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Claudio Counoupas

Researcher at University of Sydney

Publications -  36
Citations -  643

Claudio Counoupas is an academic researcher from University of Sydney. The author has contributed to research in topics: Vaccination & Mycobacterium tuberculosis. The author has an hindex of 10, co-authored 27 publications receiving 466 citations. Previous affiliations of Claudio Counoupas include Centenary Institute & University of Pisa.

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Direct Binding of Human NK Cell Natural Cytotoxicity Receptor NKp44 to the Surfaces of Mycobacteria and Other Bacteria

TL;DR: Results obtained indicate, for the first time, that at least one member of the NCR family (NKp44) may be involved in the direct recognition of bacterial pathogens by human NK cells.
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Interaction of Mycobacterium tuberculosis Cell Wall Components with the Human Natural Killer Cell Receptors NKp44 and Toll-Like Receptor 2

TL;DR: Results provide evidence that components abundant in mycobacterial cell wall are able to interact with NKp44 (AG, MA) and TLR‐2 (PG), respectively, and promote activation of resting NK cells and IFN‐γ production, and could play a secondary role in maintaining cell activation.
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A composite fibrin-based scaffold for controlled delivery of bioactive pro-angiogenetic growth factors

TL;DR: The new composite scaffolds, once implanted, providing a co-localization and temporal distribution of bioactive VEGF and bFGF in addition to good mechanical properties, may be useful to stimulate new vessels formation in ischemic tissues.
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Delta inulin-based adjuvants promote the generation of polyfunctional CD4+ T cell responses and protection against Mycobacterium tuberculosis infection.

TL;DR: If Advax displays broad applicability against important human pathogens by assessing protective immunity against infection with M. tuberculosis, CysVac2/AdvaxCpG is a strong candidate for further preclinical evaluation for progression to human trials.
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The ESX-5 Associated eccB5-eccC5 Locus Is Essential for Mycobacterium tuberculosis Viability

TL;DR: The characterization of two M. tuberculosis conditional mutant strains confirmed that the repression of eccB5-eccC5 genes is detrimental for growth of M.culosis both in vitro and in THP-1 human macrophage cell line, and revealed that both EccB5 and EccC5 are required for secretion of ESX-5 specific substrates, thus confirming that they are indeed components of the ESX -5 secretion machinery.