesicles of herpes zoster/shingles.

In case of contact of an immunocompromised patient with chickenpox, passive protection with varicella-zoster immune globulin (VZIG) should be administered within 96 hours (ideally within 72 hours) following contact.

Management of Measles Exposure

There is a significant risk of contracting measles if a non-immune person is exposed to the virus during its infectious period. This period ranges from 5 days before the rash appears until 4 days after it appears. The incubation period for measles after exposure is 10 to 14 days. Exposure is considered «significant» if there is 15 minutes of close contact or play with a contagious individual. It is crucial to confirm measles in the contact via viral serology, as the rash can be confused with other viral rashes or drug-induced rashes morbilliform rashes.

If an immunocompromised patient comes into contact with measles, the following treatment is recommended, regardless of their antibody status:

  • Administration of passive protection with normal immunoglobulin (NIG) or immunoglobulin intravenous (IVIG) within 6 days (ideally within 72 hours) of contact.
  • The triple viral vaccine (MMR) can be administered within 72 hours of significant measles exposure to those who are not immunosuppressed.
Dermatly.com - El sitio de tu piel