CS269050B1 - Lymphocyte Mice VU VIH7 - Google Patents
Lymphocyte Mice VU VIH7 Download PDFInfo
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- CS269050B1 CS269050B1 CS888955A CS895588A CS269050B1 CS 269050 B1 CS269050 B1 CS 269050B1 CS 888955 A CS888955 A CS 888955A CS 895588 A CS895588 A CS 895588A CS 269050 B1 CS269050 B1 CS 269050B1
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Abstract
Riešenie sa týká myšieho lymfocy tárneho hybridůmu, produkujúceho protilátku podtriedy IgG 2a proti nukleoproteinu virusu chřipky A. Hybridům Je uložený v zbierke hybrídůmov Virologického ústavu SAV v Bratislavě pod označením VU VIH7The solution concerns a mouse lymphocyte hybridoma producing an IgG 2a subclass antibody against the nucleoprotein of influenza A virus. The hybridoma is stored in the hybridoma collection of the Institute of Virology of the Slovak Academy of Sciences in Bratislava under the designation VU VIH7.
Description
CS 269 050 B1 1EN 269 050 B1 1
Vynález ea týká myšieho lymfocytárneho hybridámu, t. j, hybrídného jedno-bunkovóho organizmu,· zoatrojeného buňkovou fúziou myšej myelomovej linie Sp2/0a myšej slezinovej buňky, produkujúceho protilátku proti virusu chřipky A,The invention and the invention relates to a mouse lymphocyte hybridoma, i.e., a hybrid single-cell organism, driven by cell fusion of a mouse Sp2 / 0a myeloma line, and a mouse spleen cell producing an anti-influenza A antibody,
Protilátky voči proteínom virusu chřipky sa doteraz pripravojú tak, že vi-rus resp, jeho izolované proteiny sa opakované lnjikujú ako antigán pokusným zvie-ratám, najčastějšie králikom, myšiam, alebo fretkám. Sérum takto imunizovanýchzvierat, odobrate po určitej době posobenia antigénu, slúží ako zdroj protilátok,používaných predošetkým pre kvantitativná alebo kvalitativnu analýzu antigénu - virusu chřipky - vo výskume a v ímunodiagnostickej praxi. fAntibodies to influenza virus proteins have so far been prepared so that the viral or its isolated proteins are repeatedly injected as an antigen by experimental animals, most often rabbits, mice, or ferrets. The serum immunized in this way, removed after a certain period of antigen challenge, serves as a source of antibodies used primarily for the quantitative or qualitative analysis of the influenza virus - in research and practice. F
Tento postup, nazývaný konvenčnou imunizáciou, má niekolko nevýhod, V sé-re imunizovaných zvierat sa nachádza heterogenná zmes protilátok, ktorých spek-trum Je v každom jednotlivom organizme rožne a neopakovatelné. Organizmus spra-vidla vytvoří okrem protilátok voči žladanému antigénu i protilátky voči nečisto-tám antigenovóho preparátu, ktoré Je potřebné zo sér odstraňoval vysycovaním.Výrobné šarže konvenčných sér sa preto dajú lažko Standardizoval a bývajúv širokom rozmedzí kvality. Pre výrobu každej šarže třeba připravil čistý imu-nizačný antigón a 3alšie antigény na vysýtenie balastných protilátok proti ne-čistotám.This process, termed conventional immunization, has several disadvantages. A heterogeneous mixture of antibodies whose spectrum is in each individual organism is non-repeatable is found in the sera of immunized animals. Typically, the antibody creates antibodies to the antigen and antibody to the antigenic impurity impurities needed to remove them from the sera. Consequently, batches of conventional sera can be standardized and used in a wide range of quality. For the production of each batch, pure immunization antigen and 3 other antigens were prepared to saturate the non-purification ballast antibodies.
Uvedené nedostatky vyššie zmieneného a dosial používaného postupu odpadnu,ak je k dispozicii hybridám, produkujúcl monoklonélnu protilátku proti nukleoprotei-nu virusu chřipky A, uložený v zbierke hybridámov Virologického ústavu SAV v Bra-tislavě, Mlýnská dolina 1, pod označením VUVIH7,The above drawbacks of the aforementioned and hitherto used method, when hybrid is available, produce a monoclonal antibody against influenza A virus nucleoprotein, deposited in the hybrid collection of the Virological Institute of the SAS in Brač, Mill Valley 1, under the name VUVIH7,
Uvedený hybridám bol získaný spobobom známým z odbornej literatury (Kohler. G.,Milstein, C.: Continuous cultures of fused cells secreting antibody of predefinedspecificity. Nátuře, 256, (1975), 4951 Gerhard.W,: Fusion of cells in suspensionand outgrowth of hybrida in conditioned medium, In; Monoclonal antibodies, Hybrids: A New Oimension in Blological Analyses, R, H. Kennet, T.3. McKearn, K.B. Bechtol,eds. , Nex York, Plenům Press (1980), 370.) klonováním súboru hybridných buniekpo fúzii myšej myelomovej linie Sp2/0 a buniek, získaných zo sleziny myši kmeř.a BALB/c,imunizovaných virusom chřipky A/Dunadln/4/73 (H3N2), Výhodou hybrldámu podlá vynálezu je, ze produkuje homogennú protilátku, tzv,monoklonálnu protilátku, ktorá je schopná specificky reagoval s nukleoproteinomchřipkového virusu typu A. Hybridám VU VIH7 možno kultivoval in vitro v médiachvhodných pre živočišné buňky, alebo in vivo v peritoneálnej dutině myši kmefla BALB/c, Z konzerv, uchovaných v kvapalnom dusíku, možno zahájil produkciu protilátky bezáelšej imunizácie antigónom. PřikladSaid hybridoma was obtained from a known literature (Kohler, G., Milstein, C .: Continuous cultures of fused cells secreting antibodies of predefined specificity. Nature, 256, (1975), 4951 Gerhard.W ,: Fusion of cells in suspensionand outgrowth Hybrids: A New Oimension in Blological Analysis, R, H. Kennet, T.3, McKearn, KB Bechtol, eds., Nex York, Plenum Press (1980), 370.) by cloning the hybrid cell array by fusing the mouse myeloma line Sp2 / 0 and the spleen cells derived from the BALB / c mouse immunized with influenza virus A / Dunadln / 4/73 (H3N2), the advantage of which is that it produces a homogeneous antibody, a so-called monoclonal antibody that is capable of specifically reacting with a nucleoprotein-influenza virus of type A. The VU VIH7 hybrid can be cultured in vitro in animal cell media, or in vivo in the peritoneal cavity of the BALB / c mouse, conserved Preserved in liquid nitrogen, production of antibody by more immunization with antigen may be initiated. Example
Pre účel pomnoženia hybridámových buniek in vivo sa aplikovalo 5 x 106 buniekdo peritoneálnej dutiny myši, Pre lepšie uchytenie aplikovaných buniek bda myšFor the purpose of propagating hybridoma cells in vivo, 5 x 10 6 cells were injected into the peritoneal cavity of the mouse, For better attachment of the applied cells, the bda mouse
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Application Number | Priority Date | Filing Date | Title |
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CS888955A CS269050B1 (en) | 1988-12-29 | 1988-12-29 | Lymphocyte Mice VU VIH7 |
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CS888955A CS269050B1 (en) | 1988-12-29 | 1988-12-29 | Lymphocyte Mice VU VIH7 |
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CS895588A1 CS895588A1 (en) | 1989-08-14 |
CS269050B1 true CS269050B1 (en) | 1990-04-11 |
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CS888955A CS269050B1 (en) | 1988-12-29 | 1988-12-29 | Lymphocyte Mice VU VIH7 |
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