Cutting-edge assessment techniques for B cell immune memory: an overview

The adaptive humoral immune response depends on B cells. After antigens are processed and presented to naive B cells, these B cells differentiate into either surface immunoglobulin-expressing memory B cells (MBCs) or antibody-secreting plasma cells (PC) and long-lived plasma cells (LLPC). In paralle...

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Main Authors: Martina Bozhkova, Petya Gardzheva, Vanya Rangelova, Hristo Taskov, Marianna Murdjeva
Format: Article
Language:English
Published: Taylor & Francis Group 2024-12-01
Series:Biotechnology & Biotechnological Equipment
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Online Access:https://www.tandfonline.com/doi/10.1080/13102818.2024.2345119
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author Martina Bozhkova
Petya Gardzheva
Vanya Rangelova
Hristo Taskov
Marianna Murdjeva
author_facet Martina Bozhkova
Petya Gardzheva
Vanya Rangelova
Hristo Taskov
Marianna Murdjeva
author_sort Martina Bozhkova
collection DOAJ
description The adaptive humoral immune response depends on B cells. After antigens are processed and presented to naive B cells, these B cells differentiate into either surface immunoglobulin-expressing memory B cells (MBCs) or antibody-secreting plasma cells (PC) and long-lived plasma cells (LLPC). In parallel with the detection of antibodies, the detection of MBCs and LLPC is important to assess the strength and duration of the humoral immune response. The number of antigen-specific cells can be determined by the secretion of antibodies using highly sensitive techniques such as ELISpot or FluoroSpot. Flow cytometry is usually used to determine the antigen-specific MBC, PC and LLPC by binding of antigens to their surface immunoglobulins. In this technique, the antigen is either directly labelled with a fluorochrome or non-covalently linked to labelled streptavidin in a tetramer. The advantage of flow cytometry is that detailed phenotypic analysis of B cell subpopulations can be performed. Single-cell RNA Sequencing provides in-depth information about B-cell receptor diversity, functional states, transcriptomic changes associated with rare cell populations or dynamic cellular processes within the immune system. Additionally, it can lead to the discovery of novel B cell subsets previously unknown. The advantages, disadvantages and potential applications of each technique are thoroughly outlined. This overview of current knowledge on B-cell immune memory highlights some implications for advancing vaccination strategies, autoimmune disease management and personalized medicine.
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spelling doaj-art-77e4be2dbfca4ab28b5177d60ff07d442025-08-20T02:22:10ZengTaylor & Francis GroupBiotechnology & Biotechnological Equipment1310-28181314-35302024-12-0138110.1080/13102818.2024.2345119Cutting-edge assessment techniques for B cell immune memory: an overviewMartina Bozhkova0Petya Gardzheva1Vanya Rangelova2Hristo Taskov3Marianna Murdjeva4Department of Medical Microbiology and Immunology “Prof. Elisey Yanev, MD”, Medical University–Plovdiv, Plovdiv, BulgariaDepartment of Medical Microbiology and Immunology “Prof. Elisey Yanev, MD”, Medical University–Plovdiv, Plovdiv, BulgariaDepartment of Epidemiology and Disaster Medicine, Faculty of Public Health, Medical University–Plovdiv, Plovdiv, BulgariaResearch Institute, Medical University–Plovdiv, Plovdiv, BulgariaDepartment of Medical Microbiology and Immunology “Prof. Elisey Yanev, MD”, Medical University–Plovdiv, Plovdiv, BulgariaThe adaptive humoral immune response depends on B cells. After antigens are processed and presented to naive B cells, these B cells differentiate into either surface immunoglobulin-expressing memory B cells (MBCs) or antibody-secreting plasma cells (PC) and long-lived plasma cells (LLPC). In parallel with the detection of antibodies, the detection of MBCs and LLPC is important to assess the strength and duration of the humoral immune response. The number of antigen-specific cells can be determined by the secretion of antibodies using highly sensitive techniques such as ELISpot or FluoroSpot. Flow cytometry is usually used to determine the antigen-specific MBC, PC and LLPC by binding of antigens to their surface immunoglobulins. In this technique, the antigen is either directly labelled with a fluorochrome or non-covalently linked to labelled streptavidin in a tetramer. The advantage of flow cytometry is that detailed phenotypic analysis of B cell subpopulations can be performed. Single-cell RNA Sequencing provides in-depth information about B-cell receptor diversity, functional states, transcriptomic changes associated with rare cell populations or dynamic cellular processes within the immune system. Additionally, it can lead to the discovery of novel B cell subsets previously unknown. The advantages, disadvantages and potential applications of each technique are thoroughly outlined. This overview of current knowledge on B-cell immune memory highlights some implications for advancing vaccination strategies, autoimmune disease management and personalized medicine.https://www.tandfonline.com/doi/10.1080/13102818.2024.2345119B cellsB lymphocytes subpopulationsB cellular immune responseMethods for B cells assessment
spellingShingle Martina Bozhkova
Petya Gardzheva
Vanya Rangelova
Hristo Taskov
Marianna Murdjeva
Cutting-edge assessment techniques for B cell immune memory: an overview
Biotechnology & Biotechnological Equipment
B cells
B lymphocytes subpopulations
B cellular immune response
Methods for B cells assessment
title Cutting-edge assessment techniques for B cell immune memory: an overview
title_full Cutting-edge assessment techniques for B cell immune memory: an overview
title_fullStr Cutting-edge assessment techniques for B cell immune memory: an overview
title_full_unstemmed Cutting-edge assessment techniques for B cell immune memory: an overview
title_short Cutting-edge assessment techniques for B cell immune memory: an overview
title_sort cutting edge assessment techniques for b cell immune memory an overview
topic B cells
B lymphocytes subpopulations
B cellular immune response
Methods for B cells assessment
url https://www.tandfonline.com/doi/10.1080/13102818.2024.2345119
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