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Immunodeficiency

What Is Immunodeficiency?

Immunodeficiency is a condition where the immune system is weakened or not functioning properly, making it harder for the body to fight infections and diseases. It can be inherited (primary) or acquired (secondary) due to illness, medications, or other external factors.

People with immunodeficiency are more prone to frequent, severe, or unusual infections and may also have trouble recovering from them.

What Causes Immunodeficiency?

There are two main types of immunodeficiency:

1. Primary Immunodeficiency (PID)

  • Caused by genetic defects present at birth
  • Affects how immune cells develop or function
  • Examples include Severe Combined Immunodeficiency (SCID), Common Variable Immunodeficiency (CVID), and X-linked agammaglobulinemia

2. Secondary (Acquired) Immunodeficiency

  • Develops later in life due to:
    • HIV/AIDS
    • Cancer treatments (e.g., chemotherapy, radiation)
    • Immunosuppressive drugs (used after organ transplants or for autoimmune diseases)
    • Chronic illnesses (e.g., diabetes, malnutrition)
    • Aging or stress

Who Is at Risk for Immunodeficiency?

Risk depends on the type:

  • For primary immunodeficiency:
    • People with a family history of immune disorders
    • Children with frequent or severe infections
  • For secondary immunodeficiency:
    • Individuals with HIV/AIDS
    • Cancer patients undergoing treatment
    • People on long-term corticosteroids or immunosuppressive medications
    • Malnourished individuals
    • Older adults

What Are the Symptoms of Immunodeficiency?

Symptoms can vary but often include:

  • Frequent infections (e.g., respiratory, ear, skin, or sinus infections)
  • Infections that are severe, long-lasting, or hard to treat
  • Poor response to antibiotic treatment
  • Recurring fevers
  • Swollen lymph nodes or an enlarged spleen
  • Delayed growth or development in children
  • Chronic diarrhea
  • Fatigue and general weakness

In some people, symptoms may not appear until later in life, especially in secondary immunodeficiency.

How Is Immunodeficiency Diagnosed?

Doctors diagnose immunodeficiency through a combination of:

  • Medical history and physical exam
  • Blood tests to check white blood cells, antibody levels, and immune function
  • Genetic testing for inherited conditions
  • Immunoglobulin levels (IgG, IgA, IgM)
  • Response to vaccines (to test immune response)

Further tests may be done to identify specific immune defects or infections.

How Is Immunodeficiency Treated?

Treatment depends on the type and severity of the condition:

1. Treating Infections Promptly

  • Use of antibiotics, antivirals, or antifungals as needed
  • May require longer or repeated courses of treatment

2. Immunoglobulin Therapy (IVIG or SCIG)

  • Provides missing antibodies to boost the immune system
  • Used in many primary immunodeficiencies

3. Bone Marrow or Stem Cell Transplant

  • May cure certain severe primary immunodeficiencies like SCID
  • Involves replacing faulty immune cells with healthy donor cells

4. Medications and Supplements

  • Immune-boosting agents in specific cases
  • Treatment of underlying conditions causing secondary immunodeficiency

5. Lifestyle Modifications

  • Good hygiene and infection prevention (e.g., handwashing, safe food practices)
  • Avoiding crowds or sick people during outbreaks
  • Vaccinations (inactivated vaccines only for some patients)
  • Balanced nutrition and stress management

Can Immunodeficiency Be Prevented?

While primary immunodeficiencies cannot be prevented, some forms of secondary immunodeficiency can be avoided or managed:

  • Safe practices to avoid HIV infection
  • Vaccinations to prevent certain infections
  • Proper nutrition and a healthy lifestyle
  • Limiting unnecessary use of immune-suppressing medications
  • Regular medical care for chronic diseases

Genetic counseling is also recommended for families with a history of inherited immune disorders.

What Is the Outlook for People with Immunodeficiency?

  • With early diagnosis and proper treatment, many people with immunodeficiency can lead normal and productive lives
  • Children with primary immunodeficiency can thrive with regular immunoglobulin therapy or, in some cases, stem cell transplants
  • Adults with secondary immunodeficiency can often manage the condition by treating the underlying cause and avoiding infections
  • Without treatment, immunodeficiency can lead to life-threatening infections and complications

Regular follow-up and proactive management are key to living well with this condition.

When Should You See a Doctor?

See a healthcare provider if you or your child:

  • Have frequent, severe, or unusual infections
  • Aren’t responding well to antibiotics
  • Have a family history of immune problems
  • Are experiencing unexplained fatigue, weight loss, or poor growth
  • Are about to start treatments that may suppress the immune system

Early detection improves outcomes and reduces the risk of serious complications.