Evidence map›Paper›PMID 25590337›Full record

ArticlePLoS neglected tropical diseases2015

Effect of antenatal parasitic infections on anti-vaccine IgG levels in children: a prospective birth cohort study in Kenya.

Indu Malhotra, Maxim McKibben, Peter Mungai, Elisabeth McKibben, Xuelei Wang, Laura J Sutherland, Eric M Muchiri, Charles H King, Christopher L King, A Desiree LaBeaud

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
5.9field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  4. Trial
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  9. Review
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  13. Article
  14. How does geographical diversity shape vaccine efficacy?Clinical and experimental vaccine research · 2024
    Review
  15. Article
  16. The Global Prevalence ofTropical medicine and infectious disease · 2022
    Review
  17. Article
  18. Article
  19. Altered Offspring Immunity in Maternal Parasitic Infections.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Review
  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

10 authors at 4 institutions in 2 countries.

Indu MalhotraCase Western Reserve University, Center for Global Health and Diseases, Cleveland, Ohio, United States of America.
Maxim McKibbenCase Western Reserve University, Center for Global Health and Diseases, Cleveland, Ohio, United States of America.
Peter MungaiDivision of Vector Borne and Neglected Tropical Diseases, Ministry of Public Health and Sanitation, Nairobi, Kenya.
Elisabeth McKibbenCase Western Reserve University, Center for Global Health and Diseases, Cleveland, Ohio, United States of America.
Xuelei WangCase Western Reserve University, Clinical and Translational Science Collaborative, Cleveland, Ohio, United States of America.
Laura J SutherlandCase Western Reserve University, Center for Global Health and Diseases, Cleveland, Ohio, United States of America.
Eric M MuchiriDivision of Vector Borne and Neglected Tropical Diseases, Ministry of Public Health and Sanitation, Nairobi, Kenya.
Charles H KingCase Western Reserve University, Center for Global Health and Diseases, Cleveland, Ohio, United States of America.
Christopher L KingCase Western Reserve University, Center for Global Health and Diseases, Cleveland, Ohio, United States of America.
A Desiree LaBeaudCase Western Reserve University, Center for Global Health and Diseases, Cleveland, Ohio, United States of America; Children's Hospital Oakland Research Institute, Center for Immunobiology and Vaccine Development, Oakland, California, United States of America.
Case Western Reserve University · USCenter for Global Health · USMinistry of Health · KEClinical and Translational Science Collaborative of Northern Ohio

Funding

Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
Fetal Immunity to Falciparum MalariaR01AI064687 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI KING, CHRISTOPHER L · 2005 to 2015
$3.7M
The effects of polyparasitism on vaccine responseR03HD058587 · NICHD · CASE WESTERN RESERVE UNIVERSITY · PI LABEAUD, ANGELLE DESIREE, MALHOTRA, INDU · 2010 to 2011
$169k
NCATS NIH HHS UL1 TR000439NCATS NIH HHS UL1TR000439NIAID NIH HHS R01 AI064687NIAID NIH HHS R01AI064687NICHD NIH HHS R03 HD058587NICHD NIH HHS R03HD058587
6 · The paper itself

Abstract

backgroundParasitic infections are prevalent among pregnant women in sub-Saharan Africa. We investigated whether prenatal exposure to malaria and/or helminths affects the pattern of infant immune responses to standard vaccinations against Haemophilus influenzae (Hib), diphtheria (DT), hepatitis B (Hep B) and tetanus toxoid (TT). METHODS AND

findings450 Kenyan women were tested for malaria, schistosomiasis, lymphatic filariasis (LF), and intestinal helminths during pregnancy. After three standard vaccinations at 6, 10 and 14 weeks, their newborns were followed biannually to age 36 months and tested for absolute levels of IgG against Hib, DT, Hep B, and TT at each time point. Newborns' cord blood (CB) lymphocyte responses to malaria blood-stage antigens, soluble Schistosoma haematobium worm antigen (SWAP), and filaria antigen (BMA) were also assessed. Three immunophenotype categories were compared: i) tolerant (those having Plasmodium-, Schistosoma-, or Wuchereria-infected mothers but lacking respective Th1/Th2-type recall responses at birth to malaria antigens, SWAP, or BMA); ii) sensitized (those with infected/uninfected mothers and detectable Th1/Th2-type CB recall response to respective parasite antigen); or iii) unexposed (no evidence of maternal infection or CB recall response). Overall, 78.9% of mothers were infected with LF (44.7%), schistosomiasis (32.4%), malaria (27.6%) or hookworm (33.8%). Antenatal maternal malaria, LF, and hookworm were independently associated with significantly lower Hib-specific IgG. Presence of multiple maternal infections was associated with lower infant IgG levels against Hib and DT antigens post-vaccination. Post-vaccination IgG levels were also significantly associated with immunophenotype: malaria-tolerized infants had reduced response to DT, whereas filaria-tolerized infants showed reduced response to Hib.

conclusionsThere is an impaired ability to develop IgG antibody responses to key protective antigens of Hib and diphtheria in infants of mothers infected with malaria and/or helminths during pregnancy. These findings highlight the importance of control and prevention of parasitic infections among pregnant women.

Indexed as

AdolescentAdultCohort StudiesFemaleHaemophilus influenzae type bHepatitis B virusHumansImmunoglobulin GInfantInfant, NewbornKenyaPregnancyPregnancy Complications, ParasiticProspective StudiesTetanus ToxoidVaccinationImmunoglobulin GTetanus ToxoidVaccines

Identifiers

PMID25590337
PMCPMC4295886
OpenAlexW1981376031

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.