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From Selection to Use: Aptamers as Targeting Reagents in Hematology
Brandon Albert1, Fiona Ebanks1, Kimia Gharagozloo2
1Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montréal, QC H3A 0B8, Canada.
Biomedicines
|March 28, 2026
Summary
Aptamers, or synthetic nucleic acid ligands, show promise in hematology but current research unevenly covers blood cell types. This review organizes aptamer development by cell lineage, revealing gaps in targeting specific cell states and suggesting future research directions.
Area of Science:
- Biochemistry and Molecular Biology
- Hematology
- Biotechnology
Background:
- Aptamers are emerging as alternatives to antibodies for targeting cells and molecules in hematology.
- Existing reviews often categorize aptamer literature by disease or technology, masking uneven coverage of different blood cell types.
- This approach has led to a limited understanding of aptamer development across diverse hematopoietic lineages.
Purpose of the Study:
- To systematically review and organize aptamer development based on blood cell lineages (B cells, T cells, NK cells, RBCs).
- To identify gaps and limitations in current aptamer research for blood cell targeting.
- To define opportunities for advancing aptamer development for more precise and clinically relevant applications.
Main Methods:
- Literature review and analysis of developed aptamers targeting specific blood cell types.
- Categorization of aptamers by blood cell lineage and examination of targeted surface markers.
- Evaluation of reported applications, design strategies, experimental use cases, and limitations.
Main Results:
- Aptamer development is heavily concentrated on a few canonical surface markers and malignant cell models.
- Significant gaps exist in aptamers capable of distinguishing cell differentiation stages or functional states.
- Current research faces limitations in target selection and achieving adequate biological resolution.
Conclusions:
- The current organization of aptamer research by cell lineage reveals critical blind spots and practical constraints.
- There is a need to expand aptamer development beyond common markers to include cell states and differentiation.
- Future efforts should focus on creating more state-resolved, biologically informative, and clinically applicable blood-cell-targeting aptamers.

