Evidence map›Paper›PMID 41863686›Full record

ArticleJournal of clinical immunology2026

Excluded GM-specific IgG Subclass Genes in Health and Disease - Inborn Errors of Immunity.

Vivi-Anne Oxelius

Abstract read
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Article in Journal of clinical immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

1 author.

Vivi-Anne OxeliusDepartment of Pediatrics, Institute of Laboratory Medicine, University Hospital, Lund University, Lund, Se-221 85, Sweden. vivi-anne.oxelius@med.lu.se.ORCID http://orcid.org/0000-0002-2487-105X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIgG subclass genes from chromosome 14q32.3 are assessed serologically by GM allotypes, genetic markers of the Fc part of the immunoglobulin constant heavy G chains, (IGHG(Fcγ)(GM) genes. Alternative GM allotypes of IgG3, IgG1 and IgG2, respectively, define 6 unique, precise GM-specific IgG subclass genes, inherited the Mendelian way with allelic exclusion, and linkage disequilibrium of IgG3-IgG1. Increased number of homozygous GM-specific IgG subclass genotypes with total loss of alternative IgG subclass molecules, inborn errors of immunity (IEI), are found in severe immunological diseases.

methodsA novel ELISA using GM-specific myeloma proteins and GM-specific monoclonals, identifies 6 alternative GM-specific IgG subclass genes and molecules IgG3*b & IgG3*g, IgG1*f & IgG1*a and IgG2*n & IgG2*-n, with different structures and functions. 4 different IgG3-IgG1-IgG2 haplotypes encode 10 individual IGHG diplotypes from 10 innate lymphoid combined B cells in 587 healthy.

resultsThe alternative GM-specific IgG subclass genes have different structures and functions and respond differently in immunotherapy to antigen stimulation with virus, bacteria and allergens. In this report we focus on excluded GM-IgG subclass genes, inborn errors of immunity (IEI) dominating in severe immunological diseases, severe infections, primary immunodeficiencies (PIDs), JCA, asthma, diabetes type 1 and malignancy. By intravenous immunoglobulins (IVIG) the excluded IgG subclass molecules are supplied and may prevent primary virus attacks and exacerbations in autoimmune disorders. IgG subclass genes orchestrate additional immune factors of inflammation.

conclusionExcluded GM-specific IgG subclass genes, IEI explore diagnosis, pathogenesis, prognosis and different phenotypes in immunological diseases, with IVIG as treatment.

Indexed as

Immune System DiseasesImmunoglobulin GImmunoglobulin Gm AllotypesGenotypeHaplotypesHumansImmunoglobulin GImmunoglobulin Gm AllotypesBy mendelian inheritance the homozygous genotypes have excluded alternative IgG subclass genes with total loss of alternative IgG subclass moleculesIgG1 and IgG2 subclassesIgG1*f & IgG1*a and IgG2*n & IgG2*-n on chromosome 14q32.3Inborn errors of immunityPrecise alternative GM-specific Fc parts of heavy constant G chains of IgG3Respectively: IgG3*b & IgG3*gSignificantly increased in immunological diseaseWith IVIG as possible treatment

Identifiers

PMID41863686
PMCPMC13053354

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.