Abstract
Newcastle disease virus (NDV) can interact in at least two ways with rat T cells. By adsorbing to circulating lymphocytes, the virus can transiently deflect the cells from lymph nodes and inflammatory exudates induced in the peritoneal cavity. T cells are affected regardless of age, state of activation, or position in the mitotic cycle. The effect is reversible and is mediated not only by infectious (I)-NDV, but also by UV-NDV which cannot achieve a complete replication cycle in eggs. But I-NDV has another lasting effect on activated T cells. It is revealed in the failure of virus-treated thoracic duct lymphocytes to transfer cellular resistance to Listeria monocytogenes, delayed-type hypersensitivity to soluble antigens of the parasite, and the permanent exclusion of labeled S-phase lymphocytes from inflammatory foci. Activated T cells are inhibited by virus multiplicites which have little if any effect upon the proliferative potential of antigen-sensitive T cells or localization of labeled small lymphocytes in lymph nodes. The underlying mechanism has not been determined; however, there are reasons for thinking that NDV has a lethal effect upon activated T cells, because the latter are permissive for virus replication.
Full Text
The Full Text of this article is available as a PDF (1.0 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bach F. H., Bach M. L., Sondel P. M. Differential function of major histocompatibility complex antigens in T-lymphocyte activation. Nature. 1976 Jan 29;259(5541):273–281. doi: 10.1038/259273a0. [DOI] [PubMed] [Google Scholar]
- Blanden R. V., Langman R. E. Cell-mediated immunity to bacterial infection in the mouse. Thymus-derived cells as effectors of acquired resistance to Listeria monocytogenes. Scand J Immunol. 1972;1(4):379–391. doi: 10.1111/j.1365-3083.1972.tb03304.x. [DOI] [PubMed] [Google Scholar]
- Blanden R. V. T cell response to viral and bacterial infection. Transplant Rev. 1974;19(0):56–88. doi: 10.1111/j.1600-065x.1974.tb00128.x. [DOI] [PubMed] [Google Scholar]
- Bloom B. R., Jimenez L., Marcus P. I. A plaque assay for enumerating antigen-sensitive cells in delayed-type hypersensitivity. J Exp Med. 1970 Jul 1;132(1):16–30. doi: 10.1084/jem.132.1.16. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bloom B. R., Kano S., Howe M. L. Virus plaque assay and enumeration of effector cells in mixed lymphocyte cultures. Transplant Proc. 1973 Dec;5(4):1705–1709. [PubMed] [Google Scholar]
- Cantor H., Boyse E. A. Functional subclasses of T-lymphocytes bearing different Ly antigens. I. The generation of functionally distinct T-cell subclasses is a differentiative process independent of antigen. J Exp Med. 1975 Jun 1;141(6):1376–1389. doi: 10.1084/jem.141.6.1376. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Crum E. D., McGregor D. D. Functional properties of T and B cells isolated by affinity chromatography from rat thoracic duct lymph. Cell Immunol. 1976 May;23(2):211–222. doi: 10.1016/0008-8749(76)90187-8. [DOI] [PubMed] [Google Scholar]
- Howard J. C., Hunt S. V., Gowans J. L. Identification of marrow-derived and thymus-derived small lymphocytes in the lymphoid tissue and thoracic duct lymph of normal rats. J Exp Med. 1972 Feb 1;135(2):200–219. doi: 10.1084/jem.135.2.200. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Howard J. C. The life-span and recirculation of marrow-derived small lymphocytes from the rat thoracic duct. J Exp Med. 1972 Feb 1;135(2):185–199. doi: 10.1084/jem.135.2.185. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jimenez L., Bloom B. R., Blume M. R., Oettgen H. F. On the number and nature of antigen-sensitive lymphocytes in the blood of delayed-hypersensitive human donors. J Exp Med. 1971 Apr 1;133(4):740–751. doi: 10.1084/jem.133.4.740. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kano S., Bloom B. R., Howe M. L. Enumeration of activated thymus-derived lymphocytes by the virus plaque assay. Proc Natl Acad Sci U S A. 1973 Aug;70(8):2299–2303. doi: 10.1073/pnas.70.8.2299. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Koster F. T., McGregor D. D. The mediator of cellular immunity. 3. Lymphocyte traffic from the blood into the inflamed peritoneal cavity. J Exp Med. 1971 Apr 1;133(4):864–876. doi: 10.1084/jem.133.4.864. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kostiala A. A., McGregor D. D. The mediator of cellular immunity. IX. The relationship between cellular hypersensitivity and acquired cellular resistance in rats infected with Listeria monocytogenes. J Exp Med. 1975 Jun 1;141(6):1249–1260. doi: 10.1084/jem.141.6.1249. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lane F. C., Unanue E. R. Requirement of thymus (T) lymphocytes for resistance to listeriosis. J Exp Med. 1972 May 1;135(5):1104–1112. doi: 10.1084/jem.135.5.1104. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McGregor D. D., Koster F. T., Mackaness G. B. The mediator of cellular immunity. I. The life-span and circulation dynamics of the immunologically committed lymphocyte. J Exp Med. 1971 Feb 1;133(2):389–399. doi: 10.1084/jem.133.2.389. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McGregor D. D., Logie P. S. The mediator of cellular immunity. VI. Effect of the antimitotic drug vinblastine on the mediator of cellular resistance to infection. J Exp Med. 1973 Mar 1;137(3):660–674. doi: 10.1084/jem.137.3.660. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McGregor D. D., Logie P. S. The mediator of cellular immunity. VII. Localization of sensitized lymphocytes in inflammatory exudates. J Exp Med. 1974 Jun 1;139(6):1415–1430. doi: 10.1084/jem.139.6.1415. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McGregor D. D., Logie P. S. The mediator of cellular immunity. VIII. Effect of mitomycin C on specifically sensitized lymphocytes. Cell Immunol. 1975 Jan;15(1):69–81. doi: 10.1016/0008-8749(75)90165-3. [DOI] [PubMed] [Google Scholar]
- Notkins A. L., Mergenhagen S. E., Howard R. J. Effect of virus infections on the function of the immune system. Annu Rev Microbiol. 1970;24:525–538. doi: 10.1146/annurev.mi.24.100170.002521. [DOI] [PubMed] [Google Scholar]
- Nowakowski M., Feldman J. D., Kano S., Bloom B. R. The production of vesicular stomatitis virus by antigen- or mitogen-stimulated lymphocytes and continuous lymphoblastoid lines. J Exp Med. 1973 Apr 1;137(4):1042–1059. doi: 10.1084/jem.137.4.1042. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Volkert M., Marker O., Bro-Jorgensen K. Twp populations of T lymphocytes immune to the lymphocytic choriomeningitis virus. J Exp Med. 1974 May 1;139(5):1329–1343. doi: 10.1084/jem.139.5.1329. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Woodruff J. F., Woodruff J. J. Lymphocyte receptors for myxoviruses and paramyxoviruses. J Immunol. 1974 Jun;112(6):2176–2183. [PubMed] [Google Scholar]
- Woodruff J. F., Woodruff J. J. T lymphocyte interaction with viruses and virus-infected tissues. Prog Med Virol. 1975;19:120–160. [PubMed] [Google Scholar]
- Woodruff J. F., Woodruff J. J. Virus-induced alterations of lymphoid tissues. I. Modification of the recirculating pool of small lymphocytes by Newcastle disease virus. Cell Immunol. 1970 Sep;1(3):333–354. doi: 10.1016/0008-8749(70)90053-5. [DOI] [PubMed] [Google Scholar]
- Woodruff J. F., Woodruff J. J. Virus-induced alterations of lymphoid tissues. II. Lymphocyte receptors for Newcastle disease virus. Cell Immunol. 1972 Oct;5(2):296–306. doi: 10.1016/0008-8749(72)90055-x. [DOI] [PubMed] [Google Scholar]
- Woodruff J. J., Woodruff J. F. Virus-induced alterations of lymphoid tissue. IV. The effect of Newcastle disease virus on the fate of transfused thoracic duct lymphocytes. Cell Immunol. 1974 Jan;10(1):78–85. doi: 10.1016/0008-8749(74)90153-1. [DOI] [PubMed] [Google Scholar]
