Skip to main content
Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 1981 Nov;46(2):305–312.

Reactive and neoplastic human lymphoid cells producing J chain in the absence of immunoglobulin: evidence for the existence of 'J chain disease'?

D Y Mason, H Stein
PMCID: PMC1536406  PMID: 6802538

Abstract

The initiation of cytoplasmic Ig synthesis in differentiating B cells is accompanied by the start of cytoplasmic J chain production. As the cell matures further, J chain synthesis ceases (unless it is producing dimeric IgA or 19S IgM). In consequence, it is common to find Ig-positive, J chain-negative cells in reactive lymphoid tissue. However, the reverse pattern (Ig-negative/J chain-positive), which would indicate J chain production unaccompanied by Ig synthesis, has not been reported. In this paper we describe the detection of such cells in reactive human lymphoid tissue by a double immunoenzymatic labelling technique. Furthermore, retrospective immunohistological analysis of 90 cases of human high-grade lymphoma revealed three cases in which the neoplastic cells appeared to synthesize J chain but not Ig. These findings suggest that the term J chain disease might be introduced to describe this new class of lymphoid neoplasm. However, it is pointed out that immunochemical categories of human B lymphoproliferative diseases based upon patterns of Ig synthesis are often in direct conflict with histological categories (cf. mu chain-producing neoplasms) and the term J chain disease cannot therefore be recommended. It is probable that further cases of J chain-positive, Ig-negative lymphoid neoplasms, covering a range of histological categories, will be described in the future.

Full text

PDF
305

Images in this article

Selected References

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

  1. Brandtzaeg P. Presence of J chain in human immunocytes containing various immunoglobulin classes. Nature. 1974 Nov 29;252(5482):418–420. doi: 10.1038/252418a0. [DOI] [PubMed] [Google Scholar]
  2. Brouet J. C., Preud'homme J. L., Penit C., Valensi F., Rouget P., Seligmann M. Acute lymphoblastic leukemia with pre-B-cell characteristics. Blood. 1979 Jul;54(1):269–273. [PubMed] [Google Scholar]
  3. Danon F., Mihaesco C., Bouvry M., Clerc M., Seligmann M. A new case of heavy mu-chain disease. Scand J Haematol. 1975 Aug;15(1):5–9. doi: 10.1111/j.1600-0609.1975.tb01048.x. [DOI] [PubMed] [Google Scholar]
  4. Eskeland T., Brandtzaeg P. Does J chain mediate the combination of 19S IgM and dimeric IgA with the secretory component rather than being necessary for their polymerization? Immunochemistry. 1974 Mar;11(3):161–163. doi: 10.1016/0019-2791(74)90214-6. [DOI] [PubMed] [Google Scholar]
  5. Eskeland T. IgM reassociation in Vitro: no influence of J chain on the amount of polymers. Scand J Immunol. 1974;3(6):757–768. doi: 10.1111/j.1365-3083.1974.tb01311.x. [DOI] [PubMed] [Google Scholar]
  6. Frangione B., Franklin E. C. Heavy chain diseases: clinical features and molecular significance of the disordered immunoglobulin structure. Semin Hematol. 1973 Jan;10(1):53–64. [PubMed] [Google Scholar]
  7. Gordon J., Howlett A. R., Smith J. L. Free light chain synthesis by neoplastic cells in chronic lymphocytic leukaemia and non-Hodgkin's lymphoma. Immunology. 1978 Mar;34(3):397–404. [PMC free article] [PubMed] [Google Scholar]
  8. Grubb A. O. Quantitation of J chain in human biological fluids by a simple immunochemical procedure. Acta Med Scand. 1978;204(6):453–465. doi: 10.1111/j.0954-6820.1978.tb08473.x. [DOI] [PubMed] [Google Scholar]
  9. Halpern M. S., Koshland M. E. Noval subunit in secretory IgA. Nature. 1970 Dec 26;228(5278):1276–1278. doi: 10.1038/2281276a0. [DOI] [PubMed] [Google Scholar]
  10. Isaacson P. Immunochemical demonstration of J chain: a marker of B-cell malignancy. J Clin Pathol. 1979 Aug;32(8):802–807. doi: 10.1136/jcp.32.8.802. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Isaacson P., Wright D. H. Anomolous staining patterns in immunohistologic studies of malignant lymphoma. J Histochem Cytochem. 1979 Aug;27(8):1197–1199. doi: 10.1177/27.8.90079. [DOI] [PubMed] [Google Scholar]
  12. Korsrud F. R., Brandtzaeg P. Quantitative immunohistochemistry of immunoglobulin- and J-chain-producing cells in human parotid and submandibular salivary glands. Immunology. 1980 Feb;39(2):129–140. [PMC free article] [PubMed] [Google Scholar]
  13. Kownatzki E. Reassociation of IgM subunits in the presence and absence of J chain. Immunol Commun. 1973;2(1):105–113. doi: 10.3109/08820137309022886. [DOI] [PubMed] [Google Scholar]
  14. Mason D. Y., Bell J. I., Christensson B., Biberfeld P. An immunohistological study of human lymphoma. Clin Exp Immunol. 1980 May;40(2):235–248. [PMC free article] [PubMed] [Google Scholar]
  15. Mason D. Y., Sammons R. Alkaline phosphatase and peroxidase for double immunoenzymatic labelling of cellular constituents. J Clin Pathol. 1978 May;31(5):454–460. doi: 10.1136/jcp.31.5.454. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Mestecky J., Preud'homme J. L., Crago S. S., Mihaesco E., Prchal J. T., Okos A. J. Presence of J chain in human lymphoid cells. Clin Exp Immunol. 1980 Feb;39(2):371–385. [PMC free article] [PubMed] [Google Scholar]
  17. Mestecky J., Winchester R. J., Hoffman T., Kunkel H. G. Parallel synthesis of immunoglobulins and J chain in pokeweed mitogen-stimulated normal cells and in lymphoblastoid cell lines. J Exp Med. 1977 Mar 1;145(3):760–765. doi: 10.1084/jem.145.3.760. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Mestecky J., Zikan J., Butler W. T. Immunoglobulin M and secretory immunoglobulin A: presence of a common polypeptide chain different from light chains. Science. 1971 Mar 19;171(3976):1163–1165. doi: 10.1126/science.171.3976.1163. [DOI] [PubMed] [Google Scholar]
  19. Morrison S. L., Koshland M. E. Characterization of the J chain from polymeric immunoglobulins (IgA-IgM-immunological specificity-primary structure). Proc Natl Acad Sci U S A. 1972 Jan;69(1):124–128. doi: 10.1073/pnas.69.1.124. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Mosmann T. R., Gravel Y., Williamson A. R., Baumal R. Modification and fate of J chain in myeloma cells in the presence and absence of polymeric immunoglobulin secretion. Eur J Immunol. 1978 Feb;8(2):94–101. doi: 10.1002/eji.1830080205. [DOI] [PubMed] [Google Scholar]
  21. Stein H., Bonk A., Tolksdorf G., Lennert K., Rodt H., Gerdes J. Immunohistologic analysis of the organization of normal lymphoid tissue and non-Hodgkin's lymphomas. J Histochem Cytochem. 1980 Aug;28(8):746–760. doi: 10.1177/28.8.7003001. [DOI] [PubMed] [Google Scholar]
  22. Stott D. I. Biosynthesis and assembly of IgM. Addition of J chain to intracellular pools of 8S and 19S IgM. Immunochemistry. 1976 Feb;13(2):157–163. doi: 10.1016/0019-2791(76)90284-6. [DOI] [PubMed] [Google Scholar]
  23. Tomasi T. B., Czerwinski D. S. Naturally occurring polymers of IgA lacking J chain. Scand J Immunol. 1976;5(6-7):647–653. doi: 10.1111/j.1365-3083.1976.tb03014.x. [DOI] [PubMed] [Google Scholar]
  24. Yasuda N., Kanoh T., Uchino H. J chain synthesis in human myeloma cells: light and electron microscopic studies. Clin Exp Immunol. 1980 Jun;40(3):573–580. [PMC free article] [PubMed] [Google Scholar]

Articles from Clinical and Experimental Immunology are provided here courtesy of British Society for Immunology

RESOURCES