Artykuły w czasopismach na temat „Soluble CD89”
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Launay, Pierre, Béatrice Grossetête, Michelle Arcos-Fajardo, Emmanuelle Gaudin, Sonia P. Torres, Lucie Beaudoin, Natacha Patey-Mariaud de Serre, Agnès Lehuen i Renato C. Monteiro. "Fcα Receptor (Cd89) Mediates the Development of Immunoglobulin a (Iga) Nephropathy (Berger's Disease)". Journal of Experimental Medicine 191, nr 11 (6.06.1999): 1999–2010. http://dx.doi.org/10.1084/jem.191.11.1999.
Pełny tekst źródłavan Zandbergen, Ger, Ralf Westerhuis, Ngaisah Klar Mohamad, Jan G. J. van de Winkel, Mohamed R. Daha i Cees van Kooten. "Crosslinking of the Human Fc Receptor for IgA (FcαRI/CD89) Triggers FcR γ-Chain-Dependent Shedding of Soluble CD89". Journal of Immunology 163, nr 11 (1.12.1999): 5806–12. http://dx.doi.org/10.4049/jimmunol.163.11.5806.
Pełny tekst źródłaEsteve Cols, Clara, Freddzia-Amanda Graterol Torres, Bibiana Quirant Sánchez, Helena Marco Rusiñol, Maruja Isabel Navarro Díaz, Jordi Ara del Rey i Eva Mª Martínez Cáceres. "Immunological Pattern in IgA Nephropathy". International Journal of Molecular Sciences 21, nr 4 (18.02.2020): 1389. http://dx.doi.org/10.3390/ijms21041389.
Pełny tekst źródłaWu, Haiting, Xiaoyan Wang, Zhe Yang, Qing Zhao, Yubing Wen, Xuemei Li, Wei Zhang i Ruitong Gao. "Serum Soluble CD89-IgA Complexes Are Elevated in IgA Nephropathy without Immunosuppressant History". Disease Markers 2020 (16.01.2020): 1–6. http://dx.doi.org/10.1155/2020/8393075.
Pełny tekst źródłaCambier, Alexandra, Patrick J. Gleeson, Lilia Abbad, Fanny Canesi, Jennifer da Silva, Julie Bex-Coudrat, Georges Deschênes i in. "Soluble CD89 is a critical factor for mesangial proliferation in childhood IgA nephropathy". Kidney International 101, nr 2 (luty 2022): 274–87. http://dx.doi.org/10.1016/j.kint.2021.09.023.
Pełny tekst źródłaBerthelot, Laureline, Thomas Robert, Vincent Vuiblet, Thierry Tabary, Antoine Braconnier, Moustapha Dramé, Olivier Toupance, Philippe Rieu, Renato C. Monteiro i Fatouma Touré. "Recurrent IgA nephropathy is predicted by altered glycosylated IgA, autoantibodies and soluble CD89 complexes". Kidney International 88, nr 4 (październik 2015): 815–22. http://dx.doi.org/10.1038/ki.2015.158.
Pełny tekst źródłaVuong, Mai T., Mirjana Hahn-Zoric, Sigrid Lundberg, Iva Gunnarsson, Cees van Kooten, Lars Wramner, Maria Seddighzadeh i in. "Association of soluble CD89 levels with disease progression but not susceptibility in IgA nephropathy". Kidney International 78, nr 12 (grudzień 2010): 1281–87. http://dx.doi.org/10.1038/ki.2010.314.
Pełny tekst źródłaHahn-Zoric, Mirjana, Mai Vuong, Sigrid Lundberg, Lars Wramner, Jarl Ahlmen, Lars Å. Hanson, Iva Gunnarsson, Stefan Jacobson i Leonid Padyukov. "Su.82. Evidence for Genetic Regulation of Fc Alpha Receptor (CD89) Expression: Study of Soluble CD89 in Plasma of IgA Nephropathy Patients and Healthy Controls". Clinical Immunology 127 (styczeń 2008): S151. http://dx.doi.org/10.1016/j.clim.2008.03.433.
Pełny tekst źródłaHahn-Zoric, Mirjana, Neda Tahmasebifar, Cees van Kooten, Jarl Ahlmen, Svante Swerkersson, Sverker Hansson, Ulla Berg, Lars Åke Hanson, Leonid Padyukov i Stefan H. Jacobson. "Immunoassays for Detection of Soluble Fc Alpha Receptor (CD89) in Plasma of IgA Nephropathy Patients". Clinical Immunology 123 (2007): S54—S55. http://dx.doi.org/10.1016/j.clim.2007.03.335.
Pełny tekst źródłaBerthelot, Laureline, Christina Papista, Thiago T. Maciel, Martine Biarnes-Pelicot, Emilie Tissandie, Pamela H. M. Wang, Houda Tamouza i in. "Transglutaminase is essential for IgA nephropathy development acting through IgA receptors". Journal of Experimental Medicine 209, nr 4 (26.03.2012): 793–806. http://dx.doi.org/10.1084/jem.20112005.
Pełny tekst źródłaNockher, W. A., i J. E. Scherberich. "Expression and release of the monocyte lipopolysaccharide receptor antigen CD14 are suppressed by glucocorticoids in vivo and in vitro." Journal of Immunology 158, nr 3 (1.02.1997): 1345–52. http://dx.doi.org/10.4049/jimmunol.158.3.1345.
Pełny tekst źródłaBerthelot, L., P. Housset, V. Sauvaget, A. Jamin, R. C. Monteiro i E. Pillebout. "Complexes IgA-CD89 soluble comme biomarqueurs d’atteinte rénale et facteur de risque de progression au cours du purpura rhumatoïde". Néphrologie & Thérapeutique 9, nr 5 (wrzesień 2013): 278. http://dx.doi.org/10.1016/j.nephro.2013.07.184.
Pełny tekst źródłaTissandié, Emilie, Willy Morelle, Laureline Berthelot, François Vrtovsnik, Eric Daugas, Francine Walker, Didier Lebrec i in. "Both IgA nephropathy and alcoholic cirrhosis feature abnormally glycosylated IgA1 and soluble CD89–IgA and IgG–IgA complexes: common mechanisms for distinct diseases". Kidney International 80, nr 12 (grudzień 2011): 1352–63. http://dx.doi.org/10.1038/ki.2011.276.
Pełny tekst źródłaMonteiro, Renato C., Dina Rafeh i Patrick J. Gleeson. "Is There a Role for Gut Microbiome Dysbiosis in IgA Nephropathy?" Microorganisms 10, nr 4 (22.03.2022): 683. http://dx.doi.org/10.3390/microorganisms10040683.
Pełny tekst źródłaChai, Jian-Guo, Silvia Vendetti, Istvan Bartok, Diana Schoendorf, Katalin Takacs, James Elliott, Robert Lechler i Julian Dyson. "Critical Role of Costimulation in the Activation of Naive Antigen-Specific TCR Transgenic CD8+ T Cells In Vitro". Journal of Immunology 163, nr 3 (1.08.1999): 1298–305. http://dx.doi.org/10.4049/jimmunol.163.3.1298.
Pełny tekst źródłaLal, R. B., D. L. Rudolph, C. S. Dezzutti, P. S. Linsley i H. E. Prince. "Costimulatory effects of T cell proliferation during infection with human T lymphotropic virus types I and II are mediated through CD80 and CD86 ligands." Journal of Immunology 157, nr 3 (1.08.1996): 1288–96. http://dx.doi.org/10.4049/jimmunol.157.3.1288.
Pełny tekst źródłaMotta, Juliana, Morgana Castelo-Branco i Vivian Rumjanek. "Characterization of human monocyte-derived dendritic cells in the presence of leukemic cell soluble products (127.14)". Journal of Immunology 188, nr 1_Supplement (1.05.2012): 127.14. http://dx.doi.org/10.4049/jimmunol.188.supp.127.14.
Pełny tekst źródłaChai, Jian-Guo, Istvan Bartok, Diane Scott, Julian Dyson i Robert Lechler. "T:T Antigen Presentation by Activated Murine CD8+ T Cells Induces Anergy and Apoptosis". Journal of Immunology 160, nr 8 (15.04.1998): 3655–65. http://dx.doi.org/10.4049/jimmunol.160.8.3655.
Pełny tekst źródłaChung, Yeonseok, Jae-Hoon Chang, Mi-Na Kweon, Paul D. Rennert i Chang-Yuil Kang. "CD8α–11b+ dendritic cells but not CD8α+ dendritic cells mediate cross-tolerance toward intestinal antigens". Blood 106, nr 1 (1.07.2005): 201–6. http://dx.doi.org/10.1182/blood-2004-11-4240.
Pełny tekst źródłaHock, B. D., J. L. O'Donnell, K. Taylor, A. Steinkasserer, J. L. McKenzie, A. G. Rothwell i K. L. Summers. "Levels of the soluble forms of CD80, CD86, and CD83 are elevated in the synovial fluid of rheumatoid arthritis patients". Tissue Antigens 67, nr 1 (styczeń 2006): 57–60. http://dx.doi.org/10.1111/j.1399-0039.2005.00524.x.
Pełny tekst źródłaMorva, Ahsen, Sébastien Lemoine, Achouak Achour, Jacques-Olivier Pers, Pierre Youinou i Christophe Jamin. "Maturation and function of human dendritic cells are regulated by B lymphocytes". Blood 119, nr 1 (5.01.2012): 106–14. http://dx.doi.org/10.1182/blood-2011-06-360768.
Pełny tekst źródłaLi, Haiyan, Sungyoul Hong, Jianfei Qian, Yuhuan Zheng, Jing Yang i Qing Yi. "Cross talk between the bone and immune systems: osteoclasts function as antigen-presenting cells and activate CD4+ and CD8+ T cells". Blood 116, nr 2 (15.07.2010): 210–17. http://dx.doi.org/10.1182/blood-2009-11-255026.
Pełny tekst źródłaOehler, Leopold, Otto Majdic, Winfried F. Pickl, Johannes Stöckl, Elisabeth Riedl, Johannes Drach, Klemens Rappersberger, Klaus Geissler i Walter Knapp. "Neutrophil Granulocyte–committed Cells Can Be Driven to Acquire Dendritic Cell Characteristics". Journal of Experimental Medicine 187, nr 7 (6.04.1998): 1019–28. http://dx.doi.org/10.1084/jem.187.7.1019.
Pełny tekst źródłaTekguc, Murat, James Badger Wing, Motonao Osaki, Jia Long i Shimon Sakaguchi. "Treg-expressed CTLA-4 depletes CD80/CD86 by trogocytosis, releasing free PD-L1 on antigen-presenting cells". Proceedings of the National Academy of Sciences 118, nr 30 (23.07.2021): e2023739118. http://dx.doi.org/10.1073/pnas.2023739118.
Pełny tekst źródłaArcaro, Alexandre, Claude Grégoire, Talitha R. Bakker, Lucia Baldi, Martin Jordan, Laurence Goffin, Nicole Boucheron i in. "CD8β Endows CD8 with Efficient Coreceptor Function by Coupling T Cell Receptor/CD3 to Raft-associated CD8/p56lck Complexes". Journal of Experimental Medicine 194, nr 10 (19.11.2001): 1485–95. http://dx.doi.org/10.1084/jem.194.10.1485.
Pełny tekst źródłaTsuji, Shoutaro, Misako Matsumoto, Osamu Takeuchi, Shizuo Akira, Ichiro Azuma, Akira Hayashi, Kumao Toyoshima i Tsukasa Seya. "Maturation of Human Dendritic Cells by Cell Wall Skeleton of Mycobacterium bovis Bacillus Calmette-Guérin: Involvement of Toll-Like Receptors". Infection and Immunity 68, nr 12 (1.12.2000): 6883–90. http://dx.doi.org/10.1128/iai.68.12.6883-6890.2000.
Pełny tekst źródłaLechmann, Matthias, Daniëlle J. E. B. Krooshoop, Diana Dudziak, Elisabeth Kremmer, Christine Kuhnt, Carl G. Figdor, Gerold Schuler i Alexander Steinkasserer. "The Extracellular Domain of CD83 Inhibits Dendritic Cell–mediated T Cell Stimulation and Binds to a Ligand on Dendritic Cells". Journal of Experimental Medicine 194, nr 12 (17.12.2001): 1813–21. http://dx.doi.org/10.1084/jem.194.12.1813.
Pełny tekst źródłaNauta, Alma J., Ellie Lurvink, Alwine B. Kruisselbrink, Roelof Willemze i Willem E. Fibbe. "Mesenchymal Stem Cells Inhibit Generation and Function of Both Monocyte-Derived and CD34-Derived Dendritic Cells." Blood 106, nr 11 (16.11.2005): 593. http://dx.doi.org/10.1182/blood.v106.11.593.593.
Pełny tekst źródłaCorinti, Silvia, Donata Medaglini, Andrea Cavani, Maria Rescigno, Gianni Pozzi, Paola Ricciardi-Castagnoli i Giampiero Girolomoni. "Human Dendritic Cells Very Efficiently Present a Heterologous Antigen Expressed on the Surface of Recombinant Gram-Positive Bacteria to CD4+ T Lymphocytes". Journal of Immunology 163, nr 6 (15.09.1999): 3029–36. http://dx.doi.org/10.4049/jimmunol.163.6.3029.
Pełny tekst źródłaFaries, Mark B., Isabelle Bedrosian, Shuwen Xu, Gary Koski, James G. Roros, Mirielle A. Moise, Hung Q. Nguyen, Friederike H. C. Engels, Peter A. Cohen i Brian J. Czerniecki. "Calcium signaling inhibits interleukin-12 production and activates CD83+ dendritic cells that induce Th2 cell development". Blood 98, nr 8 (15.10.2001): 2489–97. http://dx.doi.org/10.1182/blood.v98.8.2489.
Pełny tekst źródłaAndersson, Anders, Apostolos Bossios, Carina Malmhäll, Margareta Sjöstrand, Maria Eldh, Britt-Marie Eldh, Pernilla Glader i in. "Effects of tobacco smoke on IL-16 in CD8+ cells from human airways and blood: a key role for oxygen free radicals?" American Journal of Physiology-Lung Cellular and Molecular Physiology 300, nr 1 (styczeń 2011): L43—L55. http://dx.doi.org/10.1152/ajplung.00387.2009.
Pełny tekst źródłaZinser, Elisabeth, Matthias Lechmann, Antje Golka, Manfred B. Lutz i Alexander Steinkasserer. "Prevention and Treatment of Experimental Autoimmune Encephalomyelitis by Soluble CD83". Journal of Experimental Medicine 200, nr 3 (2.08.2004): 345–51. http://dx.doi.org/10.1084/jem.20030973.
Pełny tekst źródłaBowman, Christine E., Ada Chen, Damie Juat, Kaustubh Parashar, Julie Clor, Hema Singh, Ritu Kushwaha i in. "Abstract 321: Inhibition of CD39 results in elevated ATP and activation of myeloid cells to promote anti-tumor immunity". Cancer Research 82, nr 12_Supplement (15.06.2022): 321. http://dx.doi.org/10.1158/1538-7445.am2022-321.
Pełny tekst źródłaTomita, Yuji, Eri Watanabe, Masumi Shimizu, Yasuyuki Negishi, Yukihiro Kondo i Hidemi Takahashi. "Induction of tumor-specific CD8+ cytotoxic T lymphocytes from naïve human T cells by using Mycobacterium-derived mycolic acid and lipoarabinomannan-stimulated dendritic cells". Cancer Immunology, Immunotherapy 68, nr 10 (17.09.2019): 1605–19. http://dx.doi.org/10.1007/s00262-019-02396-8.
Pełny tekst źródłaSimone, Rita, Giampaola Pesce, Princey Antola, Margarita Rumbullaku, Marcello Bagnasco, Nicola Bizzaro i Daniele Saverino. "The Soluble Form of CTLA-4 from Serum of Patients with Autoimmune Diseases Regulates T-Cell Responses". BioMed Research International 2014 (2014): 1–9. http://dx.doi.org/10.1155/2014/215763.
Pełny tekst źródłaButler, Marcus O., Osamu Imataki, Yoshihiro Yamashita, Makito Tanaka, Sascha Ansén, Alla Berezovskaya, Matthew I. Milstein i in. "Human CD4+ T Cells Help CD8+ T Cells Proliferate Ex Vivo by Secreting Both IL-2/IL-21 and Upregulating IL-21R". Blood 116, nr 21 (19.11.2010): 4284. http://dx.doi.org/10.1182/blood.v116.21.4284.4284.
Pełny tekst źródłaPrazma, Charlene M., i Thomas F. Tedder. "Ag-engaged B cells express CD83, a sensitive marker for B cell activation (83.15)". Journal of Immunology 178, nr 1_Supplement (1.04.2007): S114. http://dx.doi.org/10.4049/jimmunol.178.supp.83.15.
Pełny tekst źródłaPaul, Santanu, Charles C. Chu, Brian A. McCarthy, Erin Boyle, Bettie M. Steinberg, Matthew Kaufman, Jonathan Kolitz, Steven L. Allen, Kanti R. Rai i Nicholas Chiorazzi. "Activation of Nucleic Acid-Sensing Toll-Like Receptors Induces Proliferation, Cytokine Production, Immunogenic Phenotype, and Plasma Cell Differentiation of CLL Cells and Immunoglobulin Production." Blood 110, nr 11 (16.11.2007): 1137. http://dx.doi.org/10.1182/blood.v110.11.1137.1137.
Pełny tekst źródłaBjørge, Line, Tone Skeie Jensen, Christian A. Vedeler, Elling Ulvestad, Einar K. Kristoffersen i Roald Matre. "Soluble CD59 in pregnancy and infancy". Immunology Letters 36, nr 2 (maj 1993): 233. http://dx.doi.org/10.1016/0165-2478(93)90058-a.
Pełny tekst źródłaPaszkiet, Brian, Andrew Worden, Yajin Ni, Saran Bao, Franck Lemiale, Boro Dropulic i Laurent Humeau. "CD86 and CD54 Co-Expression on VSV-G Pseudotyped HIV-1 Based Vectors Improves Transduction and Activation of Human Primary CD4+ T Lymphocytes." Blood 104, nr 11 (16.11.2004): 1754. http://dx.doi.org/10.1182/blood.v104.11.1754.1754.
Pełny tekst źródłaZelek, Wioleta, Loek Willems, Ricardo Brandwijk, Sam Loveless, Neil R. Robertson i B. Paul Morgan. "High levels of soluble CD59 in CSF compared to plasma suggests intrathecal source of soluble CD59". Molecular Immunology 89 (wrzesień 2017): 186. http://dx.doi.org/10.1016/j.molimm.2017.06.179.
Pełny tekst źródłaZhu, Lv-yun, Li Nie, Tong Shao, Wei-ren Dong, Li-xin Xiang i Jian-zhong Shao. "B cells in primitive vertebrate act as pivotal antigen presenting cells in priming adaptive immunity (P5035)". Journal of Immunology 190, nr 1_Supplement (1.05.2013): 110.18. http://dx.doi.org/10.4049/jimmunol.190.supp.110.18.
Pełny tekst źródłaStachel, Daniel K., Uta Eickelmann, Rita Meilbeck, Michael H. Albert, Raymund Buhmann, Michael Hallek i Irene Schmid. "Coculture of Pediatric Acute Lymphoblastic Leukemia (ALL) Blasts with CD40 Ligand Transfected Cells Leads to Changes of Surface Antigens and RNA Expression." Blood 106, nr 11 (16.11.2005): 856. http://dx.doi.org/10.1182/blood.v106.11.856.856.
Pełny tekst źródłavan der Merwe, P. Anton, Dale L. Bodian, Susan Daenke, Peter Linsley i Simon J. Davis. "CD80 (B7-1) Binds Both CD28 and CTLA-4 with a Low Affinity and Very Fast Kinetics". Journal of Experimental Medicine 185, nr 3 (3.02.1997): 393–404. http://dx.doi.org/10.1084/jem.185.3.393.
Pełny tekst źródłaTomkinson, B. E., M. C. Brown, S. H. Ip, S. Carrabis i J. L. Sullivan. "Soluble CD8 during T cell activation." Journal of Immunology 142, nr 7 (1.04.1989): 2230–36. http://dx.doi.org/10.4049/jimmunol.142.7.2230.
Pełny tekst źródłaZelek, Wioleta M., Lewis M. Watkins, Owain W. Howell, Rhian Evans, Sam Loveless, Neil P. Robertson, Marijke Beenes, Loek Willems, Ricardo Brandwijk i B. Paul Morgan. "Measurement of soluble CD59 in CSF in demyelinating disease: Evidence for an intrathecal source of soluble CD59". Multiple Sclerosis Journal 25, nr 4 (9.02.2018): 523–31. http://dx.doi.org/10.1177/1352458518758927.
Pełny tekst źródłaNair, Jayakumar R., Louise M. Carlson, Cheryl Rozanski, Lawrence H. Boise, Asher Chanan-Khan i Kelvin P. Lee. "Direct interaction with dendritic cells through CD28-CD80/CD86 supports plasma cell survival (34.9)". Journal of Immunology 182, nr 1_Supplement (1.04.2009): 34.9. http://dx.doi.org/10.4049/jimmunol.182.supp.34.9.
Pełny tekst źródłaWong, C. K., L. C. W. Lit, L. S. Tam, E. K. Li i C. W. K. Lam. "Aberrant production of soluble costimulatory molecules CTLA-4, CD28, CD80 and CD86 in patients with systemic lupus erythematosus". Rheumatology 44, nr 8 (3.05.2005): 989–94. http://dx.doi.org/10.1093/rheumatology/keh663.
Pełny tekst źródłaButler, Marcus O., Sascha Ansén, Makito Tanaka, Osamu Imataki, Alla Berezovskaya, Mary M. Mooney, Genita Metzler, Matthew I. Milstein, Lee M. Nadler i Naoto Hirano. "A Series of Human Cell-Based Artificial APC Expands Long-Lived, Th1-Biased, Viral Antigen-Specific CD4+ T Cells with a Central/Effector Memory Phenotpype Restricted by Common HLA-DR Alleles". Blood 116, nr 21 (19.11.2010): 354. http://dx.doi.org/10.1182/blood.v116.21.354.354.
Pełny tekst źródłaEckhardt, J., S. Kreiser, M. Döbbeler, C. Nicolette, M. A. DeBenedette, I. Y. Tcherepanova, C. Ostalecki i in. "Soluble CD83 ameliorates experimental colitis in mice". Mucosal Immunology 7, nr 4 (15.01.2014): 1006–18. http://dx.doi.org/10.1038/mi.2013.119.
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