Evidence map›Paper›PMID 27007118›Full record

ArticlePloS one2016

A Comparison of the Adaptive Immune Response between Recovered Anthrax Patients and Individuals Receiving Three Different Anthrax Vaccines.

Thomas R Laws, Tinatin Kuchuloria, Nazibriola Chitadze, Stephen F Little, Wendy M Webster, Amanda K Debes, Salome Saginadze, Nikoloz Tsertsvadze, Mariam Chubinidze, Robert G Rivard and 5 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Human anthrax vaccines: Current status and future prospects.Human vaccines & immunotherapeutics · 2025
    Review
  2. Review
  3. Article
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  6. Article
  7. Article
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  10. Zoonoses under our noses.Microbes and infection
    Review
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

15 authors at 5 institutions in 3 countries.

Thomas R LawsDefence Science and Technology Laboratory, DSTL Porton Down, Salisbury, United Kingdom.
Tinatin KuchuloriaDepartment of Public Health, Tbilisi State University, Tbilisi, Georgia.
Nazibriola ChitadzeNational Center for Disease Control and Public Health (NCDC), Tbilisi, Georgia.
Stephen F LittleU. S. Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, MD, United States of America.
Wendy M WebsterU. S. Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, MD, United States of America.
Amanda K DebesU. S. Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, MD, United States of America.
Salome SaginadzeNational Center for Disease Control and Public Health (NCDC), Tbilisi, Georgia.
Nikoloz TsertsvadzeNational Center for Disease Control and Public Health (NCDC), Tbilisi, Georgia.
Mariam ChubinidzeNational Center for Disease Control and Public Health (NCDC), Tbilisi, Georgia.
Robert G RivardU. S. Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, MD, United States of America.
Shota TsanavaDepartment of Public Health, Tbilisi State University, Tbilisi, Georgia.
Edward H DysonDefence Science and Technology Laboratory, DSTL Porton Down, Salisbury, United Kingdom.
Andrew J H SimpsonDefence Science and Technology Laboratory, DSTL Porton Down, Salisbury, United Kingdom.
Matthew J HepburnU. S. Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, MD, United States of America.
Nino TrapaidzeClinical Research Unit (CRU), Technology Management Company (TMC), Tbilisi, Georgia.
National Center for Disease Control and Public Health · GEUnited States Army Medical Research Institute of Infectious Diseases · USDefence Science and Technology Laboratory · GBTbilisi State University · GETechnology Management Company (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several different human vaccines are available to protect against anthrax. We compared the human adaptive immune responses generated by three different anthrax vaccines or by previous exposure to cutaneous anthrax. Adaptive immunity was measured by ELISPOT to count cells that produce interferon (IFN)-γ in response to restimulation ex vivo with the anthrax toxin components PA, LF and EF and by measuring circulating IgG specific to these antigens. Neutralising activity of antisera against anthrax toxin was also assayed. We found that the different exposures to anthrax antigens promoted varying immune responses. Cutaneous anthrax promoted strong IFN-γ responses to all three antigens and antibody responses to PA and LF. The American AVA and Russian LAAV vaccines induced antibody responses to PA only. The British AVP vaccine produced IFN-γ responses to EF and antibody responses to all three antigens. Anti-PA (in AVA and LAAV vaccinees) or anti-LF (in AVP vaccinees) antibody titres correlated with toxin neutralisation activities. Our study is the first to compare all three vaccines in humans and show the diversity of responses against anthrax antigens.

Indexed as

Adaptive ImmunityAdultAnthraxAnthrax VaccinesAntibodies, BacterialAntigens, BacterialBacterial ToxinsFemaleHumansImmune SeraImmunoglobulin GInterferon-gammaMaleMiddle AgedSkin Diseases, BacterialVaccinationanthrax toxinAnthrax VaccinesAntibodies, BacterialAntigens, BacterialBacterial ToxinsImmune SeraImmunoglobulin GInterferon-gamma

Identifiers

PMID27007118
PMCPMC4805272
OpenAlexW2305930557

What OpenQuestion holds

Textmetadata
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.