2004Zhonghua fengshibingxue zazhiRequires access

Study of CD28,CD152 costimulatory molecules expression on subpopulation of T cells in rheumatoid arthritis patients

Zeng Ting-tin

Open publisher page 0 citations

Abstract

Objective To investigate the relationship between abnormal expression of CD28, CD152 costimulatory molecules on subpopulation of T cells and the immune dysfunction in patients with rheumatoid arthritis (RA). Methods CD3, CD4, CD8, CD28, CD152 on the surface of T cells were labeled by immuno-fluorescence and determined by flow cytometry. Results As compared with control, CD3+CD4+ T cells were significantly higher (P0.01), while CD3+CD8+ T cells were significantly lower (P0.05). CD28 on CD4+Tcells was significantly lower (P0.05), while CD28 on CD8+T cells was neither higher nor lower(P0.05).CD152 on CD4+T and CD8+T cells were both significantly higher (P0.01). Conclusion In RA patients the initial reaction of cellular immunity is B7/CD28 pathway activation. It activates T cells, then a great deal of CD152 is secreted. It combines with B7 and inhibits T cells. The decrease of CD28 causes AICD of lymphocytes in RA patients, then induces pathological injuries. Blocking of CD152/B7 pathway is helpful in RA treatment.

About this research paper

What this paper is about

Objective To investigate the relationship between abnormal expression of CD28, CD152 costimulatory molecules on subpopulation of T cells and the immune dysfunction in patients with rheumatoid arthritis (RA). Methods CD3, CD4, CD8, CD28, CD152 on the surface of T cells were labeled by immuno-fluorescence and determined by flow cytometry. Results As compared with control, CD3+CD4+ T cells were significantly higher (P0.01), while CD3+CD8+ T cells were significantly lower (P0.05). CD28 on CD4+Tcells was significantly lower (P0.05), while CD28 on CD8+T cells was neither higher nor lower(P0.05).CD152 on CD4+T and CD8+T cells were both significantly higher (P0.01). Conclusion In RA patients the initial reaction of cellular immunity is B7/CD28 pathway activation. It activates T cells, then a great deal of CD152 is secreted. It combines with B7 and inhibits T cells. The decrease of CD28 causes AICD of lymphocytes in RA patients, then induces pathological injuries. Blocking of CD152/B7 pathway is helpful in RA treatment.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To investigate the relationship between abnormal expression of CD28, CD152 costimulatory molecules on subpopulation of T cells and the immune dysfunction in patients with rheumatoid arthritis (RA). Methods CD3, CD4, CD8, CD28, CD152 on the surface of T cells were labeled by immuno-fluorescence and determined by flow cytometry. Results As compared with control, CD3+CD4+ T cells were significantly higher (P0.01), while CD3+CD8+ T cells were significantly lower (P0.05). CD28 on CD4+Tcells was significantly lower (P0.05), while CD28 on CD8+T cells was neither higher nor lower(P0.05).CD152 on CD4+T and CD8+T cells were both significantly higher (P0.01). Conclusion In RA patients the initial reaction of cellular immunity is B7/CD28 pathway activation. It activates T cells, then a great deal of CD152 is secreted. It combines with B7 and inhibits T cells. The decrease of CD28 causes AICD of lymphocytes in RA patients, then induces pathological injuries. Blocking of CD152/B7 pathway is helpful in RA treatment.

Key concepts: CD28, CD8, Flow cytometry, Immune system, Immunology, CD3, Rheumatoid arthritis, T cell

Related papers

Back to paper searchBrowse research topicsOriginal source
Study of CD28,CD152 costimulatory molecules expression on subpopulation of T cells in rheumatoid arthritis patients — Research Paper | ScholarLens