Skip to main content
Cancer Immunology, Immunotherapy : CII logoLink to Cancer Immunology, Immunotherapy : CII
. 1989 May;30(3):170–176. doi: 10.1007/BF01669426

Tumor-induced alteration in macrophage accessory cell activity on autoreactive T cells

Andrew D Yurochko 1, Prakash S Nagarkatti 1, Mitzi Nagarkatti 1, Klaus D Elgert 1,
PMCID: PMC11038806  PMID: 2598186

Abstract

Using a tumor-model system, differences in the accessory cell capabilities on autoreactive T cells of splenic macrophages from normal and tumor-bearing hosts (TBH) were assessed in the syngeneic mixed lymphocyte reaction. Tumor development caused a drop in autoreactivity. At 0 and 7 days of tumor growth, no drop in reactivity occurred when TBH macrophages were used as accessory cells and L3T4+ autoreactive T cells from normal mice were used as responder cells. However, by day 14, there was a 32% drop in reactivity, and by day 21 only 22% of the T cell reactivity remained when TBH macrophages were used as accessory cells. Alterations in macrophage Ia antigen during tumor growth were first investigated as the potential cause of reduced autoreactivity. Before tumor growth (day 0) 59% of the splenic macrophages were found to be Ia+. Day-7 TBH macrophages showed no difference in Ia antigen expression when compared to day 0 macrophages. However, by day 14, TBH macrophages showed a 9% decrease, and by day 21 they showed a 36% decrease in the number which were Ia+. Concomitant with the decrease in the number of Ia+ cells was a decrease in the density of Ia antigen expression on day-14 and -21 TBH macrophages. In day-14 and -21 TBH macrophages, two populations were seen that were Ia+. The first had a 10%–20% decrease in Ia antigen expression per cell while the second population had a >50% drop in Ia antigen expression per cell. By titrating and mixing TBH macrophages with normal host macrophages, we assessed whether they could actively mediate suppression of autoreactive T cells. A titratable suppressive phenomenon was demonstrated using day-21 TBH macrophages. In contrast, day-7 and -14 TBH macrophages titrated with normal host macrophages had no effect on the syngeneic mixed lymphocyte reactivity. Lastly, we investigated whether the macrophage-mediated suppression was caused by increased prostaglandin secretion. Addition of indomethacin to cultures increased autoreactive T cell reactivity stimulated by normal or TBH macrophages (59% and 99% increase, respectively). Although indomethacin reduced suppression mediated by TBH macrophages, autoreactivity did not return to levels induced by untreated or indomethacin-treated cells from a normal host. Taken together, the data suggested that tumor growth modulates the function of macrophage accessory cells with autoreactive T cells in at least two ways: by decreasing Ia antigen expression and by increasing suppressor activity.

Keywords: Tumor Growth, Prostaglandin, Cell Activity, Indomethacin, Tumor Development

Footnotes

This work was supported in part by an NIH Biomedical Research Support Grant and grants CA40009 and CA40010

References

  • 1.Adkinson NF, Jr, Barron T, Powell S, Cohen S. Prostaglandin production by human peripheral blood cellsin vitro . J Lab Clin Med. 1977;90:1043. [PubMed] [Google Scholar]
  • 2.Battisto JR, Ponzio NM. Autologous and syngeneic mixed lymphocyte reactions and their immunological significance. Prog Allergy. 1981;28:160. [PubMed] [Google Scholar]
  • 3.Chow K-PN, Battisto JR. Down regulation of cytotoxic T lymphocyte development by a minor stimulating locus-induced suppressor cascade that involves Lyt-1+ suppressor T cells, IA− macrophages, and their factors. J Immunol. 1988;140:1005. [PubMed] [Google Scholar]
  • 4.Clayberger C, Dekruyff RH, Cantor H. Immunoregulatory activities of autoreactive T cells: an I-A-specific T cell clone mediates both help and suppression of antibody responses. J Immunol. 1984;132:2237. [PubMed] [Google Scholar]
  • 5.Denbow CJ, Conroy JM, Elgert KD. Macrophagederived prostaglandin E modulation of the mixed-lymphocyte reaction: an anomaly of increased production and decreased T-cell susceptibility during tumor growth. Cell Immunol. 1984;84:1. doi: 10.1016/0008-8749(84)90071-6. [DOI] [PubMed] [Google Scholar]
  • 6.Elgert KD, Farrar WL. Suppressor cell activity in tumor-bearing mice. I. Dualistic inhibition by suppressor T lymphocytes and macrophages. J Immunol. 1978;120:1345. [PubMed] [Google Scholar]
  • 7.Engleman EG, Benike CJ, Hoppe RT, Kaplan HS, Berberich FR. Autologous mixed lymphocyte reaction in patients with Hodgkin's disease. Evidence for a T cell defect. J Clin Invest. 1980;66:149. doi: 10.1172/JCI109828. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Finnegan A, Hodes RJ. Antigen-induced T suppressor cells regulate the autoreactive T helper-B cell interaction. J Immunol. 1986;136:793. [PubMed] [Google Scholar]
  • 9.Garner RE, Elgert KD. Changes in splenic macrophage Mac antigen expression during tumor growth: a kinetic study of accessory cell function and antigen-defined phenotypes. J Leukocyte Biol. 1986;40:709. doi: 10.1002/jlb.40.6.709. [DOI] [PubMed] [Google Scholar]
  • 10.Garner RE, Malick AP, Elgert KD. Variations in macrophage antigen phenotype: a correlation between Ia antigen reduction and immune dysfunction during tumor growth. J Leukocyte Biol. 1986;40:561. doi: 10.1002/jlb.40.5.561. [DOI] [PubMed] [Google Scholar]
  • 11.Garner RE, Malick AP, Yurochko AD, Elgert KD. Shifts in macrophage (Mϕ) surface phenotypes during tumor growth: association of Mac-2+ and Mac-3+ Mϕ with immunosuppressive activity. Cell Immunol. 1987;108:255. doi: 10.1016/0008-8749(87)90211-5. [DOI] [PubMed] [Google Scholar]
  • 12.Goldyne ME. Lymphocyte and monocyte/macrophage interactions involving arachidonic acid metabolism. Transplant Proc. 1986;18:37. [Google Scholar]
  • 13.Goodwin JS, Messner RP, Bankhurst AD, Peake GT, Saiki JH, Williams RC., Jr Prostaglandin-producing suppressor cells in Hodgkin's disease. N Engl J Med. 1977;297:963. doi: 10.1056/NEJM197711032971802. [DOI] [PubMed] [Google Scholar]
  • 14.Grinwich KD, Plescia OJ. Tumor-mediated immunosuppression: prevention by inhibitors of prostaglandin inhibitors. Prostaglandins. 1977;14:1175. doi: 10.1016/0090-6980(77)90294-5. [DOI] [PubMed] [Google Scholar]
  • 15.Halper JP, Fu SM, Gottlieb AB, Winchester RJ, Kunkel HG. Poor mixed lymphocyte reaction stimulatory capacity of leukemic B cells of chronic lymphocytic leukemia patients despite the presence of Ia antigens. J Clin Invest. 1979;64:1141. doi: 10.1172/JCI109567. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Innes JB, Kuntz MM, Kim YT, Weksler ME. Induction of suppressor activity in the autologous mixed lymphocyte reaction and in cultures with concanavalin A. J Clin Invest. 1979;64:1608. doi: 10.1172/JCI109622. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Jerne NK. Idiotypic networks and other preconceived ideas. Immunol Rev. 1984;79:5. doi: 10.1111/j.1600-065x.1984.tb00484.x. [DOI] [PubMed] [Google Scholar]
  • 18.Kadhim SA, Rees RC. Enhancement of tumor growth in mice: evidence for the involvement of host macrophages. Cell Immunol. 1984;87:259. doi: 10.1016/0008-8749(84)90150-3. [DOI] [PubMed] [Google Scholar]
  • 19.Kennedy DW, Russo C, Kim YT, Weksler ME. T cell proliferation induced by antiself-I-A-specific T cell hybridomas: evidence of a T cell network. J Exp Med. 1986;164:490. doi: 10.1084/jem.164.2.490. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Kotani H, Mitsuya H, Jarrett RF, Yenokida GG, James SP, Strober W. An autoreactive T cell that can be activated to provide both helper and suppressor function. J Immunol. 1986;136:1951. [PubMed] [Google Scholar]
  • 21.Kurland JI, Bockman R. Prostaglandin E production by human blood monocytes and mouse peritoneal macrophages. J Exp Med. 1978;147:952. doi: 10.1084/jem.147.3.952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Malick AP, Elgert KD, Garner RE, Adkinson NF., Jr Prostaglandin E2 production by Mac-2+ macrophages: tumorinduced population shift. J Leukocyte Biol. 1987;42:673. doi: 10.1002/jlb.42.6.673. [DOI] [PubMed] [Google Scholar]
  • 23.Malick AP, Yurochko AD, Burger CJ, Askew D, Elgert KD. Tumor-induced variations in a high molecular weight inhibitory monokine. Immunobiology. 1989;178:361. doi: 10.1016/S0171-2985(89)80059-2. [DOI] [PubMed] [Google Scholar]
  • 24.Nagai H, Fisher RI, Cossman J, Oppenheim JJ. Decreased expression of class II major histocompatibility antigens on monocytes from patients with Hodgkin's disease. J Leukocyte Biol. 1986;39:313. doi: 10.1002/jlb.39.3.313. [DOI] [PubMed] [Google Scholar]
  • 25.Nagarkatti PS, Nagarkatti M, Kaplan AM. Normal Lyt-1+2− T cells have the unique capacity to respond to syngeneic autoreactive T cells. J Exp Med. 1985;162:375. doi: 10.1084/jem.162.1.375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Nagarkatti PS, Snow EC, Kaplan AM. Characterization and function of autoreactive T-lymphocyte clones isolated from normal, unprimed mice. Cell Immunol. 1985;94:32. doi: 10.1016/0008-8749(85)90083-8. [DOI] [PubMed] [Google Scholar]
  • 27.Nagarkatti PS, Nagarkatti M, Mann LW, Jones LA, Kaplan AM. Characterization of an endogenous Lyt 2+ T-suppressor-cell population regulating autoreactive T cellsin vitro andin vivo . Cell Immunol. 1988;112:64. doi: 10.1016/0008-8749(88)90276-6. [DOI] [PubMed] [Google Scholar]
  • 28.Ninneman JL. Prostaglandins in inflammation and disease. Immunol Today. 1984;5:173. doi: 10.1016/0167-5699(84)90011-2. [DOI] [PubMed] [Google Scholar]
  • 29.Palacios R, Moller G. HLA-DR antigens render resting T cells sensitive to interleukin-2 and induce production of the growth factor in the autologous mixed lymphocyte reaction. Cell Immunol. 1981;63:143. doi: 10.1016/0008-8749(81)90035-6. [DOI] [PubMed] [Google Scholar]
  • 30.Raff HV, Stobo JD. Macrophage modulation of immune reactivity in man. In: Goodwin JS, editor. Suppressor cells in human disease vol. 14. New York: Marcel Dekker; 1981. p. 65. [Google Scholar]
  • 31.Smith JB, Knowlton RP. Activation of suppressor T cells in human autologous mixed lymphocyte culture. J Immunol. 1979;123:419. [PubMed] [Google Scholar]
  • 32.Smolen JS, Sharrow SO, Reeves JP, Boegel WA, Steinberg AD. The human autologous mixed lymphocyte reaction. I. Suppression by macrophages and T cells. J Immunol. 1981;127:1987. [PubMed] [Google Scholar]
  • 33.Snyder DS, Beller DI, Unanue ER. Prostaglandins modulate macrophage Ia expression. Nature. 1982;299:163. doi: 10.1038/299163a0. [DOI] [PubMed] [Google Scholar]
  • 34.Stevenson JR, Battisto JR. In the murine syngeneic mixed lymphocyte reaction, one T cell subset replicates in the presence of B cells or macrophages and replication is inhibited by simultaneous presence of both stimulator. Eur J Immunol. 1986;16:508. doi: 10.1002/eji.1830160508. [DOI] [PubMed] [Google Scholar]
  • 35.Suzuki H, Evavold B, Swartz TJ, Latta SL, Quitans J. The syngeneic T-T lymphocyte reaction (STTLR). I. Induction of primary T anti-T cell proliferative responses in T cell cultures stimulated with self- and antigen-reactive T cells. J Mol Cell Immunol. 1986;2:331. [PubMed] [Google Scholar]
  • 36.Takemura R, Werb Z. Secretory products of macrophages and their physiological functions. Am J Physiol. 1984;246:C1. doi: 10.1152/ajpcell.1984.246.1.C1. [DOI] [PubMed] [Google Scholar]
  • 37.de Talance A, Regnier D, Spinella S, Morisset J, Seman M. Origin of autoreactive T cells. I. Characterization of Thy-1+, Lyt−, L3T4− precursors in the spleen of normal mice. J Immunol. 1986;137:1101. [PubMed] [Google Scholar]
  • 38.Ting CC, Rodrigues D. Switching on the macrophagemediated suppressor mechanism by tumor cells to evade host immune surveillance. Proc Natl Acad Sci USA. 1980;77:4265. doi: 10.1073/pnas.77.7.4265. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Tomonari K. Cytotoxic T cells generated in the autologous mixed lymphocyte reaction. I. Primary autologous mixed lymphocyte reaction. J Immunol. 1980;124:1111. [PubMed] [Google Scholar]
  • 40.Uchida A, Moore M, Klein E. Autologous mixed lymphocyte-tumor reaction and autologous mixed lymphocyte reaction. II. Generation of specific and non-specific killer T cells capable of lysing autologous tumor. Int J Cancer. 1988;41:651. doi: 10.1002/ijc.2910410502. [DOI] [PubMed] [Google Scholar]
  • 41.Unanue ER. The regulatory role of macrophages in antigenic stimulation. Part two: symbiotic relationship between lymphocytes and macrophages. Adv Immunol. 1981;31:1. doi: 10.1016/s0065-2776(08)60919-0. [DOI] [PubMed] [Google Scholar]
  • 42.Vercammen C, Ceuppens JL. Prostaglandin E2 inhibits human T-cell proliferation after crosslinking of the CD3-Ti complex by directly affecting T cells at an early step of the activation process. Cell Immunol. 1987;104:24. doi: 10.1016/0008-8749(87)90003-7. [DOI] [PubMed] [Google Scholar]
  • 43.Webb PJ, Brooks CG, Baldwin RW. Macrophage-like suppressor cells in rats. II. Evidence for a quantitative rather than a qualitative change in tumor-bearer animals. Cell Immunol. 1980;52:381. doi: 10.1016/0008-8749(80)90359-7. [DOI] [PubMed] [Google Scholar]
  • 44.Willard KE, Elgert KD. Glucocorticosteroid modification of lymphocyte blastogenesis in tumor-bearing hosts. Cell Immunol. 1980;55:355. doi: 10.1016/0008-8749(80)90167-7. [DOI] [PubMed] [Google Scholar]
  • 45.Wing EJ, Remington JS. Studies on the regulation of lymphocyte reactivity by normal and activated macrophages. Cell Immunol. 1977;30:108. doi: 10.1016/0008-8749(77)90052-1. [DOI] [PubMed] [Google Scholar]
  • 46.Wolos JA, Smith JB. Helper cells in the autologous mixed lymphocyte reaction. III. Production of helper(s) distinct from interleukin 2. J Exp Med. 1982;156:1807. doi: 10.1084/jem.156.6.1807. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Young MR, Endicott RA, Duffie GP, Wepsic HT. Suppressor alveolar macrophages in mice bearing metastatic Lewis lung carcinoma tumors. J Leukocyte Biol. 1987;42:682. doi: 10.1002/jlb.42.6.682. [DOI] [PubMed] [Google Scholar]
  • 48.Yurochko AD, Pyle RH, Elgert KD. Changes in macrophage populations: Phenotypic differences between the normal and tumor-bearing host macrophages. Immunobiology. 1989;178:416. doi: 10.1016/s0171-2985(89)80063-4. [DOI] [PubMed] [Google Scholar]
  • 49.Zlotnik A, Shimonkevitz R, Kappler J, Marrick P. Effect of prostaglandin E2 on the γ-interferon induction of antigen presenting ability in P388D1 cells and on IL-2 production by T-cell hybridomas. Cell Immunol. 1985;90:154. doi: 10.1016/0008-8749(85)90177-7. [DOI] [PubMed] [Google Scholar]

Articles from Cancer Immunology, Immunotherapy : CII are provided here courtesy of Springer

RESOURCES