Abstract
Surgical removal of the bursa of Fabricius from newly hatched chicks resulted in a depletion of immunoglobulin A (IgA) from serum and bile of 55 and 67% of the birds, respectively, up to 11 weeks of age. The occurrence of IgG and IgM in serum and IgG in bile was not affected by neonatal bursectomy (Bx). A slight compensatory increase in the occurrence of IgM in bile was noted in Bx birds. When exposed to a lentogenic strain of Newcastle disease virus by either intramuscular or intratracheal routes, the Bx group produced a level of serum hemagglutinating antibody and tracheal wash neutralizing antibody indistinguishable from that reached in the sham-Bx group. All of the vaccinated Bx birds challenged by intratracheal exposure to a velogenic strain of Newcastle disease virus remained healthy. These results suggest that IgA is not essential for the development of immunity in the chicken and that other locally produced immunoglobulins or transuded serum antibody may protect the tracheal mucosa in the absence of IgA.
Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bienenstock J., Perey D. Y., Gauldie J., Underdown B. J. Chicken immunoglobulin resembling A. J Immunol. 1972 Aug;109(2):403–406. [PubMed] [Google Scholar]
- Brandtzaeg P. Conjugates of immunoglobulin G with different fluorochromes. I. Characterization by anionic-exchange chromatography. Scand J Immunol. 1973;2(3):273–290. doi: 10.1111/j.1365-3083.1973.tb02037.x. [DOI] [PubMed] [Google Scholar]
- Cheville N. F., Beard C. W. Cytopathology of Newcastle disease. The influence of bursal and thymic lymphoid systems in the chicken. Lab Invest. 1972 Jul;27(1):129–143. [PubMed] [Google Scholar]
- Cooper M. D., Raymond D. A., Peterson R. D., South M. A., Good R. A. The functions of the thymus system and the bursa system in the chicken. J Exp Med. 1966 Jan 1;123(1):75–102. doi: 10.1084/jem.123.1.75. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eidelman S., Davis S. D. Immunoglobulin content of intestinal mucosal plasma-cells in ataxia telangiectasia. Lancet. 1968 Apr 27;1(7548):884–886. doi: 10.1016/s0140-6736(68)90238-9. [DOI] [PubMed] [Google Scholar]
- Kincade P. W., Cooper M. D. Immunoglobulin A: site and sequence of expression in developing chicks. Science. 1973 Jan 26;179(4071):398–400. doi: 10.1126/science.179.4071.398. [DOI] [PubMed] [Google Scholar]
- Kono R., Akao Y., Sasagawa A., Nomura Y. Studies on the local immunity of intestinal tract of chickens after oral administration of Newcastle disease virus. Jpn J Med Sci Biol. 1969 Aug;22(4):235–252. doi: 10.7883/yoken1952.22.235. [DOI] [PubMed] [Google Scholar]
- Lebacq-Verheyden A. M., Vaerman J. P., Heremans J. F. A possible homologue of mammalian IgA in chicken serum and secretions. Immunology. 1972 Jan;22(1):165–175. [PMC free article] [PubMed] [Google Scholar]
- Lebacq-Verheyden A. M., Vaerman J. P., Heremans J. F. Quantification and distribution of chicken immunoglobulins IgA, IgM and IgG in serum and secretions. Immunology. 1974 Oct;27(4):683–692. [PMC free article] [PubMed] [Google Scholar]
- Leslie G. A., Martin L. N. The secretory immunologic system of fowl. IV. Serum and salivary immunoglobulins in normal, agammaglobulinemic and dysgammaglobulinemic chickens. Int Arch Allergy Appl Immunol. 1974;46(6):834–841. [PubMed] [Google Scholar]
- March S. C., Parikh I., Cuatrecasas P. A simplified method for cyanogen bromide activation of agarose for affinity chromatography. Anal Biochem. 1974 Jul;60(1):149–152. doi: 10.1016/0003-2697(74)90139-0. [DOI] [PubMed] [Google Scholar]
- Martin L. N., Leslie G. A. Ontogeny of IgA in normal and neonatally bursectomized chickens, with corroborative data on IgY and IgM. Proc Soc Exp Biol Med. 1973 May;143(1):241–243. doi: 10.3181/00379727-143-37294. [DOI] [PubMed] [Google Scholar]
- Ogra P. L., Karzon D. T. Distribution of poliovirus antibody in serum, nasopharynx and alimentary tract following segmental immunization of lower alimentary tract with poliovaccine. J Immunol. 1969 Jun;102(6):1423–1430. [PubMed] [Google Scholar]
- Perey D. Y., Biennenstock J. Effects of bursectomy and thymectomy on ontogeny of fowl IgA, IgG, and IgM. J Immunol. 1973 Aug;111(2):633–637. [PubMed] [Google Scholar]
- Perey D. Y., Cleland G. B., Dent P. B. Newcastle disease in normal and immunodeficient chickens. Am J Vet Res. 1975 Apr;36(4 Pt 2):513–517. [PubMed] [Google Scholar]
- Perey D. Y., Dent P. B. Host resistance mechanisms to Newcastle disease virus in immunodeficient chickens (38540). Proc Soc Exp Biol Med. 1975 Feb;148(2):365–369. doi: 10.3181/00379727-148-38540. [DOI] [PubMed] [Google Scholar]
- Portnoy J., Bloom K., Merigan T. C. The effect of bursectomy and thymectomy on the course of avian influenza virus infection. Cell Immunol. 1973 Nov;9(2):251–262. doi: 10.1016/0008-8749(73)90076-2. [DOI] [PubMed] [Google Scholar]
- ROCKEY J. H., HANSON L. A., HEREMANS J. F., KUNKEL H. G. BETA-2A AGLOBULINEMIA IN TWO HEALTHY MEN. J Lab Clin Med. 1964 Feb;63:205–212. [PubMed] [Google Scholar]
- Stobo J. D., Tomasi T. B. A Low Molecular Weight Immunoglobulin Antigenically Related to 19 S IgM. J Clin Invest. 1967 Aug;46(8):1329–1337. doi: 10.1172/JCI105625. [DOI] [PMC free article] [PubMed] [Google Scholar]
- TOMASI T. B., Jr, ZIGELBAUM S. THE SELECTIVE OCCURENCE OF GAMMA-1A GLOBULINS IN CERTAIN BODY FLUIDS. J Clin Invest. 1963 Oct;42:1552–1560. doi: 10.1172/JCI104840. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Waldman R. H., Mann J. J., Small P. A., Jr Immunization against influenza. Prevention of illness in man by aerosolized inactivated vaccine. JAMA. 1969 Jan 20;207(3):520–524. doi: 10.1001/jama.207.3.520. [DOI] [PubMed] [Google Scholar]