From Early Diet to Immune Phenotype: Childhood Nutrition and Immunometabolic Programming Across the Life Course—A Scoping Review

Childhood diet may shape immune and inflammatory trajectories through interacting metabolic, microbial, and developmental pathways, but the long-term human evidence remains heterogeneous. This scoping review mapped longitudinal studies examining dietary exposures from birth to 18 years in relation to subsequent immune, inflammatory, allergic, autoimmune, gastrointestinal, immunometabolic, hepatic, neurocognitive, and endocrine–immunometabolic outcomes. The review was conducted in accordance with Joanna Briggs Institute guidance and reported according to PRISMA-ScR principles. A total of 403 studies were included. Evidence was concentrated in infancy and early childhood and predominantly addressed allergic and atopic outcomes; evidence on other immunological outcomes and on middle childhood and adolescence was more limited. Thirty studies provided relatively direct immunometabolic evidence, 149 contributed mechanistically indirect evidence, and 224 primarily reported longitudinal clinical diet–outcome associations. The principal mechanistic axes involved allergic sensitization and immune tolerance, lipid and fatty-acid metabolism, micronutrient and antioxidant pathways, cytokine signaling, gut microbiome and metabolite pathways, and human-milk-derived bioactive signals. Dietary diversity and overall diet quality intersected with several of these pathways. Associations were frequently context-dependent, varying according to developmental timing, host susceptibility, genetic background, immune state, and feeding context. Mechanistic interpretation rests on convergence across complementary studies rather than on complete pathways demonstrated within individual cohorts. Overall, the evidence is compatible with a proposed life-course nutritional immunology framework in which childhood diet acts as a dynamic developmental exposure interacting with microbial, metabolic, and immune processes; however, this framework derives mainly from early-life exposures and allergic and atopic outcomes, and the persistence of effects beyond early childhood remains insufficiently demonstrated. Limitations include restriction to English-language publications, marked methodological heterogeneity, residual confounding, and the absence of a formal risk-of-bias assessment.

Authors

Institutions

Publication Details

Journal
Nutrients
Published
2026-11-08
DOI
https://doi.org/10.3390/nu18213706
Primary Topic
Infant Nutrition and Health
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
NOV
article

From Early Diet to Immune Phenotype: Childhood Nutrition and Immunometabolic Programming Across the Life Course—A Scoping Review

Raluca Vasilescu, Delia-Maria Nicoară, Niculina Mang, Laura Cristina Rusu et al.
Nutrients
Infant Nutrition and Health
article

From Early Diet to Immune Phenotype: Childhood Nutrition and Immunometabolic Programming Across the Life Course—A Scoping Review

Raluca Vasilescu, Delia-Maria Nicoară, Niculina Mang, Laura Cristina Rusu, Otilia Mărginean, Iulius Jugănaru, Meda-Ada Bugi, Lucian-Ioan Cristun, Andrei-Ioan Munteanu, Alexandra-Diana Cheleș, Andrei Păun
article en

Abstract

Childhood diet may shape immune and inflammatory trajectories through interacting metabolic, microbial, and developmental pathways, but the long-term human evidence remains heterogeneous. This scoping review mapped longitudinal studies examining dietary exposures from birth to 18 years in relation to subsequent immune, inflammatory, allergic, autoimmune, gastrointestinal, immunometabolic, hepatic, neurocognitive, and endocrine–immunometabolic outcomes. The review was conducted in accordance with Joanna Briggs Institute guidance and reported according to PRISMA-ScR principles. A total of 403 studies were included. Evidence was concentrated in infancy and early childhood and predominantly addressed allergic and atopic outcomes; evidence on other immunological outcomes and on middle childhood and adolescence was more limited. Thirty studies provided relatively direct immunometabolic evidence, 149 contributed mechanistically indirect evidence, and 224 primarily reported longitudinal clinical diet–outcome associations. The principal mechanistic axes involved allergic sensitization and immune tolerance, lipid and fatty-acid metabolism, micronutrient and antioxidant pathways, cytokine signaling, gut microbiome and metabolite pathways, and human-milk-derived bioactive signals. Dietary diversity and overall diet quality intersected with several of these pathways. Associations were frequently context-dependent, varying according to developmental timing, host susceptibility, genetic background, immune state, and feeding context. Mechanistic interpretation rests on convergence across complementary studies rather than on complete pathways demonstrated within individual cohorts. Overall, the evidence is compatible with a proposed life-course nutritional immunology framework in which childhood diet acts as a dynamic developmental exposure interacting with microbial, metabolic, and immune processes; however, this framework derives mainly from early-life exposures and allergic and atopic outcomes, and the persistence of effects beyond early childhood remains insufficiently demonstrated. Limitations include restriction to English-language publications, marked methodological heterogeneity, residual confounding, and the absence of a formal risk-of-bias assessment.

NutrientsVol. 18(21)
Victor Babeș University of Medicine and Pharmacy Timișoara (RO), Vasile Goldis Western University of Arad (RO)
Infant Nutrition and Health
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon