Evidence map›Paper›PMID 42127031›Full record

ArticlePLOS global public health2026

Maternal microchimerism at birth associates with reduced odds of non-malarial fever and respiratory tract infections in Tanzanian children.

Gitte L Petersen, Paul T Edlefsen, Xiaohong Li, Robert Morrison, Edward Kabyemela, J Lee Nelson, Patrick E Duffy, Michal Fried, Whitney E Harrington

Abstract read
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Article in PLOS global public health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Gitte L PetersenDepartment of Translational Type 1 Diabetes Research, Steno Diabetes Center Copenhagen, Herlev, Denmark.ORCID https://orcid.org/0000-0001-8920-4015
Paul T EdlefsenVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Xiaohong LiDivision of Public Health Sciences, Fred Hutchinson Cancer Research Center, University of Washington, Seattle, Washington, United States of America.
Robert MorrisonLaboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
Edward KabyemelaSchool of Diagnostic Medicine, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
J Lee NelsonTranslational Science and Therapeutics, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Patrick E DuffyLaboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
Michal FriedLaboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
Whitney E HarringtonCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, Washington, United States of America.ORCID https://orcid.org/0000-0002-0121-978X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The presence of maternal cells in the offspring at birth, a phenomenon known as maternal microchimerism, has been previously associated with decreased odds of malaria and respiratory infections in early childhood suggesting a role in immunological responses to infections. Here, we assess the effect of cord blood maternal microchimerism on symptomatic non-malarial infections in Tanzanian children. We conducted a secondary analysis using a nested birth cohort of 52 children from Muheza, Tanzania, with previously measured cord blood maternal microchimerism and longitudinal records on infections in the first four years of life. The associations between maternal microchimerism and symptomatic lower and upper respiratory tract infections, diarrhea, and non-malarial fever were estimated using generalized estimating equation models. In total, 29% of the 52 children in the study screened positive for cord blood maternal microchimerism. Detected versus non-detected maternal microchimerism was associated with 58% lower odds of non-malarial fever (fully adjusted odds ratio (OR): 0.42 [95% CI: 0.18-0.98]) and 28% lower odds of respiratory tract infection (OR: 0.72 [95% CI: 0.53-0.96]). Lower and upper respiratory tract infections contributed equally to the observed association with any symptomatic respiratory tract infections (ORs respectively: 0.81 [95% CI: 0.50-1.31] and 0.71 [95% CI: 0.50-1.01]). We did not find any association between maternal microchimerism and odds of diarrhea (OR: 1.63 [95% CI: 0.85-3.13]). Detectable cord blood maternal microchimerism was associated with lower odds of non-malarial fever and symptomatic respiratory infections in Tanzanian infants. These findings emphasize that MMc may play an underrecognized role in protection from infection during early childhood.

Identifiers

PMID42127031
PMCPMC13170846

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