Hyper IgM syndrome
Hyper IgM syndrome | |
---|---|
Immunoglobulin M | |
Specialty | Immunology |
Symptoms | Chronic diarrhea[1] |
Types | Hyper-IgM syndrome type 1, 2, 3, 4 and 5[2][3][4][5][6] |
Diagnostic method | MRI, Chest radiography[1] |
Treatment | Allogeneic hematopoietic cell transplantation[7] |
Hyper IgM syndrome is a rare primary immune deficiency disorders characterized by low or absent levels of serum IgG, IgA, IgE and normal or increased levels of serum IgM.[8]
They are resulting from mutations in the pathway from B-cell activation to isotype class switching. Patients with HIGM are usually diagnosed within the first two years of life and experience severe immunosuppression. This syndrome is also known as immunoglobulin class switch recombination (Ig-CSR) deficiencies.[9] The most common causes are mutations in the CD40 Ligand (CD40LG) gene located at Xq26.3-27 leading to X-linked HIGM (XHIGM) in males.[10]
Types
Five types of hyper IgM syndrome have been characterized:
- CD40LG gene. In this type, lack of CD40L on the surfaces of T cells results in defective signaling to B cells, which do not receive the needed signal to undergo isotype switching. Therefore, the only antibody secreted by the B cell is IgM, the least specific class of antibody.[2]
- AICDA gene. In this type, B cells cannot recombine genetic material to change heavy chain production[3]
- CD40 gene and it is inherited by autosomal recessive manner. It has similar phenotype of impaired class switch recombination and somatic hyper mutation with CD40L deficiency but B cells from CD40 deficient patients are unable to undergo class switching in vitro upon activation with agonists and cytokines as per their intrinsic defect .[9]
- Hyper-IgM syndrome type 4 caused by the mutation in the NEMO (nuclear factor κB essential modulator) complex, which, when mutated, is unable to phosphorylate IκB downstream of CD40 signaling.
- Hyper-IgM syndrome type 5 characterized by mutations of the UNG gene.[5] UNG is responsible for the cleavage of cytosines that have been deaminated by AID in single-stranded DNA.
- Hyper-IgM syndrome type 6 is the least-characterized of the HIGM types, as the gene is unknown. Resembles HIGM2, but AID is normal.
Signs and symptoms
The majority of patients with HIGM syndrome present with a broad spectrum of clinical symptoms even with a same genetic defects.
- Infection/Pneumocystis pneumonia (PCP), which is common in infants with hyper IgM syndrome, is a serious illness.[14] PCP 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 PCP 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[medical citation needed]
- Hepatitis (Hepatitis C)
- Chronic diarrhea
- Hypothyroidism
- Neutropenia
- Arthritis
- Encephalopathy (degenerative)
Cause
Different genetic defects cause HIgM syndrome, the vast majority are inherited as an
IgM is the form of
Pathophysiology
Diagnosis
The diagnosis of X-linked hyper IgM syndrome (HIGM1) is established in males with typical clinical and laboratory findings by identifying a hemizygous pathogenic variant in the CD40LG gene through molecular genetic testing. In females, the diagnosis of HIGM1 is extremely rare. Heterozygous females are usually asymptomatic unless there is skewed X-chromosome inactivation.[12] The diagnosis of hyper IgM syndrome can be done via the following methods and tests:[1]
- MRI
- Chest radiography
- Pulmonary function test
- Lymph node test
- Flow Cytometry (evaluate the presence and function of certain immune cells, such as T cells and B cells)
- Genetic testing
- Blood test(Immunoglobulin levels, Antibody response, Complete blood count (CBC))
Treatment
The primary goal is to address the underlying defect in CD40L or other gene mutations causing HIGM. The potential for precise correction of the CD40LG gene in T cells and hematopoietic stem/progenitor cells (HSPC) to treat X-linked hyper-IgM Syndrome (HIGM1) is a promising avenue of research. However, the actual therapeutic efficacy of this approach is not yet fully understood and requires further investigation to determine its true potential. In addition to HSCT, supportive measures are crucial for managing infections and complications associated with HIGM. This may include
Epidemiology
All forms of hyper-IgM syndrome are rare. According to the US X-HIGM registry, the prevalence of X-linked hyper IgM syndrome (X-HIGM) during the period from 1984 to 1993 was approximately 1 in 1,000,000 live births. The estimated frequency of CD40L deficiency, a subtype of X-HIGM, is 2 in 1,000,000 in males. Limited data is available on the frequency of AICDA deficiency, another subtype of X-HIGM, but it is believed to affect less than 1 in 1,000,000 individuals. Globally, all forms of HIGM make up approximately 0.3% to 2.9% of all patients diagnosed with primary immunodeficiency disorders (PIDs).[8]
See also
References
- ^ a b c d e "X-linked Immunodeficiency With Hyper IgM Clinical Presentation: History, Physical, Causes". emedicine.medscape.com. Retrieved 27 November 2016.
- ^ a b "OMIM Entry – # 308230 – IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 1; HIGM1". omim.org. Retrieved 16 November 2016.
- ^ a b "OMIM Entry – # 605258 – IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2; HIGM2". omim.org. Retrieved 16 November 2016.
- ^ "OMIM Entry – # 606843 – IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 3; HIGM3". omim.org. Retrieved 16 November 2016.
- ^ a b "OMIM Entry – # 608106 – IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5". omim.org. Retrieved 16 November 2016.
- ^ "OMIM Entry – 608184 – IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 4; HIGM4". omim.org. Retrieved 2 January 2018.
- ^ PMID 20301576. Retrieved 12 November 2016.update 2013
- ^ S2CID 53566466.
- ^ PMID 30319630.
- PMID 27189378.
- S2CID 33972331.
- ^ PMID 20301576, retrieved 22 June 2023
- PMID 20180797.
- PMID 15319456.
- ^ Reference, Genetics Home. "X-linked hyper IgM syndrome". Genetics Home Reference. Retrieved 27 November 2016.
- ^ Reference, Genetics Home. "CD40 gene". Genetics Home Reference. Retrieved 27 November 2016.
- PMID 33475257.
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 (2008). Walker's Pediatric Gastrointestinal Disease. PMPH-USA. ISBN 9781550093643. Retrieved 27 November 2016.