Evidence map›Paper›PMID 37405655›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Antibody-Secreting Cell Isolation from Different Species for Microfluidic Antibody Hit Discovery.

Ramona Gaa, Qingyong Ji, Achim Doerner

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Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Ramona GaaProtein Engineering and Antibody Technologies, Merck Healthcare KGaA, Darmstadt, Germany.
Qingyong JiProtein Engineering and Antibody Technologies, EMD Serono, Billerica, MA, USA.
Achim DoernerProtein Engineering and Antibody Technologies, Merck Healthcare KGaA, Darmstadt, Germany. achim.doerner@merckgroup.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The recent advent of microfluidic-assisted antibody hit discovery as standard methodology accelerated pharmaceutical research. While work on compatible recombinant antibody library approaches is ongoing, the major source of antibody-secreting cells (ASCs) remains to be primary B cells of mostly rodent origin. As fainting viability and secretion rates can lead to false-negative screening results, careful preparation of these cells is an essential prerequisite for successful hit discovery. We here describe procedures to enrich plasma cells from relevant tissues of mice and rats and plasmablasts from human blood donations. Although freshly prepared ASCs yield the most robust results, suitable freezing and thawing protocols to preserve the viability and antibody secretory function can circumvent extensive process time and allow transferring of samples between laboratories. An optimized procedure is described to yield similar secretion rates after prolonged storage when compared to freshly prepared cells. Finally, the identification of ASC-containing samples can increase the probability of success of droplet-based microfluidics-two methods for pre- or in-droplet staining are described. In summary, the preparative methods described herein can facilitate robust and successful microfluidic antibody hit discovery.

Indexed as

AntibodiesMicrofluidicsAnimalsAntibody-Producing CellsB-LymphocytesHumansPlasma CellsRatsAntibodiesAntibody-secreting cell (ASC)MicrofluidicsPlasmablastPlasma cellPrimary cell isolation

Identifiers

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Registered trials

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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.