Evidence map›Paper›PMID 41915428›Full record

ArticleThe Journal of clinical investigation2026

Human antibody targeting Crimean-Congo hemorrhagic fever virus glycoprotein 38 protects mice against heterologous virus challenge.

Nathaniel S Chapman, Viktoriya Borisevich, Nurgun Kose, Luke Myers, Stephen Priest, Éric Bergeron, Elena Trigo Esteban, María Paz Sánchez-Seco, José Melero, Thomas W Geisbert and 2 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

12 authors.

Nathaniel S ChapmanDepartment of Pathology, Microbiology and Immunology and.
Viktoriya BorisevichGalveston National Laboratory and.
Nurgun KoseThe Vanderbilt Center for Antibody Therapeutics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Luke MyersThe Vanderbilt Center for Antibody Therapeutics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Stephen PriestThe Vanderbilt Center for Antibody Therapeutics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Éric BergeronDepartment of Pharmaceutical and Biomedical Sciences, College of Pharmacy, University of Georgia, Athens, Georgia, USA.
Elena Trigo EstebanNational Referral Centre for Tropical Diseases and International Health, Hospital La Paz-Carlos III, IdIPaz, CIBERInfec, Madrid, Spain.
María Paz Sánchez-SecoLaboratory of Arbovirus and Imported Viral Diseases, National Center of Microbiology, and.
José MeleroLaboratory of Arbovirus and Imported Viral Diseases, National Center of Microbiology, and.
Thomas W GeisbertGalveston National Laboratory and.
Robert W CrossGalveston National Laboratory and.
James E CroweDepartment of Pathology, Microbiology and Immunology and.

Funding

Preclinical Development of Human Monoclonal Antibodies for Postexposure Treatment of Crimean-Congo Hemorrhagic FeverR01AI132246 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI GEISBERT, THOMAS WILLIAM · 2017 to 2021
$6.0M
NIAID NIH HHS R01 AI132246
6 · The paper itself

Abstract

Crimean-Congo hemorrhagic fever virus (CCHFV) is an emerging arboviral and zoonotic bunyavirus. CCHFV can infect livestock, wild animals, and humans. Here, we report the isolation of a panel of mAbs from the B cells of an immune individual following a natural nosocomial infection. We determined that the panel comprised antibodies that bound to 2 glycoproteins: (a) the carboxy-terminal glycoprotein (Gc) that serves as the fusion protein and (b) the glycoprotein 38 (GP38). By antibody variable gene analysis, we identified genetic diversity in the B cell response to CCHFV within a single donor for both Gc- and GP38-specific responses. Protection against most bunyavirus-associated diseases is mediated principally by neutralizing antibodies, but here, we found that neutralization activity was not associated with protection. Gc-specific antibodies to diverse antigenic sites neutralized only weakly and did not protect against heterologous virus challenge. GP38-specific antibodies bound to 2 dominant antigenic sites on the glycoprotein. Although GP38-specific antibodies did not neutralize the virus, one mediated protection against heterologous virus challenge in an experimental model of infection in mice primarily by complement-mediated activity. These studies support the development of protective CCHFV countermeasures against GP38.

Indexed as

Antibodies, MonoclonalAntibodies, ViralGlycoproteinsHemorrhagic Fever, CrimeanHemorrhagic Fever Virus, Crimean-CongoAnimalsAntibodies, NeutralizingB-LymphocytesFemaleHumansMiceAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralGlycoproteinsAdaptive immunityAntigenImmunoglobulinsInfectious diseaseVirology

Identifiers

PMID41915428
PMCPMC13178664

What Socratic 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 Socratic graph.