» Articles » PMID: 25505951

Maternal and Infant Infections Stimulate a Rapid Leukocyte Response in Breastmilk

Overview
Date 2014 Dec 16
PMID 25505951
Citations 90
Authors
Affiliations
Soon will be listed here.
Abstract

Breastmilk protects infants against infections; however, specific responses of breastmilk immune factors to different infections of either the mother or the infant are not well understood. Here, we examined the baseline range of breastmilk leukocytes and immunomodulatory biomolecules in healthy mother/infant dyads and how they are influenced by infections of the dyad. Consistent with a greater immunological need in the early postpartum period, colostrum contained considerable numbers of leukocytes (13-70% out of total cells) and high levels of immunoglobulins and lactoferrin. Within the first 1-2 weeks postpartum, leukocyte numbers decreased significantly to a low baseline level in mature breastmilk (0-2%) (P<0.001). This baseline level was maintained throughout lactation unless the mother and/or her infant became infected, when leukocyte numbers significantly increased up to 94% leukocytes out of total cells (P<0.001). Upon recovery from the infection, baseline values were restored. The strong leukocyte response to infection was accompanied by a more variable humoral immune response. Exclusive breastfeeding was associated with a greater baseline level of leukocytes in mature breastmilk. Collectively, our results suggest a strong association between the health status of the mother/infant dyad and breastmilk leukocyte levels. This could be used as a diagnostic tool for assessment of the health status of the lactating breast as well as the breastfeeding mother and infant.

Citing Articles

Immunological composition of human milk before and during subclinical and clinical mastitis.

Castro-Navarro I, Pace R, Williams J, Pace C, Kaur H, Piaskowski J Front Immunol. 2025; 15:1532432.

PMID: 39896819 PMC: 11782115. DOI: 10.3389/fimmu.2024.1532432.


Infant respiratory infections modulate lymphocyte homing to breast milk.

Zheng Y, Correa-Silva S, Rodrigues R, Correa de Souza E, Macaferri da Fonseca F, Gilio A Front Immunol. 2025; 15:1481416.

PMID: 39867906 PMC: 11757141. DOI: 10.3389/fimmu.2024.1481416.


Maternal microchimeric cell trafficking and its biological consequences depend on the onset of inflammation at the feto-maternal interface.

Slaats E, Bramreiter B, Chua K, Quilang R, Sallinger K, Eikmans M Semin Immunopathol. 2025; 47(1):8.

PMID: 39820729 PMC: 11742462. DOI: 10.1007/s00281-025-01037-w.


Human breastmilk memory T cells throughout lactation manifest activated tissue-oriented profile with prominent regulation.

Saager E, Van Stigt A, Lerkvaleekul B, Lutter L, Hellinga A, Van Der Wal M JCI Insight. 2024; 9(20).

PMID: 39435660 PMC: 11530127. DOI: 10.1172/jci.insight.181788.


Maternal-Fetal Microchimerism: Impacts on Offspring's Immune Development and Transgenerational Immune Memory Transfer.

Malinska N, Grobarova V, Knizkova K, cerny J Physiol Res. 2024; 73(3):315-332.

PMID: 39027950 PMC: 11299782. DOI: 10.33549/physiolres.935296.


References
1.
Le Huerou-Luron I, Blat S, Boudry G . Breast- v. formula-feeding: impacts on the digestive tract and immediate and long-term health effects. Nutr Res Rev. 2010; 23(1):23-36. DOI: 10.1017/S0954422410000065. View

2.
Kourtis A, Ibegbu C, Theiler R, Xu Y, Bansil P, Jamieson D . Breast milk CD4+ T cells express high levels of C chemokine receptor 5 and CXC chemokine receptor 4 and are preserved in HIV-infected mothers receiving highly active antiretroviral therapy. J Infect Dis. 2007; 195(7):965-72. DOI: 10.1086/512082. View

3.
Hassiotou F, Beltran A, Chetwynd E, Stuebe A, Twigger A, Metzger P . Breastmilk is a novel source of stem cells with multilineage differentiation potential. Stem Cells. 2012; 30(10):2164-74. PMC: 3468727. DOI: 10.1002/stem.1188. View

4.
Telemo E, Hanson L . Antibodies in milk. J Mammary Gland Biol Neoplasia. 1996; 1(3):243-9. DOI: 10.1007/BF02018077. View

5.
Fetherston C . Risk factors for lactation mastitis. J Hum Lact. 1998; 14(2):101-9. DOI: 10.1177/089033449801400209. View