Skip to main content
Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 1993 Jun;92(3):442–447. doi: 10.1111/j.1365-2249.1993.tb03418.x

Mucosal macrophage subsets of the gut in HIV: decrease in antigen-presenting cell phenotype.

S G Lim 1, A Condez 1, L W Poulter 1
PMCID: PMC1554780  PMID: 8513576

Abstract

The effect of HIV infection on intestinal lamina propria macrophage subsets was investigated in 41 patients at various stages of HIV infection (asymptomatic HIV infection, n = 17; AIDS, n = 24). Duodenal biopsies taken from HIV patients at endoscopy were snap frozen and cryostat sections cut for immunohistochemical staining. MoAbs CD68 (EBM11, pan-macrophage marker), RFD1 (antigen-presenting cells) and RFD7 (mature phagocytic macrophages) were used to identify cell subsets using indirect immunoperoxidase or alkaline phosphatase. Double immunofluorescence using MoAbs to HIV proteins (p24, p17 and gp120) and RFD1 were used to identify HIV-infected antigen-presenting cells. Double immunofluorescence was also used to identify macrophages that expressed both RFD1 and RFD7 ('suppressor' macrophages). Intensity of HLA-DR expression in lamina propria cells was investigated using a MoAb to HLA-DR directly conjugated to glucose oxidase. The results show that there was no difference in overall density of macrophages, but there was a significant decrease in dendritic cells (RFD1+) in all clinical stages of HIV. There was no difference in the density of RFD7+ macrophages, nor was there a difference intensity of HLA-DR expression in lamina propria cells. Only four HIV-infected cells were positively identified in the 41 patients. This result suggests that the antigen-presenting arm of mucosal immune defences may be seriously compromised in HIV infection, and represents a further insult to mucosal immunity already impaired as a result of loss of CD4+ T lymphocytes. This may contribute to development of opportunist infection in the gut.

Full text

PDF
442

Selected References

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

  1. Allison M. C., Cornwall S., Poulter L. W., Dhillon A. P., Pounder R. E. Macrophage heterogeneity in normal colonic mucosa and in inflammatory bowel disease. Gut. 1988 Nov;29(11):1531–1538. doi: 10.1136/gut.29.11.1531. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bray D. H., Squire S. B., Bagdades E., Mulvenna P. M., Johnson M. A., Poulter L. W. Alveolar macrophage populations are distorted in immunocompromised patients with pneumonitis. Eur Respir J. 1992 May;5(5):545–552. [PubMed] [Google Scholar]
  3. Budhraja M., Levendoglu H., Kocka F., Mangkornkanok M., Sherer R. Duodenal mucosal T cell subpopulation and bacterial cultures in acquired immune deficiency syndrome. Am J Gastroenterol. 1987 May;82(5):427–431. [PubMed] [Google Scholar]
  4. Di Massimo A. M., Placido R., Bach S., Anastasi A. M., Mastino A., Capobianchi M. R., Colizzi V. Cytotoxic activity of intestinal lamina propria lymphocytes on human immunodeficiency virus (HIV)-infected cells. Immunology. 1992 May;76(1):117–121. [PMC free article] [PubMed] [Google Scholar]
  5. Eales L. J., Farrant J., Helbert M., Pinching A. J. Peripheral blood dendritic cells in persons with AIDS and AIDS related complex: loss of high intensity class II antigen expression and function. Clin Exp Immunol. 1988 Mar;71(3):423–427. [PMC free article] [PubMed] [Google Scholar]
  6. Enders G., Gottwald T., Brendel W. Induction of oral tolerance in rats without Peyer's patches. Immunology. 1986 Jun;58(2):311–314. [PMC free article] [PubMed] [Google Scholar]
  7. Gendelman H. E., Meltzer M. S. Mononuclear phagocytes and the human immunodeficiency virus. Curr Opin Immunol. 1989;2(3):414–419. doi: 10.1016/0952-7915(89)90152-0. [DOI] [PubMed] [Google Scholar]
  8. Jarry A., Cortez A., René E., Muzeau F., Brousse N. Infected cells and immune cells in the gastrointestinal tract of AIDS patients. An immunohistochemical study of 127 cases. Histopathology. 1990 Feb;16(2):133–140. doi: 10.1111/j.1365-2559.1990.tb01081.x. [DOI] [PubMed] [Google Scholar]
  9. Kelly P. M., Bliss E., Morton J. A., Burns J., McGee J. O. Monoclonal antibody EBM/11: high cellular specificity for human macrophages. J Clin Pathol. 1988 May;41(5):510–515. doi: 10.1136/jcp.41.5.510. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Knight S. C., Fryer P., Griffiths S., Harding B. Class II histocompatibility antigens on human dendritic cells. Immunology. 1987 May;61(1):21–27. [PMC free article] [PubMed] [Google Scholar]
  11. Macatonia S. E., Lau R., Patterson S., Pinching A. J., Knight S. C. Dendritic cell infection, depletion and dysfunction in HIV-infected individuals. Immunology. 1990 Sep;71(1):38–45. [PMC free article] [PubMed] [Google Scholar]
  12. Macatonia S. E., Patterson S., Knight S. C. Suppression of immune responses by dendritic cells infected with HIV. Immunology. 1989 Jul;67(3):285–289. [PMC free article] [PubMed] [Google Scholar]
  13. Mahida Y. R., Patel S., Gionchetti P., Vaux D., Jewell D. P. Macrophage subpopulations in lamina propria of normal and inflamed colon and terminal ileum. Gut. 1989 Jun;30(6):826–834. doi: 10.1136/gut.30.6.826. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Mahida Y. R., Wu K. C., Jewell D. P. Characterization of antigen-presenting activity of intestinal mononuclear cells isolated from normal and inflammatory bowel disease colon and ileum. Immunology. 1988 Dec;65(4):543–549. [PMC free article] [PubMed] [Google Scholar]
  15. Patterson S., Knight S. C. Susceptibility of human peripheral blood dendritic cells to infection by human immunodeficiency virus. J Gen Virol. 1987 Apr;68(Pt 4):1177–1181. doi: 10.1099/0022-1317-68-4-1177. [DOI] [PubMed] [Google Scholar]
  16. Pavli P., Woodhams C. E., Doe W. F., Hume D. A. Isolation and characterization of antigen-presenting dendritic cells from the mouse intestinal lamina propria. Immunology. 1990 May;70(1):40–47. [PMC free article] [PubMed] [Google Scholar]
  17. Poulter L. W., Campbell D. A., Munro C., Butcher R. G. The quantitation of HLA-DR expression on human cells using immunocytochemistry. J Immunol Methods. 1987 Apr 16;98(2):227–234. doi: 10.1016/0022-1759(87)90009-3. [DOI] [PubMed] [Google Scholar]
  18. Reed S. G., da Silva J. S., Ho J. L., Koehler J. K., Russo D. M., Pihl D. L., Coombs R. W. Cytokine activation of human macrophages infected with HIV-1 to inhibit intracellular protozoa. J Acquir Immune Defic Syndr. 1992;5(7):666–675. [PubMed] [Google Scholar]
  19. Schrappe-Bächer M., Salzberger B., Fätkenheuer G., Franzen C., Koch B., Krueger G. R., Kaufmann W. T-lymphocyte subsets in the duodenal lamina propria of patients infected with the human immunodeficiency virus type 1 and influence of high-dose immunoglobulin therapy. J Acquir Immune Defic Syndr. 1990;3(3):238–243. [PubMed] [Google Scholar]
  20. Selby W. S., Poulter L. W., Hobbs S., Jewell D. P., Janossy G. Heterogeneity of HLA-DR-positive histiocytes in human intestinal lamina propria: a combined histochemical and immunohistological analysis. J Clin Pathol. 1983 Apr;36(4):379–384. doi: 10.1136/jcp.36.4.379. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Spiteri M. A., Poulter L. W. Characterization of immune inducer and suppressor macrophages from the normal human lung. Clin Exp Immunol. 1991 Jan;83(1):157–162. doi: 10.1111/j.1365-2249.1991.tb05607.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Suffin S. C., Muck K. B., Young J. C., Lewin K., Porter D. D. Improvement of the glucose oxidase immunoenzyme technic. Use of a tetrazolium whose formazan is stable without heavey metal chelation. Am J Clin Pathol. 1979 May;71(5):492–496. doi: 10.1093/ajcp/71.5.492. [DOI] [PubMed] [Google Scholar]
  23. Ullrich R., Zeitz M., Heise W., L'age M., Ziegler K., Bergs C., Riecken E. O. Mucosal atrophy is associated with loss of activated T cells in the duodenal mucosa of human immunodeficiency virus (HIV)-infected patients. Digestion. 1990;46 (Suppl 2):302–307. doi: 10.1159/000200401. [DOI] [PubMed] [Google Scholar]

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

RESOURCES