Evidence map›Paper›PMID 25446174›Full record

ArticleActa tropica2015

Effect of transmission intensity and age on subclass antibody responses to Plasmodium falciparum pre-erythrocytic and blood-stage antigens.

Gregory S Noland, Paul Jansen, John M Vulule, Gregory S Park, Bartholomew N Ondigo, James W Kazura, Ann M Moormann, Chandy C John

Open access · greenAbstract read
In one paragraph

Article in Acta tropica, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
  2. Naturally acquired antibodies toFrontiers in immunology · 2026
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  4. Review
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  7. Review
  8. Review
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  12. Article
  13. Antibody Responses AgainstFrontiers in immunology · 2019
    Article
  14. Article
  15. Article
  16. Functional antibodies againstWellcome open research · 2018
    Article
  17. Article
  18. Article
  19. Synthetic Antigens Derived fromThe American journal of tropical medicine and hygiene · 2017
    Article
  20. 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

8 authors at 5 institutions in 2 countries.

Gregory S NolandDivision of Global Pediatrics, Department of Pediatrics, University of Minnesota Medical School, 717 Delaware Street, SE, Room 363, Minneapolis, MN 55414, USA. Electronic address: gregory.noland@emory.edu.
Paul JansenDivision of Global Pediatrics, Department of Pediatrics, University of Minnesota Medical School, 717 Delaware Street, SE, Room 363, Minneapolis, MN 55414, USA. Electronic address: jansenpa@gmail.com.
John M VululeCenter for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya. Electronic address: vulule@yahoo.com.
Gregory S ParkDivision of Global Pediatrics, Department of Pediatrics, University of Minnesota Medical School, 717 Delaware Street, SE, Room 363, Minneapolis, MN 55414, USA. Electronic address: parkx479@umn.edu.
Bartholomew N OndigoCenter for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya. Electronic address: ondigo2002@yahoo.com.
James W KazuraCenter for Global Health and Diseases, Case Western Reserve University, 10900 Euclid Avenue LC: 7286, Cleveland, OH 44106, USA. Electronic address: james.kazura@case.edu.
Ann M MoormannDivision of Pediatric Immunology & Infectious Diseases, Department of Pediatrics, University of Massachusetts Medical School - Biotech II, 373 Plantation Street, Suite 318, Worcester, MA 01605, USA. Electronic address: ann.moormann@umassmed.edu.
Chandy C JohnDivision of Global Pediatrics, Department of Pediatrics, University of Minnesota Medical School, 717 Delaware Street, SE, Room 363, Minneapolis, MN 55414, USA. Electronic address: ccj@umn.edu.
University of Minnesota · USKenya Medical Research Institute · KECenter for Global Health · USUniversity of Massachusetts Chan Medical School · USUniversity of Minnesota Medical Center · US

Funding

Naturally Acquired Immunity to Malaria during the Epidemiologic Transition in KenR01AI095192 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI KAZURA, JAMES WALTER · 2011 to 2015
$3.2M
Human immunity to MSP-1 in Western KenyaR01AI043906 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI KAZURA, JAMES WALTER · 2004 to 2008
$3.0M
Malaria transmission and immunity in highland KenyaU01AI056270 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI JOHN, CHANDY C. · 2005 to 2009
$2.9M
IMMUNOLOGIC MEMORY TO PREERYTHROCYTIC P FALCIPARUMU01AI043906 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI KAZURA, JAMES WALTER · 1998 to 2002
$1.5M
Translational Research in Malaria Transmission and Immunity in KenyaD43TW008085 · FIC · UNIVERSITY OF MINNESOTA · PI JOHN, CHANDY C. · 2008 to 2012
$752k
IMMUNE RESPONSES TO P FALCIPARUM IN HIGHLAND KENYAK08AI001572 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI JOHN, CHANDY C · 1999 to 2002
$350k
FIC NIH HHS D43 TW008085NIAID NIH HHS AI01572NIAID NIH HHS AI056270NIAID NIH HHS AI43906NIAID NIH HHS R01 AI043906NIAID NIH HHS R01 AI095192NIAID NIH HHS U01 AI043906NIAID NIH HHS U01 AI056270
6 · The paper itself

Abstract

Cytophilic immunoglobulin (IgG) subclass responses (IgG1 and IgG3) to Plasmodium falciparum antigens have been associated with protection from malaria, yet the relative importance of transmission intensity and age in generation of subclass responses to pre-erythrocytic and blood-stage antigens have not been clearly defined. We analyzed IgG subclass responses to the pre-erythrocytic antigens CSP, LSA-1, and TRAP and the blood-stage antigens AMA-1, EBA-175, and MSP-1 in asymptomatic residents age 2 years or older in stable (n=116) and unstable (n=96) transmission areas in Western Kenya. In the area of stable malaria transmission, a high prevalence of cytophilic (IgG1 and IgG3) antibodies to each antigen was seen in all age groups. Prevalence and levels of cytophilic antibodies to pre-erythrocytic and blood-stage P. falciparum antigens increased with age in the unstable transmission area, yet IgG1 and IgG3 responses to most antigens for all ages in the unstable transmission area were less prevalent and lower in magnitude than even the youngest age group from the stable transmission area. The dominance of cytophilic responses over non-cytophilic (IgG2 and IgG4) was more pronounced in the stable transmission area, and the ratio of IgG3 over IgG1 generally increased with age. In the unstable transmission area, the ratio of cytophilic to non-cytophilic antibodies did not increase with age, and tended to be IgG3-biased for pre-erythrocytic antigens yet IgG1-biased for blood-stage antigens. The differences between areas could not be attributed to active parasitemia status, as there were minimal differences in antibody responses between those positive and negative for Plasmodium infection by microscopy in the stable transmission area. Individuals in areas of unstable transmission have low cytophilic to non-cytophilic IgG subclass ratios and low IgG3:IgG1 ratios to P. falciparum antigens. These imbalances could contribute to the persistent risk of clinical malaria in these areas and serve as population-level, age-specific biomarkers of transmission.

Indexed as

AdolescentAdultAgedAged, 80 and overAge FactorsAntibodies, ProtozoanAntigens, ProtozoanChildChild, PreschoolErythrocytesFemaleHumansImmunoglobulin GKenyaMalaria, FalciparumMaleAntibodies, ProtozoanAntigens, ProtozoanImmunoglobulin GAntibodiesBlood-stage antigenImmunityMalariaPre-erythrocytic antigenSubclass

Identifiers

PMID25446174
PMCPMC4277715
OpenAlexW2012338601

What OpenQuestion holds

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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.