Thomas Balligand

ORCID: 0000-0003-0156-8936
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About
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Research Areas
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Monoclonal and Polyclonal Antibodies Research
  • Lipid metabolism and disorders
  • Cytokine Signaling Pathways and Interactions
  • Radiopharmaceutical Chemistry and Applications
  • Platelet Disorders and Treatments
  • Kruppel-like factors research
  • Acute Myeloid Leukemia Research
  • Renal Diseases and Glomerulopathies
  • Immune Cell Function and Interaction
  • Influenza Virus Research Studies
  • CAR-T cell therapy research
  • Respiratory viral infections research
  • interferon and immune responses
  • Chronic Lymphocytic Leukemia Research
  • IL-33, ST2, and ILC Pathways
  • Blood properties and coagulation
  • Hemoglobinopathies and Related Disorders
  • RNA Interference and Gene Delivery
  • Protein Tyrosine Phosphatases
  • Advanced biosensing and bioanalysis techniques
  • Endoplasmic Reticulum Stress and Disease
  • Nanowire Synthesis and Applications
  • Amino Acid Enzymes and Metabolism
  • Chronic Myeloid Leukemia Treatments

Boston Children's Hospital
2023-2025

Harvard University
2023-2025

Boston Children's Museum
2024

de Duve Institute
2016-2023

Ludwig Cancer Research
2016-2022

UCLouvain
2012-2022

Walloon Excellence in Lifesciences and Biotechnology
2019-2020

The immune system eliminates pathogen intruders such as viruses and bacteria. To recruit effectors to virus-infected cells, we conjugated a small molecule, the influenza neuraminidase inhibitor zanamivir, nanobody that recognizes kappa light chains of mouse immunoglobulins. This adduct was designed achieve half-life extension zanamivir through complex formation with much-larger immunoglobulins in circulation. moiety targets whereas anti-kappa component simultaneously delivers polyclonal...

10.1126/sciimmunol.adg9459 article EN Science Immunology 2023-06-23

The purpose of the present work was to identify catalytic activity AGXT2L1 and AGXT2L2, two closely related, putative pyridoxal-phosphate-dependent enzymes encoded by vertebrate genomes. existence bacterial homologues (40-50% identity with AGXT2L2) forming bi- or tri-functional proteins a kinase belonging family aminoglycoside phosphotransferases suggested that AGXT2L2 acted on phosphorylated aminated compounds. Vertebrate genomes were found encode homologue (AGPHD1) these kinases, which...

10.1074/jbc.m111.323485 article EN cc-by Journal of Biological Chemistry 2012-01-13

Mutant calreticulin (CALR) proteins resulting from a -1/+2 frameshifting mutation of the CALR exon 9 carry novel C-terminal amino acid sequence and drive development myeloproliferative neoplasms (MPNs). CALRs were shown to interact with activate thrombopoietin receptor (TpoR/MPL) in same cell. We report that mutant are secreted can be found patient plasma at levels up 160 ng/mL, mean 25.64 ng/mL. Plasma is complex soluble transferrin 1 (sTFR1) acts as carrier protein increases half-life....

10.1182/blood.2022016846 article EN cc-by-nc-nd Blood 2022-11-10

Abstract The glycoproteins MICA and MICB are upregulated on the surface of cells undergoing stress, for instance due to (viral) infection or malignant transformation. MICA/B ligands activating receptor NKG2D, found cytotoxic immune like NK cells, CD8+ T γδ cells. Upon engagement these activated eradicate MICA/B-positive targets, assisted by secretion cytokines. Nanobodies, VHHs, derived from variable regions camelid heavy-chain only immunoglobulins. Nanobodies characterized their small size,...

10.1093/pnasnexus/pgae184 article EN cc-by-nc PNAS Nexus 2024-04-30

Two anti-transferrin receptor (TfR) nanobodies, V H H123 specific for mouse TfR and H188 human (huTfR) were used to track transplants non-invasively by PET/CT in models, without the need genetic modification of transferred cells. We provide a comparison specificity kinetics PET signals acquired when using nanobodies radiolabeled with 89 Zr, 64 Cu 18 F. knock-in that expresses ectodomain (huTfR +/+ ) as source into C57BL/6 recipients show detects such PET/CT. Conversely, huTfR can be imaged...

10.7554/elife.104302 preprint EN 2025-01-07

Two anti-transferrin receptor (TfR) nanobodies, V H H123 specific for mouse TfR and H188 human (huTfR) were used to track transplants non-invasively by PET/CT in models, without the need genetic modification of transferred cells. We provide a comparison specificity kinetics PET signals acquired when using nanobodies radiolabeled with 89 Zr, 64 Cu 18 F. knock-in that expresses ectodomain (huTfR +/+ ) as source into C57BL/6 recipients show detects such PET/CT. Conversely, huTfR can be imaged...

10.7554/elife.104302.1 preprint EN 2025-01-07

Influenza remains a significant public health threat. Both monoclonal antibodies and small-molecule inhibitors can target the influenza surface glycoproteins hemagglutinin (HA) or neuraminidase (NA) for prevention treatment of influenza. Here, we combine strengths anti-influenza small molecules by site-specific conjugation NA inhibitor zanamivir to MEDI8852, an HA-specific fully human antibody. MEDI8852 targets conserved stem region HA inhibits HA-mediated fusion viral host cell membranes....

10.1073/pnas.2424889122 article EN cc-by-nc-nd Proceedings of the National Academy of Sciences 2025-04-07

Primary familial and congenital polycythemia is characterized by erythropoietin hypersensitivity of erythroid progenitors due to germline nonsense or frameshift mutations in the receptor gene. All so far described lead truncation C-terminal sequence that contains negative regulatory domains. Their removal presented as sufficient cause phenotype. Here we provide evidence for a new mechanism whereby presence novel sequences generated required phenotype rather than just extensive resulting from...

10.3324/haematol.2017.176370 article EN cc-by-nc Haematologica 2017-12-21

Dimerization of the thrombopoietin receptor (TpoR) is necessary for activation and downstream signaling through activated Janus kinase 2. We have shown previously that different orientations transmembrane (TM) helices within a dimer can lead to outputs. Here we addressed structural basis mutations S505N W515K induce myeloproliferative neoplasms. show using in vivo bone marrow reconstitution experiments ligand-independent TpoR by TM asparagine (Asn) substitutions proportional proximity Asn...

10.7554/elife.81521 article EN cc-by eLife 2023-06-20

Bispecific antibody engagers are fusion proteins composed of a nanobody that recognizes immunoglobulin kappa light chains (

10.21203/rs.3.rs-4792057/v1 preprint EN cc-by Research Square (Research Square) 2024-08-01

Two anti-transferrin receptor (TfR) nanobodies, V H H123 specific for mouse TfR and H188 human (huTfR) were used to track transplants non-invasively by PET/CT in models, without the need genetic modification of transferred cells. We provide a comparison specificity kinetics PET signals acquired when using nanobodies radiolabeled with 89 Zr, 64 Cu 18 F. knock-in that expresses ectodomain (huTfR +/+ ) as source into C57BL/6 recipients show detects such PET/CT. Conversely, huTfR can be imaged...

10.1101/2024.11.20.624506 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2024-11-22
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