New! Sign up for our free email newsletter.
Science News
from research organizations

A method to study immune cells offers hope for finding new disease treatments

Date:
June 26, 2024
Source:
University of Surrey
Summary:
An innovative combination of methods to identify and study how macrophages function could potentially revolutionize the diagnosis and treatment of various diseases.
Share:
FULL STORY

Macrophages play a critical role in the immune system by fighting infections and aiding in tissue repair. Understanding how these cells are activated in different scenarios is important for developing new medical treatments. However, identifying and studying macrophage activation has been challenging due to the complex nature of these cells and their responses.

The research team identified a protein called colony stimulating factor 1 receptor (CSF1R) as a reliable marker for monocytes and dendritic cells in blood and macrophages in tissues -- allowing for the clear identification and separation of different sample types. The new method works reliably for people of all ages and sexes.

Dr Fernando Martinez Estrada, who led the research project and is Senior Lecturer in Innate Immunology in the School of Biosciences at the University of Surrey, said:

"We have developed a method using CSF1R that can identify all types of Mononuclear phagocyte system cells in the body. This marker is incredibly useful for studying these cells in both health and disease, and it unlocks exciting new possibilities for cell isolation and quantification for diagnosing and monitoring various conditions with a single cell marker."

The study developed a set of tools to understand and check how these immune cells respond when they are activated. These tools focus on signals in the body, including IL-4 (involved in healing and fibrosis), steroids (deactivation), IFNγ (fights infections), and LPS (a bacterial product that causes inflammation).

The research team also described a novel concept that they call Macrophage Activation Mosaicism. This means that macrophages do not simply switch between the canonical two states previously described; instead, they can exhibit a mix of activation characteristics, reflecting the complexity of real tissue environments.

Dr Federica Orsenigo, co-author of the study, explains further:

"This discovery is significant because it changes how we perceive macrophage activation.

"Recognising that macrophages can have mixed activation status helps us better understand their roles in different diseases and could lead to more targeted and effective treatments."

Emeritus Professor Siamon Gordon, co-author of the study from the University of Oxford, said:

"Therapies that seek to re-educate macrophages are widely sought. However, the tools to measure activation are underdeveloped. Having a robust multi-gene tool to study macrophage activation can help in drug screening, identify drugs that revert macrophage activation, and eventually help with patient characterisation and personalised medicine."


Story Source:

Materials provided by University of Surrey. Note: Content may be edited for style and length.


Journal Reference:

  1. Federica Orsenigo, Alexander Stewart, Clare P. Hammer, Emma Clarke, Daniel Simpkin, Hossameldin Attia, Timothy Rockall, Siamon Gordon, Fernando O. Martinez. Unifying considerations and evidence of macrophage activation mosaicism through human CSF1R and M1/M2 genes. Cell Reports, 2024; 43 (6): 114352 DOI: 10.1016/j.celrep.2024.114352

Cite This Page:

University of Surrey. "A method to study immune cells offers hope for finding new disease treatments." ScienceDaily. ScienceDaily, 26 June 2024. <www.sciencedaily.com/releases/2024/06/240626152014.htm>.
University of Surrey. (2024, June 26). A method to study immune cells offers hope for finding new disease treatments. ScienceDaily. Retrieved July 3, 2024 from www.sciencedaily.com/releases/2024/06/240626152014.htm
University of Surrey. "A method to study immune cells offers hope for finding new disease treatments." ScienceDaily. www.sciencedaily.com/releases/2024/06/240626152014.htm (accessed July 3, 2024).

Explore More

from ScienceDaily

RELATED STORIES