Humoral immune deficiency
| Humoral immune deficiency | |
|---|---|
 | |
| B cells and antibody | |
| Specialty | Hematology  |
| Symptoms | Sinusitis |
| Causes | Absent B cells(primary), Multiple myeloma(secondary) |
| Diagnostic method | B cell count, Family medical history |
| Treatment | Immunoglobulin replacement therapy |
Humoral immune deficiencies are conditions which cause impairment of humoral immunity, which can lead to immunodeficiency. It can be mediated by insufficient number or function of B cells, the plasma cells they differentiate into, or the antibody secreted by the plasma cells. The most common such immunodeficiency is inherited selective IgA deficiency, occurring between 1 in 100 and 1 in 1000 persons, depending on population. They are associated with increased vulnerability to infection, but can be difficult to detect (or asymptomatic) in the absence of infection.
Signs and symptoms
Signs/symptoms of humoral immune deficiency depend on the cause, but generally include signs of infection such as:
Causes
Cause of this deficiency is divided into primary and secondary:
- Primary the International Union of Immunological Societies classifies primary immune deficiencies of the humoral system as follows:
- Absent B cells with a resultant severe reduction of all types of antibody: X-linked agammaglobulinemia (btk deficiency, or Bruton's agammaglobulinemia), μ-Heavy chain deficiency, l 5 deficiency, Igα deficiency, BLNK deficiency, thymoma with immunodeficiency
- B cells low but present, 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: Hyper-IgM syndromes
- 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
- Transient hypogammaglobulinemia of infancy (THI)
- Secondary secondary (or acquired) forms of humoral immune deficiency are mainly due to hematopoietic malignancies and infections that disrupt the immune system:
Diagnosis
In terms of diagnosis of humoral immune deficiency depends upon the following:
- Measure serum immunoglobulin levels
- B cell count
- Family medical history
Treatment
Treatment for B cell deficiency (humoral immune deficiency) depends on the cause, however generally the following applies:
- Treatment of infection (antibiotics)
- Surveillance for malignancies
- Immunoglobulin replacement therapy
See also
References
- 1 2 N. Franklin Adkinson Jr.; Bochner, Bruce S.; Burks, Wesley; Busse, William W.; Holgate, Stephen T. (2013-11-01). Middleton's Allergy: Principles and Practice. Elsevier Health Sciences. p. 1134. ISBN 9780323085939.
- 1 2 "Pure B-Cell Disorders: Background, Pathophysiology, Epidemiology". 2017-01-06.
{{cite journal}}: Cite journal requires|journal=(help) - 1 2 Notarangelo L, Casanova JL, Conley ME, et al. (2006). "Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee Meeting in Budapest, 2005". J. Allergy Clin. Immunol. 117 (4): 883–96. doi:10.1016/j.jaci.2005.12.1347. PMID 16680902.
- 1 2 Page 432, Chapter 22, Table 22.1 in: Jones, Jane; Bannister, Barbara A.; Gillespie, Stephen H. (2006). Infection: Microbiology and Management. Wiley-Blackwell. ISBN 978-1-4051-2665-6.
- 1 2 3 4 Fried, Ari J.; Bonilla, Francisco A. (2009-07-01). "Pathogenesis, Diagnosis, and Management of Primary Antibody Deficiencies and Infections". Clinical Microbiology Reviews. 22 (3): 396–414. doi:10.1128/CMR.00001-09. ISSN 0893-8512. PMC 2708392. PMID 19597006.
- 1 2 Cecil, Russell La Fayette; Goldman, Lee; Schafer, Andrew I. (2012-01-01). Goldman's Cecil Medicine, Expert Consult Premium Edition -- Enhanced Online Features and Print, Single Volume,24: Goldman's Cecil Medicine. Elsevier Health Sciences. p. 1618. ISBN 978-1437716047.
- ↑ Pieper, Kathrin; Grimbacher, Bodo; Eibel, Hermann (2013-04-01). "B-cell biology and development". Journal of Allergy and Clinical Immunology. 131 (4): 959–971. doi:10.1016/j.jaci.2013.01.046. ISSN 0091-6749. PMID 23465663.
- ↑ Fernandez, James (October 2024). "Selective IgA Deficiency - Allergy and Immunology". MSD Manual Professional Edition. Retrieved 2026-10-17.
- ↑ Malesza, Ida Judyta; Malesza, Michał; Krela-Kaźmierczak, Iwona; Zielińska, Aleksandra; Souto, Eliana B.; Dobrowolska, Agnieszka; Eder, Piotr (2020-07-23). "Primary Humoral Immune Deficiencies: Overlooked Mimickers of Chronic Immune-Mediated Gastrointestinal Diseases in Adults". International Journal of Molecular Sciences. 21 (15): 5223. doi:10.3390/ijms21155223. ISSN 1422-0067. PMC 7432083. PMID 32718006.
Further reading
- Ahn, Sam; Cunningham-Rundles, Charlotte (2017-05-11). "Role of B cells in common variable immune deficiency". Expert Review of Clinical Immunology. 5 (5): 557–564. doi:10.1586/eci.09.43. ISSN 1744-666X. PMC 2922984. PMID 20477641.
- Honjo, Tasuku; Reth, Michael; Radbruch, Andreas; Alt, Frederick (2014-10-09). Molecular Biology of B Cells. Elsevier. ISBN 9780123984906.
External links
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