Skip to main content
British Journal of Cancer logoLink to British Journal of Cancer
. 1984 Apr;49(4):465–476. doi: 10.1038/bjc.1984.74

Characteristics of Sternberg-Reed, and related cells in Hodgkin's disease: an immunohistological study.

M S Dorreen, J A Habeshaw, A G Stansfeld, P F Wrigley, T A Lister
PMCID: PMC1976777  PMID: 6370286

Abstract

A panel of monoclonal antileucocyte antibodies was used in a study of Hodgkin's disease (HD) to explore the phenotypic characteristics of Sternberg-Reed and related cells (collectively termed HD cells). Cryostat preparations of 31 lymph nodes and 2 spleens were obtained from 30 patients with active HD. The histological diagnoses were: lymphocyte predominance (LP), 4 patients; nodular sclerosis (NS), 22; mixed cellularity (MC), 2; lymphocyte depletion (LD), 2. The monoclonal antibodies used were: OKT3, T11, Leu-1 (pan T cell specific); Leu-3A (T "helper" specific); Leu-2A, OKT8 (T "suppressor" specific); immunoglobulin (Ig) antibodies: anti kappa and lambda light chains, anti mu and delta heavy chains; B1 (anti B lymphocyte); CA2-11 (anti HLA-DR); OKM1, Mo-2 (anti myeloid/monocyte); OKT9 (anti transferrin receptor); Leu-7 (anti "NK" cell) and J5 (anti common ALL antigen). Reactions with peanut lectin (PNL) were also studied. The reactions were developed using a modified "ABC" immunoperoxidase technique. Specific attention was paid to the cell surface phenotype and anatomical localisation of HD cells in relation to surrounding T and B lymphocytes. HD cells formed distinct "rosettes" with T cells of "helper" phenotype although in 3 cases (1: LP, 2: NS) Leu-7 positive cells formed a prominent component of these interactions. In partially involved lymph node and spleen, HD cells were prominently distributed in a perifollicular distribution. In addition follicular mantle zones were frequently infiltrated by HD cells, the degree of ensuing destruction being related to the extent of lymph node effacement by HD. In 2 cases (1: NS, 1: LD) HD cells expressed clear, positive reactions with B1 although in neither of these cases nor in any other instance, was surface Ig expressed on the HD cell surface. The great majority of HD cells reacted positively with both OKT9 and, as previously reported, with anti HLA-DR antibody. In addition, HD cells demonstrated intense surface and cytoplasmic staining with PNL. HD cells were negative with all other antibodies. On the basis of these findings, no lineage specificity can confidently be attributed to the HD cell. However, the pattern of immunohistological reactions suggest that it is related to a cell of B follicular origins.

Full text

PDF
465

Images in this article

Selected References

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

  1. Abo T., Balch C. M. A differentiation antigen of human NK and K cells identified by a monoclonal antibody (HNK-1). J Immunol. 1981 Sep;127(3):1024–1029. [PubMed] [Google Scholar]
  2. Agliozzo C. M., Reingold I. M. Infectious mononucleosis simulating Hodgkin's disease: a patient with Reed-Sternbery cells. Am J Clin Pathol. 1971 Dec;56(6):730–735. doi: 10.1093/ajcp/56.6.730. [DOI] [PubMed] [Google Scholar]
  3. Anagnostou D., Parker J. W., Taylor C. R., Tindle B. H., Lukes R. J. Lacunar cells of nodular sclerosing Hodgkin's disease: an ultrastructural and immunohistologic study. Cancer. 1977 Mar;39(3):1032–1043. doi: 10.1002/1097-0142(197703)39:3<1032::aid-cncr2820390306>3.0.co;2-x. [DOI] [PubMed] [Google Scholar]
  4. Banerjee D., Thibert R. F. Natural killer-like cells found in B-cell compartments of human lymphoid tissues. Nature. 1983 Jul 21;304(5923):270–272. doi: 10.1038/304270a0. [DOI] [PubMed] [Google Scholar]
  5. Beverley P. C., Callard R. E. Distinctive functional characteristics of human "T" lymphocytes defined by E rosetting or a monoclonal anti-T cell antibody. Eur J Immunol. 1981 Apr;11(4):329–334. doi: 10.1002/eji.1830110412. [DOI] [PubMed] [Google Scholar]
  6. Bhan A. K., Nadler L. M., Stashenko P., McCluskey R. T., Schlossman S. F. Stages of B cell differentiation in human lymphoid tissue. J Exp Med. 1981 Sep 1;154(3):737–749. doi: 10.1084/jem.154.3.737. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Biniaminov M., Ramot B. Letter: Possible T-lymphocyte origin of Reed-Sternberg cells. Lancet. 1974 Mar 2;1(7853):368–368. doi: 10.1016/s0140-6736(74)93138-9. [DOI] [PubMed] [Google Scholar]
  8. Borowitz M. J., Croker B. P., Metzgar R. S. Immunohistochemical analysis of the distribution of lymphocyte subpopulations in Hodgkin's disease. Cancer Treat Rep. 1982 Apr;66(4):667–674. [PubMed] [Google Scholar]
  9. Bramwell V. H., Crowther D., Gallagher J., Stoddart R. W. Studies of lectin binding to normal and neoplastic lymphoid tissues. I. Normal nodes and Hodgkin's disease. Br J Cancer. 1982 Oct;46(4):568–581. doi: 10.1038/bjc.1982.241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Brooks J. S. Leukophagocytosis by Reed-Sternberg cells in Hodgkin's disease. N Engl J Med. 1979 May 10;300(19):1115–1116. doi: 10.1056/nejm197905103001919. [DOI] [PubMed] [Google Scholar]
  11. Carbone P. P., Kaplan H. S., Musshoff K., Smithers D. W., Tubiana M. Report of the Committee on Hodgkin's Disease Staging Classification. Cancer Res. 1971 Nov;31(11):1860–1861. [PubMed] [Google Scholar]
  12. Charron D. J., McDevitt H. O. Analysis of HLA-D region-associated molecules with monoclonal antibody. Proc Natl Acad Sci U S A. 1979 Dec;76(12):6567–6571. doi: 10.1073/pnas.76.12.6567. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Cossman J., Deegan M. J., Schnitzer B. Complement receptor B lymphocytes in nodular sclerosing Hodgkin's disease. Cancer. 1977 May;39(5):2166–2173. doi: 10.1002/1097-0142(197705)39:5<2166::aid-cncr2820390533>3.0.co;2-6. [DOI] [PubMed] [Google Scholar]
  14. Curran R. C., Jones E. L. Dendritic cells and B lymphocytes in Hodgkin's disease. Lancet. 1977 Aug 13;2(8033):349–349. doi: 10.1016/s0140-6736(77)91502-1. [DOI] [PubMed] [Google Scholar]
  15. Curran R. C., Jones E. L. Hodgkin's disease: an immunohistochemical and histological study. J Pathol. 1978 May;125(1):39–51. doi: 10.1002/path.1711250107. [DOI] [PubMed] [Google Scholar]
  16. DeVita V. T., Jr Lymphocyte reactivity in Hodgkin's disease: a lymphocyte civil war. N Engl J Med. 1973 Oct 11;289(15):801–802. doi: 10.1056/NEJM197310112891510. [DOI] [PubMed] [Google Scholar]
  17. Diehl V., Kirchner H. H., Burrichter H., Stein H., Fonatsch C., Gerdes J., Schaadt M., Heit W., Uchanska-Ziegler B., Ziegler A. Characteristics of Hodgkin's disease-derived cell lines. Cancer Treat Rep. 1982 Apr;66(4):615–632. [PubMed] [Google Scholar]
  18. Evans R. L., Faldetta T. J., Humphreys R. E., Pratt D. M., Yunis E. J., Schlossman S. F. Peripheral human T cells sensitized in mixed leukocyte culture synthesize and express Ia-like antigens. J Exp Med. 1978 Nov 1;148(5):1440–1445. doi: 10.1084/jem.148.5.1440. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Garvin A. J., Spicer S. S., Parmley R. T., Munster A. M. Immunohistochemical demonstration of IgG in Reed-Sternberg and other cells in Hodgkin's disease. J Exp Med. 1974 May 1;139(5):1077–1083. doi: 10.1084/jem.139.5.1077. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Greaves M. F., Delia D., Robinson J., Sutherland R., Newman R. Exploitation of monoclonal antibodies: a "who's who" of haemopoietic malignancy. Blood Cells. 1981;7(2):257–280. [PubMed] [Google Scholar]
  21. Habeshaw J. A., Bailey D., Stansfeld A. G., Greaves M. F. The cellular content of non Hodgkin lymphomas: a comprehensive analysis using monoclonal antibodies and other surface marker techniques. Br J Cancer. 1983 Mar;47(3):327–351. doi: 10.1038/bjc.1983.52. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Habeshaw J. A., Lister T. A., Stansfeld A. G., Greaves M. F. Correlation of transferrin receptor expression with histological class and outcome in non-Hodgkin lymphoma. Lancet. 1983 Mar 5;1(8323):498–501. doi: 10.1016/s0140-6736(83)92191-8. [DOI] [PubMed] [Google Scholar]
  23. Halie M. R., Thiadens J., Eibergen R., van den Broek A. A. Hodgkin's disease in the spleen. Investigation of Hodgkin foci and areas for the immune response. Virchows Arch B Cell Pathol. 1978 Mar 2;27(1):39–48. [PubMed] [Google Scholar]
  24. Hartsock R. J. Postvaccinial lymphadenitis. Hyperplasia of lymphoid tissue that simulates malignant lymphomas. Cancer. 1968 Apr;21(4):632–649. doi: 10.1002/1097-0142(196804)21:4<632::aid-cncr2820210415>3.0.co;2-o. [DOI] [PubMed] [Google Scholar]
  25. Hsu S. M., Raine L., Fanger H. The use of antiavidin antibody and avidin-biotin-peroxidase complex in immunoperoxidase technics. Am J Clin Pathol. 1981 Jun;75(6):816–821. doi: 10.1093/ajcp/75.6.816. [DOI] [PubMed] [Google Scholar]
  26. Kadin M. E., Billing R. J. B lymphocyte antigens in the differential diagnosis of human neoplasia. Blood. 1978 May;51(5):813–823. [PubMed] [Google Scholar]
  27. Kadin M. E., Newcom S. R., Gold S. B., Stites D. P. Letter: Origin of Hodgkin's cell. Lancet. 1974 Jul 20;2(7873):167–168. doi: 10.1016/s0140-6736(74)91602-x. [DOI] [PubMed] [Google Scholar]
  28. Kadin M. E. Possible origin of the Reed-Sternberg cell from an interdigitating reticulum cell. Cancer Treat Rep. 1982 Apr;66(4):601–608. [PubMed] [Google Scholar]
  29. Kadin M. E., Stites D. P., Levy R., Warnke R. Exogenous immunoglobulin and the macrophage origin of Reed-Sternberg cells in Hodgkin's disease. N Engl J Med. 1978 Nov 30;299(22):1208–1214. doi: 10.1056/NEJM197811302992203. [DOI] [PubMed] [Google Scholar]
  30. Katz D. R. The macrophage in Hodgkin's disease. J Pathol. 1981 Feb;133(2):145–159. doi: 10.1002/path.1711330206. [DOI] [PubMed] [Google Scholar]
  31. Leech J. Immunoglobulin-positive Reed Sternberg cells in Hodgkin's disease. Lancet. 1973 Aug 4;2(7823):265–266. doi: 10.1016/s0140-6736(73)93173-5. [DOI] [PubMed] [Google Scholar]
  32. Lukes R. J., Tindle B. H., Parker J. W. Reed-Sternberg-like cells in infectious mononucleosis. Lancet. 1969 Nov 8;2(7628):1003–1004. doi: 10.1016/s0140-6736(69)90552-2. [DOI] [PubMed] [Google Scholar]
  33. Order S. E., Hellman S. Pathogenesis of Hodgkin's disease. Lancet. 1972 Mar 11;1(7750):571–573. doi: 10.1016/s0140-6736(72)90360-1. [DOI] [PubMed] [Google Scholar]
  34. Payne S. V., Jones D. B., Haegert D. G., Smith J. L., Wright D. H. T and B lymphocytes and Reed-Sternberg cells in Hodgkin's disease lymph nodes and spleens. Clin Exp Immunol. 1976 May;24(2):280–286. [PMC free article] [PubMed] [Google Scholar]
  35. Payne S. V., Newell D. G., Jones D. B., Wright D. H. The Reed-Sternberg cell/lymphocyte interaction: ultrastructure and characteristics of binding. Am J Pathol. 1980 Jul;100(1):7–24. [PMC free article] [PubMed] [Google Scholar]
  36. Payne S. V., Wright D. H., Jones K. J., Judd M. A. Macrophage origin of Reed-Sternberg cells: an immunohistochemical study. J Clin Pathol. 1982 Feb;35(2):159–166. doi: 10.1136/jcp.35.2.159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Poppema S., Bhan A. K., Reinherz E. L., McCluskey R. T., Schlossman S. F. Distribution of T cell subsets in human lymph nodes. J Exp Med. 1981 Jan 1;153(1):30–41. doi: 10.1084/jem.153.1.30. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Poppema S., Bhan A. K., Reinherz E. L., Posner M. R., Schlossman S. F. In situ immunologic characterization of cellular constituents in lymph nodes and spleens involved by Hodgkin's disease. Blood. 1982 Feb;59(2):226–232. [PubMed] [Google Scholar]
  39. Poppema S., Elema J. D., Halie M. R. The localization of Hodgkin's disease in lymph nodes. A study with immunohistological, enzyme histochemical and rosetting techniques on frozen sections. Int J Cancer. 1979 Nov 15;24(5):532–540. doi: 10.1002/ijc.2910240503. [DOI] [PubMed] [Google Scholar]
  40. Poppema S., Elema J. D., Halie M. R. The significance of intracytoplasmic proteins in Reed-Sternberg cells. Cancer. 1978 Oct;42(4):1793–1803. doi: 10.1002/1097-0142(197810)42:4<1793::aid-cncr2820420418>3.0.co;2-l. [DOI] [PubMed] [Google Scholar]
  41. Poppema S., Kaiserling E., Lennert K. Hodgkin's disease with lymphocytic predominance, nodular type (nodular paragranuloma) and progressively transformed germinal centres--a cytohistological study. Histopathology. 1979 Jul;3(4):295–308. doi: 10.1111/j.1365-2559.1979.tb03011.x. [DOI] [PubMed] [Google Scholar]
  42. Poppema S., Kaiserling E., Lennert K. Nodular paragranuloma and progressively transformed germinal centers. Ultrastructural and immunohistologic findings. Virchows Arch B Cell Pathol Incl Mol Pathol. 1979;31(3):211–225. doi: 10.1007/BF02889938. [DOI] [PubMed] [Google Scholar]
  43. Resnick G. D., Nachman R. L. Reed-Sternberg cells in Hodgkin's disease contain fibronectin. Blood. 1981 Feb;57(2):339–342. [PubMed] [Google Scholar]
  44. Roder J. C., Pross H. F. The biology of the human natural killer cell. J Clin Immunol. 1982 Oct;2(4):249–263. doi: 10.1007/BF00915064. [DOI] [PubMed] [Google Scholar]
  45. Rose M. L., Habeshaw J. A., Kennedy R., Sloane J., Wiltshaw E., Davies A. J. Binding of peanut lectin to germinal-centre cells: a marker for B-cell subsets of follicular lymphoma? Br J Cancer. 1981 Jul;44(1):68–74. doi: 10.1038/bjc.1981.149. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. SALTZSTEIN S. L., ACKERMAN L. V. Lymphadenopathy induced by anticonvulsant drugs and mimicking clinically pathologically malignant lymphomas. Cancer. 1959 Jan-Feb;12(1):164–182. doi: 10.1002/1097-0142(195901/02)12:1<164::aid-cncr2820120122>3.0.co;2-y. [DOI] [PubMed] [Google Scholar]
  47. SALTZSTEIN S. L., JAUDON J. C., LUSE S. A., ACKERMAN L. V. Lymphadenopathy induced by ethotoin (peganone); clinical and pathological mimicking of malignant lymphoma. J Am Med Assoc. 1958 Jul 26;167(13):1618–1620. doi: 10.1001/jama.1958.72990300001010. [DOI] [PubMed] [Google Scholar]
  48. Schwab U., Stein H., Gerdes J., Lemke H., Kirchner H., Schaadt M., Diehl V. Production of a monoclonal antibody specific for Hodgkin and Sternberg-Reed cells of Hodgkin's disease and a subset of normal lymphoid cells. Nature. 1982 Sep 2;299(5878):65–67. doi: 10.1038/299065a0. [DOI] [PubMed] [Google Scholar]
  49. Si L., Whiteside T. L. Tissue distribution of human NK cells studied with anti-Leu-7 monoclonal antibody. J Immunol. 1983 May;130(5):2149–2155. [PubMed] [Google Scholar]
  50. Stashenko P., Nadler L. M., Hardy R., Schlossman S. F. Characterization of a human B lymphocyte-specific antigen. J Immunol. 1980 Oct;125(4):1678–1685. [PubMed] [Google Scholar]
  51. 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]
  52. Stein H., Gerdes J., Kirchner H., Diehl V., Schaadt M., Bonk A., Steffen T. Immunohistological analysis of Hodgkin's and Sternberg-reed cells: detection of a new antigen and evidence for selective IgG uptake in the absence of B cell, T cell and histiocytic markers. J Cancer Res Clin Oncol. 1981;101(1):125–134. doi: 10.1007/BF00405073. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Stein H., Gerdes J., Schwab U., Lemke H., Mason D. Y., Ziegler A., Schienle W., Diehl V. Identification of Hodgkin and Sternberg-reed cells as a unique cell type derived from a newly-detected small-cell population. Int J Cancer. 1982 Oct 15;30(4):445–459. doi: 10.1002/ijc.2910300411. [DOI] [PubMed] [Google Scholar]
  54. Stein H., Papadimitriou C. S., Bouman H., Lennert K., Fuchs J. Demonstration of immunoglobulin production by tumor cells in non-Hodgkin's and Hodgkin's malignant lymphomas and its significance for their classification. Recent Results Cancer Res. 1978;64:158–175. doi: 10.1007/978-3-642-81246-0_18. [DOI] [PubMed] [Google Scholar]
  55. Stein H., Uchánska-Ziegler B., Gerdes J., Ziegler A., Wernet P. Hodgkin and Sternberg-Reed cells contain antigens specific to late cells of granulopoiesis. Int J Cancer. 1982 Mar 15;29(3):283–290. doi: 10.1002/ijc.2910290310. [DOI] [PubMed] [Google Scholar]
  56. Strum S. B., Park J. K., Rappaport H. Observation of cells resembling Sternberg-Reed cells in conditions other than Hodgkin's disease. Cancer. 1970 Jul;26(1):176–190. doi: 10.1002/1097-0142(197007)26:1<176::aid-cncr2820260123>3.0.co;2-i. [DOI] [PubMed] [Google Scholar]
  57. Stuart A. E., Dewar A. E. Properties of anti-hairy cell serum. Br J Haematol. 1979 Feb;41(2):163–168. doi: 10.1111/j.1365-2141.1979.tb05844.x. [DOI] [PubMed] [Google Scholar]
  58. Stuart A. E., Jackson E., Morris C. S. The reaction of xenogeneic and monoclonal antisera with Reed-Sternberg cells. J Pathol. 1982 Jun;137(2):129–138. doi: 10.1002/path.1711370206. [DOI] [PubMed] [Google Scholar]
  59. Stuart A. E., Volsen S. G., Zola H. The reactivity of Reed-Sternberg cells with monoclonal antisera at thin section and ultrastructural levels. J Pathol. 1983 Sep;141(1):71–82. doi: 10.1002/path.1711410108. [DOI] [PubMed] [Google Scholar]
  60. Stuart A. E., Williams A. R., Habeshaw J. A. Rosetting and other reactions of the Reed-Sternberg cell. J Pathol. 1977 Jun;122(2):81–90. doi: 10.1002/path.1711220205. [DOI] [PubMed] [Google Scholar]
  61. Sutherland R., Delia D., Schneider C., Newman R., Kemshead J., Greaves M. Ubiquitous cell-surface glycoprotein on tumor cells is proliferation-associated receptor for transferrin. Proc Natl Acad Sci U S A. 1981 Jul;78(7):4515–4519. doi: 10.1073/pnas.78.7.4515. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Taylor C. R. An immunohistological study of follicular lymphoma, reticulum cell sarcoma and Hodgkin's disease. Eur J Cancer. 1976 Jan;12(1):61–75. doi: 10.1016/0014-2964(76)90125-0. [DOI] [PubMed] [Google Scholar]
  63. Taylor C. R. The nature of Reed-Sternberg cells and other malignant "reticulum" cells. Lancet. 1974 Oct 5;2(7884):802–807. doi: 10.1016/s0140-6736(74)91071-x. [DOI] [PubMed] [Google Scholar]
  64. Taylor C. R. Upon the nature of Hodgkin's disease and the Reed-Sternberg cell. Recent Results Cancer Res. 1978;64:214–231. doi: 10.1007/978-3-642-81246-0_26. [DOI] [PubMed] [Google Scholar]
  65. Tindle B. H., Parker J. W., Lukes R. J. "Reed-Sternberg cells" in infectious mononucleosis? Am J Clin Pathol. 1972 Dec;58(6):607–617. doi: 10.1093/ajcp/58.6.607. [DOI] [PubMed] [Google Scholar]
  66. Trowbridge I. S., Omary M. B. Human cell surface glycoprotein related to cell proliferation is the receptor for transferrin. Proc Natl Acad Sci U S A. 1981 May;78(5):3039–3043. doi: 10.1073/pnas.78.5.3039. [DOI] [PMC free article] [PubMed] [Google Scholar]
  67. Verbi W., Greaves M. F., Schneider C., Koubek K., Janossy G., Stein H., Kung P., Goldstein G. Monoclonal antibodies OKT 11 and OKT 11A have pan-T reactivity and block sheep erythrocyte "receptors". Eur J Immunol. 1982 Jan;12(1):81–86. doi: 10.1002/eji.1830120115. [DOI] [PubMed] [Google Scholar]
  68. Vodinelich L., Sutherland R., Schneider C., Newman R., Greaves M. Receptor for transferrin may be a "target" structure for natural killer cells. Proc Natl Acad Sci U S A. 1983 Feb;80(3):835–839. doi: 10.1073/pnas.80.3.835. [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. Yamashita U., Shevach E. M. The expression of Ia antigens on immunocompetent cells in the guinea pig. II. Ia antigens on macrophages. J Immunol. 1977 Nov;119(5):1584–1588. [PubMed] [Google Scholar]

Articles from British Journal of Cancer are provided here courtesy of Cancer Research UK

RESOURCES