Primary Immunodeficiency PRIMARY IMMUNODEFICIENCY by Justina May 13, 2024 May 13, 2024 A+A- Reset 34 Primary immunodeficiency (PID) is a group of disorders characterized by a weakened immune system due to genetic defects. These disorders impair the body’s ability to fight infections, leaving individuals vulnerable to recurrent and severe infections. PID encompasses over 400 conditions that disrupt the functioning of your immune system, making you more vulnerable to infections and certain ailments like autoimmune disorders and cancers. Also known as primary immunodeficiency disease, disorder, or inborn errors of immunity (IEI), these conditions stem from genetic mutations. While often hereditary, they can also arise sporadically. PIDD can affect babies, young children, or even adults for the first time. Treatment involves managing and preventing infections and compensating for deficient immune components. Examples of primary immunodeficiency are diverse, varying in severity and age of onset. Some manifest early in infancy, while others remain latent until adulthood. Here are a few examples: Common variable immunodeficiency (CVID) Ataxia-telangiectasia Chronic granulomatous disease (CGD) DiGeorge syndrome Hemophagocytic lymphohistiocytosis Selective IgA deficiency X-linked agammaglobulinemia Causes of Primary immunodeficiency Primary immunodeficiency stems from genetic mutations affecting various components of the immune system, such as cells and proteins. These mutations can lead to immune system components being: Less active than normal. Defective. Completely absent. In approximately 50% to 60% of cases, primary immunodeficiency is associated with abnormalities in B lymphocytes (B cells). These cells are responsible for producing antibodies, specialized proteins crucial for the immune system’s defense against pathogens like bacteria and viruses. Prevalence Primary immunodeficiency is considered rare, with prevalence estimates varying depending on the specific type of disorder. However, advancements in genetic testing have led to the identification of more cases in recent years. It is believed that many cases go undiagnosed or misdiagnosed, leading to underestimations of prevalence. Symptoms of Primary immunodeficiency Recognizing primary immunodeficiency often begins with experiencing recurrent, stubborn, or uncommon infections that prove challenging to treat. These infections may be severe and may also affect other family members. Additional symptoms of primary immunodeficiency can include: Requiring multiple rounds of antibiotics to combat infections effectively. Experiencing complications following administration of live vaccines. Enlargement of the spleen. Swollen lymph nodes. Weight loss or inadequate growth. Persistent digestive issues like chronic diarrhea. Development of autoimmune diseases. Recurrent infections, such as respiratory infections, ear infections, sinus infections, and skin infections. Slow wound healing, Gastrointestinal issues Growth delays. Risk Factors Risk factors for primary immunodeficiency include having a family history of the condition, which increases the likelihood of being affected. PID typically manifests before the age of 20 and is more prevalent among individuals assigned male at birth compared to those assigned female at birth. Additionally, certain environmental factors and infections may exacerbate symptoms in individuals with PID. Diagnosis Diagnosing PID involves a thorough assessment by your healthcare provider, which includes reviewing your medical history, conducting a physical examination, and performing laboratory tests. Your doctor will conduct a physical examination and inquire about your child’s medical history, focusing on: Frequency and duration of severe infections. Persistence of illness despite antibiotic treatment. Family history of frequent illnesses. To confirm the diagnosis, your provider may recommend: Blood tests to detect specific abnormalities in the immune system. Genetic testing to identify mutations in genes. Flow cytometry, a specialized technique using laser technology to analyze immune system cell samples. Additionally, newborn screening in all U.S. states includes testing for severe combined immunodeficiency (SCID), a type of primary immunodeficiency. Treatments for Primary immunodeficiency Treatment for PID aims to manage existing infections and prevent future ones. The specific approach depends on the type of infection and may involve: Antibiotics to prevent or treat bacterial infections. Antiviral medications to combat viral infections. While infections are inevitable, treatments can effectively manage symptoms, allowing your child to recover swiftly and resume their favorite activities. For severe infections, your child may require higher doses of infection-fighting medications administered for an extended duration. In critical cases, antibiotics may need to be delivered intravenously through an IV. Even if your child is currently asymptomatic, your doctor may recommend prophylactic antibiotics or other preventive medications to ward off potential illnesses. To enhance your child’s immune function, your doctor may propose the following treatments: Immunoglobulin (Ig) replacement therapy: This involves administering disease-fighting antibodies, known as immunoglobulins, through intravenous infusion or subcutaneously, to replace deficient immune components.. These antibodies typically require replenishment every 3 to 4 weeks. While generally safe, this therapy may result in side effects such as muscle or joint pain, headaches, or low-grade fever. Stem cell transplant: Reserved for severe cases of PID, a stem cell transplant offers a potential cure. Stem cells, which originate from the bone marrow, play a crucial role in producing new blood cells. During a transplant, stem cells from a compatible donor, ideally a close relative or someone with a similar genetic background, are infused into your child’s bloodstream through an IV. Following the transplant, it may take 2 to 6 weeks for the new stem cells to proliferate and begin generating healthy blood cells. During this period, your child may need hospitalization or frequent monitoring by the transplant team. It could take 6 months to a year for the number of functioning blood cells to normalize. In some cases, surgery may be necessary to address complications from infections, such as draining abscesses to promote healing. Additionally, gene therapy has shown promise as a treatment option for certain types of primary immunodeficiency. Home Care Tips With appropriate treatment, most individuals with primary immunodeficiency can lead healthy lives. In some cases, lifelong medication may be necessary. Preventing infections becomes crucial, and some strategies to achieve this include: Maintaining good hand hygiene by washing hands with soap and water frequently, especially before and after meals, after using the restroom, after handling pets, and after touching contaminated surfaces. Avoiding crowded places and contact with sick individuals. Adhering to vaccination schedules as advised by healthcare providers. Ensuring adequate rest and following a healthy diet and exercise regimen. Complications of primary immunodeficiency This may arise later in life, potentially leading to the development of autoimmune disorders or certain types of cancer. Untreated primary immunodeficiency can also heighten the risk of severe infections. Prevention While primary immunodeficiency cannot be prevented, early diagnosis and appropriate management can help minimize complications and improve outcomes. Genetic counseling may be recommended for individuals with a family history of PID to assess their risk and explore options for family planning. When to See a Doctor It is important to consult a healthcare professional if you or your child experience recurrent or severe infections, unexplained symptoms such as chronic fatigue or slow wound healing, or have a family history of primary immunodeficiency. Early diagnosis and intervention can help prevent complications and improve quality of life. Outlook/Prognosis The outlook for individuals with primary immunodeficiency varies depending on the specific disorder, its severity, and the effectiveness of treatment. With proper management, many individuals with PID can lead relatively normal lives and maintain good health. However, some forms of PID may be associated with significant complications and require ongoing medical care. Sources Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015 National Institute of Allergy and Infectious Diseases (NIAID) – Primary Immunodeficiency Diseases American Academy of Allergy, Asthma & Immunology (AAAAI) – Primary Immunodeficiency Disorders Immune Deficiency Foundation (IDF) – About Primary Immunodeficiency Diseases Centers for Disease Control and Prevention (U.S.). Primary Immunodeficiency (PI) Primary immunodeficiency 0 FacebookTwitterPinterestLinkedinEmail Justina previous post PRIMARY SCLEROSING CHOLANGITIS next post PRIMARY BILIARY CIRRHOSIS(PBC)
