Human immunoglobulin constant heavy G chain (IGHG) (Fcγ) (GM) genes, defining innate variants of IgG molecules and B cells, have impact on disease and therapy.
(2013) In Clinical Immunology 149(3). p.475-486- Abstract
- The distinguished alternative GM allotypes localized in immunoglobulin constant heavy G chain IGHG (Fcγ) (GM) genes on chromosome 14q32.3 define two unique variants of respectively IgG3, IgG1 and IgG2 subclasses, with different structures and functions. The IGHG allele (allotypes), expressed in homozygous or heterozygous forms, are assessed by new serological methods. Fixed combinations of γ3, γ1 and γ2 allotypes constitute the haplotypes, which are indirect markers of B cells. We highlight the role of homozygous IGHG genes with restricted qualities of IgG subclass molecules and B cells. These common Mendelian IGHG genes respond differently to allergens and infections, both bacterial and viral, and to active and passive immunotherapies.... (More)
- The distinguished alternative GM allotypes localized in immunoglobulin constant heavy G chain IGHG (Fcγ) (GM) genes on chromosome 14q32.3 define two unique variants of respectively IgG3, IgG1 and IgG2 subclasses, with different structures and functions. The IGHG allele (allotypes), expressed in homozygous or heterozygous forms, are assessed by new serological methods. Fixed combinations of γ3, γ1 and γ2 allotypes constitute the haplotypes, which are indirect markers of B cells. We highlight the role of homozygous IGHG genes with restricted qualities of IgG subclass molecules and B cells. These common Mendelian IGHG genes respond differently to allergens and infections, both bacterial and viral, and to active and passive immunotherapies. IGHG genes have an impact on diseases such as allergy, immunodeficiency, autoimmunity and malignancy. Association/linkage of different IGHG genes gives information about risk/protection, good or bad prognosis, for improvement of clinical care. The IGHG gene map of healthy Caucasians is registered. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/4179272
- author
- Oxelius, Vivi-Anne LU and Pandey, Janardan P
- organization
- publishing date
- 2013
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Clinical Immunology
- volume
- 149
- issue
- 3
- pages
- 475 - 486
- publisher
- Elsevier
- external identifiers
-
- wos:000328874800013
- pmid:24239836
- scopus:84887564125
- pmid:24239836
- ISSN
- 1521-6616
- DOI
- 10.1016/j.clim.2013.10.003
- language
- English
- LU publication?
- yes
- id
- 1ae5a763-e5f8-450b-9b38-7e1cea7f7295 (old id 4179272)
- alternative location
- http://www.ncbi.nlm.nih.gov/pubmed/24239836?dopt=Abstract
- date added to LUP
- 2016-04-01 10:57:50
- date last changed
- 2022-01-26 04:14:35
@article{1ae5a763-e5f8-450b-9b38-7e1cea7f7295, abstract = {{The distinguished alternative GM allotypes localized in immunoglobulin constant heavy G chain IGHG (Fcγ) (GM) genes on chromosome 14q32.3 define two unique variants of respectively IgG3, IgG1 and IgG2 subclasses, with different structures and functions. The IGHG allele (allotypes), expressed in homozygous or heterozygous forms, are assessed by new serological methods. Fixed combinations of γ3, γ1 and γ2 allotypes constitute the haplotypes, which are indirect markers of B cells. We highlight the role of homozygous IGHG genes with restricted qualities of IgG subclass molecules and B cells. These common Mendelian IGHG genes respond differently to allergens and infections, both bacterial and viral, and to active and passive immunotherapies. IGHG genes have an impact on diseases such as allergy, immunodeficiency, autoimmunity and malignancy. Association/linkage of different IGHG genes gives information about risk/protection, good or bad prognosis, for improvement of clinical care. The IGHG gene map of healthy Caucasians is registered.}}, author = {{Oxelius, Vivi-Anne and Pandey, Janardan P}}, issn = {{1521-6616}}, language = {{eng}}, number = {{3}}, pages = {{475--486}}, publisher = {{Elsevier}}, series = {{Clinical Immunology}}, title = {{Human immunoglobulin constant heavy G chain (IGHG) (Fcγ) (GM) genes, defining innate variants of IgG molecules and B cells, have impact on disease and therapy.}}, url = {{https://lup.lub.lu.se/search/files/2270248/4391246.pdf}}, doi = {{10.1016/j.clim.2013.10.003}}, volume = {{149}}, year = {{2013}}, }