The more you understand about primary immunodeficiency (PI), the better you can live with the disease or support others in your life with PI. Learn more about PI, including the various diagnoses and treatment options.
Living with primary immunodeficiency (PI) can be challenging, but you’re not alone—many people with PI lead full and active lives. With the right support and resources, you can, too.
Be a hero for those with PI. Change lives by promoting primary immunodeficiency (PI) awareness and taking action in your community through advocacy, donating, volunteering, or fundraising.
Whether you’re a clinician, researcher, or an individual with primary immunodeficiency (PI), IDF has resources to help you advance the field. Get details on surveys, grants, and clinical trials.
ALPS is a rare genetic disorder in which lymphocytes, a type of white blood cell, increase and accumulate in the spleen and lymph nodes. This is due to the failure of the mechanism that normally causes lymphocytes to die naturally.
See if you qualify to participate in clinical trials evaluating new treatments and/or diagnostics for autoimmune lymphoproliferative syndrome.
Two of the key manifestations of the disease, lymphoproliferation and splenomegaly, are especially difficult to treat but may not always cause severe harm without treatment. Treatments for ALPS usually focus on the complications due to autoimmune conditions associated with ALPS, especially severe autoimmune cytopenias, which can be life threatening.
Splenectomy (removal of spleen by surgery) was often used to treat the autoimmune cytopenias until the early 2000s. However, since then, spleen-sparing immunomodulatory regimens have become the mainstay of long-term therapy for these complications in individuals with ALPS. The shift away from splenectomy was driven by the observation that individuals with ALPS had a greater than normal risk of suffering a severe and potentially life-threatening infection after splenectomy.
The drugs used to treat autoimmune cytopenias include corticosteroids, mycophenolate mofetil (MMF), and rapamycin (also known as sirolimus). Rapamycin has been shown to reduce spleen and lymph node size over the long term. MMF does not reduce lymph node or spleen size and can cause hypogammaglobulinemia, which is a condition of a low level of immunoglobulins and may require immunoglobulin (Ig) replacement therapy.
Rapamycin has been used to resolve 90% of autoimmune symptoms as well as enlargement of lymph nodes and spleen. This drug may cause immune suppression leading to an increased risk for infections, though it has not been reported to cause hypogammaglobulinemia. Individuals taking rapamycin require careful monitoring as the drug can increase the risk of various cancers, cause mucositis (painful inflammation and ulceration of the digestive tract), diarrhea, hyperlipidemia (increased lipid/fat levels in blood), and slow the healing of wounds.
Corticosteroids can and should be used only as a short-term pulse therapy to address cytopenias and organ enlargement, and overall they have been met with limited success. Hematopoietic stem cell transplantation (HSCT) has also been used for some individuals. However, generally, HSCT is not advised because the good prognosis of most individuals with ALPS usually doesn’t warrant the challenges and risks associated with HSCT.
The spleen plays a critical role in fighting a common bacteria called pneumococci. If ALPS-related splenomegaly becomes severe enough, long-term rapamycin and short-term corticosteroids should be used to shrink the spleen. As noted above, splenectomy can result in a significant risk of sepsis with encapsulated bacteria, which is a lifethreatening condition in which tissues and organs are infected by bacteria and damaged by the body’s response to it. Therefore, individuals whose spleens have been removed should employ long-term antibiotic treatment and consult a healthcare provider immediately upon developing a fever. More individuals with ALPS-FAS have died due to infection developed many years after splenectomy than from any other cause, including lymphoma.
Unlike many forms of primary immunodeficiency, ALPS itself does not significantly raise the risk of severe or frequent infection. Individuals who have undergone splenectomy should wear a medical alert bracelet, take prophylactic antibiotics, and seek immediate medical care for any fevers.
Complications associated with ALPS, including autoimmune hepatitis, vasculitis, uveitis, and others, should be managed just as they would be in people who do not have ALPS.
Because of its genetic nature, ALPS often affects more than one family member. Prompt recognition and treatment of any symptoms is important for optimal outcomes. Symptoms associated with ALPS are sometimes most severe in early childhood, when the lymphatic system is expanding, but may improve during adolescence and adulthood.
Individuals with ALPS have a higher risk of developing B cell lymphomas (Hodgkin and non-Hodgkin lymphoma), and they require frequent screening and monitoring for these cancers on a lifelong basis. Whenever individuals with ALPS develop systemic symptoms (like fever, night sweats, weight loss, or loss of appetite) and/or sudden focal enlargement of a group of their lymph nodes beyond their norm of clinical and seasonal variability, they should undergo further medical evaluations. These may include radiological imaging with computerized tomography (CT) and/or positron emission tomography (PET) scans followed by a biopsy of an appropriate lymph node(s). Routine frequent whole-body imaging on a yearly basis only for monitoring lymph nodes for lymphoma yields little benefit, and it is not recommended for individuals with ALPS.
In children, the enlargement of lymph nodes can be severe enough to be visible, resulting in potential anxiety and embarrassment. Shrinkage of the nodes for cosmetic reasons is not recommended, although attention to the child or young adult’s overall well-being and emotional concerns is equally vital. The nodes should be carefully watched for any sudden and significant changes in size, which should be promptly reported to the healthcare provider. The size of the lymph nodes and the spleen should also be regularly monitored through measurement by the medical team.
Although there are reports of successful use of rapamycin and MMF, the long-term toxicities of these therapies remain unknown. Through proper care, ALPS is usually manageable, and most individuals can have a relatively normal lifestyle and life span. However, this does not preclude the need for careful lifelong monitoring for possible progression to autoimmune and malignant diseases, particularly in children and young adults.
More recently, additional genetic variants have been discovered that mimic ALPS with similar clinical findings. For the sake of this material, they will be referred as ALPS related disorders (Table 17:1). Knowing the genetic basis of many of these lymphoproliferative disorders with autoimmune problems may facilitate better and more targeted treatment of these individuals.
This page contains general medical and/or legal information that cannot be applied safely to any individual case. Medical and/or legal knowledge and practice can change rapidly. Therefore, this page should not be used as a substitute for professional medical and/or legal advice. Additionally, links to other resources and websites are shared for informational purposes only and should not be considered an endorsement by the Immune Deficiency Foundation.
Adapted from the IDF Patient & Family Handbook for Primary Immunodeficiency Diseases, Sixth Edition.
Copyright ©2019 by Immune Deficiency Foundation, USA
Receive news and helpful resources to your cell phone or inbox. You can change or cancel your subscription at any time.
