# From Selection to Use: Aptamers as Targeting Reagents in Hematology

**Authors:** Brandon Albert, Fiona Ebanks, Kimia Gharagozloo, Xinying Hai, Raymond Ngu, Sietse Munting, Maureen McKeague

PMC · DOI: 10.3390/biomedicines14030534 · Biomedicines · 2026-02-27

## TL;DR

This review analyzes how aptamers are used to target different blood cells, revealing gaps in current research and suggesting ways to improve their development.

## Contribution

The paper introduces a novel organization of aptamer research by blood cell lineages, highlighting biases and opportunities in hematology.

## Key findings

- Aptamer research is heavily focused on a few surface markers and cancerous cells.
- There is a lack of aptamers that distinguish cell differentiation stages or functional states.
- Current aptamer development has practical and conceptual limitations in biological resolution.

## Abstract

Aptamers are synthetic nucleic acid ligands that have been proposed as alternatives to antibodies for targeting molecules and cells. In hematology, most reviews have organized aptamer literature around diseases or technological platforms. This framing has obscured how unevenly different blood cell types have been covered. In this review, we present developed aptamers organized by blood cell lineages. Specifically, we examine aptamers for B cells, T cells, natural killer cells, and red blood cells. This organization revealed a strong concentration on a small set of canonical surface markers and on malignant cell models. A parallel gap appeared in aptamers that distinguish differentiation stages or functional cell states. Within this framework, we evaluated reported applications, design strategies, and experimental use cases alongside persistent limitations in target selection and biological resolution. Our analysis highlighted both practical constraints and conceptual blind spots in current blood-cell-targeting aptamer research. Together, these observations defined a set of clear opportunities for expanding aptamer development toward more state-resolved, biologically informative, and clinically relevant targeting strategies.

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13023674/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13023674/full.md

## References

187 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023674/full.md

---
Source: https://tomesphere.com/paper/PMC13023674