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WO1994011507A3 - Production of monoclonal recombinant antibodies without the use of hybridomas by in vitro spleen fragment culture combined with isothermal self-sustained sequence replication of rna - Google Patents

Production of monoclonal recombinant antibodies without the use of hybridomas by in vitro spleen fragment culture combined with isothermal self-sustained sequence replication of rna Download PDF

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Publication number
WO1994011507A3
WO1994011507A3 PCT/US1993/011295 US9311295W WO9411507A3 WO 1994011507 A3 WO1994011507 A3 WO 1994011507A3 US 9311295 W US9311295 W US 9311295W WO 9411507 A3 WO9411507 A3 WO 9411507A3
Authority
WO
WIPO (PCT)
Prior art keywords
rna
hybridomas
production
recombinant antibodies
sequence replication
Prior art date
Application number
PCT/US1993/011295
Other languages
French (fr)
Other versions
WO1994011507A2 (en
Inventor
Thomas R Gingeras
Norman R M D Klinman
Cathy A Stillman
Phyllis-Jean Linton
Debra J Decker
Matthew C Biery
Original Assignee
Thomas R Gingeras
Norman R M D Klinman
Cathy A Stillman
Linton Phyllis Jean
Debra J Decker
Matthew C Biery
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Thomas R Gingeras, Norman R M D Klinman, Cathy A Stillman, Linton Phyllis Jean, Debra J Decker, Matthew C Biery filed Critical Thomas R Gingeras
Priority to EP94902330A priority Critical patent/EP0628076A1/en
Priority to AU56737/94A priority patent/AU5673794A/en
Publication of WO1994011507A2 publication Critical patent/WO1994011507A2/en
Publication of WO1994011507A3 publication Critical patent/WO1994011507A3/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6844Nucleic acid amplification reactions
    • C12Q1/6865Promoter-based amplification, e.g. nucleic acid sequence amplification [NASBA], self-sustained sequence replication [3SR] or transcription-based amplification system [TAS]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Wood Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Immunology (AREA)
  • Biochemistry (AREA)
  • Zoology (AREA)
  • Biophysics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Microbiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Analytical Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Peptides Or Proteins (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

The invention is directed to a method for producing a recombinant protein having a preselected binding affinity and specificity for a given antigen. Generally, the method combines spleen fragment culture for the in vitro somatic mutation of B cells in response to antigen, followed by preferential amplification of RNA encoding heavy and light chains of desired antibodies produced by those B cells. The amplified RNA is then converted to DNA and incorporated into expression vectors; transfected host cells then express the antibody chains or a single chain antibody having preselected characteristics. Also disclosed are generic degenerate primer pools for the efficient amplification of RNA encoding mouse IgG.
PCT/US1993/011295 1992-11-19 1993-11-19 Production of monoclonal recombinant antibodies without the use of hybridomas by in vitro spleen fragment culture combined with isothermal self-sustained sequence replication of rna WO1994011507A2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP94902330A EP0628076A1 (en) 1992-11-19 1993-11-19 PRODUCTION OF MONOCLONAL RECOMBINANT ANTIBODIES WITHOUT THE USE OF HYBRIDOMAS BY $i(IN VITRO) SPLEEN FRAGMENT CULTURE COMBINED WITH ISOTHERMAL SELF-SUSTAINED SEQUENCE REPLICATION OF RNA
AU56737/94A AU5673794A (en) 1992-11-19 1993-11-19 Production of monoclonal recombinant antibodies without the use of hybridomas by (in vitro) spleen fragment culture combined with isothermal self-sustained sequence replication of rna

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US97883592A 1992-11-19 1992-11-19
US07/978,835 1992-11-19

Publications (2)

Publication Number Publication Date
WO1994011507A2 WO1994011507A2 (en) 1994-05-26
WO1994011507A3 true WO1994011507A3 (en) 1994-07-07

Family

ID=25526436

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1993/011295 WO1994011507A2 (en) 1992-11-19 1993-11-19 Production of monoclonal recombinant antibodies without the use of hybridomas by in vitro spleen fragment culture combined with isothermal self-sustained sequence replication of rna

Country Status (3)

Country Link
EP (1) EP0628076A1 (en)
AU (1) AU5673794A (en)
WO (1) WO1994011507A2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU6266899A (en) * 1998-10-05 2000-04-26 Ludwig Institute For Cancer Research Methods for producing human tumor antigen specific antibodies
EP1392866B1 (en) * 2001-05-14 2012-03-28 Henry Hongjun Ji Novel method for cloning variable domain sequences of immunological gene repertoire
GB0701253D0 (en) 2007-01-23 2007-02-28 Diagnostics For The Real World Nucleic acid amplification and testing
EP3961214A1 (en) 2010-12-31 2022-03-02 BioAtla, Inc. Comprehensive monoclonal antibody generation

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992008800A1 (en) * 1990-11-13 1992-05-29 Siska Diagnostics, Inc. Nucleic acid amplification by two-enzyme, self-sustained sequence replication

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992008800A1 (en) * 1990-11-13 1992-05-29 Siska Diagnostics, Inc. Nucleic acid amplification by two-enzyme, self-sustained sequence replication

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
LINTON, P-J. ET AL.;: "Primary antibody-forming cells and secondary B cells are generated from separate precursor cell populations", CELL, vol. 59, 22 December 1989 (1989-12-22), CAMBRIDGE, NA US, pages 1049 - 1059 *

Also Published As

Publication number Publication date
AU5673794A (en) 1994-06-08
EP0628076A1 (en) 1994-12-14
WO1994011507A2 (en) 1994-05-26

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