Institution
Swiss Red Cross
Nonprofit•Bern, Switzerland•
About: Swiss Red Cross is a nonprofit organization based out in Bern, Switzerland. It is known for research contribution in the topics: Population & Antibody. The organization has 407 authors who have published 420 publications receiving 10285 citations. The organization is also known as: Red Cross of Switzerland & Switzerland Red Cross.
Topics: Population, Antibody, Antigen, ABO blood group system, Transplantation
Papers published on a yearly basis
Papers
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TL;DR: The glycosylation pattern of chCE7 was engineered in Chinese hamster ovary cells with tetracycline–regulated expression of GnTIII to optimize the ADCC activity, and this activity correlated with the level of constant region–associated, bisected complex oligosaccharides determined by matrix–assisted laser desorption/ionization time–of–flight mass spectrometry.
Abstract: The glycosylation pattern of chCE7, an antineuroblastoma chimeric IgG1, was engineered in Chinese hamster ovary cells with tetracycline-regulated expression of beta(1,4)-N-acetylglucosaminyltransferase III (GnTIII), a glycosyltransferase catalyzing formation of bisected oligosaccharides that have been implicated in antibody-dependent cellular cytotoxicity (ADCC). Measurement of the ADCC activity of chCE7 produced at different tetracycline levels showed an optimal range of GnTIII expression for maximal chCE7 in vitro ADCC activity, and this activity correlated with the level of constant region-associated, bisected complex oligosaccharides determined by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. The new optimized variants of chCE7 exhibit substantial ADCC activity and, hence, may be useful for treatment of neuroblastoma. The strategy presented here should be applicable to optimize the ADCC activity of other therapeutic IgGs.
1,034 citations
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TL;DR: It is suggested that IVIg contains anti-idiotypes against autoantibodies and may be effective in the treatment of some autoimmune diseases through idiotypic/anti-IDiotypic interactions.
466 citations
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TL;DR: The modifications put on the alcohol fractionation procedure of Nitschmann.
Abstract: ummary
The modifications put on the alcohol fractionation procedure of Nitschmann., Kistler and Lergier [8] since 1954 are communicated. The yields and purities realised were calculated from the results of about 150 fractionation runs, 100 1 of plasma each. The actual method allows the isolation of 48% of the total plasmaproteins as albumin (98% pure in electrophoretic analysis), 9,8% as γ-Globulin (practically 100% pure) and 3,4% as clottable fibrinogen. A scheme summarizes the details of the entire procedure.
Resume
Les modifications apportees depuis 1954 a la methode de fractionnement de Nitschmann, Kistler et Lergier [8] sont decrites. Le rendement et la purete des differents fractions ont ete calculees a partir des resultats de 150 fractionnements de 100 litres chacun. La methode actuelle permet d'obtenir 48% des proteines plasmatiques totales sous forme d'albumine (degre de purete electrophoretique de 98%), 9,8% sous forme de γ-globuline (degre de purete pratiquement de 100%) et 3,4% sous forme de fibrinogene coagulable. Un schema detaille risume l'ensemble du procede de fractionnement.
Zusammenfassung:
Die seit 1954 vorgenommenen Veranderungen der Alkoholfraktionierungsmethode nach Nitschmann, Kistler und Lergier [8] werden dargelegt. Die mit der Methode praktisch erzielten Ausbeuten und Reinheiten wurden aus den Ergebnissen von and 150 100-Liter-Plasma-Ansatzen ermittelt: Nnch dem heutigen Verfahren lassen sich etwa 48% der totalen Plasmaproteine als Albumin (ungefahr 98% elektrophoretisch rein), 9,80/, als γ-Globulin (praktisch 100prozentig rein) und 3,4% als gerinnbares Fibrinogen gewinnen. Das ganze Fraktionierverfahren ist in Form eines detaillierten Schemas zusammenfassend dargestellt.
327 citations
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TL;DR: Preclinical and clinical studies using MSCs applied intravenously or intra-arterially are discussed in the context of the current understanding of how M SCs might work in physiological and pathological situations.
Abstract: Mesenchymal stem/stromal cells (MSCs) are increasingly used as an intravenously applied cellular therapeutic. They were found to be potent in situations such as tissue repair or severe inflammation. Still, data are lacking with regard to the biodistribution of MSCs, their cellular or molecular target structures, and the mechanisms by which MSCs reach these targets. This review discusses current hypotheses for how MSCs can reach tissue sites. Both preclinical and clinical studies using MSCs applied intravenously or intra-arterially are discussed in the context of our current understanding of how MSCs might work in physiological and pathological situations.
271 citations
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TL;DR: Aprotinin reduced postoperative blood loss by 50% and blood pressure, hemoglobin value and serum protein concentration were higher after operation in the aProtinin group.
222 citations
Authors
Showing all 407 results
Name | H-index | Papers | Citations |
---|---|---|---|
Michel D. Kazatchkine | 77 | 364 | 20502 |
Roland B. Walter | 51 | 356 | 10786 |
Alberto Vierucci | 40 | 159 | 5516 |
Jean-Daniel Tissot | 40 | 225 | 5281 |
Reinhard Henschler | 39 | 144 | 4848 |
Andreas Buser | 34 | 180 | 7749 |
Sylvia Miescher | 32 | 96 | 2938 |
Lorenz Risch | 31 | 188 | 4281 |
Christoph Kempf | 31 | 82 | 2324 |
Urs E. Nydegger | 28 | 137 | 2910 |
Michael Medinger | 25 | 109 | 2184 |
Beatrice Drexler | 22 | 58 | 2220 |
Laura Infanti | 20 | 68 | 1667 |
Beat M. Frey | 20 | 58 | 1332 |
Bart Jacobs | 20 | 42 | 1582 |