Academic literature on the topic 'INKT cells'

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Journal articles on the topic "INKT cells"

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Uddin, Mohammad Nizam, Dil Afroz Sultana, Kyle J. Lorentsen, et al. "Transcription factor Bcl11b sustains iNKT1 and iNKT2 cell programs, restricts iNKT17 cell program, and governs iNKT cell survival." Proceedings of the National Academy of Sciences 113, no. 27 (2016): 7608–13. http://dx.doi.org/10.1073/pnas.1521846113.

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Invariant natural killer T (iNKT) cells are innate-like T cells that recognize glycolipid antigens and play critical roles in regulation of immune responses. Based on expression of the transcription factors (TFs) Tbet, Plzf, and Rorγt, iNKT cells have been classified in effector subsets that emerge in the thymus, namely, iNKT1, iNKT2, and iNKT17. Deficiency in the TF Bcl11b in double-positive (DP) thymocytes has been shown to cause absence of iNKT cells in the thymus and periphery due to defective self glycolipid processing and presentation by DP thymocytes and undefined intrinsic alterations
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Maas-Bauer, Kristina, Juliane K. Lohmeyer, Toshihito Hirai, et al. "Invariant natural killer T-cell subsets have diverse graft-versus-host-disease–preventing and antitumor effects." Blood 138, no. 10 (2021): 858–70. http://dx.doi.org/10.1182/blood.2021010887.

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Abstract Invariant natural killer T (iNKT) cells are a T-cell subset with potent immunomodulatory properties. Experimental evidence in mice and observational studies in humans indicate that iNKT cells have antitumor potential as well as the ability to suppress acute and chronic graft-versus-host-disease (GVHD). Murine iNKT cells differentiate during thymic development into iNKT1, iNKT2, and iNKT17 sublineages, which differ transcriptomically and epigenomically and have subset-specific developmental requirements. Whether distinct iNKT sublineages also differ in their antitumor effect and their
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Maas-Bauer, Kristina, Federico Simonetta, Toshihito Hirai, et al. "Invariant Natural Killer T Cell Subsets Have Diverse Functions: iNKT2 and iNKT17 Protect from Graft-Versus-Host-Disease, Whereas iNKT1 Have Antitumor Potential." Blood 132, Supplement 1 (2018): 475. http://dx.doi.org/10.1182/blood-2018-99-113673.

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Abstract Invariant natural killer T (iNKT) cells are an interesting subpopulation of T cells that can potently inhibit graft-versus-host-disease (GVHD) through the production of Interleukin 4 (IL-4), while also carrying anti-tumor potential (Leveson-Gower et al. Blood. 2011;117:3220-9; Schneidawind et al. Blood. 2014;124:3320-8). Murine iNKT cells differentiate during thymic development into three distinct sublineages, named according to the classification of conventional T cells: Th1-like iNKT (iNKT1) cells, Th2-like iNKT (iNKT2) cells, and Th-17 like iNKT (iNKT17) cells (Brennan et al. Nat R
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Patel, Nishant P., Peng Guan, Devika Bahal, et al. "Cancer Immunotherapeutic Potential of NKTT320, a Novel, Invariant, Natural Killer T Cell-Activating, Humanized Monoclonal Antibody." International Journal of Molecular Sciences 21, no. 12 (2020): 4317. http://dx.doi.org/10.3390/ijms21124317.

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Invariant natural killer T cells (iNKTs) directly kill tumor cells and trans-activate the anti-tumor functions of dendritic cells (DC), natural killer (NK) cells, and T and B cells. As such, iNKTs serve as a powerful tool for use in cell-based cancer immunotherapy. iNKT cell activation commonly requires engagement of the invariant T cell receptor (iTCR) by CD1d presenting glycolipid antigens. However, transformed cells often down-regulate CD1d expression, which results in a reduction of iNKT cell anti-tumor functions. One approach to circumvent this critical barrier to iNKT cell activation is
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Chen, Dongzhi, Wenbin Xu, Jingfang Teng, et al. "Migration, Distribution, and Safety Evaluation of Specific Phenotypic and Functional Mouse Spleen-Derived Invariant Natural Killer T2 Cells after Adoptive Infusion." Mediators of Inflammation 2021 (December 8, 2021): 1–11. http://dx.doi.org/10.1155/2021/5170123.

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Herein, the migration distribution and safety of specific phenotypic and functionally identified spleen-derived invariant natural killer T2 (iNKT2) cells after adoptive infusion in mice were studied. The proliferation and differentiation of iNKT cells were induced by intraperitoneal injection of α-galactosylceramide (α-GalCer) in vivo. Mouse spleens were isolated in a sterile environment. iNKT cells were isolated by magnetic-activated cell sorting columns (MS columns). Cytometric bead array (CBA) assay was used to detect cytokine secretion in the supernatant stimulated by iNKT cells. The basic
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Jahnke, Simona, Hannes Schmid, Kathy-Ann Secker, et al. "Invariant Natural Killer T Cells from Donor Lymphocyte Infusions (DLI-iNKTs) Contribute to Anti-Tumor Immunity after Allogeneic Hematopoietic Cell Transplantation." Blood 132, Supplement 1 (2018): 3340. http://dx.doi.org/10.1182/blood-2018-99-111745.

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Abstract Allogeneic hematopoietic cell transplantation (HCT) is a curative treatment option for hematologic malignancies but relapse remains the most common cause of death. Infusion of donor lymphocytes (DLIs) can induce remission and prolong survival by exerting potent graft-versus-leukemia (GVL) effects. However, sufficient tumor control cannot be established in all patients. We showed previously that invariant natural killer T (iNKT) cells promote anti-tumor immunity in murine models of allogeneic HCT without exacerbating graft-versus-host disease (GVHD). We therefore studied iNKT cells in
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Castillo, Eliseo F., Luis F. Acero, Spencer W. Stonier, Dapeng Zhou, and Kimberly S. Schluns. "Thymic and peripheral microenvironments differentially mediate development and maturation of iNKT cells by IL-15 transpresentation." Blood 116, no. 14 (2010): 2494–503. http://dx.doi.org/10.1182/blood-2010-03-277103.

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Abstract Invariant NKT (iNKT) cells are an innate type of T cells, which respond rapidly on activation. iNKT cells acquire these innate-like abilities during development; however, the signals driving development and functional maturation remain only partially understood. Because interleukin-15 (IL-15) is crucial for iNKT development and is delivered by transpresentation, we set out to identify the cell types providing IL-15 to developing iNKT cells and determine their role at the various states of development and maturation. We report here that transpresentation of IL-15 by parenchymal cells w
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Kanda, Masatoshi, Hiroyuki Yamanaka, Satoshi Kojo та ін. "Transcriptional regulator Bhlhe40 works as a cofactor of T-bet in the regulation of IFN-γ production in iNKT cells". Proceedings of the National Academy of Sciences 113, № 24 (2016): E3394—E3402. http://dx.doi.org/10.1073/pnas.1604178113.

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Invariant natural killer T (iNKT) cells are a subset of innate-like T cells that act as important mediators of immune responses. In particular, iNKT cells have the ability to immediately produce large amounts of IFN-γ upon activation and thus initiate immune responses in various pathological conditions. However, molecular mechanisms that control IFN-γ production in iNKT cells are not fully understood. Here, we report that basic helix–loop–helix transcription factor family, member e40 (Bhlhe40), is an important regulator for IFN-γ production in iNKT cells. Bhlhe40 is highly expressed in stage 3
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Purbhoo, Marco, Burcu Yigit, Darrian Moskowitz, et al. "400 Persistence and tissue distribution of agent-797 – a native allogeneic iNKT cell-therapy drug product." Journal for ImmunoTherapy of Cancer 9, Suppl 2 (2021): A432. http://dx.doi.org/10.1136/jitc-2021-sitc2021.400.

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BackgroundInvariant Natural Killer T (iNKT) cells are key effectors and regulators of immune responses, making them an ideal immunotherapy. There is a paucity of evidence describing the persistence and trafficking of these cells in humans to inform the optimal clinical application. Here, we describe the development of a murine Xenograft model for the study of an unmodified human iNKT cell therapy (Agent-797) and present data on the persistence and tissue distribution of human iNKT cells in this model. We further describe the development and validation of a digital PCR-based methodology to trac
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Metelitsa, Leonid S., Hong-Wei Wu, Hong Wang, et al. "Natural Killer T Cells Infiltrate Neuroblastomas Expressing the Chemokine CCL2." Journal of Experimental Medicine 199, no. 9 (2004): 1213–21. http://dx.doi.org/10.1084/jem.20031462.

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CD1d-restricted Vα24-Jα18–invariant natural killer T cells (iNKTs) are potentially important in tumor immunity. However, little is known about their localization to tumors. We analyzed 98 untreated primary neuroblastomas from patients with metastatic disease (stage 4) for tumor-infiltrating iNKTs using TaqMan® reverse transcription polymerase chain reaction and immunofluorescent microscopy. 52 tumors (53%) contained iNKTs, and oligonucleotide microarray analysis of the iNKT+ and iNKT− tumors revealed that the former expressed higher levels of CCL2/MCP-1, CXCL12/SDF-1, CCL5/RANTES, and CCL21/SL
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Dissertations / Theses on the topic "INKT cells"

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Lopes, Nuno Duarte Ribeiro. "iNKT cells in mucopolysaccharidosis type II patients." Master's thesis, Universidade de Aveiro, 2013. http://hdl.handle.net/10773/11621.

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Mestrado em Biomedicina Molecular<br>A Mucopolissacaridose tipo II (MPS II) é uma Doença de Sobrecarga Lisossomal (LSD) pertencente às mucopolissacaridoses. É caracterizada pela acumulação de sulfato de heparan e dermatan devido à deficiência na enzima lisossomal Iduronato 2-Sulfatase. O lisossoma é um compartimento importante para a atividade dos linfócitos iNKT (iNKT). Os linfócitos iNKT são linfócitos T restritos a lípidos envolvidos na infeção, autoimunidade e vigilância tumoral. Estudos anteriores em modelos de murganhos de LSDs demonstraram uma redução do número de linfócitos iNKT assim
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Rothchild, Alissa Chen. "Antimicrobial Roles for iNKT Cells and GM-CSF in Mycobacterium Tuberculosis Infection." Thesis, Harvard University, 2014. http://dissertations.umi.com/gsas.harvard:11371.

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Despite effective antibiotics, Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis, still infects nearly one-third of the world's population. While key immune factors including CD4+ T cells and IFNg production have been identified, there are still many antimicrobial mechanisms yet to be explored. Here we characterized the role of invariant natural killer T (iNKT) cells and GM-CSF during Mtb infection.
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Arscott, Ramon. "The influence of invariant natural killer T cells on myeloid-derived suppressor cell generation and function." Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:07ab563a-7455-4f69-bca0-3b409b72d2f7.

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The absence of invariant Natural Killer T cells (iNKT cells) in mice infected with Influenza A virus (flu) has previously been shown to augment the expansion of Myeloid-derived suppressor cells (MDSCs), a bone marrow derived population that powerfully suppress the development of viral and tumor immune responses. Moreover, iNKT cell adoptive transfer into flu-infected mice has been shown to abolish the expansion and flu-induced suppressive activity of the MDSCs in a CD1d- and CD40-dependent manner. However, the mechanisms by which this relatively small subset of T cells influence myelopoiesis a
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Al, Dulaimi Dina. "Développement et fonction des cellules INKT." Thesis, Sorbonne Paris Cité, 2018. http://www.theses.fr/2018USPCC116.

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Les cellules invariantes « natural killer » T (iNKT) constituent une population particulière de LT non conventionnelle qui exprime un récepteur TCRαβ semi-invariant composé de la chaine Vα14-Jα18 associée aux chaines Vβ8, -7 ou -2 chez la souris et dont le développement a lieu dans le thymus. Ainsi, les cellules iNKT sont capables de reconnaitre via leur TCR des antigènes de type glycolipidique présentés par une molécule de classe I non polymorphique : le CD1d. Ces cellules sont connues pour être impliquées dans diverses réponses immunes grâce à leur capacité à produire rapidement des cytokine
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Correa, Frederico José Silva. "Avaliação das células iNKT em pacientes com endometriose." Universidade de São Paulo, 2018. http://www.teses.usp.br/teses/disponiveis/5/5139/tde-13022019-145705/.

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Introdução: A endometriose é uma doença com características inflamatórias que atinge as mulheres em idade reprodutiva. A patogênese da endometriose não está esclarecida. Tem sido demonstrada associação entre distúrbios imunológicos e endometriose, como alterações nos macrófagos, células NK, citocinas e nas repostas Th1, Th2 e Th17. As células iNKT, um tipo especial de linfócitos T, tem importante papel na resposta inflamatória como mediadores das repostas Th1, Th2 e Th17. Objetivos: o objetivo principal deste estudo foi comparar as frequências das células iNKT e seus subtipos entre pacientes c
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Wu, Ching-Lien. "Study of the immune checkpoint HLA-G/ILT2 : soluble receptors, inhibition of iNKT cells." Thesis, Sorbonne Paris Cité, 2018. http://www.theses.fr/2018USPCC188.

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HLA-G est une molécule checkpoint immunologique tolérogène connue pour son rôle dans la tolerance materno-foetale, puis comme mécanisme d’échappement immunitaire des tumeurs. HLA-G exerce ses fonctions via avec deux récepteurs inhibiteurs principaux, ILT2 et ILT4, différentiellement exprimés par les effecteurs immunitaires. L’expression de HLA-G par les tumeurs solides est associée à de plus hauts grades et à un pronostic plus sévère. Pour ces raisons, HLA-G et ses récepteurs pourraient constituer de bonnes cibles immuno-thérapeutiques en oncologie.Ce travail de doctorat a porté sur 1) l’exist
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Costa, Renata Cardoso Belo da. "Leishmania infantum extracellular material and human invariant natural killer T cells : a functional study." Thesis, Sorbonne Paris Cité, 2017. http://www.theses.fr/2017USPCB022/document.

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Les cellules iNKT (de l’anglais invariant Natural Killer T) constituent un sous-type particulier de lymphocytes T caractérisé par un profil de type inné. Ces cellules répondent rapidement à des antigènes lipidiques et glycolipidique présentés par le CD1d, une glycoprotéine exprimée par les différentes cellules présentatrices d'antigène. Suite à l’activation, les cellules iNKT sont capables de produire de grandes quantités de cytokines anti-inflammatoires et pro-inflammatoires et elles sont impliquées dans différentes maladies, telles que l'allergie, l'auto-immunité, le cancer
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Dempsey, Claire. "An investigation into the phenotype, function and immunomodulatory properties of in vitro expanded iNKT cells." Thesis, University of Birmingham, 2019. http://etheses.bham.ac.uk//id/eprint/8843/.

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Invariant natural killer T (iNKT) cells are endowed with features of both innate and adaptive immunity. They are activated by the recognition of glycolipid agonists presented by CD1d which makes them excellent candidates for cellular therapies. In order to investigate the ability of iNKT cells to suppress experimental acute Graft versus host disease (GVHD), iNKT cells were first expanded in vitro, which is likely to be required prior to their use as a cellular therapeutic. Interestingly, the expanded cells showed increased frequencies of IL-10, IL-13 and IL-17 producing cells and were found to
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Costa, Renata Cardoso Belo da. "Leishmania infantum extracellular material and human invariant natural killer T cells: a functional study." Doctoral thesis, Sorbonne Paris Cité, 2017. https://hdl.handle.net/10216/107808.

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Les cellules iNKT (de l’anglais invariant Natural Killer T) constituent un sous-type particulier de lymphocytes T caractérisé par un profil de type inné. Ces cellules répondent rapidement à des antigènes lipidiques et glycolipidique présentés par le CD1d, une glycoprotéine exprimée par les différentes cellules présentatrices d'antigène. Suite à l’activation, les cellules iNKT sont capables de produire de grandes quantités de cytokines anti-inflammatoires et pro-inflammatoires et elles sont impliquées dans différentes maladies, telles que l'allergie, l'auto-immunité, le cancer
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Marante, Tânia Alves. "The impact of chronic obstructive pulmonary disease on iNKT lymphocytes." Master's thesis, Universidade de Aveiro, 2017. http://hdl.handle.net/10773/17144.

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Mestrado em Biomedicina Molecular<br>A doença pulmonar obstrutiva crónica (DPOC) é uma das doenças inflamatórias mais comuns das vias aéreas e uma das principais causas de morbidade e mortalidade em todo o mundo. A doença é caracterizada por uma limitação persistente do fluxo aéreo, geralmente progressiva. As respostas inflamatórias crónicas e imunes desempenham papéis fundamentais no desenvolvimento e progressão da DPOC. A inflamação é uma resposta protetora normal, mas na DPOC esta inflamação é amplificada. Várias células inflamatórias, seus mediadores e enzimas participam na resposta inflam
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Books on the topic "INKT cells"

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Hikaru, Koide, Endou Hitoshi, and Kurokawa Kiyoshi, eds. Cellular and molecular biology of the kidney: Int. Symposium on Cell Biology of Nephron Heterogeneity--Fine Structure and Functions, Shizuoka, July 22-25, 1990. Karger, 1991.

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Douglas, Kenneth. Bioprinting. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780190943547.001.0001.

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Abstract: This book describes how bioprinting emerged from 3D printing and details the accomplishments and challenges in bioprinting tissues of cartilage, skin, bone, muscle, neuromuscular junctions, liver, heart, lung, and kidney. It explains how scientists are attempting to provide these bioprinted tissues with a blood supply and the ability to carry nerve signals so that the tissues might be used for transplantation into persons with diseased or damaged organs. The book presents all the common terms in the bioprinting field and clarifies their meaning using plain language. Readers will lear
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Foray, June, writer of foreword, Disney Walt 1901-1966, and Walt Disney Productions, eds. Ink & paint: The women of Walt Disney's animation. Disney Editions, 2017.

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Kong, X. Y., Y. C. Wang, X. F. Fan, G. F. Guo, and L. M. Tong. Free-standing grid-like nanostructures assembled into 3D open architectures for photovoltaic devices. Edited by A. V. Narlikar and Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533060.013.22.

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This article describes three-dimensional open architectures with free-standing grid-like nanostructure arrays as photocatalytic electrodes for a new type of dye-sensitized solar cell. It introduces a novel technique for fabricating a series of semiconducting oxides with grid-like nanostructures replicated from the biotemplates. These semiconducting oxides, including n-type titanium dioxide or p-type nickel oxide nanogrids, were sensitized with the dye molecules, then assembled into 3D stacked-grid arrays on a flexible substrate by means of the Langmuir–Blodgett method or the ink-jet printing t
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Book chapters on the topic "INKT cells"

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Ly, Dalam, and Terry L. Delovitch. "Innate Regulatory iNKT Cells." In Regulatory T Cells and Clinical Application. Springer US, 2008. http://dx.doi.org/10.1007/978-0-387-77909-6_27.

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Michel, Marie-Laure, and Maria C. Leite-de-Moraes. "Other Sources of IL-17: iNKT Cells." In IL-17, IL-22 and Their Producing Cells: Role in Inflammation and Autoimmunity. Springer Basel, 2012. http://dx.doi.org/10.1007/978-3-0348-0522-3_7.

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Wang, Jing, Chen Zhao, and Jianqing Xu. "Expansion of Human iNKT Cells Ex Vivo." In Methods in Molecular Biology. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1775-5_11.

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Chiba, Asako, and Sachiko Miyake. "Basic Techniques for Studies of iNKT Cells and MAIT Cells." In Methods in Molecular Biology. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0404-4_9.

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Cheng, Xue, Xiaosheng Tan, Rui Dou, Xiongwen Wu, and Xiufang Weng. "The Expansion and Cytotoxicity Detection of Human iNKT Cells." In Methods in Molecular Biology. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1775-5_12.

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Cong, Mengqing, Xiang Li, Haopeng Fang, Li Bai, Xucai Zheng, and Bofeng Li. "Isolation and Detection of Murine iNKT Cells in Different Organs." In Methods in Molecular Biology. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1775-5_5.

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He, Wenjing, Dongmei Ye, and Yifang Gao. "Identifying, Isolation, and Functional Use of Human Liver iNKT Cells." In Methods in Molecular Biology. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1775-5_6.

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Joshi, Vibhuti, and Masaki Terabe. "Detection of Mouse Type I NKT (iNKT) Cells by Flow Cytometry." In Methods in Molecular Biology. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1775-5_8.

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Khatwani, Natasha K., Kelly J. Andrews, and Asha B. Pillai. "Ex Vivo Expansion of Th2-Polarizing Immunotherapeutic iNKT Cells from Human Peripheral Blood." In Methods in Molecular Biology. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1775-5_13.

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Sahler, Julie, Orchi Anannya, Candice Limper, Brian Imbiakha, Tim Pierpont, and Avery August. "Genetic Analysis of iNKT Cell Development and Function." In Methods in Molecular Biology. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1775-5_1.

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Conference papers on the topic "INKT cells"

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Wongkajornsilp, Adisak, Khin Su Su Htwe, Nathawadee Sawatpiboon, Sunisa Duangsa-ard, and Kanda Kasetsinsombat. "Abstract 4141: The induction of iNKT cells and CIK cells toward anti-tumor phenotypes." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-4141.

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Wongkajornsilp, Adisak, Khin Su Su Htwe, Nathawadee Sawatpiboon, Sunisa Duangsa-ard, and Kanda Kasetsinsombat. "Abstract 4141: The induction of iNKT cells and CIK cells toward anti-tumor phenotypes." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-4141.

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Yamamoto, N., SM Kerfoot, T. Aoyagi, et al. "Transfer therapy of Immune B-1 cells triggered by activated iNKT cells for acute lung infection withS. pneumoniae." In American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a5746.

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Adenugba, A., M. Hornung, H. Schlitt, E. Geissler, J. Hutchinson, and J. Werner. "Lipid-loaded Hepatocytes fail to Suppress IL-4 Production by Human CD4+ iNKT Cells." In 36. Jahrestagung der Deutschen Arbeitsgemeinschaft zum Studium der Leber. Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0039-3402168.

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Luszczek, Wioleta, Vanessa Morales-Tirado, Marie van der Merwe, Ko Kudo, Dario Campana, and Asha Pillai. "Abstract 3512: Expanded human regulatory iNKT cells exhibit direct cytotoxicity against hematolymphoid tumor targets." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-3512.

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Rijavec, Matija, Katarina Osolnik, Mitja Košnik, and Peter Korošec. "Factors Involved In Development Of INKT Cells Are Differently Expressed In Patients With Sarcoidosis." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a5700.

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Tercelj, Marjeta, Barbara Salobir, Matija Rijavec, Izidor Kern, Ragnar Rylander та Peter Korosec. "iNKT cells are inversely related to β-glucan in BALF and granuloma formation in patients with sarcoidosis". У Annual Congress 2015. European Respiratory Society, 2015. http://dx.doi.org/10.1183/13993003.congress-2015.pa3309.

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Constable, Laura, Nusrat Iqbal, Domenico Cozzetto, Ailsa Hart, Phillip Tozer, and Nick Powell. "O39 IL22 producing iNKT and CD4+ T-cells drive dysregulation of the extracellular matrix in perianal fistulas." In Abstracts of the BSG Annual Meeting, 20–23 June 2022. BMJ Publishing Group Ltd and British Society of Gastroenterology, 2022. http://dx.doi.org/10.1136/gutjnl-2022-bsg.39.

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Su, W. J., S. F. Huang, J. Y. Feng, and Y. Y. Yang. "Isoniazid as an Immunomodulatory Agent for Latent Tuberculosis Infection Treatment in View of Invariant Natural Killer T (iNKT Cells." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a4427.

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Hix, Laura M., Yihui H. Shi, Paul L. Stein, Chyung-Ru Wang, and Ming Zhang. "Abstract B21: CD1 d-expressing breast cancer cells promote iNKT-mediated antitumor immunity in a mouse model of breast cancer bone metastasis." In Abstracts: AACR International Conference on Translational Cancer Medicine-- Jul 11-14, 2010; San Francisco, CA. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1078-0432.tcmusa10-b21.

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Reports on the topic "INKT cells"

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Ginley, David S. Inks for Ink Jet Printed Contacts for High Performance Silicon Solar Cells: Cooperative Research and Development Final Report, CRADA No. CRD-06-199. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1062460.

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van Hest, M. Metallic Inks for Solar Cells: Cooperative Research and Development Final Report, CRADA Number CRD-10-370. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1076645.

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Antoniadis, H. High Efficiency, Low Cost Solar Cells Manufactured Using 'Silicon Ink' on Thin Crystalline Silicon Wafers. Office of Scientific and Technical Information (OSTI), 2011. http://dx.doi.org/10.2172/1010461.

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Silicon Ink for High-Efficiency Solar Cells Captures a Share of the Market (Fact Sheet). Office of Scientific and Technical Information (OSTI), 2011. http://dx.doi.org/10.2172/1022295.

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