Evidence map›Paper›PMID 38167935›Full record

ArticleNature medicine2024

A candidate antibody drug for prevention of malaria.

Katherine L Williams, Steve Guerrero, Yevel Flores-Garcia, Dongkyoon Kim, Kevin S Williamson, Christine Siska, Pauline Smidt, Sofia Z Jepson, Kan Li, S Moses Dennison and 20 more

Open access · hybridAbstract read
In one paragraph

Article in Nature medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
25.0field-weighted citation impact, top 1% of its field
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

39 citing papers in PubMed, 46 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Machine learning enables de novo multiepitope design ofProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors at 11 institutions in 2 countries.

Katherine L WilliamsAtreca, Inc., San Carlos, CA, USA. kwilliams@atreca.com.ORCID 0000-0003-1657-6795
Steve GuerreroAtreca, Inc., San Carlos, CA, USA.ORCID 0009-0006-6748-8153
Yevel Flores-GarciaDepartment of Molecular Microbiology and Immunology, Malaria Research Institute, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Dongkyoon KimAtreca, Inc., San Carlos, CA, USA.
Kevin S WilliamsonAtreca, Inc., San Carlos, CA, USA.
Christine SiskaJust - Evotec Biologics, Seattle, WA, USA.
Pauline SmidtJust - Evotec Biologics, Seattle, WA, USA.
Sofia Z JepsonJust - Evotec Biologics, Seattle, WA, USA.ORCID 0000-0003-2435-4906
Kan LiDuke Center for Human Systems Immunology, Department of Surgery, Duke University, Durham, NC, USA.
S Moses DennisonDuke Center for Human Systems Immunology, Department of Surgery, Duke University, Durham, NC, USA.ORCID 0000-0003-1198-9179
Shamika Mathis-TorresDepartment of Molecular Microbiology and Immunology, Malaria Research Institute, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Xiaomu ChenAtreca, Inc., San Carlos, CA, USA.
Ulrike Wille-ReeceBioNTech US, Inc., Cambridge, MA, USA.
Randall S MacGillPATH Center for Vaccine Innovation and Access, Washington DC, USA.ORCID 0000-0002-4566-1481
Michael WalkerWalker Bioscience, Carlsbad, CA, USA.
Erik JongertGSK, Rixensart, Belgium.
C Richter KingPATH Center for Vaccine Innovation and Access, Washington DC, USA.
Christian OckenhousePATH Center for Vaccine Innovation and Access, Washington DC, USA.
Jacob GlanvilleCentivax, Inc., South San Francisco, CA, USA.
James E MoonCenter for Enabling Capabilities, Walter Reed Army Institute of Research, Silver Spring, MD, USA.
Jason A RegulesWalter Reed Army Institute of Research, Silver Spring, MD, USA.
Yann Chong TanAtreca, Inc., San Carlos, CA, USA.
Guy CavetAtreca, Inc., San Carlos, CA, USA.
Shaun M LippowAtreca, Inc., San Carlos, CA, USA.
William H RobinsonDivision of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0003-4385-704X
Sheetij DuttaWalter Reed Army Institute of Research, Silver Spring, MD, USA.
Georgia D TomarasDuke Center for Human Systems Immunology, Department of Surgery, Duke University, Durham, NC, USA.ORCID 0000-0001-8076-1931
Fidel ZavalaDepartment of Molecular Microbiology and Immunology, Malaria Research Institute, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.ORCID 0000-0002-1414-6196
Randal R KetchemJust - Evotec Biologics, Seattle, WA, USA.ORCID 0000-0002-7821-2682
Daniel E EmerlingAtreca, Inc., San Carlos, CA, USA. danielemerling@biosimplify.com.ORCID 0000-0002-8754-9201
Evotec (United States) · USProgram for Appropriate Technology in Health · USDuke University · USJohns Hopkins University · USWalter Reed Army Institute of Research · USArcher Daniels Midland (United States) · USGlaxoSmithKline (Belgium) · BEKaryopharm Therapeutics (United States) · USMental Illness Research, Education and Clinical Centers · USStanford University · USWalker (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over 75% of malaria-attributable deaths occur in children under the age of 5 years. However, the first malaria vaccine recommended by the World Health Organization (WHO) for pediatric use, RTS,S/AS01 (Mosquirix), has modest efficacy. Complementary strategies, including monoclonal antibodies, will be important in efforts to eradicate malaria. Here we characterize the circulating B cell repertoires of 45 RTS,S/AS01 vaccinees and discover monoclonal antibodies for development as potential therapeutics. We generated >28,000 antibody sequences and tested 481 antibodies for binding activity and 125 antibodies for antimalaria activity in vivo. Through these analyses we identified correlations suggesting that sequences in Plasmodium falciparum circumsporozoite protein, the target antigen in RTS,S/AS01, may induce immunodominant antibody responses that limit more protective, but subdominant, responses. Using binding studies, mouse malaria models, biomanufacturing assessments and protein stability assays, we selected AB-000224 and AB-007088 for advancement as a clinical lead and backup. We engineered the variable domains (Fv) of both antibodies to enable low-cost manufacturing at scale for distribution to pediatric populations, in alignment with WHO's preferred product guidelines. The engineered clone with the optimal manufacturing and drug property profile, MAM01, was advanced into clinical development.

Indexed as

Antibodies, MonoclonalMalariaAnimalsB-LymphocytesChild, PreschoolHumansInfantMalaria VaccinesMiceAntibodies, MonoclonalMalaria Vaccines

Identifiers

PMID38167935
PMCPMC10803262
OpenAlexW4390501289

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.