Evidence map›Paper›PMID 35059561›Full record

ArticleAntibody therapeutics2022

CellCelector™ as a platform in isolating primary B cells for antibody discovery.

Wadim L Matochko, Constantin Nelep, Weihsu C Chen, Stephanie Grauer, Karyn McFadden, Vicki Wilson, Kirill Oxenoid

Abstract read
In one paragraph

Article in Antibody therapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

7 authors.

Wadim L MatochkoBiologics Discovery, Department of Therapeutic Discovery, Amgen British Columbia Inc., Burnaby, Canada.ORCID https://orcid.org/0000-0001-7387-9106
Constantin NelepMarketing and Application Development, ALS Automated Lab Solutions GmbH, Jena, Germany.
Weihsu C ChenBiologics Discovery, Department of Therapeutic Discovery, Amgen British Columbia Inc., Burnaby, Canada.
Stephanie GrauerBiologics Discovery, Department of Therapeutic Discovery, Amgen British Columbia Inc., Burnaby, Canada.
Karyn McFaddenBiologics Discovery, Department of Therapeutic Discovery, Amgen British Columbia Inc., Burnaby, Canada.
Vicki WilsonBiologics Discovery, Department of Therapeutic Discovery, Amgen British Columbia Inc., Burnaby, Canada.
Kirill OxenoidBiologics Discovery, Department of Therapeutic Discovery, Amgen British Columbia Inc., Burnaby, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The most robust strategy in antibody discovery is the use of immunized animals and the ability to isolate and immortalize immune B-cells to hybridoma for further interrogation. However, capturing the full repertoire of an immunized animal is labor intensive, time consuming and limited in throughput. Therefore, techniques to directly mine the antibody repertoire of primary B-cells are of great importance in antibody discovery. In the current study, we present a method to isolate individual antigen-specific primary B-cells using the CellCellector™ single-cell isolation platform from XenoMouse® (XM) immunized with a recombinant therapeutic protein, EGFR. We screened a subset of CD138+ B-cells and identified 238 potential EGFR-specific B-cells from 1189 antibody-secreting cells (ASCs) and isolated 94 by CellCellector. We identified a diverse set of heavy chain complementarity-determining region sequences and cloned and expressed 20 into a standard human immunoglobulin G1 antibody format. We further characterized and identified 13 recombinant antibodies that engage soluble and native forms of EGFR. By extrapolating the method to all 400 000 CD138+ B-cells extracted from one EGFR immunized XM, a potential 1196 unique EGFR-specific antibodies could be discovered. CellCelector allows for interrogating the B-cell pool directly and isolating B-cells specific to the therapeutic target of interest. Furthermore, antibody sequences recovered from isolated B-cells engage the native and recombinant target, demonstrating the CellCellector can serve as a platform in antibody discovery.

Indexed as

antibody discoveryantibody generationASCB-cellCellCelector™

Identifiers

PMID35059561
PMCPMC8764991

What OpenQuestion holds

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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.