Hyper IgM syndrome

Hyper IgM syndrome
Immunoglobulin M
Classification and external resources
Specialty	hematology
ICD-10	D80.5
ICD-9-CM	279.05
eMedicine	ped/2457
MeSH	D053306

Hyper IgM syndromes is a group of primary immune deficiency disorders characterized by defective CD40 signaling; via B cells affecting class switch recombination(CSR) and somatic hypermutation. Immunoglobulin (Ig) class switch recombination deficiencies are characterized by elevated serum Immunoglobulin M (IgM) levels and a considerable deficiency in Immunoglobulins G (IgG), A (IgA) and E (IgE). As a consequence, people with HIGM have decreased concentrations of serum IgG and IgA and normal or elevated IgM, leading to increased susceptibility to infections.^[1][2][3]

Types

Five types of hyper IgM syndrome have been characterized:

• Hyper-IgM syndrome type 1 (X-linked), characterized by mutations of the CD40LG gene. In this type, T cells cannot tell B cells to switch classes.^[4]
• Hyper-IgM syndrome type 2 (autosomal recessive), characterized by mutations of the AICDA gene. In this type, B cells cannot recombine genetic material to change heavy chain production^[5]
• Hyper-IgM syndrome type 3 characterized by mutations of the CD40 gene. In this type, B cells cannot receive the signal from T cells to switch classes.^[6]
• Hyper-IgM syndrome type 4 which is a defect in class switch recombination downstream of the AICDA gene that does not impair Somatic Hypermutation.^[7]
• Hyper-IgM syndrome type 5 characterized by mutations of the UNG gene.^[8]

Signs/symptoms

Among the presentation consistent with hyper IgM syndrome are the following:^[9][10]

Pneumocystis pneumonia

• Infection/Pneumocystis pneumonia (common in infants with hyper IgM syndrome, Pneumocystis carinii pneumonia (PJP or PCP) is a serious illness.^[1] PJP is one of the most frequent and severe opportunistic infections in people with weakened immune systems. Many CD40 Ligand Deficiency are first diagnosed after having PJP in their first year of life. The fungus is common and is present in over 70% of healthy people’s lungs, however, Hyper IgM patients are not able to fight it off without the administration of Bactrim)
• Hepatitis (Hepatitis C)
• Chronic diarrhea
• Hypothyroidism
• Neutropenia
• Arthritis
• Encephalopathy (degenerative)

Cause

Class switch recombination

Different genetic defects cause HIgM syndrome, the vast majority are inherited as an X-linked recessive genetic trait and most sufferers are male.^[2]

IgM is the form of antibody that all B cells produce initially, before they undergo class switching due to exposure to a recognized antigen. Healthy B cells efficiently switch to other types of antibodies as needed to attack invading bacteria, viruses, and other pathogens. In people with hyper IgM syndromes, the B cells keep making IgM antibodies because they can't switch to a different antibody. This results in an overproduction of IgM antibodies and an underproduction of IgA, IgG, and IgE.^[11][2]

Pathophysiology

In the mechanism one sees that CD40, protein is a receptor for cells of the human immune system, furthermore, is important in immune and inflammatory response.^[12] When CD40L is not working properly, this then leads to defective T-cell interaction with monocytes. Consequently, resulting cell-mediated immune response is affected, therefore certain infections have a greater opportunity to invade the human body.^[9]

Diagnosis

The diagnosis of hyper IgM syndrome can be done via the following methods and tests:^[9]

• MRI
• Chest radiography
• Pulmonary function test
• Lymph node test
• Laboratory test (to measure CD40)

Treatment

In terms of treatment for hyper Igm syndrome there is the use of allogeneic hematopoietic cell transplantation. Additionally anti-microbial therapy, use of granulocyte colony-stimulating factor, immunosuppressants, as well as, other treatments may be needed.^[2]

See also

• X-linked agammaglobulinemia
• Common variable immunodeficiency CVID)

References

Further reading

• Strober, Warren; Gottesman, Susan R. (2014). Immunology: Clinical Case Studies and Disease Pathophysiology. John Wiley & Sons. ISBN 9781118966006. Retrieved 27 November 2016. 
• Kleinman, Ronald (Professor of Paediatrics (2008). Walker's Pediatric Gastrointestinal Disease. PMPH-USA. ISBN 9781550093643. Retrieved 27 November 2016.