Evidence map›Paper›PMID 30247686›Full record

ArticleThe Journal of nutrition2018

Human Breast-Milk Feeding Enhances the Humoral and Cell-Mediated Immune Response in Neonatal Piglets.

John J Miklavcic, Thomas M Badger, Anne K Bowlin, Katelin S Matazel, Mario A Cleves, Tanya LeRoith, Manish K Saraf, Sree V Chintapalli, Brian D Piccolo, Kartik Shankar and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of nutrition, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 23 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

11 authors at 3 institutions in 1 country.

John J MiklavcicArkansas Children's Nutrition Center, Little Rock, AR.
Thomas M BadgerArkansas Children's Nutrition Center, Little Rock, AR.
Anne K BowlinArkansas Children's Nutrition Center, Little Rock, AR.
Katelin S MatazelArkansas Children's Nutrition Center, Little Rock, AR.
Mario A ClevesArkansas Children's Nutrition Center, Little Rock, AR.
Tanya LeRoithDepartment of Biomedical Science and Pathobiology, Virginia Polytechnic Institute and State University, Blacksburg, VA.
Manish K SarafArkansas Children's Nutrition Center, Little Rock, AR.
Sree V ChintapalliArkansas Children's Nutrition Center, Little Rock, AR.
Brian D PiccoloArkansas Children's Nutrition Center, Little Rock, AR.
Kartik ShankarArkansas Children's Nutrition Center, Little Rock, AR.
Laxmi YeruvaArkansas Children's Nutrition Center, Little Rock, AR.
Arkansas Children's Nutrition Center · USArkansas Children's Hospital · USVirginia Tech · US

Funding

Translational Regulation in Normal Erythropoiesis and Diamond Blackfan AnemiaP20GM121293 · NIGMS · ARKANSAS CHILDREN'S HOSPITAL RES INST · PI Alan Tackett, Sean D. Taverna · 2017 to 2026
$27.6M
NIGMS NIH HHS P20 GM121293
6 · The paper itself

Abstract

Background: The benefits of breastfeeding infants are well characterized, including those on the immune system. However, determining the mechanism by which human breast milk (HBM) elicits effects on immune response requires investigation in an appropriate animal model. Objective: The primary aim of this study was to develop a novel porcine model and to determine the differential effects of feeding HBM and a commercial milk formula (MF) on immune response and gastrointestinal microbial colonization in a controlled environment. Methods: Male piglets were fed HBM (n = 26) or MF (n = 26) from day 2 through day 21. Piglets were vaccinated (n = 9/diet group) with cholera toxin and cholera toxin subunit B (CTB) and tetanus toxoid at 21 d or were fed placebo (n = 6/diet group) and then weaned to a standard solid diet at the age of 21 d. Humoral and cell-mediated immune responses were assessed from blood on days 35 and 48. Immune response was further examined from tissues, including mesenteric lymph nodes (MLNs), Peyer's patches (PPs), and spleen. The colonization of gut microbiota was characterized from feces on days 16 and 49. Results: Serum antibody titers in piglets fed HBM were 4-fold higher (P < 0.05) to CTB and 3-fold higher (P < 0.05) to tetanus toxoid compared with piglets fed MF on day 48. Compared with MF, the numbers of immunoglobulin A antibody-producing cells to CTB were 13-fold higher (P < 0.05) in MLNs and 11-fold higher (P < 0.05) in PPs in the HBM diet group on day 51. In addition, significantly increased T cell proliferation was observed in the HBM group relative to the MF group. Furthermore, microbial diversity in the HBM group was lower (P < 0.05) than in the MF group. Conclusions: This porcine model appears to be valid for studying the effects of early postnatal diet on immune responses and the gastrointestinal microbiome. Our results lay the groundwork for future studies defining the role of infant diet on microbiota and immune function.

Indexed as

Animals, NewbornImmunity, CellularImmunity, HumoralMilk, HumanAnimal FeedAnimalsHumansMaleSwine

Identifiers

PMID30247686
PMCPMC6209812
OpenAlexW2892598048

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.