Evidence map›Paper›PMID 10648934›Full record

ReviewJournal of immunological methods1999

Transgenic milk as a method for the production of recombinant antibodies.

D P Pollock, J P Kutzko, E Birck-Wilson, J L Williams, Y Echelard, H M Meade

Abstract readReview
In one paragraph

Review in Journal of immunological methods, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed.

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  12. Investigation of hFVIII production in mammary glands of transgenic mice.Monoclonal antibodies in immunodiagnosis and immunotherapy · 2014
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

D P PollockGenzyme Transgenics, One Mountain Rd, Framingham, MA 01701-9322, USA.
J P Kutzko
E Birck-Wilson
J L Williams
Y Echelard
H M Meade

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recombinant antibodies and their derivatives are increasingly being used as therapeutic agents. Clinical applications of antibodies often require large amounts of highly purified molecules, sometimes for multiple treatments. The development of very efficient expression systems is essential to the full exploitation of the antibody technology. Production of recombinant protein in the milk of transgenic dairy animals is currently being tested as an alternative to plasma fractionation for the manufacture of a number of blood factors (human antithrombin, human alpha-1-antitrypsin, human serum albumin, factor IX). The ability to routinely yield mg/ml levels of antibodies and the scale-up flexibility make transgenic production an attractive alternative to mammalian cell culture as a source of large quantities of biotherapeutics. The following review examines the potential of transgenic expression for the production of recombinant therapeutic antibodies.

Indexed as

Animals, Genetically ModifiedAntibody FormationAnimalsCloning, MolecularFemaleGene ExpressionGerm CellsGoatsHumansMammary Glands, AnimalMilkRecombinant Fusion ProteinsTransgenesRecombinant Fusion Proteins

Identifiers

PMID10648934
PMCPMC7125573

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.