Cargando…

Tradeoffs in milk immunity affect infant infectious disease risk

BACKGROUND AND OBJECTIVES: The human immune system has evolved to balance protection against infection with control of immune-mediated damage and tolerance of commensal microbes. Such tradeoffs between protection and harm almost certainly extend to the immune system of milk. METHODOLOGY: Among breas...

Descripción completa

Detalles Bibliográficos
Autores principales: Wander, Katherine, Fujita, Masako, Mattison, Siobhan M, Duris, Margaret, Gauck, Megan, Hopt, Tessa, Lacy, Katherine, Foligno, Angela, Ulloa, Rebecca, Dodge, Connor, Mowo, Frida, Kiwelu, Ireen, Mmbaga, Blandina T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233416/
https://www.ncbi.nlm.nih.gov/pubmed/35769951
http://dx.doi.org/10.1093/emph/eoac020
_version_ 1784735762124636160
author Wander, Katherine
Fujita, Masako
Mattison, Siobhan M
Duris, Margaret
Gauck, Megan
Hopt, Tessa
Lacy, Katherine
Foligno, Angela
Ulloa, Rebecca
Dodge, Connor
Mowo, Frida
Kiwelu, Ireen
Mmbaga, Blandina T
author_facet Wander, Katherine
Fujita, Masako
Mattison, Siobhan M
Duris, Margaret
Gauck, Megan
Hopt, Tessa
Lacy, Katherine
Foligno, Angela
Ulloa, Rebecca
Dodge, Connor
Mowo, Frida
Kiwelu, Ireen
Mmbaga, Blandina T
author_sort Wander, Katherine
collection PubMed
description BACKGROUND AND OBJECTIVES: The human immune system has evolved to balance protection against infection with control of immune-mediated damage and tolerance of commensal microbes. Such tradeoffs between protection and harm almost certainly extend to the immune system of milk. METHODOLOGY: Among breastfeeding mother–infant dyads in Kilimanjaro, Tanzania, we characterized in vitro proinflammatory milk immune responses to Salmonella enterica (an infectious agent) and Escherichia coli (a benign target) as the increase in interleukin-6 after 24 h of incubation with each bacterium. We characterized incident infectious diseases among infants through passive monitoring. We used Cox proportional hazards models to describe associations between milk immune activity and infant infectious disease. RESULTS: Among infants, risk for respiratory infections declined with increasing milk in vitro proinflammatory response to S. enterica (hazard ratio [HR]: 0.68; 95% confidence interval [CI]: 0.54, 0.86; P: 0.001), while risk for gastrointestinal infections increased with increasing milk in vitro proinflammatory response to E. coli (HR: 1.44; 95% CI: 1.05, 1.99; P: 0.022). Milk proinflammatory responses to S. enterica and E. coli were positively correlated (Spearman’s rho: 0.60; P: 0.000). CONCLUSIONS AND IMPLICATIONS: These findings demonstrate a tradeoff in milk immune activity: the benefits of appropriate proinflammatory activity come at the hazard of misdirected proinflammatory activity. This tradeoff is likely to affect infant health in complex ways, depending on prevailing infectious disease conditions. How mother–infant dyads optimize proinflammatory milk immune activity should be a central question in future ecological–evolutionary studies of the immune system of milk.
format Online
Article
Text
id pubmed-9233416
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-92334162022-06-28 Tradeoffs in milk immunity affect infant infectious disease risk Wander, Katherine Fujita, Masako Mattison, Siobhan M Duris, Margaret Gauck, Megan Hopt, Tessa Lacy, Katherine Foligno, Angela Ulloa, Rebecca Dodge, Connor Mowo, Frida Kiwelu, Ireen Mmbaga, Blandina T Evol Med Public Health Original Research Article BACKGROUND AND OBJECTIVES: The human immune system has evolved to balance protection against infection with control of immune-mediated damage and tolerance of commensal microbes. Such tradeoffs between protection and harm almost certainly extend to the immune system of milk. METHODOLOGY: Among breastfeeding mother–infant dyads in Kilimanjaro, Tanzania, we characterized in vitro proinflammatory milk immune responses to Salmonella enterica (an infectious agent) and Escherichia coli (a benign target) as the increase in interleukin-6 after 24 h of incubation with each bacterium. We characterized incident infectious diseases among infants through passive monitoring. We used Cox proportional hazards models to describe associations between milk immune activity and infant infectious disease. RESULTS: Among infants, risk for respiratory infections declined with increasing milk in vitro proinflammatory response to S. enterica (hazard ratio [HR]: 0.68; 95% confidence interval [CI]: 0.54, 0.86; P: 0.001), while risk for gastrointestinal infections increased with increasing milk in vitro proinflammatory response to E. coli (HR: 1.44; 95% CI: 1.05, 1.99; P: 0.022). Milk proinflammatory responses to S. enterica and E. coli were positively correlated (Spearman’s rho: 0.60; P: 0.000). CONCLUSIONS AND IMPLICATIONS: These findings demonstrate a tradeoff in milk immune activity: the benefits of appropriate proinflammatory activity come at the hazard of misdirected proinflammatory activity. This tradeoff is likely to affect infant health in complex ways, depending on prevailing infectious disease conditions. How mother–infant dyads optimize proinflammatory milk immune activity should be a central question in future ecological–evolutionary studies of the immune system of milk. Oxford University Press 2022-06-13 /pmc/articles/PMC9233416/ /pubmed/35769951 http://dx.doi.org/10.1093/emph/eoac020 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Foundation for Evolution, Medicine, and Public Health. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Wander, Katherine
Fujita, Masako
Mattison, Siobhan M
Duris, Margaret
Gauck, Megan
Hopt, Tessa
Lacy, Katherine
Foligno, Angela
Ulloa, Rebecca
Dodge, Connor
Mowo, Frida
Kiwelu, Ireen
Mmbaga, Blandina T
Tradeoffs in milk immunity affect infant infectious disease risk
title Tradeoffs in milk immunity affect infant infectious disease risk
title_full Tradeoffs in milk immunity affect infant infectious disease risk
title_fullStr Tradeoffs in milk immunity affect infant infectious disease risk
title_full_unstemmed Tradeoffs in milk immunity affect infant infectious disease risk
title_short Tradeoffs in milk immunity affect infant infectious disease risk
title_sort tradeoffs in milk immunity affect infant infectious disease risk
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233416/
https://www.ncbi.nlm.nih.gov/pubmed/35769951
http://dx.doi.org/10.1093/emph/eoac020
work_keys_str_mv AT wanderkatherine tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk
AT fujitamasako tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk
AT mattisonsiobhanm tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk
AT durismargaret tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk
AT gauckmegan tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk
AT hopttessa tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk
AT lacykatherine tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk
AT folignoangela tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk
AT ulloarebecca tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk
AT dodgeconnor tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk
AT mowofrida tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk
AT kiweluireen tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk
AT mmbagablandinat tradeoffsinmilkimmunityaffectinfantinfectiousdiseaserisk