Presentation

Contact
Isabelle Andre is a research director at INSERM and leads the research Human Lymphohematopoiesis laboratory at Imagine Institute.
Her main research focuses on the development of the human hematopoietic immune system, and cell therapy pre-clinical studies for inherited and acquired disease of the hematopoietic system. The research group she leads studies not only how to succeed hematopoietic stem cell transplantation in humans but also the differentiation of mouse and human stem cells towards lymphocyte lineages. She has identified key steps in the production of T cells, key players of immunity generated throughout the life of an individual within the thymus. This work led to the development of an artificial thymus, which will be tested in a clinical trial to reduce the immune deficiency period after bone marrow transplantation. Her team also identified new genes involved in severe forms of inherited immune deficiencies in children and demonstrated genotoxicity of anti-viral drugs, such as AZT, used to prevent transmission of HIV during pregnancy.
She is involved in several clinical trials that are based on the use of ex vivo gene modified hematopoietic stem cells to treat patients with inherited disorders. She is the author or co-author of several patents and of about 60 publications in peer-reviewed journals and was awarded with several national and European grants.
Resources & publications
-
Journal (source)Blood
Clonal tracking in gene therapy patients reveals a diversity of human hematop...
-
Journal (source)Cancer Res
Comprehensive Genetic Profiling Reveals Frequent Alterations of Driver Genes ...
-
Journal (source)Nat Commun
Transient mTOR inhibition rescues 4-1BB CAR-Tregs from tonic signal-induced d...
-
Journal (source)Cell Mol Immunol
A DL-4- and TNFα-based culture system to generate high numbers of nonmodified...
-
Journal (source)Nat Immunol
Single-cell analysis of FOXP3 deficiencies in humans and mice unmasks intrins...
-
Journal (source)Am J Transplant
Donor-targeted serotherapy as a rescue therapy for steroid-resistant acute GV...
-
Journal (source)Bone Marrow Transplant
Ex vivo generated human T-lymphoid progenitors as a tool to accelerate immune...
-
Journal (source)Blood
A combination of cyclophosphamide and interleukin-2 allows CD4+ T cells conve...
-
Journal (source)J Allergy Clin Immunol
Improving the diagnostic efficiency of primary immunodeficiencies with target...
-
Journal (source)Blood Adv
Baboon envelope LVs efficiently transduced human adult, fetal, and progenitor...
-
Journal (source)J Allergy Clin Immunol
Improving the diagnostic efficiency of primary immunodeficiencies with target...
-
Journal (source)Top Curr Chem
Sucrose-utilizing transglucosidases for biocatalysis.
-
Journal (source)Blood
Clonal tracking in gene therapy patients reveals a diversity of human hematop...
-
Journal (source)Haematologica
A gain-of-function RAC2 mutation is associated with bone-marrow hypoplasia an...
-
Journal (source)Blood Adv
Gene transfer into hematopoietic stem cells reduces HLH manifestations in a m...
-
Journal (source)Stem Cells
Human T-lymphoid progenitors generated in a feeder-cell-free Delta-like-4 cul...
-
Journal (source)Cell Death Dis
AK2 deficiency compromises the mitochondrial energy metabolism required for d...
-
Journal (source)Blood Adv
Gene transfer into hematopoietic stem cells reduces HLH manifestations in a m...
-
Journal (source)J. Allergy Clin. Immunol.
X-linked primary immunodeficiency associated with hemizygous mutations in the...
-
Journal (source)J. Clin. Invest.
Loss of ARHGEF1 causes a human primary antibody deficiency.
-
Journal (source)Blood
Gene-corrected human Munc13-4-deficient CD8+ T cells can efficiently restrict...
-
Journal (source)Stem Cells Dev.
Gene Therapy with Hematopoietic Stem Cells: The Diseased Bone Marrow's Point ...
-
Journal (source)Hum. Gene Ther.
Gene Therapy for X-Linked Severe Combined Immunodeficiency: Where Do We Stand?
-
Journal (source)J. Allergy Clin. Immunol.
Generation of adult human T-cell progenitors for immunotherapeutic applications.
-
Journal (source)Haematologica
Plerixafor enables safe, rapid, efficient mobilization of hematopoietic stem ...
-
Journal (source)Mol Ther Methods Clin Dev
A Nontoxic Transduction Enhancer Enables Highly Efficient Lentiviral Transduc...
-
Journal (source)Nat Rev Drug Discov
Gene therapy targeting haematopoietic stem cells for inherited diseases: prog...