Skip to main content
Canadian Journal of Veterinary Research logoLink to Canadian Journal of Veterinary Research
. 1993 Jan;57(1):1–8.

Immunomodulating effects of intestinal absorbed maternal colostral leukocytes by neonatal pigs.

P P Williams 1
PMCID: PMC1263580  PMID: 8431798

Abstract

Intestinal absorption of fluorescein isothiocyanate-labelled maternal colostral leukocytes (FITC-CL) was studied in 49 neonatal colostrum-deprived (CD) pigs from nine Minnesota miniature sows. Within 2 h postfeeding (pf), maternal FITC-CL were absorbed from the sibling's digestive tract and migrated into blood. The peak appearance of FITC-CL in blood occurred in samples at 5 and 7 h pf. By 24 h pf, cells were detected in liver, lung, lymph nodes, spleen and gastrointestinal tissues. To confirm intercellular migration of FITC-CL, gastrointestinal explant cultures from neonatal CD pigs were used. Maternal FITC-CL were observed to intercellularly migrate in 24 to 48 h pf between duodenal- and jejunal-epithelial cells to lamina propria cells and submucosal spaces. Fluorescein isothiocyanate-labelled maternal colostral leukocytes were not absorbed via ileal explant cultures. Unlike FITC-CL, maternal FITC-peripheral blood mononuclear leukocytes (FITC-PBL) were not absorbed either in vivo or in vitro by gastrointestinal tissues. When maternal FITC-PBL were intravenously administered to siblings they were distributed in blood and organs similar to FITC-CL. Following exposure to FITC-labelled cells, treated- and mock (untreated)-pigs were compared on the basis of PBL proliferative responses to phytomitogens. Sibling CD-pigs fed maternal FITC-CL showed higher PBL T-cell responses to phytohemagglutinin (PHA) and concanavalin A (ConA), and a significant stimulation (p < or = 0.01) of B-cell responses to pokeweed mitogen (PWM). Pigs fed FITC-PBL showed little PBL responses to PHA, ConA and PWM over PBL from mock pigs. Similarly, the influence of noncellular constituents of colostrum were also assessed by proliferative studies.(ABSTRACT TRUNCATED AT 250 WORDS)

Full text

PDF
1

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Banks K. L. Host defense in the newborn animal. J Am Vet Med Assoc. 1982 Nov 15;181(10):1053–1056. [PubMed] [Google Scholar]
  2. Butcher E. C., Weissman I. L. Direct fluorescent labeling of cells with fluorescein or rhodamine isothiocyanate. I. Technical aspects. J Immunol Methods. 1980;37(2):97–108. doi: 10.1016/0022-1759(80)90195-7. [DOI] [PubMed] [Google Scholar]
  3. Evans P. A., Newby T. J., Stokes C. R., Bourne F. J. A study of cells in the mammary secretions of sows. Vet Immunol Immunopathol. 1982 Sep;3(5):515–527. doi: 10.1016/0165-2427(82)90017-4. [DOI] [PubMed] [Google Scholar]
  4. Head J. R., Beer A. E., Billingham R. E. Significance of the cellular component of the maternal immunologic endowment in milk. Transplant Proc. 1977 Jun;9(2):1465–1471. [PubMed] [Google Scholar]
  5. Jeurissen S. H., Duijvestijn A. M., Sontag Y., Kraal G. Lymphocyte migration into the lamina propria of the gut is mediated by specialized HEV-like blood vessels. Immunology. 1987 Oct;62(2):273–277. [PMC free article] [PubMed] [Google Scholar]
  6. Klobasa F., Butler J. E., Werhahn E., Habe F. Maternal-neonatal immunoregulation in swine. II. Influence of multiparity on de novo immunoglobulin synthesis by piglets. Vet Immunol Immunopathol. 1986 Feb;11(2):149–159. doi: 10.1016/0165-2427(86)90094-2. [DOI] [PubMed] [Google Scholar]
  7. Mohr J. A. The possible induction and-or acquisition of cellular hypersensitivity associated with ingestion of colostrum. J Pediatr. 1973 Jun;82(6):1062–1064. doi: 10.1016/s0022-3476(73)80448-2. [DOI] [PubMed] [Google Scholar]
  8. Ogra S. S., Weintraub D., Ogra P. L. Immunologic aspects of human colostrum and milk. III. Fate and absorption of cellular and soluble components in the gastrointestinal tract of the newborn. J Immunol. 1977 Jul;119(1):245–248. [PubMed] [Google Scholar]
  9. Porter P. Transfer of immunoglobulins IgG, IgA and IgM to lacteal secretions in the parturient sow and their absorption by the neonatal piglet. Biochim Biophys Acta. 1969 Jul 1;181(2):381–392. doi: 10.1016/0005-2795(69)90271-2. [DOI] [PubMed] [Google Scholar]
  10. Reyero C., Thalhammer J. G., Reszler G., Stöckl W. Development of peripheral B and T lymphocytes in piglets. Z Immunitatsforsch Immunobiol. 1978 Sep;154(5):409–415. [PubMed] [Google Scholar]
  11. SEGRE D., KAEBERLE M. L. The immunologic behavior of baby pigs. II. Production of antibodies in newborn pigs. J Immunol. 1962 Dec;89:790–793. [PubMed] [Google Scholar]
  12. SPEER V. C., BROWN H., QUINN L., CATRON D. V. The cessation of antibody absorption in the young pig. J Immunol. 1959 Dec;83:632–634. [PubMed] [Google Scholar]
  13. Sachs D. H., Leight G., Cone J., Schwarz S., Stuart L., Rosenberg S. Transplantation in miniature swine. I. Fixation of the major histocompatibility complex. Transplantation. 1976 Dec;22(6):559–567. doi: 10.1097/00007890-197612000-00004. [DOI] [PubMed] [Google Scholar]
  14. Schnorr K. L., Pearson L. D. Intestinal absorption of maternal leucocytes by newborn lambs. J Reprod Immunol. 1984 Aug;6(5):329–337. doi: 10.1016/0165-0378(84)90031-7. [DOI] [PubMed] [Google Scholar]
  15. Schnorr K. L., Pearson L. D., Knisley K. A., DeMartini J. C. Fluorescein isothiocyanate as a cell marker for tracing lymphocyte circulation in sheep. Int Arch Allergy Appl Immunol. 1983;72(3):239–242. doi: 10.1159/000234874. [DOI] [PubMed] [Google Scholar]
  16. Sheldrake R. F., Husband A. J. Intestinal uptake of intact maternal lymphocytes by neonatal rats and lambs. Res Vet Sci. 1985 Jul;39(1):10–15. [PubMed] [Google Scholar]
  17. Smith J. W., Schultz R. D. Mitogen- and antigen-responsive milk lymphocytes. Cell Immunol. 1977 Mar 1;29(1):165–173. doi: 10.1016/0008-8749(77)90285-4. [DOI] [PubMed] [Google Scholar]
  18. Taura Y., Mullen Y., Papoian T., Tsunoda T., Shiogama T. Early in vitro detection of interleukin-2-like activities by pretreatment with allogeneic blood lymphocytes in miniature swine. J Vet Med Sci. 1991 Jun;53(3):365–369. doi: 10.1292/jvms.53.365. [DOI] [PubMed] [Google Scholar]
  19. Tuboly S., Bernáth S., Glávits R., Medveczky I. Intestinal absorption of colostral lymphoid cells in newborn piglets. Vet Immunol Immunopathol. 1988 Dec;20(1):75–85. doi: 10.1016/0165-2427(88)90027-x. [DOI] [PubMed] [Google Scholar]
  20. Valpotić I., Gerencer M., Basić I. In vitro modulating effects of porcine immunoglobulin G on mitogens-induced lymphocyte response in precolostral, suckling and weaned piglets. Vet Immunol Immunopathol. 1989 Sep;22(2):113–122. doi: 10.1016/0165-2427(89)90054-8. [DOI] [PubMed] [Google Scholar]
  21. Watson D. L., Bennell M. A., Chaniago T. D. Effect of circulating, maternally derived antibody on the development of a local immune response in the intestine of the neonatal pig. Am J Vet Res. 1979 Jan;40(1):61–65. [PubMed] [Google Scholar]
  22. Williams P. P., Hall M. R., McFarland M. D. Immunological responses of cross-bred and in-bred miniature pigs to swine poxvirus. Vet Immunol Immunopathol. 1989 Nov 30;23(1-2):149–159. doi: 10.1016/0165-2427(89)90117-7. [DOI] [PubMed] [Google Scholar]

Articles from Canadian Journal of Veterinary Research are provided here courtesy of Canadian Veterinary Medical Association

RESOURCES