Abstract
Rats regularly develop evidence of allergic encephalomyelitis (AE) 2 to 3 weeks following sensitization to nervous tissue plus adjuvant. Independent of the severity of AE which occurs, gradual recovery is the rule and by the 6th to 9th week after sensitization rats appear clinically well and microscopic lesions of AE have virtually disappeared. Pooled serum collected from rats 3 or 6 weeks after sensitization contains complement-fixing (CF) antibrain antibodies. Such pooled serum exerts a striking suppressive influence on development of AE when passively administered to rats actively sensitized to nervous tissue. Serum pools which contain CF antibrain antibody suppress the disease. Serum pools lacking CF antibody do not suppress the disease. Serum containing CF antibrain antibody after treatment with 2-mercaptoethanol no longer fixes complement with brain antigen in vitro and no longer suppresses AE in vivo. The data suggest that transfer of protection against AE by passively administered antibrain rat serum is due to an antibrain antibody, possibly the CF antibodies. The meaning of these findings is discussed in terms of the role(s) of circulating antibrain antibody in the pathogenesis of AE.
Full Text
The Full Text of this article is available as a PDF (1.2 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- ALVORD E. C., Jr, KIES M. W. Clinico-pathologic correlations in experimental allergic encephalomyelitis. II. Development of an index for quantitative assay of encephalitogenic activity of antigens. J Neuropathol Exp Neurol. 1959 Jul;18(3):447–457. doi: 10.1097/00005072-195907000-00007. [DOI] [PubMed] [Google Scholar]
- BELL J., PATERSON P. Y. Rapid induction of allergic encephalomyelitis in rats without the use of mycobacteria. Science. 1960 May 13;131(3411):1448–1448. doi: 10.1126/science.131.3411.1448. [DOI] [PubMed] [Google Scholar]
- FREUND J., LIPTON M. M., THOMPSON G. E. Aspermatogenesis in the guinea pig induced by testicular tissue and adjuvants. J Exp Med. 1953 May;97(5):711–726. doi: 10.1084/jem.97.5.711. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HARWIN S. M., PATERSON P. Y. Antibrain antibodies of the 19S gamma-globulin type in rats with allergic encephalomyelitis. Nature. 1962 Apr 28;194:391–392. doi: 10.1038/194391a0. [DOI] [PubMed] [Google Scholar]
- HARWIN S. M., PATERSON P. Y., DIDAKOW N. C. Antibodies against autologous brain in rats with allergic encephalomyelitis. Nature. 1961 Jan 28;189:322–323. doi: 10.1038/189322a0. [DOI] [PubMed] [Google Scholar]
- KABAT E. A., WOLF A., BEZER A. E. Studies on acute disseminated encephalomyelitis produced experimentally in rhesus monkeys; disseminated encephalomyelitis produced in monkeys with their own brain tissue. J Exp Med. 1949 Apr 1;89(4):395–398. doi: 10.1084/jem.89.4.395. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KALISS N. The survival of homografts in mice pretreated with antisera to mouse tissue. Ann N Y Acad Sci. 1957 Mar 22;64(5):977-90; discussion, 990-3. doi: 10.1111/j.1749-6632.1957.tb52489.x. [DOI] [PubMed] [Google Scholar]
- NEIDERS M. E., ROWLEY D. A., FITCH F. W. The sustained suppression of hemolysin response in passively immunized rats. J Immunol. 1962 Jun;88:718–724. [PubMed] [Google Scholar]
- NELSON D. S. Immunological enhancement of skin homografts in guinea-pigs. Br J Exp Pathol. 1962 Feb;43:1–11. [PMC free article] [PubMed] [Google Scholar]
- PATERSON P. Y. A study of experimental encephalomyelitis employing mammalian and nonmammalian nervous tissues. J Immunol. 1957 Jun;78(6):472–475. [PubMed] [Google Scholar]
- PATERSON P. Y., BELL J. Studies of induction of allergic encephalomyelities in rats and guinea pigs without the use of Mycobacteria. J Immunol. 1962 Jul;89:72–79. [PubMed] [Google Scholar]
- PATERSON P. Y., DIDAKOW N. C. Transfer of allergic encephalomyelitis using splenectomized albino rats. Proc Soc Exp Biol Med. 1961 Dec;108:768–771. doi: 10.3181/00379727-108-27061. [DOI] [PubMed] [Google Scholar]
- PATERSON P. Y. Transfer of allergic encephalomyelitis in rats by means of lymph node cells. J Exp Med. 1960 Jan 1;111:119–136. doi: 10.1084/jem.111.1.119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Snell G. D., Winn H. J., Stimpfling J. H., Parker S. J. DEPRESSION BY ANTIBODY OF THE IMMUNE RESPONSE TO HOMOGRAFTS AND ITS ROLE IN IMMUNOLOGICAL ENHANCEMENT. J Exp Med. 1960 Aug 1;112(2):293–314. doi: 10.1084/jem.112.2.293. [DOI] [PMC free article] [PubMed] [Google Scholar]
- THOMAS L., PATERSON P. Y., SMITHWICK B. Acute disseminated encephalomyelitis following immunization with homologous brain extracts; studies on the role of a circulating antibody in the production of the condition in dogs. J Exp Med. 1950 Aug;92(2):133–152. doi: 10.1084/jem.92.2.133. [DOI] [PMC free article] [PubMed] [Google Scholar]
- UHR J. W., BAUMANN J. B. Antibody formation. I. The suppression of antibody formation by passively administered antibody. J Exp Med. 1961 May 1;113:935–957. doi: 10.1084/jem.113.5.935. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WAKSMAN B. H. Further study of skin reactions in rabbits with experimental allergic encephalomyelitis: reactions to tests with purified white matter fractions; use of a quantitative technique for evaluating sensitivity production of sensitization and disease by intradermal injection of antigen without adjuvants. J Infect Dis. 1956 Nov-Dec;99(3):258–269. doi: 10.1093/infdis/99.3.258. [DOI] [PubMed] [Google Scholar]
- WITEBSKY E., ROSE N. R. Studies on organ specificity. IV. Production of rabbit thyroid antibodies in the rabbit. J Immunol. 1956 Jun;76(6):408–416. [PubMed] [Google Scholar]
