Publications by authors named "Orly Gershoni-Yahalom"

Stem cells are the foundation for cell therapy due to their ability to self-renew, differentiate into other cell types, and persist throughout the life of an organism. Stem cell isolation and transplantation have not yet been established in Hexacorallia, a cnidarian subclass containing stony corals and sea anemones. Here, we demonstrate that candidate stem cells in the hexacorallian Nematostella vectensis can be transplanted into adult animals.

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  • The study investigates how glycosphingolipids (GSLs), specifically α1,2-fucosylated GSLs, influence the differentiation of human pluripotent cells (hPCs) during early embryogenesis.
  • Overexpression of these GSLs hinders hPC differentiation into mesodermal cells and cardiomyocytes, while their reduction enhances differentiation and responsiveness to external signals such as BMP4.
  • The research suggests that α1,2-fucosylated GSLs play a crucial role in regulating cell signaling pathways involved in early embryo development and cell fate decisions.
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  • Climate change is causing more coral bleaching due to heat stress, and this involves immune genes that respond to that stress.
  • Researchers studied two types of sea anemones to see how heat affects their immune functions, specifically looking at immune cell activity and its relation to the presence of algal symbionts.
  • Their findings suggest that the immune response to heat stress is a fundamental reaction that occurs regardless of whether bleaching is happening, which helps in understanding coral immunity better.
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  • - The immune system protects organisms from infections and helps in tissue maintenance and regeneration, with key processes like phagocytosis and cytotoxicity serving as foundational functions in mammals.
  • - This review examines the evolution of immune cell lineages responsible for fighting pathogens and clearing damaged cells, comparing examples from various multicellular organisms, including invertebrates and vertebrates.
  • - It highlights shared features and divergent functions of immune cells, discussing the trade-offs between enhanced pathogen defense and potential limitations in tissue regeneration.
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  • - Understanding how the immune system remains nonreactive is vital for successful organ transplants and pregnancy, as rejections are mainly due to the adaptive immune system, which needs innate immunity to activate.
  • - A colonial tunicate, closely related to vertebrates, lacks T- and B-cell adaptive immunity, making it ideal for researching innate immunity; it shows unique behaviors like natural allogeneic transplantation and regeneration.
  • - Recent studies have revealed key molecular and cellular mechanisms behind the tunicate's innate immunity tolerance, and exploring these could lead to better strategies for managing immune responses in human transplantation and hematopoietic stem cell transplants.
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  • Phagocytosis is a key defense mechanism in innate immunity where cells engulf and break down harmful particles, like antigens from damaged cells and pathogens.
  • In hexacorallians, such as corals and sea anemones, the specific phagocytic processes are not well understood, although certain immune cells called amoebocytes have been identified.
  • The study characterizes different types of phagocytic cells that can engulf various materials and shows how cellular changes affect this process, laying groundwork for better understanding hexacorallian immune systems.
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mAb-based blocking of the immune checkpoints involving the CTLA4-B7 and PD1-PDL1 inhibitory axes enhance T-cell-based adaptive immune responses in patients with cancer. We show here that antitumor responses by natural killer (NK) cells can be enhanced by a checkpoint-blocking mAb, 14-25-9, which we developed against proliferating cell nuclear antigen (PCNA). PCNA is expressed on the surface of cancer cells and acts as an inhibitory ligand for the NK-cell receptor, NKp44-isoform1.

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The Ebola virus (EBOV) uses evasion mechanisms that directly interfere with host T-cell antiviral responses. By steric shielding of human leukocyte antigen class-1, the Ebola glycoprotein (GP) blocks interaction with T-cell receptors (TCRs), thus rendering T cells unable to attack virus-infected cells. It is likely that this mechanism could promote increased natural killer (NK) cell activity against GP-expressing cells by preventing the engagement of NK inhibitory receptors; however, we found that primary human NK cells were less reactive to GP-expressing HEK293T cells.

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Proliferating cell nuclear antigen (PCNA) is considered as a hub protein and is a key regulator of DNA replication, repair, cell cycle control, and apoptosis. PCNA is overexpressed in many cancer types, and PCNA overexpression is correlated with cancer virulence. Membrane-associated PCNA is a ligand for the NKp44 (NCR2) innate immune receptor.

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Ebolavirus is a highly lethal pathogen, causing a severe hemorrhagic disease with a high fatality rate. To better understand immune correlates of protection by virus specific IgG, we investigated the evolution of the Fcγ receptors (FcγRs)-activating capabilities of antiviral IgG in serum samples of long recovered survivors. To this end, longitudinal serum samples from survivors of Sudan ebolavirus (SUDV) infection, studied over years, were examined for the presence of Ebola-GP specific IgG subclasses, and for their binding to FcγRs.

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The natural killer (NK) cell activating receptor NKp46/NCR1 plays a critical role in elimination of virus-infected and tumor cells. The gene can be transcribed into five different splice variants, but the functional importance and physiological distribution of NKp46 isoforms are not yet fully understood. Here, we shed light on differential expression of NKp46 splice variants in viral respiratory tract infections and their functional difference at the cellular level.

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The protective efficacy and immunogenicity of a chimeric peptide against West Nile virus (WNV) was evaluated. This virus is the aetiological agent of West Nile fever, which has recently emerged in the western hemisphere. The rapid spread of WNV throughout North America, as well as the constantly changing epidemiology and transmission of the virus by blood transfusion and transplantation, have raised major public-health concerns.

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Natural killer (NK) cells serve as a crucial first-line defense against tumors and virus-infected cells. We previously showed that lysis of influenza virus (IV)-infected cells is mediated by the interaction between the NK receptor, NKp46, and the IV hemagglutinin (HA) type 1 expressed by the infected cells. This interaction requires the presence of sialyl groups on the NKp46-T225 O-glycoforms.

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Dengue virus (DV) and West Nile virus (WNV) have become a global concern due to their widespread distribution and their ability to cause a variety of human diseases. Antiviral immune defenses involve NK cells. In the present study, we investigated the interaction between NK cells and these two flaviviruses.

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  • West Nile Virus (WNV) is common in Israel, and many people have developed antibodies against it through exposure, leading researchers to explore its use in treating severe infections.
  • OMRIX Biopharmaceuticals developed a method to select plasma from Israeli blood donors with anti-WNV antibodies to create a more potent treatment known as WNIG, which is significantly stronger than regular IVIG.
  • In experiments on mice, WNIG demonstrated much higher effectiveness in preventing and treating WNV infections, especially in immunosuppressed mice, suggesting it could be a valuable therapy for patients with severe WNV.
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