Evidence map›Paper›PMID 38954386›Full record

ReviewBioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy2024

Monoclonal Antibody Generation Using Single B Cell Screening for Treating Infectious Diseases.

John S Schardt, Neelan S Sivaneri, Peter M Tessier

Erratum issuedAbstract readReview
In one paragraph

Review in BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Discovery of Therapeutic Antibodies Targeting Complex Multi-Spanning Membrane Proteins.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

John S SchardtDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI, 48109, USA.
Neelan S SivaneriDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
Peter M TessierDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI, 48109, USA. ptessier@umich.edu.ORCID http://orcid.org/0000-0002-3220-007X

Funding

CD98hc Brain Shuttles for Delivering Off-the-shelf Neuroprotective Antibodies in Alzheimer's DiseaseR01AG080016 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Colin Fred Greineder, Peter M Tessier · 2023 to 2026
$3.2M
Structure-guided antibody targeting of pre-selected epitopes in amyloidogenic aggregatesR35GM136300 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TESSIER, PETER M · 2020 to 2024
$1.5M
Neuronal Silencing of ATXN3 Using Peripherally Administered Antibody/ASO Conjugates That Penetrate the Blood-Brain BarrierR21NS132018 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TESSIER, PETER M · 2023 to 2024
$429k
Mutational Analysis of Tradeoffs between Receptor Affinity and Antibody Escape for SARS-CoV-2 Variants of ConcernR21AI171844 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TESSIER, PETER M · 2022 to 2023
$405k
Administrative Supplement: Activity-based Discovery and OptimizationF32GM137513 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCHARDT, JOHN SAMUEL · 2020 to 2022
$141k
Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases R21AI171844NIAID NIH HHS R21 AI171844NIA NIH HHS R01 AG080016NIA NIH HHS R01AG080016NIGMS NIH HHS F32 GM137513NIGMS NIH HHS R35 GM136300NIGMS NIH HHS R35GM136300NINDS NIH HHS R21 NS132018NINDS NIH HHS R21NS132018
6 · The paper itself

Abstract

The screening of antigen-specific B cells has been pivotal for biotherapeutic development for over four decades. Conventional antibody discovery strategies, including hybridoma technology and single B cell screening, remain widely used based on their simplicity, accessibility, and proven track record. Technological advances and the urgent demand for infectious disease applications have shifted paradigms in single B cell screening, resulting in increased throughput and decreased time and labor, ultimately enabling the rapid identification of monoclonal antibodies with desired biological and biophysical properties. Herein, we provide an overview of conventional and emergent single B cell screening approaches and highlight their potential strengths and weaknesses. We also detail the impact of innovative technologies-including miniaturization, microfluidics, multiplexing, and deep sequencing-on the recent identification of broadly neutralizing antibodies for infectious disease applications. Overall, the coronavirus disease 2019 (COVID-19) pandemic has reinvigorated efforts to improve the efficiency of monoclonal antibody discovery, resulting in the broad application of innovative antibody discovery methodologies for treating a myriad of infectious diseases and pathological conditions.

Indexed as

Antibodies, MonoclonalB-LymphocytesAnimalsAntibodies, NeutralizingCommunicable DiseasesCOVID-19COVID-19 Drug TreatmentHumansSARS-CoV-2Single-Cell AnalysisAntibodies, MonoclonalAntibodies, Neutralizing

Identifiers

PMID38954386
PMCPMC11645890

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.