-
Instruments
-
Flow Cytometers
- Clinical Cell Analyzers
-
Research Cell Analyzers
- BD® LSR II Flow Cytometer
- BD FACSCelesta™ Cell Analyzer
- BD FACSLyric™ Research System
- LSRFortessa™ Cell Analyzer
- LSRFortessa™ X-20
- FACSymphony™ A5
- BD Accuri™ C6
- FACSVerse™
- FACSymphony™ A3
- BD Accuri™ C6 Plus
- FACSymphony™ A5 SE Cell Analyzer
- FACSymphony™ A1 Cell Analyzer
- BD FACSDiscover™ A8 Research Cell Analyzer
- Research Cell Sorters
- Clinical Sample Prep Systems
- Single-Cell Multiomics Systems
-
Flow Cytometers
-
Reagents
-
Flow Cytometry Reagents
- Clinical Diagnostics
-
Research Reagents
- BD Horizon RealViolet™ 828 for Flow Cytometry
- Quality and Reproducibility
- Single Color Antibodies RUO
- Panels Multicolor Cocktails RUO
- Flow Cytometry Controls and Lysates
- buffers and Supporting Reagents RUO
- Cell Function Analysis Stains Dyes
- Single Color Antibodies
- Compensation Beads
- BD Horizon™ Human T Cell Backbone Panel
- BD Pharmingen™ MonoBlock™ Leukocyte Staining Buffer
- BV605 Transition
- BD Horizon RealBlue™ 670 for Flow Cytometry
- BD Horizon RealBlue™ 780 for Flow Cytometry
- BD Horizon RealYellow™ 586
- BD Horizon RealYellow™ 610
- BD Horizon RealYellow™ 703
- Clinical Discovery
-
Western Blotting and Molecular Reagents
- Immunoassay Reagents
-
Single-Cell Multiomics Reagents
- BD® AbSeq Assay
-
BD® Single-Cell Multiplexing Kit
-
BD Rhapsody™ ATAC-Seq Assays
-
BD Rhapsody™ Whole Transcriptome Analysis (WTA) Amplification Kit
-
BD Rhapsody™ TCR/BCR Next Multiomic Assays
-
BD Rhapsody™ Targeted mRNA Kits
-
BD Rhapsody™ Accessory Kits
-
BD Rhapsody™ TCR/BCR Profiling Assays for Human and Mouse
- BD® OMICS-One Protein Panels
-
Functional Assays
-
Microscopy and Imaging Reagents
-
Cell Preparation and Separation Reagents
-
Flow Cytometry Reagents
-
-
- BD® LSR II Flow Cytometer
- BD FACSCelesta™ Cell Analyzer
- BD FACSLyric™ Research System
- LSRFortessa™ Cell Analyzer
- LSRFortessa™ X-20
- FACSymphony™ A5
- BD Accuri™ C6
- FACSVerse™
- FACSymphony™ A3
- BD Accuri™ C6 Plus
- FACSymphony™ A5 SE Cell Analyzer
- FACSymphony™ A1 Cell Analyzer
- BD FACSDiscover™ A8 Research Cell Analyzer
-
-
-
- BD Horizon RealViolet™ 828 for Flow Cytometry
- Quality and Reproducibility
- Single Color Antibodies RUO
- Panels Multicolor Cocktails RUO
- Flow Cytometry Controls and Lysates
- buffers and Supporting Reagents RUO
- Cell Function Analysis Stains Dyes
- Single Color Antibodies
- Compensation Beads
- BD Horizon™ Human T Cell Backbone Panel
- BD Pharmingen™ MonoBlock™ Leukocyte Staining Buffer
- BV605 Transition
- BD Horizon RealBlue™ 670 for Flow Cytometry
- BD Horizon RealBlue™ 780 for Flow Cytometry
- BD Horizon RealYellow™ 586
- BD Horizon RealYellow™ 610
- BD Horizon RealYellow™ 703
-
-
-
- Brazil (English)
-
Change location/language
Old Browser
Looks like you're visiting us from {countryName}.
Would you like to stay on the current location site or be switched to your location?
The Complex Interplay of Immune Dysfunction in
B-Cell Malignancies
The spectrum of secondary immunodeficiency (SID) associated with B-cell lymphoproliferative diseases (B-CLPD) encompasses defects primarily in antibody production and hypogammaglobulinemia, alongside varying T cell and innate immunity defects. Like primary immunodeficiency disorders (PID), a classification system is warranted to categorize SID defects and assess infection risk.
Despite similarities in infection profiles between PID and SID to B-CLPD, it is of utmost importance to rule out PID at B-CLPD diagnosis, which has clinical and prognostic implications for the patients and their families. An integrated approach that incorporates immunological biomarkers alongside traditional prognostic indicators is essential for enhancing diagnostic accuracy and tailoring risk-adapted therapies in patients with B-CLPD and concurrent immune dysfunction. Collaboration between hematologists and immunologists is imperative for navigating the complex landscape of immune dysfunction in cancer.
Join us to learn:
- The clinical relevance of an adequate assessment and classification of the immunodeficiency in B-CLPD in predicting disease progression and guiding treatment decisions.
- The challenges in diagnosing primary versus secondary immunodeficiency and the importance of early recognition.
- Through exploration of the genomic landscape of B-CLPD and its intersection with PID, potential shared pathways and therapeutic targets are underscored, highlighting the relevance of interdisciplinary collaboration and integrated approaches to patient care.
Speakers
Silvia Sánchez-Ramón, MD, Ph.D.
Head Immunology Department, Hospital Clínico San Carlos, Madrid
Associate Professor, Complutense University of Madrid
Silvia Sánchez Ramón is the Head of the Immunology Department at the Hospital Clínico San Carlos, and an associate professor at the Faculty of Medicine of the Universidad Complutense de Madrid. She works as a clinical immunologist and researcher in the field of primary and secondary immunodeficiencies and immunoregulation.