Introduction
SIDs, also known as acquired immunodeficiencies are caused by external factors, rather than being caused by a hereditary or intrinsic defect.
Estimated to be 30 times more common than PIDs.
SIDs arise from various factors that weaken the immune system. SID may occur when the immune system is compromised by external factors such as malnutrition, treatments for other diseases or chronic infections1.
Causes of SID include:
Possible manifestations of SID:
SID may manifest as an antibody deficiency, which can mimic any of the primary antibody deficiencies. Vaccine response assessment may be used to determine whether these patients are able to mount a response to specific protein or polysaccharide vaccinations. Prophylactic antibiotics and immunoglobulin replacement therapy may be required in some patients.
It may also present as neutropenia. Low neutrophil counts can be caused by immunosuppression or other medical treatments. Therapy may be changed and if not possible, prophylactic antibiotics and antifungals may be required or a neutrophil stimulating treatment.
It may also present as a T cell deficiency. Patients with reduced T cells may suffer from multiple infections. If the underlying cause of this immunodeficiency cannot be removed, then the patient may be treated with antiviral, antifungal, or antibiotic therapies.
As there are many different possible causes, epidemiological data is very difficult to obtain. These patients may be found in a number of different situations, or clinics, and may have a number of other problems that clinicians are trying to manage.
An algorithm was proposed for the identification of secondary antibody deficiency and provides guidance for treatment options and monitoring.2
Treatment or management of the underlying cause of SID will often lead to improvement in symptoms, as the immune system is able to recover. However, sometimes this is not feasible, and treatment for the immunodeficiency may be required in order to prevent serious infections.
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