Human Primary Mast Cells for Research
Reliable human data on drug efficacy & toxicity

Today’s research on new drugs is often complicated by a consistent lack of relevant study tools. This is also the case when it comes to research on mast cells, where rodent and human cell line models are still the standard and human primary mast cells remain notoriously hard to obtain. Genoskin provides a reliable solution to help you study human primary mast cell response to your compound or formula. You’ll find a quick overview of our offer below.
In Vitro
Genoskin provides unique access to connective-tissue type human primary mast cells for drug candidate screening.
Human
Our research consistently focuses on human tools to generate reliable data on your compound or formula.
Mast Cells
Mast cells are immunological key players in a wide range of pathologies, including allergic reactions.
For Research
Our mast cells are designed for in vitro research on drug efficacy and toxicity.
First-in-human data on drug efficacy and toxicity
A unique platform to de-risk drug development

As human primary mast cells are notoriously hard to obtain for research purposes, Genoskin has developed a unique process using peripheral blood samples from healthy adult donors. This 1-month process yields mature mast cells that show the same metabolism and expression as the mast cells in the human body, with the phenotype of connective tissue-type mast cells:
- The granules are filed with heparin, tryptase and chymase
- They express the high affinity receptor for IgE (FcɛR1⍺), MRGPRX2 (specifically expressed by skin mast cells), FcgRs and many G protein-coupled receptors including receptors for complement anaphylatoxins
- They can degranulate and produce cytokines/chemokines in response to many stimuli including IgE/anti-IgE, cationic molecules that bind to MRGPRX2 (e.g neuropeptide substance P and FDA-approved drugs), C3a and C5a, endothelin-1,…

First-in-human data on drug efficacy and toxicity
A unique platform to de-risk drug development

As human primary mast cells are notoriously hard to obtain for research purposes, Genoskin has developed a unique process using peripheral blood samples from healthy adult donors. This 1-month process yields mature mast cells that show the same metabolism and expression as the mast cells in the human body, with the phenotype of connective tissue-type mast cells:
- The granules are filed with heparin, tryptase and chymase
- They express the high affinity receptor for IgE (FcɛR1⍺), MRGPRX2 (specifically expressed by skin mast cells), FcgRs and many G protein-coupled receptors including receptors for complement anaphylatoxins
- They can degranulate and produce cytokines/chemokines in response to many stimuli including IgE/anti-IgE, cationic molecules that bind to MRGPRX2 (e.g neuropeptide substance P and FDA-approved drugs), C3a and C5a, endothelin-1,…

Pharmacological validation
Mast cell degranulation & dose-effect experiments

Genoskin’s in vitro primary mast cells degranulate upon stimulation with compounds known to trigger mast cell degranulation. The platform also allows to perform dose-effect experiments.

Relevant Scientific Publications
Literature on mast cells by Dr. Gaudenzio, our CSO

Below you’ll find relevant literature on mast cells by our Chief Scientific Officer and immunology expert, Dr. Nicolas Gaudenzio.
September 2016 - Different activation signals induce distinct mast cell degranulation strategies
- Different activation signals induce distinct mast cell degranulation strategies
- Published in The Journal of Clinical Investigation – September 19, 2016
- Nicolas Gaudenzio, Riccardo Sibilano, Thomas Marichal, Philipp Starkl, Laurent L. Reber, Nicolas Cenac, Benjamin D. McNeil, Xinzhong Dong, Joseph D. Hernandez, Ronit Sagi-Eisenberg, Ilan Hammel, Axel Roers, Salvatore Valitutti, Mindy Tsai, Eric Espinosa, and Stephen J. Galli.
- Published in The Journal of Clinical Investigation – September 19, 2016
March 2013 - Human mast cells drive memory CD4+ T cells toward an inflammatory IL-22+ phenotype
- Human mast cells drive memory CD4+ T cells toward an inflammatory IL-22+ phenotype
- Published in The Journal of Allergy and Clinical Immunology – March 20,2013
- Nicolas Gaudenzio, PhD, Camille Laurent, MD, Salvatore Valitutti, MD, Eric Espinosa, PhD
- Published in The Journal of Allergy and Clinical Immunology – March 20,2013