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Published on: September 14, 2010
The role of immunosuppression and immune-activation in classic Kaposi's sarcoma
G Touloumi1, A Hatzakis, I Potouridou
1Department of Hygiene and Epidemiology, Athens Medical School, Athens, Greece.
Insights
Classic Kaposi's sarcoma (CKS) patients exhibit immune activation, indicated by elevated neopterin and beta(2)-microglobulin levels. While not definitively immunosuppressed, CKS may involve some immune deficiency alongside this activation.
Area of Science:
- Immunology
- Oncology
- Virology
Background:
- Immunodeficiency and elevated cytokines are linked to Kaposi's sarcoma (KS) in AIDS and iatrogenic cases.
- The role of these factors in classic KS (CKS) remains unclear.
- CKS is a distinct clinical entity from AIDS-related KS.
Purpose of the Study:
- To investigate immune status in HIV-negative patients with classic Kaposi's sarcoma (CKS).
- To compare immune markers in CKS patients versus age- and sex-matched controls.
- To determine if CKS is associated with immune activation or suppression.
Main Methods:
- Measured peripheral blood cell counts, including T-cell subsets (CD4, CD8).
- Assessed levels of neopterin and beta(2)-microglobulin in 91 CKS patients and 107 controls.
- Analyzed data for significant differences between CKS cases and controls.
Main Results:
- CKS patients showed slightly lower leukocyte and lymphocyte counts.
- CD4 T-lymphocyte counts were significantly lower in CKS patients.
- Neopterin and beta(2)-microglobulin levels were considerably elevated in CKS patients compared to controls.
Conclusions:
- Classic Kaposi's sarcoma is predominantly characterized by immune activation.
- A degree of minor immunosuppression may also be present in CKS.
- Immune dysregulation, rather than profound immunodeficiency, appears central to CKS pathogenesis.
Abstract:
Immunodeficiency and elevated levels of cytokines have been associated with the development of Kaposi's sarcoma (KS) lesions in patients with AIDS and iatrogenic immunodeficiency. However, their role in classic KS (CKS) is unclear. We measured peripheral blood cell levels, including T-cell subsets, as well as neopterin and beta(2)-microglobulin in 91 HIV-negative Greek patients with histologically confirmed CKS and in 107 controls matched for age and sex. CKS cases had slightly lower leukocyte counts (p = 0.08) and lymphocyte counts (p = 0.02). Although the percentage of CD4 and CD8 T-lymphocytes were not significantly different from controls (p = 0.10 and p = 0.45, respectively), CD4 T-lymphocytes were lower in cases than controls (812 cells/microliter and 1,009 cells/microliter, respectively; p = 0.01); part of this difference resulted from the lower lymphocyte counts (p = 0.07 after adjusting for lymphocyte counts). However, neopterin and beta(2)-microglobulin were both considerably elevated [geometric mean (95% CI): 8.35 (7.27-9.73) nmol/L and 2,904 (2,479-3,401) microgram/L in cases and 5.86 (5.40-6. 35) nmol/L and 2,042 (1,880-2,218) microgram/L in controls, respectively]. We conclude that CKS patients are predominantly characterised by immune activation, although an element of minor immunosupression may also be present.
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