In order to gain further insight on the role of Kaposi’ s sarcoma associated herpesvirus (KSHV) in classic and endemic Kaposi’ s sarcoma (KS) pathogenesis, we aimed to determine (i) whether KSHV is detectable in p...In order to gain further insight on the role of Kaposi’ s sarcoma associated herpesvirus (KSHV) in classic and endemic Kaposi’ s sarcoma (KS) pathogenesis, we aimed to determine (i) whether KSHV is detectable in peripheral blood mononuclear cells (PBMCs), (ii) which PBMCs subpopulation harbor the virus, (iii) which clinical, histologic, and immunologic parameters are associated with KSHV viremia in a population of classic and endemic KS. KSHV viremia and various immunologic parameters were screened on 81 patients. KSHV viremia was positive in 58% of the patients. KSHV was detected in B cells, T cells, and monocytes. CD34+ cells depleted in circulating endothelial cells (CECs) were never infected and 50% of the patients tested had CECs infected by KSHV. We observed a significant increase of IL-2 and IFN-γ production by CD4 T cells and an increase of IFN-γ production by CD8 T cells compared to control patients. KS progression (P=0.001) and KS staging (P=0.03) were significantly and independently associated with positive KSHV viremia. Our results show that there is no specific immunosuppression in classic or endemic KS. We showed that KSHV can be detected within CECs and that KSHV viremia could be an indicator of circulating mature or precursor spindle cells.展开更多
文摘In order to gain further insight on the role of Kaposi’ s sarcoma associated herpesvirus (KSHV) in classic and endemic Kaposi’ s sarcoma (KS) pathogenesis, we aimed to determine (i) whether KSHV is detectable in peripheral blood mononuclear cells (PBMCs), (ii) which PBMCs subpopulation harbor the virus, (iii) which clinical, histologic, and immunologic parameters are associated with KSHV viremia in a population of classic and endemic KS. KSHV viremia and various immunologic parameters were screened on 81 patients. KSHV viremia was positive in 58% of the patients. KSHV was detected in B cells, T cells, and monocytes. CD34+ cells depleted in circulating endothelial cells (CECs) were never infected and 50% of the patients tested had CECs infected by KSHV. We observed a significant increase of IL-2 and IFN-γ production by CD4 T cells and an increase of IFN-γ production by CD8 T cells compared to control patients. KS progression (P=0.001) and KS staging (P=0.03) were significantly and independently associated with positive KSHV viremia. Our results show that there is no specific immunosuppression in classic or endemic KS. We showed that KSHV can be detected within CECs and that KSHV viremia could be an indicator of circulating mature or precursor spindle cells.
