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    <title>Immunotherapy</title>
    <description></description>
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    <item>
      <title>GABA signaling linked to immune resistance in some tumors</title>
      <description>Certain cancers that contain organized clusters of immune cells known as tertiary lymphoid structures (TLS) do not respond to treatment as well as expected. Even though they have TLS that support the elimination of cancer cells, they remain resistant to immunotherapy. γ-Aminobutyric acid (GABA), better known as the brain’s major inhibitory neurotransmitter, may play a role in this lack of response by acting as an immunoregulatory metabolite, according to a study led by scientists at Sorbonne Université.</description>
      <content:encoded>
        <![CDATA[Certain cancers that contain organized clusters of immune cells known as tertiary lymphoid structures (TLS) do not respond to treatment as well as expected. Even though they have TLS that support the elimination of cancer cells, they remain resistant to immunotherapy. γ-Aminobutyric acid (GABA), better known as the brain’s major inhibitory neurotransmitter, may play a role in this lack of response by acting as an immunoregulatory metabolite, according to a study led by scientists at Sorbonne Université.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732642</guid>
      <pubDate>Wed, 15 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732642-gaba-signaling-linked-to-immune-resistance-in-some-tumors</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Immuno-oncology-TCells-attacking-cancer.webp?t=1784126243" type="image/jpeg" medium="image" fileSize="1371026">
        <media:title type="plain">Illustration of T cells attacking cancer</media:title>
      </media:content>
    </item>
    <item>
      <title>ASCO 2026: PD-(L)1 x VEGF bispecifics fight it out</title>
      <description>Multiple companies are chasing Akeso Inc. and Summit Therapeutics Inc. in the battle to potentially dethrone Keytruda (pembrolizumab, Merck &amp; Co. Inc.) as the top cancer immunotherapy for patients with non-small-cell lung cancer with bispecific antibodies targeting PD-(L)1 and VEGF.</description>
      <content:encoded>
        <![CDATA[Multiple companies are chasing Akeso Inc. and Summit Therapeutics Inc. in the battle to potentially dethrone Keytruda (pembrolizumab, Merck & Co. Inc.) as the top cancer immunotherapy for patients with non-small-cell lung cancer with bispecific antibodies targeting PD-(L)1 and VEGF.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731513</guid>
      <pubDate>Mon, 01 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731513-asco-2026-pd-l1-x-vegf-bispecifics-fight-it-out</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/3D-bispecific-antibody-immuno-oncology.webp?t=1695826102" type="image/jpeg" medium="image" fileSize="199545">
        <media:title type="plain">Bispecific antibodies with heavy chain in green and pink, light chain in blue and yellow</media:title>
      </media:content>
    </item>
    <item>
      <title>Valo raises €19M for immunotherapy work</title>
      <description>Finnish cancer immunotherapy specialist Valo Therapeutics Oy has raised €19 million (US$20.7 million) in a round that attracted Italian and Australian investors, and funding the company to the completion of the ongoing phase Ib trial of its lead program in the treatment of solid tumors.</description>
      <content:encoded>
        <![CDATA[Finnish cancer immunotherapy specialist Valo Therapeutics Oy has raised €19 million (US$20.7 million) in a round that attracted Italian and Australian investors, and funding the company to the completion of the ongoing phase Ib trial of its lead program in the treatment of solid tumors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/718113</guid>
      <pubDate>Tue, 11 Mar 2025 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/718113-valo-raises-19m-for-immunotherapy-work</link>
    </item>
    <item>
      <title>LTZ completes series A of more than $20M</title>
      <description>LTZ Therapeutics Inc. has completed a series A financing of more than $20 million to advance the development of its myeloid engager pipeline to treat cancer and autoimmune diseases. The closing of this round brings LTZ’s total funding to about $50 million.</description>
      <content:encoded>
        <![CDATA[LTZ Therapeutics Inc. has completed a series A financing of more than $20 million to advance the development of its myeloid engager pipeline to treat cancer and autoimmune diseases. The closing of this round brings LTZ’s total funding to about $50 million.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/711096</guid>
      <pubDate>Thu, 01 Aug 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/711096-ltz-completes-series-a-of-more-than-20m</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/finance-dollar-growth.webp?t=1638226495" type="image/png" medium="image" fileSize="416016">
        <media:title type="plain">Hand holding dollar sign</media:title>
      </media:content>
    </item>
    <item>
      <title>IAS 2024: Seventh HIV cure reported, but broad reach will take other approaches </title>
      <description>The 2024 meeting of the International AIDS Society (IAS), which is being held in Munich this week, began with the announcement of another curative bone marrow transplant. The new case brings the total number of patients cured of HIV via a bone marrow transplant up to 7 since “Berlin patient” Timothy Ray Brown became the first such person in 2007.</description>
      <content:encoded>
        <![CDATA[The 2024 meeting of the International AIDS Society (IAS), which is being held in Munich this week, began with the announcement of another curative bone marrow transplant. The new case brings the total number of patients cured of HIV via a bone marrow transplant up to 7 since “Berlin patient” Timothy Ray Brown became the first such person in 2007.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/710677</guid>
      <pubDate>Mon, 22 Jul 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/710677-ias-2024-seventh-hiv-cure-reported-but-broad-reach-will-take-other-approaches</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/HIV-AIDS-viral-structure.webp?t=1707321297" type="image/jpeg" medium="image" fileSize="238698">
        <media:title type="plain">Cross section illustration of HIV virus parts</media:title>
      </media:content>
    </item>
    <item>
      <title>Cancervax announces discovery of bispecific antibody vaccine for Ewing sarcoma</title>
      <description>A research team at University of California, Los Angeles (UCLA), funded by Cancervax Inc., has created a promising new bispecific antibody vaccine for treating recurrent Ewing sarcoma.</description>
      <content:encoded>
        <![CDATA[A research team at University of California, Los Angeles (UCLA), funded by Cancervax Inc., has created a promising new bispecific antibody vaccine for treating recurrent Ewing sarcoma. ]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/707627</guid>
      <pubDate>Tue, 16 Apr 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/707627-cancervax-announces-discovery-of-bispecific-antibody-vaccine-for-ewing-sarcoma</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Vaccine-research-vial-syringe.webp?t=1670859743" type="image/png" medium="image" fileSize="1080600">
        <media:title type="plain">Vaccine vial and syringe</media:title>
      </media:content>
    </item>
    <item>
      <title>New funding at Conformation-X supports pipeline of immune checkpoint inhibitors</title>
      <description>Conformation-X Therapeutics LLC has closed an oversubscribed funding tranche of $3.65 million to support the company’s development of a pipeline of immunotherapies that activate both the innate and adaptive arms of the immune system.</description>
      <content:encoded>
        <![CDATA[Conformation-X Therapeutics LLC has closed an oversubscribed funding tranche of $3.65 million to support the company’s development of a pipeline of immunotherapies that activate both the innate and adaptive arms of the immune system.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/707230</guid>
      <pubDate>Thu, 04 Apr 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/707230-new-funding-at-conformation-x-supports-pipeline-of-immune-checkpoint-inhibitors</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Immuno-oncology-checkpoint-inhibitors-PD-1-CTLA-4-PD-L1.webp?t=1666968950" type="image/png" medium="image" fileSize="1192319">
        <media:title type="plain">Immune checkpoint inhibitors illustration of PD-1, CTLA-4 and PD-L1.</media:title>
      </media:content>
    </item>
    <item>
      <title>Epitope editing in hematopoietic cells provides CAR T immunotherapy against all types of blood cancer</title>
      <description>A new method of CAR T-cell immunotherapy developed by researchers at the University of Pennsylvania Perelman School of Medicine could serve as a treatment for most blood cancers. Until now, CAR T-based immunotherapy for hematological malignancies has targeted the antigens CD19 for B cells, CD7 for T cells, BCMA for myeloma, and CD33 for AML.</description>
      <content:encoded>
        <![CDATA[A new method of CAR T-cell immunotherapy developed by researchers at the University of Pennsylvania Perelman School of Medicine could serve as a treatment for most blood cancers. Until now, CAR T-based immunotherapy for hematological malignancies has targeted the antigens CD19 for B cells, CD7 for T cells, BCMA for myeloma, and CD33 for AML.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/701164</guid>
      <pubDate>Fri, 22 Sep 2023 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/701164-epitope-editing-in-hematopoietic-cells-provides-car-t-immunotherapy-against-all-types-of-blood-cancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Genes-cells-DNA.webp?t=1588872593" type="image/png" medium="image" fileSize="499588">
        <media:title type="plain">Cells, DNA illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Hanchorbio and Henlius collaborate to develop novel cancer immunotherapies</title>
      <description>Hanchorbio Inc. and Shanghai Henlius Biotech Inc. have entered into a strategic framework agreement for collaboration to combine Hanchorbio’s protein engineering expertise and proprietary Fc-based designer biologics (FBDB) technology platform with Henlius’ integrated product development and commercialization capabilities.</description>
      <content:encoded>
        <![CDATA[Hanchorbio Inc. and Shanghai Henlius Biotech Inc. have entered into a strategic framework agreement for collaboration to combine Hanchorbio’s protein engineering expertise and proprietary Fc-based designer biologics (FBDB) technology platform with Henlius’ integrated product development and commercialization capabilities.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/700414</guid>
      <pubDate>Tue, 29 Aug 2023 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/700414-hanchorbio-and-henlius-collaborate-to-develop-novel-cancer-immunotherapies</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Cancer-cells-and-immunotherapy.webp?t=1623784162" type="image/png" medium="image" fileSize="495987">
        <media:title type="plain">Illustration of cancer cells and immunotherapy treatment</media:title>
      </media:content>
    </item>
    <item>
      <title>Killer T cells go after MHC-I-deficient tumors through NKG2D receptor</title>
      <description>Adaptative immune response mediated by NKG2D receptor and its ligand NKG2DL could be the clue for CD8-expressing “killer” T cells to kill tumors lacking the major histocompatibility complex (MHC) class I, according to a group of researchers at Duke University.</description>
      <content:encoded>
        <![CDATA[Adaptative immune response mediated by NKG2D receptor and its ligand NKG2DL could be the clue for CD8-expressing “killer” T cells to kill tumors lacking the major histocompatibility complex (MHC) class I, according to a group of researchers at Duke University.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/700309</guid>
      <pubDate>Thu, 24 Aug 2023 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/700309-killer-t-cells-go-after-mhc-i-deficient-tumors-through-nkg2d-receptor</link>
    </item>
    <item>
      <title>FDA clears Georgiamune’s IND application for GIM-122</title>
      <description>Georgiamune Inc. announced that the FDA cleared its IND application for GIM-122, a first-in-class dual-functioning monoclonal antibody designed to target a highly novel mechanism to overcome immunotherapy resistance.</description>
      <content:encoded>
        <![CDATA[Georgiamune Inc. announced that the FDA cleared its IND application for GIM-122, a first-in-class dual-functioning monoclonal antibody designed to target a highly novel mechanism to overcome immunotherapy resistance.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/699822</guid>
      <pubDate>Thu, 10 Aug 2023 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/699822-fda-clears-georgiamunes-ind-application-for-gim-122</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Antibodies-attacking-cancer-cell.webp?t=1621365766" type="image/png" medium="image" fileSize="566115">
        <media:title type="plain">Antibodies attacking cancer cell</media:title>
      </media:content>
    </item>
    <item>
      <title>Precision target discovery at forefront for immunotherapy startup Cartography</title>
      <description>Most drug developers working in the immunotherapy space focus on existing therapeutic targets when developing cancer drugs, optimizing ways of drugging them via engineering modalities such as CAR T-cell approaches, CRISPR editing or antibody-drug conjugates that deliver toxic payloads. The angle of one company – Cartography Biosciences – is the opposite to this. Its modus operandi is to pinpoint the immunological targets first, leveraging tools that already exist, before building therapies around them.</description>
      <content:encoded>
        <![CDATA[Most drug developers working in the immunotherapy space focus on existing therapeutic targets when developing cancer drugs, optimizing ways of drugging them via engineering modalities such as CAR T-cell approaches, CRISPR editing or antibody-drug conjugates that deliver toxic payloads. The angle of one company – Cartography Biosciences – is the opposite to this. Its modus operandi is to pinpoint the immunological targets first, leveraging tools that already exist, before building therapies around them.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/698815</guid>
      <pubDate>Tue, 11 Jul 2023 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/698815-precision-target-discovery-at-forefront-for-immunotherapy-startup-cartography</link>
      <media:content url="https://www.bioworld.com/ext/resources/BW-source/2023/Cartography-immunotherapy-target-illustration-7-5.webp?t=1688587139" type="image/jpeg" medium="image" fileSize="115012">
        <media:title type="plain">Cartography immunotherapy target illustratio</media:title>
        <media:description type="plain">Credit: Cartography Biosciences</media:description>
      </media:content>
    </item>
    <item>
      <title>Precision target discovery at forefront for immunotherapy startup Cartography</title>
      <description>Most drug developers working in the immunotherapy space focus on existing therapeutic targets when developing cancer drugs, optimizing ways of drugging them via engineering modalities such as CAR T-cell approaches, CRISPR editing or antibody-drug conjugates that deliver toxic payloads. The angle of one company – Cartography Biosciences – is the opposite to this. Its modus operandi is to pinpoint the immunological targets first, leveraging tools that already exist, before building therapies around them.</description>
      <content:encoded>
        <![CDATA[Most drug developers working in the immunotherapy space focus on existing therapeutic targets when developing cancer drugs, optimizing ways of drugging them via engineering modalities such as CAR T-cell approaches, CRISPR editing or antibody-drug conjugates that deliver toxic payloads. The angle of one company – Cartography Biosciences – is the opposite to this. Its modus operandi is to pinpoint the immunological targets first, leveraging tools that already exist, before building therapies around them.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/698678</guid>
      <pubDate>Wed, 05 Jul 2023 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/698678-precision-target-discovery-at-forefront-for-immunotherapy-startup-cartography</link>
      <media:content url="https://www.bioworld.com/ext/resources/BW-source/2023/Cartography-immunotherapy-target-illustration-7-5.webp?t=1688587139" type="image/jpeg" medium="image" fileSize="115012">
        <media:title type="plain">Cartography immunotherapy target illustratio</media:title>
        <media:description type="plain">Credit: Cartography Biosciences</media:description>
      </media:content>
    </item>
    <item>
      <title>Macrophages drive invasive breast cancer</title>
      <description>T cells do not have the last word in some breast cancers. According to a study from the University of Pittsburgh, the key to estrogen receptor positive (ER+) breast tumors are macrophages, not T cells, and targeting them could prevent immunotherapy failure in this type of cancer.</description>
      <content:encoded>
        <![CDATA[T cells do not have the last word in some breast cancers. According to a study from the University of Pittsburgh, the key to estrogen receptor positive (ER+) breast tumors are macrophages, not T cells, and targeting them could prevent immunotherapy failure in this type of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/695254</guid>
      <pubDate>Mon, 20 Mar 2023 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/695254-macrophages-drive-invasive-breast-cancer</link>
    </item>
    <item>
      <title>Releasing T cells from neutrophil traps restores immunotherapy in pancreatic cancer</title>
      <description>The traps that neutrophils develop against microorganisms also hold T cells and prevent the success of immunotherapy in pancreatic cancer. To free the immune system from itself, scientists at the Istituto Oncologico Veneto in Italy made a key that unlocked this sticky dungeon from an antibody against arginase-1 (ARG1), an enzyme also present in the trap.</description>
      <content:encoded>
        <![CDATA[The traps that neutrophils develop against microorganisms also hold T cells and prevent the success of immunotherapy in pancreatic cancer. To free the immune system from itself, scientists at the Istituto Oncologico Veneto in Italy made a key that unlocked this sticky dungeon from an antibody against arginase-1 (ARG1), an enzyme also present in the trap.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/695194</guid>
      <pubDate>Thu, 16 Mar 2023 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/695194-releasing-t-cells-from-neutrophil-traps-restores-immunotherapy-in-pancreatic-cancer</link>
    </item>
    <item>
      <title>Rise Therapeutics to advance R-3750 immunotherapy for ulcerative colitis</title>
      <description>Rise Therapeutics LLC has received FDA clearance for its IND application to proceed with a phase I trial of R-3750, a synthetic biology-based cellular immunotherapy being developed for the treatment of inflammatory bowel disease. The phase I trial will enroll patients with mild to moderate ulcerative.</description>
      <content:encoded>
        <![CDATA[Rise Therapeutics LLC has received FDA clearance for its IND application to proceed with a phase I trial of R-3750, a synthetic biology-based cellular immunotherapy being developed for the treatment of inflammatory bowel disease. The phase I trial will enroll patients with mild to moderate ulcerative.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/693835</guid>
      <pubDate>Wed, 01 Feb 2023 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/693835-rise-therapeutics-to-advance-r-3750-immunotherapy-for-ulcerative-colitis</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/IBD-ulcerative-colitis.webp?t=1668182386" type="image/png" medium="image" fileSize="1246429">
        <media:title type="plain">Gastrointestinal system with ulcerative colitis.</media:title>
      </media:content>
    </item>
    <item>
      <title>Redeeming neutrophils could be anticancer approach</title>
      <description>Unexpected behavior of neutrophils unveiled by researchers at Stanford University could lead to a new type of immunotherapy to treat cancer. Although various studies have suggested that these cells are harmful due to their immunosuppressive characteristics, the scientists saw in them an opportunity to redirect them and eliminate tumors.</description>
      <content:encoded>
        <![CDATA[Unexpected behavior of neutrophils unveiled by researchers at Stanford University could lead to a new type of immunotherapy to treat cancer. Although various studies have suggested that these cells are harmful due to their immunosuppressive characteristics, the scientists saw in them an opportunity to redirect them and eliminate tumors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/693677</guid>
      <pubDate>Fri, 27 Jan 2023 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/693677-redeeming-neutrophils-could-be-anticancer-approach</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Hematologic/Neutrophil-and-red-blood-cells.webp?t=1665000404" type="image/png" medium="image" fileSize="335030">
        <media:title type="plain">Neutrophil and red blood cells</media:title>
      </media:content>
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    <item>
      <title>Oncogene activation during immunotherapy triggers cancer hyperprogression</title>
      <description>Immunotherapy, a treatment that increases the survival of cancer patients to the point of remission of the disease, can also have the opposite effect. In some patients, immune checkpoint blockade accelerates cancer. Now, researchers at the University of Michigan Medical School have discovered that the answer to this hyperprogressive disease (HPD) lies in the interconnection of the molecular pathways of interferon signaling (IFNγ), fibroblast growth factor 2 (FGF2) and the β-catenin protein.</description>
      <content:encoded>
        <![CDATA[Immunotherapy, a treatment that increases the survival of cancer patients to the point of remission of the disease, can also have the opposite effect. In some patients, immune checkpoint blockade accelerates cancer. Now, researchers at the University of Michigan Medical School have discovered that the answer to this hyperprogressive disease (HPD) lies in the interconnection of the molecular pathways of interferon signaling (IFNγ), fibroblast growth factor 2 (FGF2) and the β-catenin protein.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/693355</guid>
      <pubDate>Fri, 20 Jan 2023 06:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/693355-oncogene-activation-during-immunotherapy-triggers-cancer-hyperprogression</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Cancer-cell-under-magnifying-glass.webp?t=1611092780" type="image/png" medium="image" fileSize="453785">
        <media:title type="plain">Cancer cells under magnifying glass</media:title>
      </media:content>
    </item>
    <item>
      <title>Cofactor Genomics expands PREDAPT study to NSCLC</title>
      <description>Cofactor Genomics Inc. opened the non-small-cell lung cancer portion of its study of the Oncoprism test, which predicts response to immunotherapy. The Predicting Immunotherapy Efficacy from Analysis of Pre-treatment Tumor Biopsies (PREDAPT) trial will study the test’s predictive ability in 11 cancers in total.</description>
      <content:encoded>
        <![CDATA[Cofactor Genomics Inc. opened the non-small-cell lung cancer portion of its study of the Oncoprism test, which predicts response to immunotherapy. The Predicting Immunotherapy Efficacy from Analysis of Pre-treatment Tumor Biopsies (PREDAPT) trial will study the test’s predictive ability in 11 cancers in total.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/692557</guid>
      <pubDate>Fri, 16 Dec 2022 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/692557-cofactor-genomics-expands-predapt-study-to-nsclc</link>
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    <item>
      <title>Blocking the KIR2DL5/PVR pathway boosts NK cell-based cancer immunotherapy</title>
      <description>NK cell-based cancer immunotherapy has emerged as an anticancer treatment approach and is currently being tested in clinical trials. KIR2DL5, a member of the human killer cell immunoglobulin-like receptor (KIR) family, has recently been identified as a binding partner for poliovirus receptor (PVR). However, the biology and therapeutic potential of the KIR2DL5/PVR pathway remain widely unexplored.</description>
      <content:encoded>
        <![CDATA[NK cell-based cancer immunotherapy has emerged as an anticancer treatment approach and is currently being tested in clinical trials. KIR2DL5, a member of the human killer cell immunoglobulin-like receptor (KIR) family, has recently been identified as a binding partner for poliovirus receptor (PVR). However, the biology and therapeutic potential of the KIR2DL5/PVR pathway remain widely unexplored.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/692084</guid>
      <pubDate>Wed, 07 Dec 2022 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/692084-blocking-the-kir2dl5-pvr-pathway-boosts-nk-cell-based-cancer-immunotherapy</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Human-natural-killer-cell.webp?t=1613505013" type="image/png" medium="image" fileSize="207424">
        <media:title type="plain">Human natural killer cell</media:title>
        <media:description type="plain">Colorized scanning electron micrograph of a natural killer cell from a human donor. Credit: NIAID</media:description>
      </media:content>
    </item>
    <item>
      <title>New hydrogel-based delivery platform exploits gasdermin-induced tumor pyroptosis to kill tumor cells</title>
      <description>Previous research has shown that cytotoxic lymphocytes rely on gasdermin-mediated pyroptosis to kill tumor cells. Pyroptosis appears to be closely involved in anticancer immune response and has therefore emerged as a promising strategy for cancer treatment. In a recently published study, scientists at the University of Wisconsin-Madison aimed to leverage gasdermin-triggered pyroptosis for antitumor immunotherapy.</description>
      <content:encoded>
        <![CDATA[Previous research has shown that cytotoxic lymphocytes rely on gasdermin-mediated pyroptosis to kill tumor cells. Pyroptosis appears to be closely involved in anticancer immune response and has therefore emerged as a promising strategy for cancer treatment. In a recently published study, scientists at the University of Wisconsin-Madison aimed to leverage gasdermin-triggered pyroptosis for antitumor immunotherapy.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/692078</guid>
      <pubDate>Wed, 07 Dec 2022 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/692078-new-hydrogel-based-delivery-platform-exploits-gasdermin-induced-tumor-pyroptosis-to-kill-tumor-cells</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Cancer-cells-and-immunotherapy.webp?t=1623784162" type="image/png" medium="image" fileSize="495987">
        <media:title type="plain">Illustration of cancer cells and immunotherapy treatment</media:title>
      </media:content>
    </item>
    <item>
      <title>Sana outlines preclinical pipeline progress following portfolio prioritization</title>
      <description>Sana Biotechnology Inc. has outlined the status of its pipeline following a portfolio prioritization. The company remains on track to file an IND this year for SC-291, the company's HIP-modified, CD19-targeted allogeneic chimeric antigen receptor (CAR) T therapy, with initial clinical data expected next year.</description>
      <content:encoded>
        <![CDATA[Sana Biotechnology Inc. has outlined the status of its pipeline following a portfolio prioritization. The company remains on track to file an IND this year for SC-291, the company's HIP-modified, CD19-targeted allogeneic chimeric antigen receptor (CAR) T therapy, with initial clinical data expected next year.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/691980</guid>
      <pubDate>Wed, 30 Nov 2022 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/691980-sana-outlines-preclinical-pipeline-progress-following-portfolio-prioritization</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/CAR-T-cell-with-gene-strand.webp?t=1663195081" type="image/png" medium="image" fileSize="367541">
        <media:title type="plain">CAR T cell with implanted gene strand</media:title>
      </media:content>
    </item>
    <item>
      <title>[177Lu]PNT-6555 with immunotherapy increases survival benefit in anti-PD-1 resistant tumor model</title>
      <description>Point Biopharma Global Inc. has released new preclinical data from its pan-cancer fibroblast activation protein-α (FAP-α) targeted program, PNT-2004. The preclinical study focused on assessing the potential of the lead candidate in the PNT-2004 clinical program, [177Lu]PNT-6555, in combination with anti-programmed cell death protein 1 (PD-1) immunotherapy.</description>
      <content:encoded>
        <![CDATA[Point Biopharma Global Inc. has released new preclinical data from its pan-cancer fibroblast activation protein-α (FAP-α) targeted program, PNT-2004. The preclinical study focused on assessing the potential of the lead candidate in the PNT-2004 clinical program, [177Lu]PNT-6555, in combination with anti-programmed cell death protein 1 (PD-1) immunotherapy.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/691979</guid>
      <pubDate>Wed, 30 Nov 2022 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/691979-177lupnt-6555-with-immunotherapy-increases-survival-benefit-in-anti-pd-1-resistant-tumor-model</link>
    </item>
    <item>
      <title>Umoja and Iaso partner to advance off-the-shelf therapies for hematological malignancies</title>
      <description>Umoja Biopharma Inc. and Nanjing Iaso Biotherapeutics Co. Ltd. have entered into a research agreement to evaluate Umoja's ICIL (induced cytotoxic innate lymphocytes) platform with Iaso's best-in-class chimeric antigen receptors (CARs).</description>
      <content:encoded>
        <![CDATA[Umoja Biopharma Inc. and Nanjing Iaso Biotherapeutics Co. Ltd. have entered into a research agreement to evaluate Umoja's ICIL (induced cytotoxic innate lymphocytes) platform with Iaso's best-in-class chimeric antigen receptors (CARs).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/691804</guid>
      <pubDate>Tue, 22 Nov 2022 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/691804-umoja-and-iaso-partner-to-advance-off-the-shelf-therapies-for-hematological-malignancies</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Acute-myeloid-leukemia.webp?t=1588879994" type="image/png" medium="image" fileSize="485631">
        <media:title type="plain">Acute myeloid leukemia illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Sensei collaborates with Washington University to elucidate SNS-101's mechanism of antitumor activity</title>
      <description>Sensei Biotherapeutics Inc. has entered into a sponsored research agreement with Washington University in St. Louis to support development of SNS-101, a conditionally active V-type immunoglobulin domain-containing suppressor of T-cell activation (VISTA)-blocking antibody.</description>
      <content:encoded>
        <![CDATA[Sensei Biotherapeutics Inc. has entered into a sponsored research agreement with Washington University in St. Louis to support development of SNS-101, a conditionally active V-type immunoglobulin domain-containing suppressor of T-cell activation (VISTA)-blocking antibody.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/691803</guid>
      <pubDate>Tue, 22 Nov 2022 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/691803-sensei-collaborates-with-washington-university-to-elucidate-sns-101s-mechanism-of-antitumor-activity</link>
    </item>
    <item>
      <title>FDA approves orphan drug application for TLR-AD1 immunotherapy</title>
      <description>Novaccess Global Inc. has announced the approval of its application with the FDA for orphan drug designation for TLR-AD1, a vaccine immunotherapy for the treatment of aggressive brain cancers, including glioblastoma and other high-grade gliomas. The company’s therapeutic path involves a unique transformational process, which involves the addition of proprietary substances to create a cocktail for more personalized treatment that substantially increases clinical benefits for patients.</description>
      <content:encoded>
        <![CDATA[Novaccess Global Inc. has announced the approval of its application with the FDA for orphan drug designation for TLR-AD1, a vaccine immunotherapy for the treatment of aggressive brain cancers, including glioblastoma and other high-grade gliomas. The company’s therapeutic path involves a unique transformational process, which involves the addition of proprietary substances to create a cocktail for more personalized treatment that substantially increases clinical benefits for patients.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/691009</guid>
      <pubDate>Thu, 27 Oct 2022 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/691009-fda-approves-orphan-drug-application-for-tlr-ad1-immunotherapy</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/3D-head-brain-cancer.webp?t=1588879177" type="image/png" medium="image" fileSize="203697">
        <media:title type="plain">Brain cancer illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>LB-101, a novel LockBody immunotherapy candidate targeting solid tumors</title>
      <description>Researchers from Centessa Pharmaceuticals plc presented preclinical data for LB-101, a novel first-in-class immunotherapy targeting solid tumors.</description>
      <content:encoded>
        <![CDATA[Researchers from Centessa Pharmaceuticals plc presented preclinical data for LB-101, a novel first-in-class immunotherapy targeting solid tumors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/689684</guid>
      <pubDate>Thu, 15 Sep 2022 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/689684-lb-101-a-novel-lockbody-immunotherapy-candidate-targeting-solid-tumors</link>
    </item>
    <item>
      <title>Bioengineered multifunctional exosomes evoke cancer immunity</title>
      <description>The design of genetically modified exosomes that combine multiple targets killed cancer cells and conferred immunity against them. Scientists at the University of Southern California (USC) applied bioengineering techniques to introduce up to four antitumor functions in the same type of extracellular vesicles and destroy EGFR-positive triple-negative breast cancer (TNBC) tumor cells.</description>
      <content:encoded>
        <![CDATA[The design of genetically modified exosomes that combine multiple targets killed cancer cells and conferred immunity against them. Scientists at the University of Southern California (USC) applied bioengineering techniques to introduce up to four antitumor functions in the same type of extracellular vesicles and destroy EGFR-positive triple-negative breast cancer (TNBC) tumor cells.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/689626</guid>
      <pubDate>Wed, 14 Sep 2022 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/689626-bioengineered-multifunctional-exosomes-evoke-cancer-immunity</link>
    </item>
    <item>
      <title>MC5R antagonism enhances tumor immunity in ICT-resistant cancers</title>
      <description>Previous research has revealed that some downstream hormones or effectors of the hypothalamic-pituitary (HP) unit, such as glucocorticoids, estrogen and progesterone, are elevated in patients with cancer. It was also shown that these hormones regulate the function of immune cells in the tumor microenvironment, suggesting that the neuroendocrine system and HP unit might modulate tumor immunity. In the current study, researchers from the University of Science and Technology of China aimed to investigate the role of HP unit in tumor immunity.</description>
      <content:encoded>
        <![CDATA[Previous research has revealed that some downstream hormones or effectors of the hypothalamic-pituitary (HP) unit, such as glucocorticoids, estrogen and progesterone, are elevated in patients with cancer. It was also shown that these hormones regulate the function of immune cells in the tumor microenvironment, suggesting that the neuroendocrine system and HP unit might modulate tumor immunity. In the current study, researchers from the University of Science and Technology of China aimed to investigate the role of HP unit in tumor immunity.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/689575</guid>
      <pubDate>Tue, 13 Sep 2022 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/689575-mc5r-antagonism-enhances-tumor-immunity-in-ict-resistant-cancers</link>
    </item>
    <item>
      <title>NR2F6 antagonist TES-4207 shows promising preclinical results for cancer</title>
      <description>The interaction of immune checkpoints, such as programmed cell death protein 1 (PD-1) or cytotoxic T-lymphocyte antigen-4 (CTLA-4), with their ligands leads to T-cell deactivation, allowing cancer cells to escape from the immune system.</description>
      <content:encoded>
        <![CDATA[The interaction of immune checkpoints, such as programmed cell death protein 1 (PD-1) or cytotoxic T-lymphocyte antigen-4 (CTLA-4), with their ligands leads to T-cell deactivation, allowing cancer cells to escape from the immune system.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/689500</guid>
      <pubDate>Fri, 09 Sep 2022 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/689500-nr2f6-antagonist-tes-4207-shows-promising-preclinical-results-for-cancer</link>
    </item>
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