New research characterizes bone marrow mast cells in systemic mastocytosis

Bone marrow mast cells have different properties in different mast cell disease types.

In a research letter recently published in Clinical & Experimental Allergy, scientists reported that the mast cells in the bone marrow of patients with systemic mastocytosis (SM) have a complex picture, with differences in size, granularity and histamineHistamine A chemical released by mast cells when they are activated. Histamine causes many of the allergy-type symptoms in mastocytosis, including flushing, itching and hives. content. 

Mast cells are immune cells that play an important role in releasing histamine and other substances that counter allergic reactions and inflammation. However, when these mast cells do not function as they should or if there is an abnormal, excessive accumulation of these cells in the body, various symptoms may appear, such as itching, fatigue, abdominal pain and diarrhea and flushing. 

The team of scientists conducted a study to better understand the characteristics of bone marrow mast cells in patients with clonal mast cellMast cell A type of white blood cell produced in the bone marrow. They help defend against infections and play a key role in allergic reactions. In SM, mast cells become overactive and build up throughout the body. disorders, which includes SM, as well as idiopathic mast cell activationMast cell activation Describes when mast cells release histamine and other mediators into the blood stream in response to an allergen or other trigger. This leads to symptoms like fatigue, rash and, in severe cases, anaphylaxis. syndrome (meaning that the root cause of the disease is unknown). 

A detailed laboratory analysis allowed scientists to observe anomalies in the bone marrow mast cells of affected patients. Through these efforts, they identified that mast cell characteristics varied between different disease subtypes; for example, mast cells were found to be larger in some conditions than others. The granularity of certain mast cells differed as well. 

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The research team carrying out this study found that clonal mast cells had reduced membrane-bound and intracellular histamine content. They concluded that these observations, seen in larger and more granulated bone marrow mast cells that were aberrantly activated, was an intrinsic feature. 

Scientists also discovered that the mast cells in the bone marrow of patients with idiopathic mast cell activated syndrome showed no significant changes compared with non-clonal subjects. 

The characterizing of bone marrow mast cells in mast cell disorders is of particular importance to researchers because they may help shape clinical decision-making. Continued research into this area will allow clinicians to gain a better grasp of how mast cells behave and how these can be best addressed. 

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