Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1980 Sep 1;152(3):581–593. doi: 10.1084/jem.152.3.581

Macrophage heterogeneity in man. A subpopulation of HLA-DR-bearing macrophages required for antigen-induced T cell activation also contains stimulators for autologous-reactive T cells

PMCID: PMC2185930  PMID: 6997424

Abstract

Utilizing somatic cell hybridization, we have developed a monoclonal antibody that interacts only with cells of the monocyte/macrophage (M phi) line and not with other myeloid or lymphoid cells. This antibody detects a 120,000-dalton determinant present on 37 +/- 2.8% of the peripheral blood M phi from several (HLA-DR)-disparate individuals and only depicts a subpopulation (approximately 30%) of HLA-DR-bearing M phi from any single subject. Cytolytic removal of this subpopulation of HLA-DR-bearing cells markedly diminished antigen-induced T cell reactivity, a deficiency that can be reconstituted with autologous M phi but not with either their soluble products containing lymphocyte- activating factor or with intact HLA-DR-disparate M phi. Whereas M phi bearing both the 120,000-dalton determinant and HLA-DR serve as effective stimulators for autologous mixed lymphocyte reactions. M phi bearing only HLA-DR determinants do not. However, this latter population of M phi can stimulate proliferation among alloreactive T cells. These studies indicate that the Mac-120 monoclonal antibody detects a subpopulation of HLA-DR-bearing M phi that is required for the genetically restricted presentation of conventional antigen to reactive T cells. Within the M phi population, these Mac-120+ cells constitute the most effective stimulators for autologous mixed lymphocyte reactions.

Full Text

The Full Text of this article is available as a PDF (847.8 KB).

Selected References

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

  1. Ahmann G. B., Sachs D. H., Hodes R. J. Requirement for an Ia-bearing accessory cell in Con A-induced T cell proliferation. J Immunol. 1978 Nov;121(5):1981–1989. [PubMed] [Google Scholar]
  2. Breard J., Fuks A., Friedman S. M., Schlossman S. F., Chess L. The role of p23,30-bearing human macrophages in antigen-induced T lymphocyte responses. Cell Immunol. 1979 Jun;45(1):108–119. doi: 10.1016/0008-8749(79)90366-6. [DOI] [PubMed] [Google Scholar]
  3. Calderon J., Kiely J. M., Lefko J. L., Unanue E. R. The modulation of lymphocyte functions by molecules secreted by macrophages. I. Description and partial biochemical analysis. J Exp Med. 1975 Jul 1;142(1):151–164. doi: 10.1084/jem.142.1.151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cowing C., Pincus S. H., Sachs D. H., Dickler H. B. A subpopulation of adherent accessory cells bearing both I-A and I-E or C subregion antigens is required for antigen-specific murine T lymphocyte proliferation. J Immunol. 1978 Nov;121(5):1680–1686. [PubMed] [Google Scholar]
  5. Gery I., Waksman B. H. Potentiation of the T-lymphocyte response to mitogens. II. The cellular source of potentiating mediator(s). J Exp Med. 1972 Jul 1;136(1):143–155. doi: 10.1084/jem.136.1.143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gottlieb A. B., Fu S. M., Yu D. T., Wang C. Y., Halper J. P., Kunkel H. G. The nature of the stimulatory cell in human allogeneic and autologous MLC reactions; role of isolated IgM-bearing B cells. J Immunol. 1979 Oct;123(4):1497–1503. [PubMed] [Google Scholar]
  7. Hausman P. B., Stobo J. D. Specificity and function of a human autologous reactive T cell. J Exp Med. 1979 Jun 1;149(6):1537–1542. doi: 10.1084/jem.149.6.1537. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Köhler G., Milstein C. Continuous cultures of fused cells secreting antibody of predefined specificity. Nature. 1975 Aug 7;256(5517):495–497. doi: 10.1038/256495a0. [DOI] [PubMed] [Google Scholar]
  9. Maurer B. A., Siwarski D. F., Fischetti G. P., McCoy J. L., Dean J. H., Herberman R. B. Conditions for generating and assaying human leukocyte inhibitory factor (LIF) induced by purified protein derivative (PPD). Immunopharmacology. 1978 Dec;1(1):57–69. doi: 10.1016/0162-3109(78)90009-7. [DOI] [PubMed] [Google Scholar]
  10. Picker L. J., Raff H. V., Goldyne M. E., Stobo J. D. Metabolic heterogeneity among human monocytes and its modulation by PGE2. J Immunol. 1980 Jun;124(6):2557–2562. [PubMed] [Google Scholar]
  11. Raff H. V., Cochrum K. C., Stobo J. D. Macrophage-T cell interactions in the Con A induction of human suppressive T cells. J Immunol. 1978 Dec;121(6):2311–2315. [PubMed] [Google Scholar]
  12. Rosenstreich D. L., Farrar J. J., Dougherty S. Absolute macrophage dependency of T lymphocyte activation by mitogens. J Immunol. 1976 Jan;116(1):131–139. [PubMed] [Google Scholar]
  13. Rosenwasser L. J., Rosenthal A. S. Adherent cell function in murine T lymphocyte antigen recognition. II. Definition of genetically restricted and nonrestricted macrophage functions in T cell proliferation. J Immunol. 1978 Dec;121(6):2497–2501. [PubMed] [Google Scholar]
  14. Steinman R. M., Kaplan G., Witmer M. D., Cohn Z. A. Identification of a novel cell type in peripheral lymphoid organs of mice. V. Purification of spleen dendritic cells, new surface markers, and maintenance in vitro. J Exp Med. 1979 Jan 1;149(1):1–16. doi: 10.1084/jem.149.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Stobo J. D., Paul S., Van Scoy R. E., Hermans P. E. Suppressor thymus-derived lymphocytes in fungal infection. J Clin Invest. 1976 Feb;57(2):319–328. doi: 10.1172/JCI108283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Togawa A., Oppenheim J. J., Mizel S. B. Characterization of lymphocyte-activating factor (LAF) produced by human mononuclear cells: biochemical relationship of high and low molecular weight forms of LAF. J Immunol. 1979 May;122(5):2112–2118. [PubMed] [Google Scholar]
  17. Unanue E. R. The regulatory role of macrophages in antigenic stimulation. Adv Immunol. 1972;15:95–165. doi: 10.1016/s0065-2776(08)60684-7. [DOI] [PubMed] [Google Scholar]

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

RESOURCES