Evidence map›Paper›PMID 30597938›Full record

ArticleViruses2018

Pre-Existing Dengue Immunity Drives a DENV-Biased Plasmablast Response in ZIKV-Infected Patient.

Siddhartha K Bhaumik, Lalita Priyamvada, Robert C Kauffman, Lilin Lai, Muktha S Natrajan, Alice Cho, Nadine Rouphael, Mehul S Suthar, Mark J Mulligan, Jens Wrammert

Open access · goldAbstract readCase Reports
In one paragraph

Article in Viruses, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Siddhartha K BhaumikDivision of Infectious Disease, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA. siddharthabhaumik@gmail.com.
Lalita PriyamvadaDivision of Infectious Disease, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA. odk7@cdc.gov.ORCID 0000-0002-0479-0164
Robert C KauffmanDivision of Infectious Disease, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA. robert.kauffman@emory.edu.
Lilin LaiHope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, School of Medicine, Emory University, Decatur, GA 30033, USA. llai@emory.edu.
Muktha S NatrajanHope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, School of Medicine, Emory University, Decatur, GA 30033, USA. muktha.natrajan@emory.edu.
Alice ChoDivision of Infectious Disease, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA. alice.hong.cho@emory.edu.
Nadine RouphaelHope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, School of Medicine, Emory University, Decatur, GA 30033, USA. nroupha@emory.edu.
Mehul S SutharDivision of Infectious Disease, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA. mehul.s.suthar@emory.edu.
Mark J MulliganHope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, School of Medicine, Emory University, Decatur, GA 30033, USA. mark.mulligan@nyulangone.org.
Jens WrammertDivision of Infectious Disease, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA. jwramme@emory.edu.
Emory University · US

Funding

VACCINE INDUCED IMMUNITY IN THE YOUNG AND AGEDU19AI057266 · NIAID · EMORY UNIVERSITY · PI Rafi Ahmed · 2003 to 2026
$81.7M
ALABAMA/ZAMBIA HIV VACCINE CLINICAL TRIALS UNIT (HVTU)U01AI047996 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GOEPFERT, PAUL A. · 2000 to 2006
$8.4M
Intervention to Reduce Dietary Sodium in HemodialysisR01NR010135 · NINR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SEVICK, MARY A · 2008 to 2011
$2.3M
NIAID NIH HHS U01 AI047996NIH HHS 1U01AI115651NIH HHS HHSN272201300018INIH HHS U19AI057266NINR NIH HHS R01 NR010135
6 · The paper itself

Abstract

The re-emergence of Zika virus (ZIKV) in the western hemisphere has most significantly affected dengue virus (DENV) endemic regions. Due to the geographical overlap between these two closely related flaviviruses, numerous individuals who suffered ZIKV infection during recent outbreaks may have also previously been exposed to DENV. As such, the impact of pre-existing dengue immunity on immune responses to ZIKV has been an area of focused research and interest. To understand how B cell responses to a ZIKV infection may be modulated by prior dengue exposures, we compared and contrasted plasmablast repertoire and specificity between two ZIKV-infected individuals, one dengue-naïve (ZK018) and the other dengue-experienced (ZK016). In addition to examining serological responses, we generated 59 patient plasmablast-derived monoclonal antibodies (mAbs) to define the heterogeneity of the early B cell response to ZIKV. Both donors experienced robust ZIKV-induced plasmablast expansions early after infection, with comparable mutational frequencies in their antibody variable genes. However, notable differences were observed in plasmablast clonality and functional reactivity. Plasmablasts from the dengue-experienced donor ZK016 included cells with shared clonal origin, while ZK018 mAbs were entirely clonally unrelated. Both at the mAb and plasma level, ZK016 antibodies displayed extensive cross-reactivity to DENV1-4, and preferentially neutralized DENV compared to ZIKV. In contrast, the neutralization activity of ZK018 mAbs was primarily directed towards ZIKV, and fewer mAbs from this donor were cross-reactive, with the cross-reactive phenotype largely limited to fusion loop-specific mAbs. ZK016 antibodies caused greater enhancement of DENV2 infection of FcRγ-expressing cells overall compared to ZK018, with a striking difference at the plasma level. Taken together, these data strongly suggest that the breadth and protective capacity of the initial antibody responses after ZIKV infection may depend on the dengue immune status of the individual. These findings have implications for vaccine design, given the likelihood that future epidemics will involve both dengue-experienced and naïve populations.

Indexed as

Cross ReactionsImmunologic MemoryAdultAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralB-LymphocytesDengueDengue VirusFemaleHumansPlasma CellsZika Virus InfectionAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralantibodiesB-cellcross-reactivityDENVplasmablastZIKV

Identifiers

PMID30597938
PMCPMC6356269
OpenAlexW2906919037

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.