Spleen lymphocytes from normal subjects who suddenly died were used as cells producing gamma-interferon. One spleen yielded (3-8) X 10(8) viable cells which made it possible to prepare from 3 to 81 of splenocyte suspension culture. Staphylococcal enterotoxin A (SEA) and B (SEB) were used as gamma-interferon inducers. Stimulation of splenocyte suspension culture with SEA and SEB resulted in production of gamma-interferon with an average activity of 640-2560 units/ml. A partially purified interferon preparation with an activity of 2 X 10(4) units/ml was obtained by sorption of gamma-interferon on porous glass CPG-200-240 followed by elution with a buffer containing 50% ethylene glycol and Sephadex G-25 gel chromatography. As a result of 11 successive intramuscular immunizations of rabbits at 2-week intervals with a partially purified and concentrated preparation of gamma-interferon with Freund's complete adjuvant, blood serum was obtained which was capable of neutralizing 32 units of gamma-interferon up to a dilution of 1:128. The serum was highly specific: it showed no specific interaction with antigenic determinants of either natural alpha- and beta- or plasmid alpha-F and alpha-F/D human interferons.
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Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi
September 2024
Department of Urology, Peking University First Hospital; Institute of Urology, Peking University; National Urological Cancer Center, Beijing 100034, China. *Corresponding authors, E-mail:
Clin Transl Oncol
September 2024
Department of Hematology, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, NO.19 Xiuhua Road, Xiuying District, Haikou, 570311, Hainan Province, China.
Objective: Chronic graft-versus-host disease (cGVHD) is a significant complication following allogenic hematopoietic stem cell transplantation, often necessitating therapeutic interventions such as rituximab (RTX) and cyclosporin A (CsA). This study aims to elucidate the mechanisms by which RTX and CsA jointly address B-cell dysregulation in cGVHD, providing a theoretical foundation and scientific rationale for the treatment and prognostic evaluation of this condition.
Methods: A total of 30 cGVHD mouse models were established by subjecting recipient mice to total body irradiation followed by injection of a mixed suspension of bone marrow cells and splenocytes from donor mice.
Small
August 2024
Institute of Biomedical Engineering, University of Toronto, Toronto, ON, M5S 3G9, Canada.
Structural DNA nanotechnology enables custom fabrication of nanoscale devices and promises diverse biological applications. However, the effects of design on DNA nanostructure (DN)-cell interactions in vitro and in vivo are not yet well-characterized. origamiFISH is a recently developed technique for imaging DNs in cells and tissues.
View Article and Find Full Text PDFXi Bao Yu Fen Zi Mian Yi Xue Za Zhi
November 2023
Department of Comprehensive Basic Experiment (Division Two), Strategic Support Force Medical Center, Beijing 100101, China. *Corresponding authors, E-mail:
Objective To investigate the effects of collagen peptides on the immune function of mice under the condition of X-ray irradiation combined with simulated weightlessness. Methods Mice were randomly divided into control group, modelling group and collagen peptide group. Mice in collagen peptide group were intraperitoneally injected with collagen peptide (600 mg/kg) once a day from the first day of the experiment, while mice in the other two groups were intraperitoneally injected with normal saline.
View Article and Find Full Text PDFIn the present study, for the first time, we released and assembled the particles of three major structural proteins of velogenic NDV (M, HN, and F glycoproteins) as a NDV-VLPs. The ElISA result of the cytokines of splenocyte suspension cells showed that IL2, IL10, TNF-α, and IFN- ˠ titers were significantly higher (p ≤ 0.05) in mice that were immunized only with NDV-VLPs three times with a 10-day interval, in comparison to those that were immunized with NDV-VLPs twice in a 10-day interval and received a B1 live vaccine boost on the third interval.
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