Selection and validation of antibody clones against IgG and IgA subclasses in switched memory B-cells and plasma cells
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, validační studie
PubMed
28965920
DOI
10.1016/j.jim.2017.09.008
PII: S0022-1759(17)30079-0
Knihovny.cz E-zdroje
- Klíčová slova
- Antibody clones, EuroFlow, Flow cytometry, IgG and IgA subclasses, Immune monitoring, Immunophenotyping,
- MeSH
- B-lymfocyty imunologie MeSH
- dospělí MeSH
- imunofenotypizace metody MeSH
- imunoglobulin A analýza MeSH
- imunoglobulin G analýza MeSH
- lidé středního věku MeSH
- lidé MeSH
- monoklonální protilátky * MeSH
- plazmatické buňky imunologie MeSH
- předškolní dítě MeSH
- průtoková cytometrie metody normy MeSH
- senioři MeSH
- specificita protilátek * MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- validační studie MeSH
- Názvy látek
- imunoglobulin A MeSH
- imunoglobulin G MeSH
- monoklonální protilátky * MeSH
The clinical value of assessing immunoglobulin (Ig)G and IgA subclasses in addition to the isotypes of soluble Igs in serum has been well established. >20years ago, the International Union of Immunological Societies and the World Health Organization performed collaborative studies in order to validate antibody (Ab) clones for the detection of IgG and IgA subclasses for a broad range of laboratory assays, except for flow cytometry. Here we analyzed the performance of commercially available Ab clones to detect IgG and IgA subclasses in memory B-cells and plasma cells (PCs) by flow cytometry. In a first step, 28 Ab clones were evaluated in peripheral blood from healthy donors. Only 17/28 clones showed reactivity against IgG and IgA subclasses expressed on the B-cell and PC surface membrane, including Ab clones for IgG1 (SAG1, HP6188, HP6001 and HP6186), IgG2 (SAG2, HP6014 and HP6002), IgG3 (SAG3, HP6095 and HP6050), IgG4 (SAG4), IgA1 (SAA1, H69-11.4 and B3506B4) and IgA2 (SAA2, 2E2, and A9604D2). In a second step, for each Ig subclass a single clone was selected according to its specificity and fluorescence intensity (resolution power), for further more detailed validation (SAG1, SAG2, SAG3, SAG4, SAA1 and SAA2). This validation process was carried out in 4 different laboratories by testing the selected Ab clones in human peripheral blood, bone marrow and tonsil samples, using different staining protocols (e.g. surface membrane and/or cytoplasmic staining). All selected Ab clones displayed strong positivity, high specificity and optimal resolution between negative and positive cells. Alternative Ab clones were also validated. Thus, our results show the feasibility of using the validated Ig subclass Ab clones in combination with other B cell-associated markers for detailed dissection of the memory B-cell and PC compartments that express distinct Ig subclasses in different human tissues.
Cancer Research Centre Salamanca Spain
Departamento de Inmunología Hospital Universitario La Paz Madrid Spain
Servicio de Hematología Hospital Universitario Salamanca Spain
Servicio de ORL Hospital Universitario Salamanca Spain
Servicio de Pediatría Hospital Universitario Salamanca Spain
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