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The Journal of veterinary medical science2026; 88(8); 1134-1143; doi: 10.1292/jvms.26-0023

Short-interval longitudinal analysis of immune cell dynamics in heavy draft foals after colostrum intake.

Abstract: Maternal cells and antibodies are present in equine colostrum, but their relationship with immune cells in foals after colostrum ingestion remains unclear. This study longitudinally analyzed immune cells in the peripheral blood of neonatal foals at short intervals and investigated their relationship with colostral immune cells. Eleven clinically healthy draft mares and their foals were examined. Foal blood was collected before colostrum intake (0 hr) and at 2-3, 6, 12, 36-48 hr, and 3 and 7 days after ingestion. Mare blood and milk (0, 36-48 hr; 0 hr milk defined as colostrum) were also collected. Mononuclear cells were analyzed by flow cytometry using cluster of differentiation (CD) 5, CD4, CD8, CD21, CD172a, and CD45RO, with double-staining for major histocompatibility complex class II (MHC II). Total leukocytes and CD4, CD5, CD8, and CD45RO cells significantly increased during the first week of life, whereas MHC II CD5, MHC II CD8, and MHC II CD45RO cells increased earlier at 12 hr. CD5, CD4, and CD8 cells were more abundant in colostrum than in milk. CD8 cells were more abundant in colostrum than in blood, whereas CD21 and CD45RO cells were more abundant in blood than in colostrum, with no correlation. An early increase in CD8 MHC II T cells before gut closure is a novel finding and suggests possible migration of colostrum-derived CD8 T cells into neonatal circulation.
Publication Date: 2026-06-01 PubMed ID: 42219339DOI: 10.1292/jvms.26-0023Google Scholar: Lookup
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  • Journal Article

Summary

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Overview

  • This study investigated how immune cells in newborn foals change shortly after they consume colostrum and examined the relationship between immune cells found in colostrum and those present in the foals’ blood over the first week of life.

Background and Purpose

  • Equine colostrum (the first milk produced by the mare after birth) contains maternal immune cells and antibodies, which are critical for protecting the newborn foal.
  • The exact relationship between these maternal immune components and the foal’s own immune cells after colostrum ingestion is not well understood.
  • The research aimed to perform a detailed, short-interval, longitudinal analysis of immune cells in foals’ peripheral blood to understand how these populations change over time and how they relate to cells found in the mother’s colostrum.

Study Design

  • Subjects included 11 healthy draft horse mares and their foals.
  • Blood samples were collected from foals at multiple time points: before colostrum intake (0 hr), then at 2-3, 6, 12, 36-48 hours, and finally at 3 and 7 days after birth.
  • Samples were also taken from mares’ blood and their milk at 0 hr (defined as colostrum) and 36-48 hr postpartum.

Methods

  • Mononuclear immune cells in the samples were analyzed using flow cytometry with specific markers: CD5, CD4, CD8, CD21, CD172a, and CD45RO.
  • Double-staining was performed to detect the expression of major histocompatibility complex class II (MHC II), an important molecule involved in immune activation.

Key Findings on Immune Cell Dynamics in Foals

  • There was a significant increase in total leukocytes, as well as specific T cell subsets (CD4+, CD5+, CD8+) and memory T cells (CD45RO+) during the first week of life.
  • Certain MHC II-positive T cell populations (MHC II CD5, MHC II CD8, MHC II CD45RO) increased earlier, around 12 hours after birth, suggesting early activation or influx of these cells.

Differences Between Colostrum and Blood Immune Cells

  • CD5, CD4, and CD8 T cell populations were more abundant in colostrum than in later milk samples, indicating these cells are delivered to foals shortly after birth via colostrum.
  • CD8 T cells were more numerous in colostrum compared to maternal blood, possibly implying selective enrichment or migration mechanisms.
  • Conversely, CD21 (a B cell marker) and CD45RO cells were more abundant in blood than colostrum, and there was no correlation between their levels in blood and colostrum.

Novel Insights

  • An early rise in CD8+ MHC II+ T cells detected in foals’ blood before the gut closure (the period when the foal’s intestine stops allowing large molecules and cells to pass) is a novel finding.
  • This early increase suggests that some CD8 T cells originating from the colostrum might migrate across the intestinal barrier and enter the foal’s circulation, potentially helping to jumpstart neonatal immunity.

Conclusion

  • The study provides new insights into the early immune development of foals and the role of maternally-derived immune cells from colostrum.
  • Understanding these cellular dynamics could help improve neonatal foal health and inform management practices regarding colostrum feeding.

Cite This Article

APA
Yoshida S, Takeyama A, Maeda Y, Nambo Y. (2026). Short-interval longitudinal analysis of immune cell dynamics in heavy draft foals after colostrum intake. J Vet Med Sci, 88(8), 1134-1143. https://doi.org/10.1292/jvms.26-0023

Publication

ISSN: 1347-7439
NlmUniqueID: 9105360
Country: Japan
Language: English
Volume: 88
Issue: 8
Pages: 1134-1143

Researcher Affiliations

Yoshida, Sakura
  • Department of Clinical Veterinary Sciences, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido, Japan.
Takeyama, Akiko
  • Department of Clinical Veterinary Sciences, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido, Japan.
Maeda, Yosuke
  • Laboratory of Clinical Veterinary Medicine for Large Animals, Kitasato University School of Veterinary Medicine, Aomori, Japan.
Nambo, Yasuo
  • Department of Clinical Veterinary Sciences, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido, Japan.

MeSH Terms

  • Animals
  • Colostrum / immunology
  • Colostrum / cytology
  • Horses / immunology
  • Horses / blood
  • Female
  • Animals, Newborn / immunology
  • Longitudinal Studies
  • Flow Cytometry / veterinary
  • Milk / immunology

Citations

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