Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1964 Oct 1;120(4):547–560. doi: 10.1084/jem.120.4.547

PASSIVE TRANSFER OF ADJUVANT ARTHRITIS BY LYMPH NODE OR SPLEEN CELLS

Carl M Pearson 1, Fae D Wood 1
PMCID: PMC2137780  PMID: 14212118

Abstract

All adjuvant-induced arthritis has been passively transferred in a highly inbred strain of rats by transfer of viable lymph node or spleen cells, but not thymus cells, to normal recipients. After an interval averaging 4.3 days recipients developed arthritis, whereas animals actively sensitized with adjuvant never developed disease before the 9th day (average 11.3 days). The transferred disease had all of the gross and pathological characteristics of primary disease, except for a lesser severity. Control studies using non-viable cells either of lymphoidal or other tissue origin were always negative. It is concluded that adjuvant arthritis is the result of an immunologic reaction which is perhaps similar to delayed hypersensitivity. The antigen in this reaction so far remains obscure.

Full Text

The Full Text of this article is available as a PDF (1.4 MB).

Selected References

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

  1. FLAX M., WAKSMAN B. H. FURTHER IMMUNOLOGIC STUDIES OF ADJUVANT DISEASE IN THE RAT. Int Arch Allergy Appl Immunol. 1963;23:331–347. doi: 10.1159/000229438. [DOI] [PubMed] [Google Scholar]
  2. HANKS J. H., WALLACE J. H. Determination of cell viability. Proc Soc Exp Biol Med. 1958 May;98(1):188–192. doi: 10.3181/00379727-98-23985. [DOI] [PubMed] [Google Scholar]
  3. HESS E. V., ASHWORTH C. T., ZIFF M. Transfer of an autoimmune nephrosis in the rat by means of lymph node cells. J Exp Med. 1962 Feb 1;115:421–438. doi: 10.1084/jem.115.2.421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. NEWBOULD B. B. CHEMOTHERAPY OF ARTHRITIS INDUCED IN RATS BY MYCOBACTERIAL ADJUVANT. Br J Pharmacol Chemother. 1963 Aug;21:127–136. doi: 10.1111/j.1476-5381.1963.tb01508.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. 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]
  6. PEARSON C. M., WAKSMAN B. H., SHARP J. T. Studies of arthritis and other lesions induced in rats by injection of mycobacterial adjuvant. V. Changes affecting the skin and mucous membranes. Comparison of the experimental process with human disease. J Exp Med. 1961 Mar 1;113:485–510. doi: 10.1084/jem.113.3.485. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. SNELL G. D. A cytosieve permitting sterile preparation of suspensions of tumor cells for transplantation. J Natl Cancer Inst. 1953 Jun;13(6):1511–1515. [PubMed] [Google Scholar]
  8. TANAKA A. FRACTIONATION OF WAX D, A PEPTIDOGLYCOLIPID OF MYCOBACTERIUM TUBERCULOSIS. Biochim Biophys Acta. 1963 Aug 27;70:483–485. doi: 10.1016/0006-3002(63)90784-4. [DOI] [PubMed] [Google Scholar]
  9. WAKSMAN B. H., PEARSON C. M., SHARP J. T. Studies of arthritis and other lesions induced in rats by injection of mycobacterial adjuvant. II. Evidence that the disease is a disseminated immunologic response to exogenous antigen. J Immunol. 1960 Oct;85:403–417. [PubMed] [Google Scholar]
  10. WAKSMAN B. H., WENNERSTEN C. PASSIVE TRANSFER OF ADJUVANT ARTHRITIS IN RATS WITH LIVING LYMPHOID CELLS OF SENSITIZED DONORS. Int Arch Allergy Appl Immunol. 1963;23:129–139. doi: 10.1159/000229412. [DOI] [PubMed] [Google Scholar]
  11. WARD J. R., JONES R. S. Studies on adjuvant-induced polyarthritis in rats. I. Adjuvant composition, route of injection, and removal of depot site. Arthritis Rheum. 1962 Dec;5:557–564. doi: 10.1002/art.1780050604. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES