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. 1971 Jun 1;133(6):1242–1263. doi: 10.1084/jem.133.6.1242

THE NATURE AND THE SPECIFICITY OF MONONUCLEAR CELLS IN EXPERIMENTAL AUTOIMMUNE INFLAMMATIONS AND THE MECHANISMS LEADING TO THEIR ACCUMULATION

Ole Werdelin 1, Robert T McCluskey 1
PMCID: PMC2138938  PMID: 5576333

Abstract

The nature and specificity of the mononuclear cells in passively transferred autoimmune encephalomyelitis and adrenalitis were studied. The recipients were prepared by production of a small heat lesion in the target tissue 5 days before transfer. Within 24 hr after transfer of lymph node cells from donors sensitized with the corresponding tissue antigen, a dense mononuclear cell infiltrate developed around the lesion. When lymph node cells labeled in vitro with 3H-thymidine or 3H-adenosine were transferred, a significant number of labeled lymphocytes was found in the infiltrate at 24 or 48 hr. Lymphocytes labeled with 3H-thymidine showed a greater tendency to accumulate than cells labeled with 3H-adenosine, indicating that newly formed lymphocytes were more prone to enter the reaction than older cells. Labeled lymphocytes and macrophages of recipient origin and labeled lymphocytes from donors stimulated with B. pertussis were also shown to accumulate around the heat lesion provided the reaction had been initiated by transfer of unlabeled lymphocytes from donors sensitized to the appropriate tissue-specific antigen. In recipients which were given lymph node cells from two groups of donors, sensitized either to spinal cord or to adrenal antigens, with cells from only one group of donors labeled, equal percentages of labeled cells were found around each lesion. Thus, no evidence of preferential accumulation of specifically sensitized lymphocytes was obtained. In recipients which received whole body irradiation on the day of production of the heat lesions, 5 days before transfer of lymph node cells from appropriately sensitized donors, neither monocytes nor lymphocytes accumulated around the lesion. However, if the tibial bone marrow was shielded or if bone marrow cells were given to the recipients shortly after irradiation, inflammation developed as in normal recipients. In recipients which were irradiated 24 hr after the transfer of unlabeled lymph node cells from donors sensitized to the appropriate tissue antigen and then given labeled lymph node cells from B. pertussis-stimulated donors, labeled lymphocytes were found in the reaction 24 hr later. This accumulation occurred although virtually all the lymphocytes present in the lesion at 24 hr after the first transfer were destroyed by the irradiation. The results are interpreted as follows. The autoimmune reaction is initiated by the arrival at the site of a few specifically sensitized lymphocytes, probably on a random basis. After contact with antigen, factors are produced and released which cause the influx of monocytes and of lymphocytes, in particular newly formed ones, of various specificities. There is no preferential accumulation of specifically sensitized cells. The influx of lymphocytes appears to require the presence of monocytes or macrophages in the reaction.

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Selected References

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  1. Aström K. E., Webster H. D., Arnason B. G. The initial lesion in experimental allergic neuritis. A phase and electron microscopic study. J Exp Med. 1968 Sep 1;128(3):469–495. doi: 10.1084/jem.128.3.469. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bennett B., Bloom B. R. Reactions in vivo and in vitro produced by a soluble substance associated with delayed-type hypersensitivity. Proc Natl Acad Sci U S A. 1968 Mar;59(3):756–762. doi: 10.1073/pnas.59.3.756. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bloom B. R., Chase M. W. Transfer of delayed-type hypersensitivity. A critical review and experimental study in the guinea pig. Prog Allergy. 1967;10:151–255. [PubMed] [Google Scholar]
  4. Bosman C., Feldman J. D. Composition, morphology, and source of cells in delayed skin reactions. Am J Pathol. 1970 Feb;58(2):201–218. [PMC free article] [PubMed] [Google Scholar]
  5. Chase M. W. Delayed sensitivity. Med Clin North Am. 1965 Nov;49(6):1613–1646. doi: 10.1016/s0025-7125(16)33249-7. [DOI] [PubMed] [Google Scholar]
  6. Cohen S., McCluskey R. T., Benacerraf B. Studies on the specificity of the cellular infiltrate of delayed hypersensitivity reactions. J Immunol. 1967 Feb;98(2):269–273. [PubMed] [Google Scholar]
  7. David J. R. Delayed hypersensitivity in vitro: its mediation by cell-free substances formed by lymphoid cell-antigen interaction. Proc Natl Acad Sci U S A. 1966 Jul;56(1):72–77. doi: 10.1073/pnas.56.1.72. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. David J. R., Paterson P. Y. In vitro demonstration of cellular sensitivity in allergic encephalomyelitis. J Exp Med. 1965 Dec 1;122(6):1161–1171. doi: 10.1084/jem.122.6.1161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. GOWANS J. L., McGREGOR D. D., COWEN D. M. Initiation of immune responses by small lymphocytes. Nature. 1962 Nov 17;196:651–655. doi: 10.1038/196651a0. [DOI] [PubMed] [Google Scholar]
  10. Gallily R., Feldman M. The role of macrophages in the induction of antibody in x-irradiated animals. Immunology. 1967 Feb;12(2):197–206. [PMC free article] [PubMed] [Google Scholar]
  11. Hall J. G. Studies of the cells in the afferent and efferent lymph of lymph nodes draining the site of skin homografts. J Exp Med. 1967 May 1;125(5):737–754. doi: 10.1084/jem.125.5.737. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Koster F. T., McGregor D. D., Mackaness G. B. The mediator of cellular immunity. II. Migration of immunologically committed lymphocytes into inflammatory exudates. J Exp Med. 1971 Feb 1;133(2):400–409. doi: 10.1084/jem.133.2.400. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Koster F., McGregor D. D. Rat thoracic duct lymphocytes: types that participate in inflammation. Science. 1970 Feb 20;167(3921):1137–1139. doi: 10.1126/science.167.3921.1137. [DOI] [PubMed] [Google Scholar]
  14. Levine S., Hoenig E. M. Induced localization of allergic adrenalitis and encephalomyelitis at sites of thermal injury. J Immunol. 1968 Jun;100(6):1310–1318. [PubMed] [Google Scholar]
  15. Levine S., Prineas J., Scheinberg L. C. Allergic encephalomyelitis: inhibition of cellular passive transfer by x-irradiation. Proc Soc Exp Biol Med. 1969 Jul;131(3):986–990. doi: 10.3181/00379727-131-34024. [DOI] [PubMed] [Google Scholar]
  16. Levine S., Wenk E. J. The production and passive transfer of allergic adrenalitis. Am J Pathol. 1968 Jan;52(1):41–54. [PMC free article] [PubMed] [Google Scholar]
  17. Lubaroff D. M., Waksman B. H. Bone marrow as a source of cells in reactions of cellular hypersensitivity. I. Passive transfer of tuberculin sensitivity in syngeneic systems. J Exp Med. 1968 Dec 1;128(6):1425–1435. doi: 10.1084/jem.128.6.1425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lubaroff D. M., Waksman B. H. Bone marrow as source of cells in reactions of cellular hypersensitivity. II. Identification of allogeneic or hybrid cells by immunofluorescence in passively transferred tuberculin reactions. J Exp Med. 1968 Dec 1;128(6):1437–1447. doi: 10.1084/jem.128.6.1437. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. MCCLUSKEY R. T., BENACERRAF B., MCCLUSKEY J. W. STUDIES ON THE SPECIFICITY OF THE CELLULAR INFILTRATE IN DELAYED HYPERSENSITIVITY REACTIONS. J Immunol. 1963 Mar;90:466–477. [PubMed] [Google Scholar]
  20. McMaster P. R., Lerner E. M., 2nd The transfer of allergic thyroiditis in histocompatible guinea pigs by lymph node cells. J Immunol. 1967 Jul;99(1):208–213. [PubMed] [Google Scholar]
  21. 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]
  22. PORTER K. A., CALNE R. Y. Origin of the infiltrating cells in skin and kidney homografts. Transplant Bull. 1960 Oct;26:458–464. doi: 10.1097/00006534-196010000-00041. [DOI] [PubMed] [Google Scholar]
  23. PRENDERGAST R. A. CELLULAR SPECIFICITY IN THE HOMOGRAFT REACTION. J Exp Med. 1964 Mar 1;119:377–388. doi: 10.1084/jem.119.3.377. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Paterson P. Y. Experimental allergic encephalomyelitis and autoimmune disease. Adv Immunol. 1966;5:131–208. doi: 10.1016/s0065-2776(08)60273-4. [DOI] [PubMed] [Google Scholar]
  25. Spector W. G., Walters M. N., Willoughby D. A. The origin of the mononuclear cells in inflammatory exudates induced by fibrinogen. J Pathol Bacteriol. 1965 Jul;90(1):181–192. doi: 10.1002/path.1700900119. [DOI] [PubMed] [Google Scholar]
  26. VOLKMAN A., GOWANS J. L. THE ORIGIN OF MACROPHAGES FROM BONE MARROW IN THE RAT. Br J Exp Pathol. 1965 Feb;46:62–70. [PMC free article] [PubMed] [Google Scholar]
  27. Ward P. A., Remold H. G., David J. R. Leukotactic factor produced by sensitized lymphocytes. Science. 1969 Mar 7;163(3871):1079–1081. doi: 10.1126/science.163.3871.1079. [DOI] [PubMed] [Google Scholar]
  28. Werdelin O., Witebsky E. Experimental allergic rat adrenalitis. A study on its elicitation and lymphokinetics. Lab Invest. 1970 Aug;23(2):136–143. [PubMed] [Google Scholar]
  29. Wiener J., Spiro D., Zunker H. O. A cellular study of tuberculin sensitivity. Am J Pathol. 1965 Nov;47(5):723–763. [PMC free article] [PubMed] [Google Scholar]

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