Hereditary alpha tryptasemia: genoty** and associated clinical features
JJ Lyons - Immunology and Allergy Clinics, 2018 - immunology.theclinics.com
Tryptase is a protein expressed by mast cells and basophils. 1, 2 Mature, enzymatically
active tryptases are tetrameric serine proteases that are stored in mast cell secretory …
active tryptases are tetrameric serine proteases that are stored in mast cell secretory …
The normal range of baseline tryptase should be 1-15 ng/ml and covers healthy individuals with hereditary alpha tryptasemia
P Valent, G Hoermann, P Bonadonna… - The Journal of Allergy …, 2023 - Elsevier
Physiologic levels of basal serum tryptase vary among healthy individuals, depending on
the numbers of mast cells, basal secretion rate, copy numbers of the TPSAB1 gene …
the numbers of mast cells, basal secretion rate, copy numbers of the TPSAB1 gene …
Is it time for a new classification of mast cells? What do we know about mast cell heterogeneity?
B Frossi, F Mion, R Sibilano, L Danelli… - Immunological …, 2018 - Wiley Online Library
Mast cells (MC s) are derived from committed precursors that leave the hematopoietic tissue,
migrate in the blood, and colonize peripheral tissues where they terminally differentiate …
migrate in the blood, and colonize peripheral tissues where they terminally differentiate …
Human mast cell tryptase in biology and medicine
J Vitte - Molecular immunology, 2015 - Elsevier
The most abundant prestored enzyme of human mast cell secretory granules is the serine-
protease tryptase. In humans, there are four tryptase isoforms, but only two of them, namely …
protease tryptase. In humans, there are four tryptase isoforms, but only two of them, namely …
The genetic basis and clinical impact of hereditary alpha-tryptasemia
KT Luskin, AA White, JJ Lyons - The Journal of Allergy and Clinical …, 2021 - Elsevier
Hereditary alpha-tryptasemia (HαT) is an autosomal dominant genetic trait found in 4% to
6% of the general population and defined by excess copies of alpha-tryptase at TPSAB1 …
6% of the general population and defined by excess copies of alpha-tryptase at TPSAB1 …
Elevated basal serum tryptase: disease distribution and variability in a regional health system
AM Waters, HJ Park, AL Weskamp, A Mateja… - The Journal of Allergy …, 2022 - Elsevier
Background Hereditary-alpha tryptasemia (HαT) is the most common etiology for elevated
basal serum tryptase (BST). However, the utility of tryptase genoty** of individuals with …
basal serum tryptase (BST). However, the utility of tryptase genoty** of individuals with …
Drug hypersensitivity in clonal mast cell disorders: ENDA/EAACI position paper
P Bonadonna, M Pagani, W Aberer, MB Bilò… - Allergy, 2015 - Wiley Online Library
Mastocytosis is a clonal disorder characterized by the proliferation and accumulation of mast
cells (MC) in different tissues, with a preferential localization in skin and bone marrow (BM) …
cells (MC) in different tissues, with a preferential localization in skin and bone marrow (BM) …
Inherited and acquired determinants of serum tryptase levels in humans
JJ Lyons - Annals of Allergy, Asthma & Immunology, 2021 - Elsevier
Objective To aid the clinician in correctly interpreting serum tryptase levels. Data Sources
Primary peer-reviewed literature. Study Selections Clinical and basic science peer-reviewed …
Primary peer-reviewed literature. Study Selections Clinical and basic science peer-reviewed …
Elevated serum tryptase in non-anaphylaxis cases: a concise review
A Lee - International Archives of Allergy and Immunology, 2020 - karger.com
One of the most important blood tests in the field of allergy, mast cell tryptase has numerous
diagnostic uses, particularly for anaphylactic reactions and for the diagnosis of mastocytosis …
diagnostic uses, particularly for anaphylactic reactions and for the diagnosis of mastocytosis …
The serum tryptase test: an emerging robust biomarker in clinical hematology
P Valent, WR Sperr, K Sotlar, A Reiter… - Expert review of …, 2014 - Taylor & Francis
During the past few years, a number of molecular markers have been developed in clinical
hematology, most of them related to specific gene defects. However, there is also an unmet …
hematology, most of them related to specific gene defects. However, there is also an unmet …