Primary immunodeficiency

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Primary immunodeficiencies are disorders in which part of the body's immune system is missing or does not function properly. To be considered a primary immunodeficiency, the cause of the immune deficiency must not be secondary in nature (i.e., caused by other disease, drug treatment, or environmental exposure to toxins). Most primary immunodeficiencies are genetic disorders; the majority are diagnosed in children under the age of one, although milder forms may not be recognised until adulthood. About 1 in 500 people is born with a primary immunodeficiency.^[1]

1 Signs and symptoms
2 Diagnosis
3 Conditions
4 Treatment
5 Epidemiology
6 References
7 External links

[edit] Signs and symptoms

The kind of defect to the immune system determines the symptoms of immunodeficiency. Generally, the problems that lead to the diagnosis of an immunodeficiency include recurrent or persistent infections, or developmental delay as a result of infection. Particular organ problems (e.g. diseases involving the skin, heart, facial development and skeletal system) may be present in certain conditions. Others predispose to autoimmune disease, where the immune system attacks the body's own tissues, or tumours (sometimes specific forms of cancer, such as lymphoma). The nature of the infections, as well as the additional features, may provide clues as to the exact nature of the immune defect.^[1]

[edit] Diagnosis

The basic tests performed when an immunodeficiency is suspected should include a full blood count (including accurate lymphocyte and granulocyte counts) and immunoglobulin levels (the three most important types of antibodies: IgG, IgA and IgM).^[1]

Other tests are performed depending on the suspected disorder:^[1]

Quantification of the different types of mononuclear cells in the blood (i.e. lymphocytes and monocytes): different groups of T lymphocytes (dependent on their cell surface markers, e.g. CD4+, CD8+, CD3+, TCRαβ and TCRγδ), groups of B lymphocytes (CD19, CD20, CD21 and Immunoglobulin), natural killer cells and monocytes (CD15+), as well as activation markers (HLA-DR, CD25, CD80 (B cells).
Tests for T cell function: skin tests for delayed-type hypersensitivity, cell responses to mitogens and allogeneic cells, cytokine production by cells
Tests for B cell function: antibodies to routine immunisations and commonly acquired infections, quantification of IgG subclasses
Tests for phagocyte function: reduction of nitro blue tetrazolium chloride, assays of chemotaxis, bactericidal activity.

Due to the rarity of many primary immunodeficiencies, many of the above tests are highly specialised and tend to be performed in research laboratories.^[1]

Criteria for diagnosis were agreed in 1999. For instance, an antibody deficiency can be diagnosed in the presence of low immunoglobulins, recurrent infections and failure of the development of antibodies on exposure to antigens. The 1999 criteria also distinguish between "definitive", "probable" and "possible" in the diagnosis of primary immunodeficiency. "Definitive" diagnosis is made when it is likely that in 20 years, the patient has a >98% chance of the same diagnosis being made; this level of diagnosis is achievable with the detection of a genetic mutation or very specific circumstantial abnormalities. "Probable" diagnosis is made when no genetic diagnosis can be made, but the patient has all other characteristics of a particular disease; the chance of the same diagnosis being made 20 years later is estimated to be 85-97%. Finally, a "possible" diagnosis is made when the patient has only some of the characteristics of a disease are present, but not all.^[2]

[edit] Conditions

The International Union of Immunological societies recognises eight classes of primary immunodeficiencies, totaling over 120 conditions.^[3]

[edit] Combined T- and B-cell immunodeficiencies

In these disorders both T lymphocytes and often B lymphocytes, regulators of adaptive immunity, are dysfunctional or decreased in number. The main members are various types of severe combined immunodeficiency (SCID).^[3]

T-/B+ SCID (T cells predominantly absent): γc deficiency, JAK3 deficiency, interleukin 7 receptor chain α deficiency, CD45 deficiency, CD3δ/CD3ε deficiency.
T-/B- SCID (both T and B cells absent): RAG 1/2 deficiency, DCLRE1C deficiency, adenosine deaminase (ADA) deficiency, reticular dysgenesis
Omenn syndrome
DNA ligase type IV deficiency
CD40 ligand deficiency
CD40 deficiency
Purine nucleoside phosphorylase (PNP) deficiency
MHC class II deficiency
CD3γ deficiency
CD8 deficiency
ZAP-70 deficiency
TAP-1/2 deficiency
Winged helix deficiency

[edit] Antibody deficiencies

In antibody deficiencies, one or more isotypes of immunoglobulin are decreased or don't function properly. These proteins, generated by plasma cells, normally bind to pathogens, targeting them for destruction.^[3]

Absent B cells with a resultant severe reduction of all types of antibody: X-linked agammaglobulinemia (btk deficiency), μ-Heavy chain deficiency, l 5 deficiency, Igα deficiency, BLNK deficiency, thymoma with immunodeficiency
B cells low but present or normal, but with reduction in 2 or more isotypes (usually IgG & IgA, sometimes IgM): common variable immunodeficiency (CVID), ICOS deficiency, CD19 deficiency, TACI (TNFRSF13B) deficiency, BAFF receptor deficiency.
Normal numbers of B cells with decreased IgG and IgA and increased IgM: AID deficiency, UNG deficiency
Normal numbers of B cells with isotype or light chain deficiencies: heavy chain deletions, kappa chain deficiency, isolated IgG subclass deficiency, IgA with IgG subsclass deficiency, selective immunoglobulin A deficiency
Specific antibody deficiency to specific antigens with normal B cell and normal Ig concentrations
Transient hypogammaglobulinemia of infancy (THI)

[edit] Well-defined syndromes

A number of syndromes escape formal classification but are otherwise recognisable by particular clinical or immunological features.^[3]

Wiskott-Aldrich syndrome
DNA repair defects not causing isolated SCID: ataxia telangiectasia, ataxia-like syndrome, Nijmegen breakage syndrome, Bloom syndrome
DiGeorge syndrome (when associated with thymic defects)
Various immuno-osseous dysplasias (abnormal development of the skeleton with immune problems): cartilage-hair hypoplasia, Schimke syndrome
Hermansky-Pudlak syndrome type 2
Hyper-IgE syndrome
Chronic mucocutaneous candidiasis

[edit] Immune dysregulation diseases

In certain conditions, the regulation rather than the intrinsic activity of parts of the immune system is the predominant problem.^[3]

Immunodeficiency with hypopigmentation or albinism: Chediak-Higashi syndrome, Griscelli syndrome type 2
familial hemophagocytic lymphohistiocytosis: perforin deficiency, MUNC13D deficiency, syntaxin 11 deficiency
X-linked lymphoproliferative syndrome
Syndromes with autoimmunity:
- Autoimmune lymphoproliferative syndrome: type 1a (CD95 defects), type 1b (Fas ligand defects), type 2a (CASP10 defects), type 2b (CASP8 defects)
- APECED (autoimmune polyendocrinopathy with candidiasis and ectodermal dystrophy)
- IPEX (immunodysregulation polyendocrinopathy enteropathy X-linked syndrome)

[edit] Phagocyte disorders

Phagocytes are the cells that engulf and ingest pathogens (phagocytosis), and destroy them with chemicals. Monocytes/macrophages as well as granulocytes are capable of this process. In certain conditions, either the number of phagocytes is reduced or their functional capacity is impaired.^[3]

Severe congenital neutropenia: due to ELA2 deficiency (with myelodysplasia), GFI1 deficiency (with T/B lymphopenia) or G-CSFR deficiency (G-CSF-unresponsive)
Kostmann syndrome
Cyclic neutropenia
X-linked neutropenia/myelodysplasia
Leukocyte adhesion deficiency types 1, 2 and 3
RAC2 deficiency
Beta-actin deficiency
Localized juvenile periodontitis
Papillon-Lefèvre syndrome
Specific granule deficiency
Shwachman-Diamond syndrome
Chronic granulomatous disease: X-linked and autosomal forms
Neutrophil glucose-6-phosphate dehydrogenase deficiency
IL-12 and IL-23 β1 chain deficiency
IL-12p40 deficiency
Interferon γ receptor 1 deficiency
Interferon γ receptor 2 deficiency
STAT1 deficiency (2 forms)

[edit] Innate immunity deficiencies

Several rare conditions are due to defects in the innate immune system, which is a basic line of defence that is independent on the more advanced lymphocyte-related systems. Many of these conditions are associated with skin problems.^[3]

Hypohidrotic ectodermal dysplasia
- NEMO deficiency
- IKBA deficiency
IRAK-4 deficiency
WHIM syndrome (warts, hypogammaglobulinaemia, infections, myleokathexis)
Epidermodysplasia verruciformis

[edit] Autoinflammatory disorders

Rather than predisposing for infections, most of the autoinflammatory disorders lead to excessive inflammation. Many manifest themselves as periodic fever syndromes. They may involve various organs directly, as well as predisposing for long-term damage (e.g. by leading to amyloid deposition).^[3]

Familial Mediterranean fever
TNF receptor associated periodic syndrome (TRAPS)
Hyper-IgD syndrome (HIDS)
CIAS1-related diseases:
- Muckle-Wells syndrome
- Familial cold autoinflammatory syndrome
- Neonatal onset multisystem inflammatory disease
PAPA syndrome (pyogenic sterile arthritis, pyoderma gangrenosum, acne)
Blau syndrome

[edit] Complement deficiencies

The complement system is part of the innate as well as the adaptive immune system; it is a group of circulating proteins that can bind pathogens and form a membrane attack complex. Complement deficiencies are the result of a lack of any of these proteins. They may predispose to infections but also to autoimmune conditions.^[3]

C1q deficiency (lupus-like syndrome, rheumatoid disease, infections)
C1r deficiency (idem)
C4 deficiency (idem)
C2 deficiency (lupus-like syndrome, vasculitis, polymyositis, pyogenic infections)
C3 deficiency (recurrent pyogenic infections)
C5 deficiency (Neisserial infections, SLE)
C6 deficiency (idem)
C7 deficiency (idem, vasculitis)
C8a and C8b deficiency (idem)
C9 deficiency (Neisserial infections)
C1-inhibitor deficiency (hereditary angioedema)
Factor I deficiency (pyogenic infections)
Factor H deficiency (haemolytic-uraemic syndrome, membranoproliferative glomerulonephritis)
Factor D deficiency (Neisserial infections)
Properdin deficiency (Neisserial infections)
MBP deficiency (pyogenic infections)
MASP2 deficiency

[edit] Treatment

The treatment of primary immunodeficiencies depends foremost on the nature of the abnormality. This may range from immunoglobulin replacement therapy intravenous immunoglobulin (IVIG) or subcutaneous immunoglobulin (SCIG) in antibody deficiencies to hematopoietic stem cell transplantation (for SCID). Reduction of exposure to pathogens may be recommended, and in many situations prophylactic antibiotics may be advised.

[edit] Epidemiology

A survey of 10,000 American households revealed that the prevalence of diagnosed primary immunodeficiency approaches 1 in 1200. This figure does not take into account people with mild immune system defects who have not received a formal diagnosis.^[4]

Milder forms of primary immunodeficiency, such as selective immunoglobulin A deficiency, are fairly common, with random groups of people (such as otherwise healthy blood donors) having a rate of 1:600. Other disorders are distinctly more uncommon, with incidences between 1:100,000 and 1:2,000,000 being reported.^[1]