keyword
https://read.qxmd.com/read/38651308/antibody-drug-conjugates-design-implications-for-clinicians
#21
REVIEW
Stephanie Pang, Arianne Duong, Chloe Siu, Amy Indorf
OBJECTIVE: There are currently 11 antibody-drug conjugates (ADC) that are FDA approved for use in oncologic disease states, with many more in the pipeline. The authors aim to review the pharmacokinetic profiles of the components of ADCs to engage pharmacist practitioners in practical considerations in the care of patients. This article provides an overview on the use of ADCs in the setting of organ dysfunction, drug-drug interactions, and management of on- and off-target adverse effects...
April 23, 2024: Journal of Oncology Pharmacy Practice
https://read.qxmd.com/read/38651269/accelerated-generation-of-gene-engineered-monoclonal-cho-cell-lines-using-fluidfm-nanoinjection-and-crispr-cas9
#22
JOURNAL ARTICLE
Justin S Antony, Anabel Migenda Herranz, Tahereh Mohammadian Gol, Susanne Mailand, Paul Monnier, Jennifer Rottenberger, Alicia Roig-Merino, Bettina Keller, Claudia Gowin, Maria Milla, Tobias A Beyer, Markus Mezger
Chinese hamster ovary (CHO) cells are the commonly used mammalian host system to manufacture recombinant proteins including monoclonal antibodies. However unfavorable non-human glycoprofile displayed on CHO-produced monoclonal antibodies have negative impacts on product quality, pharmacokinetics, and therapeutic efficiency. Glycoengineering such as genetic elimination of genes involved in glycosylation pathway in CHO cells is a viable solution but constrained due to longer timeline and laborious workflow. Here, in this proof-of-concept (PoC) study, we present a novel approach coined CellEDIT to engineer CHO cells by intranuclear delivery of the CRISPR components to single cells using the FluidFM technology...
April 2024: Biotechnology Journal
https://read.qxmd.com/read/38651187/pd-1-inhibition-with-retifanlimab-and-or-arginase-inhibition-with-incb001158-in-japanese-patients-with-solid-tumors-a-phase-i-study
#23
JOURNAL ARTICLE
Yasutoshi Kuboki, Takafumi Koyama, Nobuaki Matsubara, Yoichi Naito, Shunsuke Kondo, Kenichi Harano, Kan Yonemori, Kiyotaka Yoh, Yuan Gu, Tetsuya Mita, Xuejun Chen, Eiji Ueda, Noboru Yamamoto, Toshihiko Doi, Toshio Shimizu
BACKGROUND: Retifanlimab is a humanized monoclonal antibody targeting programmed death protein-1, and INCB001158 is an oral arginase inhibitor. This phase Ib study investigated retifanlimab, INCB001158, and their combination in Japanese patients with advanced solid tumors. METHODS: Patients received retifanlimab (500 mg every 4 weeks [Q4W] i.v.) or escalating doses of INCB001158 (75 or 100 mg twice daily [BID]) monotherapy in Part 1 and combination of retifanlimab (500 mg Q4W) and INCB001158 (100 mg BID) in Part 2...
April 2024: Cancer Medicine
https://read.qxmd.com/read/38650925/bi-isotype-immunoglobulins-enhance-antibody-mediated-neutrophil-activity-against-plasmodium-falciparum-parasites
#24
JOURNAL ARTICLE
Rodney Ogwang, Lewis Murugu, Irene N Nkumama, Lydia Nyamako, Oscar Kai, Kennedy Mwai, Linda Murungi, Richard Idro, Philip Bejon, James Tuju, Sam Muchina Kinyanjui, Faith H A Osier
BACKGROUND: Malaria remains a major global health priority, and monoclonal antibodies (mAbs) are emerging as potential new tools to support efforts to control the disease. Recent data suggest that Fc-dependent mechanisms of immunity are important mediators of protection against the blood stages of the infection, but few studies have investigated this in the context of mAbs. We aimed to isolate mAbs agnostic to cognate antigens that target whole merozoites and simultaneously induce potent neutrophil activity measured by the level of reactive oxygen species (ROS) production using an antibody-dependent respiratory burst (ADRB) assay...
2024: Frontiers in Immunology
https://read.qxmd.com/read/38650754/pd-1-blockade-induced-hemophagocytic-lymphohistiocytosis-a-dilemma-therapeutic-outcome-in-2-patients-with-caebv-a-case-series
#25
LeiLei Chen, Jingshi Wang, Zhao Wang
Hemophagocytic lymphohistiocytosis (HLH), whether primary or secondary, is a rare and fatal clinical syndrome of uncontrolled immune activation and inflammatory cascade. Immune checkpoint inhibitors (ICIs) induced HLH has no standard diagnostic and treatment guidelines. Early diagnosis and appropriate treatment according to different disease backgrounds are crucial. Herein, we first report 2 cases of patients with chronic active Epstein-Barr virus infection (CAEBV) who developed HLH after the use of sintilimab, a monoclonal antibody against programmed cell death protein 1 (PD-1), and the DEP (liposomal doxorubicin, etoposide, methylprednisolone) chemotherapy regimen in combination with ruxolitinib were used to successfully control the disease...
2024: Infection and Drug Resistance
https://read.qxmd.com/read/38650583/the-cost-effectiveness-of-a-bimekizumab-versus-il-17a-inhibitors-treatment-pathway-in-patients-with-active-axial-spondyloarthritis-in-scotland
#26
JOURNAL ARTICLE
Michael F Mørup, Vanessa Taieb, Damon Willems, Micah Rose, Nikos Lyris, Mark Lamotte, Laetitia Gerlier, Howard Thom
AIMS: To estimate the cost-effectiveness of a treatment-pathway initiated with bimekizumab, a monoclonal IgG1 antibody that selectively inhibits interleukin (IL)-17F in addition to IL-17A, in patients with axial spondyloarthritis (axSpA) compared with IL-17A inhibitors, ixekizumab, and secukinumab, from the National Health Service (NHS) of Scotland perspective. METHODS: The axSpA treatment-pathway was modeled using a one-year decision tree followed by a lifetime Markov model...
April 23, 2024: Journal of Medical Economics
https://read.qxmd.com/read/38650451/alternative-splicing-for-tuneable-expression-of-protein-subunits-at-desired-ratios
#27
JOURNAL ARTICLE
Christel Aebischer-Gumy, Pierre Moretti, Timothee Brunstein Laplace, Jana Frank, Ysaline Grand, Farid Mosbaoui, Emilie Hily, Anna Galea, Megane Peltret, Carole Estoppey, Daniel Ayoub, Roberto Giovannini, Martin Bertschinger
The controlled expression of two or more proteins at a defined and stable ratio remains a substantial challenge, particularly in the bi- and multispecific antibody field. Achieving an optimal ratio of protein subunits can facilitate the assembly of multimeric proteins with high efficiency and minimize the production of by-products. In this study, we propose a solution based on alternative splicing, enabling the expression of a tunable and predefined ratio of two distinct polypeptide chains from the same pre-mRNA under the control of a single promoter...
2024: MAbs
https://read.qxmd.com/read/38650002/correction-vegf-a-vegfr-1-signalling-and-chemotherapy-induced-neuropathic-pain-therapeutic-potential-of-a-novel-anti-vegfr-1-monoclonal-antibody
#28
Laura Micheli, Carmen Parisio, Elena Lucarini, Alessia Vona, Alessandra Toti, Alessandra Pacini, Tommaso Mello, Serena Boccella, Flavia Ricciardi, Sabatino Maione, Grazia Graziani, Pedro Miguel Lacal, Paola Failli, Carla Ghelardini, Lorenzo Di Cesare Mannelli
No abstract text is available yet for this article.
April 23, 2024: Journal of Experimental & Clinical Cancer Research: CR
https://read.qxmd.com/read/38649824/characteristics-and-outcomes-of-covid-19-patients-presumed-to-be-treated-with-sotrovimab-in-nhs-hospitals-in-england
#29
JOURNAL ARTICLE
Vishal Patel, Bethany Levick, Stephen Boult, Daniel C Gibbons, Myriam Drysdale, Emily J Lloyd, Moushmi Singh, Helen J Birch
BACKGROUND: The impact of the constantly evolving severe acute respiratory syndrome coronavirus 2 on the effectiveness of early coronavirus disease 2019 (COVID-19) treatments is unclear. Here, we report characteristics and acute clinical outcomes of patients with COVID-19 treated with a monoclonal antibody (mAb; presumed to be sotrovimab) across six distinct periods covering the emergence and predominance of Omicron subvariants (BA.1, BA.2, and BA.5) in England. METHODS: Retrospective cohort study using data from the Hospital Episode Statistics database from January 1-July 31, 2022...
April 22, 2024: BMC Infectious Diseases
https://read.qxmd.com/read/38649079/structural-basis-for-the-recognition-of-ifnar1-by-the-humanized-therapeutic-monoclonal-antibody-qx006n-for-the-treatment-of-systemic-lupus-erythematosus
#30
JOURNAL ARTICLE
Xiaorong Chen, Huimin Ke, Wei Li, Lu Yin, Wei Chen, Tao Chen, Yiliang Wu, Jiwan Qiu, Wei Feng
Interferon (IFN) alpha/beta receptor 1 (IFNAR1) is indispensable for antiviral responses and the immune regulation. Dysregulation of the IFNAR1-mediaetd signaling pathways leads to deleterious autoimmune diseases such as systemic lupus erythematosus (SLE). QX006N, a humanized therapeutic monoclonal antibody, specifically targets human IFNAR1 and is in the clinical trial phase for treating SLE, but the molecular mechanism underlying the QX006N-mediated recognition of IFNAR1 remains unclear. Here, we report the high neutralization activities of QX006N against IFNAR1-mediated signal transduction...
April 20, 2024: International Journal of Biological Macromolecules
https://read.qxmd.com/read/38648796/tight-junction-proteins-as-therapeutic-targets-to-treat-liver-fibrosis-and-hepatocellular-carcinoma
#31
JOURNAL ARTICLE
Antonio Saviano, Natascha Roehlen, Thomas F Baumert
In the last decade tight junction proteins exposed at the surface of liver or cancer cells have been uncovered as mediators of liver disease biology: Claudin-1 and Occludin are host factors for hepatitis C virus entry and Claudin-1 has been identified as a driver for liver fibrosis and hepatocellular carcinoma (HCC). Moreover, Claudins have emerged as therapeutic targets for liver disease and HCC. CLDN1 expression is upregulated in liver fibrosis and HCC. Monoclonal antibodies (mAbs) targeting Claudin-1 have completed preclinical proof-of-concept studies for treatment of liver fibrosis and HCC and are currently in clinical development for advanced liver fibrosis...
April 22, 2024: Seminars in Liver Disease
https://read.qxmd.com/read/38648728/research-strategies-of-small-molecules-as-chemotherapeutics-to-overcome-multiple-myeloma-resistance
#32
REVIEW
Jin Yang, Yan-Cheng Yu, Zi-Xuan Wang, Qing-Qing Li, Ning Ding, Xue-Jiao Leng, Jiao Cai, Meng-Yuan Zhang, Jing-Jing Wang, Yun Zhou, Tian-Hua Wei, Xin Xue, Wei-Chen Dai, Shan-Liang Sun, Ye Yang, Nian-Guang Li, Zhi-Hao Shi
Multiple myeloma (MM), a cancer of plasma cells, is the second most common hematological malignancy which is characterized by aberrant plasma cells infiltration in the bone marrow and complex heterogeneous cytogenetic abnormalities. Over the past two decades, novel treatment strategies such as proteasome inhibitors, immunomodulators, and monoclonal antibodies have significantly improved the relative survival rate of MM patients. However, the development of drug resistance results in the majority of MM patients suffering from relapse, limited treatment options and uncontrolled disease progression after relapse...
April 20, 2024: European Journal of Medicinal Chemistry
https://read.qxmd.com/read/38648666/best-practice-for-therapeutic-drug-monitoring-of-infliximab-position-statement-from-the-international-association-of-therapeutic-drug-monitoring-and-clinical-toxicology
#33
JOURNAL ARTICLE
Dahham Alsoud, Dirk Jan A R Moes, Zhigang Wang, Rani Soenen, Zohra Layegh, Murray Barclay, Tomoyuki Mizuno, Iris K Minichmayr, Ron J Keizer, Sebastian G Wicha, Gertjan Wolbink, Jo Lambert, Séverine Vermeire, Annick de Vries, Konstantinos Papamichael, Núria Padullés-Zamora, Erwin Dreesen
BACKGROUND: Infliximab, an anti-tumor necrosis factor monoclonal antibody, has revolutionized the pharmacological management of immune-mediated inflammatory diseases (IMIDs). This position statement critically reviews and examines existing data on therapeutic drug monitoring (TDM) of infliximab in patients with IMIDs. It provides a practical guide on implementing TDM in current clinical practices and outlines priority areas for future research. METHODS: The endorsing TDM of Biologics and Pharmacometrics Committees of the International Association of TDM and Clinical Toxicology collaborated to create this position statement...
April 17, 2024: Therapeutic Drug Monitoring
https://read.qxmd.com/read/38648663/tacrolimus-monitoring-in-liver-transplant-recipients-posttransplant-cholestasis-a-comparative-between-2-commercial-immunoassays-and-a-liquid-chromatography-tandem-mass-spectrometry-method
#34
JOURNAL ARTICLE
François Parant, Marie-Charlotte Delignette, Bruno Charpiat, Louis Lacaille, Fanny Lebosse, Guillaume Monneret, Kayvan Mohkam, Jean-Yves Mabrut, Frederic Aubrun, Laurent Heyer, Teresa Antonini
BACKGROUND: Cholestasis commonly occurs after orthotopic liver transplantation. It can be extrahepatic because of mechanical obstruction or intrahepatic because of various causes. During cholestasis episodes, blood concentrations of tacrolimus (TAC) metabolites may increase, potentially affecting TAC concentrations measured by immunoassays. This study aimed to simultaneously evaluate the analytical performance of 2 TAC immunoassays, a quantitative microsphere system (QMS) immunoassay, and chemiluminescence microparticle immunoassay, using liquid chromatography-tandem mass spectrometry (LC-MS/MS) as a reference method in liver transplant recipients...
April 19, 2024: Therapeutic Drug Monitoring
https://read.qxmd.com/read/38648242/risankizumab-as-a-therapeutic-approach-for-recalcitrant-pyoderma-gangrenosum
#35
JOURNAL ARTICLE
Alessandra Michelucci, Flavia Manzo Margiotta, Giammarco Granieri, Giorgia Salvia, Cristian Fidanzi, Matteo Bevilacqua, Salvatore Panduri, Marco Romanelli, Valentina Dini
Pyoderma gangrenosum (PG) is a neutrophilic dermatosis that is challenging to diagnose and treat. Clinicians frequently use fast-acting corticosteroids, which are subsequently combined with slower-acting immunosuppressants to progressively taper the corticosteroid dosage. Current research is focused on the use of monoclonal antibodies (mAbs) directed against target molecules involved in the pathogenesis of PG. However, available data on their efficacy are based on sporadic case reports and clinical experiences, so the authors aimed to evaluate the efficacy of risankizumab, an anti-interleukin-23 mAb, in the management of two complex PG cases...
May 1, 2024: Advances in Skin & Wound Care
https://read.qxmd.com/read/38648067/anti-tumor-activity-of-a-novel-lair1-antagonist-in-combination-with-anti-pd-1-to-treat-collagen-rich-solid-tumors
#36
JOURNAL ARTICLE
B Leticia Rodriguez, Jiawei Huang, Laura Gibson, Jared J Fradette, Hung-I H Chen, Kikuye Koyano, Czrina Cortez, Betty Li, Carmence Ho, Amir M Ashique, Vicky Y Lin, Suzanne Crawley, Julie M Roda, Peirong Chen, Bin Fan, Jeong Kim, James Sissons, Jonathan Sitrin, Daniel D Kaplan, Don L Gibbons, Lee B Rivera
We recently reported that resistance to PD-1-blockade in a refractory lung cancer-derived model involved increased collagen deposition and the collagen-binding inhibitory receptor leukocyte-associated immunoglobulin-like receptor 1 (LAIR1), and thus we hypothesized that LAIR1 and collagen cooperated to suppress therapeutic response. Here, we report LAIR1 is associated with tumor stroma and is highly expressed by intratumoral myeloid cells in both human tumors and mouse models of cancer. Stroma-associated myeloid cells exhibit a suppressive phenotype and correlate with LAIR1 expression in human cancer...
April 22, 2024: Molecular Cancer Therapeutics
https://read.qxmd.com/read/38647975/sustained-improvements-in-clinical-and-patient-reported-outcomes-and-quality-of-life-through-5%C3%A2-years-among-ixekizumab-treated-patients-with-complete-clearance-of-scalp-psoriasis-by-week-60
#37
JOURNAL ARTICLE
Alexander Egeberg, Jason E Hawkes, Najwa Somani, Russel Burge, Kyoungah See, Gaia Gallo, Missy McKean-Matthews, Melinda Gooderham, George Han, April Armstrong
INTRODUCTION: Ixekizumab, a high-affinity monoclonal antibody that selectively targets interleukin-17A, is approved for the treatment of moderate-to-severe plaque psoriasis. Since scalp psoriasis can be burdensome and challenging to treat with non-systemic therapies, this post hoc analysis focused on scalp psoriasis in patients with moderate-to-severe plaque psoriasis and baseline scalp involvement. The analysis considered a holistic concept of clearance through 5 years of ixekizumab treatment...
April 22, 2024: Dermatology and Therapy
https://read.qxmd.com/read/38647931/modeling-the-behavior-of-monoclonal-antibodies-on-hydrophobic-interaction-chromatography-resins
#38
JOURNAL ARTICLE
Douglas Nolan, Thomas R Chin, Mick Eamsureya, Sheldon Oppenheim, Olga Paley, Christina Alves, George Parks
Monoclonal antibodies (mAbs) require a high level of purity for regulatory approval and safe administration. High-molecular weight (HMW) species are a common impurity associated with mAb therapies. Hydrophobic interaction chromatography (HIC) resins are often used to remove these HMW impurities. Determination of a suitable HIC resin can be a time and resource-intensive process. In this study, we modeled the chromatographic behavior of seven mAbs across 13 HIC resins using measurements of surface hydrophobicity, surface charge, and thermal stability for mAbs, and hydrophobicity and zeta-potential for HIC resins with high fit quality (adjusted R2  > 0...
February 15, 2024: Bioresources and Bioprocessing
https://read.qxmd.com/read/38647666/-cochlear-implantation-in-patients-with-autoimmune-hearing-loss
#39
JOURNAL ARTICLE
Maximilian Armstorfer, Lennart Weitgasser, Stefan Tschani, Sebastian Rösch
BACKGROUND: Autoimmune inner ear disease (AIED) manifests with recurrent fluctuating sensorineural hearing loss and vestibular symptoms. Treatment includes steroids and a variety of immunosuppressants. Despite adequate treatment, sensorineural hearing loss can be progressive to the point of deafness. In these patients, a cochlear implant (CI) is indicated. We present the case of a 25-year-old male who underwent cochlear implantation in the left ear. After implantation we noticed brisk variations in impedances which were related to application of the previously prescribed tumor necrosis alpha (TNFα) inhibitor adalimumab...
April 22, 2024: HNO
https://read.qxmd.com/read/38647528/a-bispecific-antibody-that-targets-the-membrane-proximal-region-of-mesothelin-and-retains-high-anticancer-activity-in-the-presence-of-shed-mesothelin
#40
JOURNAL ARTICLE
Anirban Chakraborty, Masanori Onda, Tara O'Shea, Junxia Wei, Xiufen Liu, Tapan K Bera, Ira Pastan
Mesothelin (MSLN) is a cell-surface protein that is expressed on many cancers, which makes it a popular target for antibody-based cancer therapy. However, MSLN is shed from cancer cells at high levels via proteases that cleave at its membrane-proximal C-terminal region. Shed MSLN accumulates in patient fluids and tumors and can block antibody-based MSLN-targeting drugs from killing cancer cells. A previously established monoclonal antibody (mAb), 15B6, binds MSLN at its protease-sensitive C-terminal region and does not bind shed MSLN...
April 22, 2024: Molecular Cancer Therapeutics
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