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Institution

Swiss Red Cross

NonprofitBern, 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.


Papers
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Journal ArticleDOI
Pablo Umaña1, Joel Jean-Mairet1, R Moudry2, H Amstutz2, James E. Bailey1 
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

Journal ArticleDOI
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

Journal ArticleDOI
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

Journal ArticleDOI
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

Journal ArticleDOI
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

NameH-indexPapersCitations
Michel D. Kazatchkine7736420502
Roland B. Walter5135610786
Alberto Vierucci401595516
Jean-Daniel Tissot402255281
Reinhard Henschler391444848
Andreas Buser341807749
Sylvia Miescher32962938
Lorenz Risch311884281
Christoph Kempf31822324
Urs E. Nydegger281372910
Michael Medinger251092184
Beatrice Drexler22582220
Laura Infanti20681667
Beat M. Frey20581332
Bart Jacobs20421582
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20221
202113
202019
201912
201817
201721