Evidence map›Paper›PMID 26850066›Full record

ArticleMalaria journal2016

Acquired immune responses to three malaria vaccine candidates and their relationship to invasion inhibition in two populations naturally exposed to malaria.

Otchere Addai-Mensah, Melanie Seidel, Nafiu Amidu, Dominika J Maskus, Stephanie Kapelski, Gudrun Breuer, Carmen Franken, Ellis Owusu-Dabo, Margaret Frempong, Raphaël Rakotozandrindrainy and 6 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

16 authors at 5 institutions in 3 countries.

Otchere Addai-MensahFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074, Aachen, Germany. oaddai-mensah.chs@knust.edu.gh.
Melanie SeidelFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074, Aachen, Germany. melanie.seidel@ime.fraunhofer.de.
Nafiu AmiduDepartment of Biomedical Laboratory Science, School of Medicine and Health Science, University for Development Studies, Tamale, Ghana. nafamidu@yahoo.com.
Dominika J MaskusFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074, Aachen, Germany. dominika.maskus@rwth-aachen.de.
Stephanie KapelskiFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074, Aachen, Germany. stephanie.kapelski@rwth-aachen.de.
Gudrun BreuerFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074, Aachen, Germany. gudrun.breuer@ime.fraunhofer.de.
Carmen FrankenFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074, Aachen, Germany. carmen.franken@ime.fraunhofer.de.
Ellis Owusu-DaboKumasi Centre for Collaborative Research, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana. owusudabo@kccr.de.
Margaret FrempongDepartment of Molecular Medicine, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana. mtfrempong@gmail.com.
Raphaël RakotozandrindrainyLaboratoire de Microbiologie et de Parasitologie, ESSAGRO-Faculté de Médecine, Université d'Antananarivo, Antananarivo, Madagascar. rakrapha13@gmail.com.
Helga SchinkelFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074, Aachen, Germany. helga.schinkel@ime.fraunhofer.de.
Andreas ReimannFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074, Aachen, Germany. andreas.reimann@ime.fraunhofer.de.
Torsten KlockenbringFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074, Aachen, Germany. torsten.klockenbring@ime.fraunhofer.de.
Stefan BarthFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074, Aachen, Germany. stefan.barth@uct.ac.za.
Rainer FischerFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074, Aachen, Germany. rainer.fischer@ime.fraunhofer.de.
Rolf FendelFraunhofer Institute for Molecular Biology and Applied Ecology IME, Forckenbeckstraße 6, 52074, Aachen, Germany. rolf.fendel@ime.fraunhofer.de.
Fraunhofer Institute for Molecular Biology and Applied Ecology · DERWTH Aachen University · DEKwame Nkrumah University of Science and Technology · GHUniversity for Development Studies · GHUniversity of Antananarivo · MG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMalaria still represents a major cause of morbidity and mortality predominantly in several developing countries, and remains a priority in many public health programmes. Despite the enormous gains made in control and prevention the development of an effective vaccine represents a persisting challenge. Although several parasite antigens including pre-erythrocytic antigens and blood stage antigens have been thoroughly investigated, the identification of solid immune correlates of protection against infection by Plasmodium falciparum or clinical malaria remains a major hurdle. In this study, an immuno-epidemiological survey was carried out between two populations naturally exposed to P. falciparum malaria to determine the immune correlates of protection.

methodsPlasma samples of immune adults from two countries (Ghana and Madagascar) were tested for their reactivity against the merozoite surface proteins MSP1-19, MSP3 and AMA1 by ELISA. The antigens had been selected on the basis of cumulative evidence of their role in anti-malarial immunity. Additionally, reactivity against crude P. falciparum lysate was investigated. Purified IgG from these samples were furthermore tested in an invasion inhibition assay for their antiparasitic activity.

resultsSignificant intra- and inter- population variation of the reactivity of the samples to the tested antigens were found, as well as a significant positive correlation between MSP1-19 reactivity and invasion inhibition (p < 0.05). Interestingly, male donors showed a significantly higher antibody response to all tested antigens than their female counterparts. In vitro invasion inhibition assays comparing the purified antibodies from the donors from Ghana and Madagascar did not show any statistically significant difference. Although in vitro invasion inhibition increased with breadth of antibody response, the increase was not statistically significant.

conclusionsThe findings support the fact that the development of semi-immunity to malaria is probably contingent on the development of antibodies to not only one, but a range of antigens and that invasion inhibition in immune adults may be a function of antibodies to various antigens. This supports strategies of vaccination including multicomponent vaccines as well as passive vaccination strategies with antibody cocktails.

Indexed as

AdultAntigens, ProtozoanChromatography, AffinityEnzyme-Linked Immunosorbent AssayFemaleHumansMalaria, FalciparumMalaria VaccinesMaleMiddle AgedPlasmodium falciparumProtozoan ProteinsAntigens, ProtozoanMalaria VaccinesProtozoan Proteins

Identifiers

PMID26850066
PMCPMC4743426
OpenAlexW2253770298

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.