Effect of maternal cells transferred with colostrum on cellular responses to pathogen antigens in neonatal calves

Douglas C. Donovan Department of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602
Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens, GA 30602

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Adrian J. Reber Department of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602
Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens, GA 30602

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Jon D. Gabbard Department of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602

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Maria Aceves-Avila Department of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602

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Kimberly L. Galland Department of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602

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Katheryn A. Holbert Department of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602

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Lane O. Ely Department of Animal and Dairy Science, College of Agricultural and Environmental Sciences, University of Georgia, Athens, GA 30602

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David J. Hurley Department of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602
Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens, GA 30602

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Abstract

Objective—To assess the effect of maternal cells or cellular components on neonatal immune responses to intracellular pathogens in calves.

Animals—15 Holstein calves.

Procedures—Calves were fed whole colostrum, frozen colostrum, or cell-free colostrum within 4 hours after birth. Leukocytes were obtained from calves before feeding colostrum and 1, 2, 7, 14, 21, and 28 days after ingestion. Proliferative responses against bovine viral diarrhea virus (BVDV) and mycobacterial purified protein derivatives were evaluated. Dams received a vaccine containing inactivated BVDV, but were not vaccinated against mycobacterial antigens.

Results—All calves had essentially no IgG in circulation at birth, but comparable and substantial concentrations by day 1. Calves that received whole colostrum had enhanced responses to BVDV antigen 1 and 2 days after ingestion of colostrum. In contrast, calves that received frozen colostrum or cell-free colostrum did not respond to BVDV. No differences were identified among the 3 groups in response to mycobacterial antigens.

Conclusions and Clinical Relevance—Results indicated that transfer of live maternal cells from colostrum to neonatal calves enhanced responses to antigens against which the dams had previously responded (BVDV), but not to antigens to which the dams were naïve (mycobacterial purified protein derivatives). Results suggested that cell-mediated immune transfer to neonates can be enhanced by maternal vaccination.

Abstract

Objective—To assess the effect of maternal cells or cellular components on neonatal immune responses to intracellular pathogens in calves.

Animals—15 Holstein calves.

Procedures—Calves were fed whole colostrum, frozen colostrum, or cell-free colostrum within 4 hours after birth. Leukocytes were obtained from calves before feeding colostrum and 1, 2, 7, 14, 21, and 28 days after ingestion. Proliferative responses against bovine viral diarrhea virus (BVDV) and mycobacterial purified protein derivatives were evaluated. Dams received a vaccine containing inactivated BVDV, but were not vaccinated against mycobacterial antigens.

Results—All calves had essentially no IgG in circulation at birth, but comparable and substantial concentrations by day 1. Calves that received whole colostrum had enhanced responses to BVDV antigen 1 and 2 days after ingestion of colostrum. In contrast, calves that received frozen colostrum or cell-free colostrum did not respond to BVDV. No differences were identified among the 3 groups in response to mycobacterial antigens.

Conclusions and Clinical Relevance—Results indicated that transfer of live maternal cells from colostrum to neonatal calves enhanced responses to antigens against which the dams had previously responded (BVDV), but not to antigens to which the dams were naïve (mycobacterial purified protein derivatives). Results suggested that cell-mediated immune transfer to neonates can be enhanced by maternal vaccination.

Contributor Notes

Supported by a Veterinary Medical Experiment Station Grant and an unrestricted gift from Pfizer Animal Health.

Address correspondence to Dr. Hurley.
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