Evidence map›Paper›PMID 42239768›Full record

ArticleResearch square2026

Crimean-Congo hemorrhagic fever virus protein GP38 from isolate M18-China confers broad immunological breadth.

Albert Wang, Stephanie R Monticelli, Christy K Hjorth, Thomas G Batchelor, Alexandra L Tse, Ana I Keuhne, Russell R Bakken, N A Saavedra-Avila, Gorka Lasso, Jacob Berrigan and 4 more

Abstract readPreprint
In one paragraph

Article in Research square, 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

14 authors.

Albert WangAlbert Einstein College of Medicine.
Stephanie R MonticelliU.S. Army Medical Research Institute of Infectious Diseases.
Christy K HjorthThe University of Texas at Austin.
Thomas G BatchelorU.S. Army Medical Research Institute of Infectious Diseases.
Alexandra L TseAlbert Einstein College of Medicine.
Ana I KeuhneU.S. Army Medical Research Institute of Infectious Diseases.
Russell R BakkenU.S. Army Medical Research Institute of Infectious Diseases.
N A Saavedra-AvilaAlbert Einstein College of Medicine.
Gorka LassoAlbert Einstein College of Medicine.
Jacob BerriganAlbert Einstein College of Medicine.
Steven A PorcelliAlbert Einstein College of Medicine.
Jason S McLellanThe University of Texas at Austin.
Andrew S HerbertU.S. Army Medical Research Institute of Infectious Diseases.
Kartik ChandranAlbert Einstein College of Medicine.

Funding

Research Project 4: Mining human antibody responses to inform vaccine and therapeutic designU19AI181977 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Kartik Chandran · 2024 to 2026
$56.1M
Medical Scientist Training ProgramT32GM149364 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Myles H. Akabas · 2023 to 2026
$7.5M
Structure-based Vaccine Design for CCHFVR01AI152246 · NIAID · UNIVERSITY OF TEXAS AT AUSTIN · PI CHANDRAN, KARTIK, MCLELLAN, JASON SCOTT · 2020 to 2024
$2.2M
NIAID NIH HHS R01 AI152246NIAID NIH HHS U19 AI181977NIGMS NIH HHS T32 GM149364
6 · The paper itself

Abstract

Crimean-Congo hemorrhagic fever virus (CCHFV) is a tick-borne, negative-strand RNA virus that causes outbreaks of lethal hemorrhagic fever. No approved vaccines or specific antiviral treatments are available. CCHFV glycoprotein GP38 is an integral component of the pre-fusion glycoprotein entry complex, plays roles in viral pathogenesis, and is a key target of antibody-mediated protection. Herein, we investigated the hypothesis that recombinant GP38 itself could elicit protection against divergent CCHFV isolates/strains in an animal model. Accordingly, we generated GP38 immunogens from six CCHFV clades and showed that GP38 from the isolate M18-China induces a broad immunological response in mice despite its lower amino acid sequence similarity to other isolates. We identified sequences in M18-China GP38 associated with this immunological breadth and evaluated it as a vaccine candidate. Although M18-China GP38 was not protective in isolation, our findings warrant further exploration of its utility as one component of a broadly protective CCHFV vaccine.

Identifiers

PMID42239768
PMCPMC13228812

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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.