Increased expression of interferon-gamma in hyperplastic lymph nodes from HIV-infected patients

Clin Exp Immunol. 1993 Apr;92(1):100-5. doi: 10.1111/j.1365-2249.1993.tb05954.x.

Abstract

Polyclonal B cell activation is characteristic of HIV infection and occurs in the presence of severe CD4+ lymphocyte depletion. In contrast, CD4+ lymphocytes are the dominant T cell in the reactive lymphoid tissues of patients not infected with HIV. In this study, lymph node biopsies from eight HIV-infected patients with persistent generalized lymphadenopathy syndrome (PGL) were assessed for IL-1 beta, IL-2, IL-4, IL-6, IL-10, interferon-gamma (IFN-gamma) and tumour necrosis factor-beta (TNF-beta) gene expression using the polymerase chain reaction (PCR). The cytokine gene expression of two cases of reactive adenopathy in patients not infected with HIV was assessed for comparison. IFN-gamma was expressed much more strongly in the PGL samples than in control reactive lymphoid tissues, whereas the other cytokines were expressed to a similar extent in both types of tissues. IFN-gamma may have an important role in maintaining the adenopathy of HIV-infected patients. Expression of cytokines such as IL-2, IL-4 and IL-10 in HIV nodes may be adequate to allow the recruitment of naive B cells to the reactive process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AIDS-Related Complex / immunology*
  • Actins / biosynthesis
  • Actins / genetics
  • Base Sequence
  • DNA / analysis
  • DNA / isolation & purification
  • Gene Expression
  • HIV Infections / immunology*
  • Humans
  • Hyperplasia
  • Interferon-gamma / biosynthesis*
  • Interferon-gamma / genetics
  • Interleukins / biosynthesis
  • Interleukins / genetics
  • Lymph Nodes / injuries*
  • Lymph Nodes / pathology
  • Lymphatic Diseases / immunology
  • Lymphotoxin-alpha / biosynthesis
  • Lymphotoxin-alpha / genetics
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • RNA, Messenger / analysis
  • RNA, Messenger / isolation & purification

Substances

  • Actins
  • Interleukins
  • Lymphotoxin-alpha
  • RNA, Messenger
  • Interferon-gamma
  • DNA