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. 1975 Aug;29(2):307–318.

The bursal origin of an immunocompetent cell for antibody formation in the chicken.

H Matsuda, T Baba, Y Bito
PMCID: PMC1445945  PMID: 808466

Abstract

Surgically bursectomized and irradiated chickens were given bursal, splenic, bone marrow or thymic cells taken from syngeneic donors, together with killed Brucella abortus and Salmonella pullorum. Blood samples were taken from those chickens 7 days later, and the serum agglutinin titres were determined. The cells of any lymphoid organ taken from 28-day-old chickens were more effective in restoring antibody response than those from 18-day-old ones. The restorative capacities of the bursa and splenic cells were greater than those of the bone marrow and thymic cells. On the other hand, splenic, bone marrow or thymic cells taken from bursa-less chickens, and lymphoid cells taken from normal chickens but treated with anti-bursa serum in the persence of complement, were virtually incapable of restoring the immune response. Bursal, splenic or bone marrow cells taken from neonatally thymectomized chickens, and bursal or thymic cells treated with anti-thymus serum were effective, being comparable with the corresponding cells taken from normal chickens or treated with normal sera, in restoring the suppressed immune response in chickens devoid of the lymphoid system. These facts clearly indicate that the primary and central agent crucial for development of the humoral immune response against the two bacterial antigens tested is the bursa. It is strongly suggested from the results of adoptive immunization using intrabursally primed cells that the cells recognizing Brucella abortus exist within the bursa of 4-day-old chicken.

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Selected References

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

  1. Choi Y. S., Good R. A. Development of chicken lymphoid system. II. Synthesis of primordial immunoglobulin M by the bursa cells of chick embryo. J Exp Med. 1972 Jul 1;136(1):8–20. doi: 10.1084/jem.136.1.8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cooper M. D., Schwartz M. L., Good R. A. Restoration of gamma globulin production in agammaglobulinemic chickens. Science. 1966 Jan 28;151(3709):471–473. doi: 10.1126/science.151.3709.471. [DOI] [PubMed] [Google Scholar]
  3. Durkin H. G., Theis G. A., Thorbecke G. J. Bursa of fabricius as site of origin of germinal centre cells. Nat New Biol. 1972 Jan 26;235(56):118–119. doi: 10.1038/newbio235118a0. [DOI] [PubMed] [Google Scholar]
  4. Dwyer J. M., Warner N. L. Antigen binding cells in embryonic chicken bursa and thymus. Nat New Biol. 1971 Feb 17;229(7):210–211. doi: 10.1038/newbio229210a0. [DOI] [PubMed] [Google Scholar]
  5. Gilmour D. G., Theis G. A., Thorbecke G. J. Transfer of antibody production with cells from bursa of Fabricius. J Exp Med. 1970 Jul 1;132(1):134–147. doi: 10.1084/jem.132.1.134. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hemmingsson E. J., Linna T. J. Ontogenetic studies on lymphoid cell traffic in the chicken. I. Cell migration from the bursa of Fabricius. Int Arch Allergy Appl Immunol. 1972;42(5):693–710. doi: 10.1159/000230650. [DOI] [PubMed] [Google Scholar]
  7. Ivanyi J., Lydyard P. M. Delineation of chicken lymphocyte populations by specific anti-thymus and anti-bursa sera. Cell Immunol. 1972 Sep;5(1):180–189. doi: 10.1016/0008-8749(72)90094-9. [DOI] [PubMed] [Google Scholar]
  8. Ivanyi J., Murgatroyd L. B., Lydyard P. M. Bursal origin of bone marrow cells with competence for antibody formation. Immunology. 1972 Jul;23(1):107–111. [PMC free article] [PubMed] [Google Scholar]
  9. Kincade P. W., Cooper M. D. Development and distribution of immunoglobulin-containing cells in the chicken. An immunofluorescent analysis using purified antibodies to mu, gamma and light chains. J Immunol. 1971 Feb;106(2):371–382. [PubMed] [Google Scholar]
  10. Kincade P. W., Lawton A. R., Bockman D. E., Cooper M. D. Suppression of immunoglobulin G synthesis as a result of antibody-mediated suppression of immunoglobulin M synthesis in chickens. Proc Natl Acad Sci U S A. 1970 Dec;67(4):1918–1925. doi: 10.1073/pnas.67.4.1918. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Matsuda H., Bito Y. Different effects of bursectomy of chickens on immune response to Newcastle disease virus and Salmonella pullorum antigens. Poult Sci. 1973 May;52(3):1042–1052. doi: 10.3382/ps.0521042. [DOI] [PubMed] [Google Scholar]

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