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Related Concept Videos

B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
Cells of the Adaptive Immune Response01:23

Cells of the Adaptive Immune Response

The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...
Classification of Leukocytes01:30

Classification of Leukocytes

Leukocytes are classified into two groups based on the presence or absence of cytoplasmic granules. Granular leukocytes, which contain granules, belong to the myeloid lineage and are divided into three subtypes: neutrophils, eosinophils, and basophils. These cells are roughly spherical and characterized by the granules in their cytoplasm.
Neutrophils are the most abundant type of granular leukocytes, comprising 50-70% of all leukocytes. They feature small, evenly distributed granules and a...
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
Cellular Adaptation IV: Dysplasia and Metaplasia01:24

Cellular Adaptation IV: Dysplasia and Metaplasia

DysplasiaDysplasia refers to abnormal changes in the size, shape, and organization of mature cells, characterized by pleomorphism, nuclear abnormalities, and increased mitotic activity. It commonly affects epithelial tissues, including the cervix, gastrointestinal tract, respiratory mucosa, and endometrium. Although it may occur alongside hyperplasia, dysplasia is not a true adaptive response but a preneoplastic change with potential to progress to cancer.When confined above the basement...

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Related Experiment Video

Updated: May 13, 2026

In Vitro Differentiation Model of Human Normal Memory B Cells to Long-lived Plasma Cells
10:26

In Vitro Differentiation Model of Human Normal Memory B Cells to Long-lived Plasma Cells

Published on: January 20, 2019

[B-cell neoplasms with plasmacellular and plasmablastic differentiation].

F Fend1, L Quintanilla-Martínez

  • 1Institut für Pathologie und Neuropathologie, Universitätsklinik und Comprehensive Cancer Center Tübingen, Liebermeisterstr. 8, 72076 Tübingen, Deutschland. falko.fend@med.uni-tuebingen.de

Der Pathologe
|March 7, 2013
PubMed
Summary

Diagnosing plasma cell myeloma (PCM) and B-cell lymphomas requires careful integration of clinical, morphological, and immunophenotypic data. This review aids in distinguishing these conditions and related entities for accurate diagnosis.

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Flow Cytometric Characterization of Murine B Cell Development
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The Isolation, Differentiation, and Quantification of Human Antibody-secreting B Cells from Blood: ELISpot as a Functional Readout of Humoral Immunity

Published on: December 14, 2016

Related Experiment Videos

Last Updated: May 13, 2026

In Vitro Differentiation Model of Human Normal Memory B Cells to Long-lived Plasma Cells
10:26

In Vitro Differentiation Model of Human Normal Memory B Cells to Long-lived Plasma Cells

Published on: January 20, 2019

Flow Cytometric Characterization of Murine B Cell Development
08:25

Flow Cytometric Characterization of Murine B Cell Development

Published on: January 22, 2021

The Isolation, Differentiation, and Quantification of Human Antibody-secreting B Cells from Blood: ELISpot as a Functional Readout of Humoral Immunity
08:26

The Isolation, Differentiation, and Quantification of Human Antibody-secreting B Cells from Blood: ELISpot as a Functional Readout of Humoral Immunity

Published on: December 14, 2016

Area of Science:

  • Hematology
  • Oncology
  • Immunology

Context:

  • Plasma cell malignancies, including plasma cell myeloma (PCM), originate from terminally differentiated B-cells.
  • Distinguishing PCM from mature B-cell lymphomas with plasmablastic differentiation presents diagnostic challenges.
  • Accurate diagnosis relies on integrating clinical, morphological, and immunophenotypic analyses.

Purpose:

  • To review common diagnostic challenges in differentiating plasma cell myeloma from B-cell lymphomas.
  • To provide criteria for distinguishing small B-cell lymphomas, PCM, and high-grade B-cell lymphomas with plasmablastic differentiation.
  • To highlight the role of molecular markers and viral detection in diagnosing these hematological neoplasms.

Summary:

  • Plasma cell malignancies are neoplastic proliferations of plasma cells, with PCM being a common hematological neoplasm.
  • Morphological and immunophenotypic plasmablastic differentiation is observed in various mature B-cell lymphomas, complicating diagnosis.
  • Integration of clinical findings, morphology, immunophenotyping, viral detection, and molecular markers like MYD88 L265P is crucial for accurate differentiation.

Impact:

  • Improved diagnostic accuracy for plasma cell myeloma and related B-cell lymphomas.
  • Enhanced ability to differentiate between aggressive PCM and B-cell lymphomas with plasmablastic features.
  • Provides practical criteria for routine diagnostics in hematopathology.