TY - JOUR
T1 - Analysis of human herpesvirus type 8 infection in AIDS-related and AIDS- unrelated primary central nervous system lymphoma
AU - Gaidano, Gianluca
AU - Capello, Daniela
AU - Pastore, Cristina
AU - Antinori, Andrea
AU - Gloghini, Annunziata
AU - Carbone, Antonino
AU - Larocca, Luigi Maria
AU - Saglio, Giuseppe
PY - 1997
Y1 - 1997
N2 - Human herpesvirus type 8 (HHV-8) has been proposed as a pathogenetic factor for immunosuppression-associated primary central nervous system lymphoma (PCNSL). To verify this hypothesis, HHV-8 infection was investigated in 31 persons with PCNSL (16 AIDS-related, 15 AIDS-unrelated) and in 30 persons with systemic B cell non-Hodgkin's lymphomas (B-NHL; 15 AIDS-related, 15 AIDS-unrelated). All subjects with PCNSL scored negative by single-step polymerase chain reaction (PER), suggesting a tumor virus load of < 100 vital copies/200,000 human haploid genome equivalents (HHGE). By applying Poisson assumptions to nested PeR, 16 of 31 persons with PCNSL were devoid of HHV-8 sequences: 1 subject with AIDS and PCNSL had 1-100 viral copies/200,000 HHGE, and 14 with PCNSL had <1 viral copy/200,000 HHGE. Similarly, 10 of 30 persons with systemic B-NHL were devoid of HHV-8 sequences; 20 had <1 vital copy/200,000 HHGE. The extremely low levels of infection rule out a role of HHV-8 in PCNSL pathogenesis and are consistent with HHV-8 infection of bystander cells contaminating the tumor clone.
AB - Human herpesvirus type 8 (HHV-8) has been proposed as a pathogenetic factor for immunosuppression-associated primary central nervous system lymphoma (PCNSL). To verify this hypothesis, HHV-8 infection was investigated in 31 persons with PCNSL (16 AIDS-related, 15 AIDS-unrelated) and in 30 persons with systemic B cell non-Hodgkin's lymphomas (B-NHL; 15 AIDS-related, 15 AIDS-unrelated). All subjects with PCNSL scored negative by single-step polymerase chain reaction (PER), suggesting a tumor virus load of < 100 vital copies/200,000 human haploid genome equivalents (HHGE). By applying Poisson assumptions to nested PeR, 16 of 31 persons with PCNSL were devoid of HHV-8 sequences: 1 subject with AIDS and PCNSL had 1-100 viral copies/200,000 HHGE, and 14 with PCNSL had <1 viral copy/200,000 HHGE. Similarly, 10 of 30 persons with systemic B-NHL were devoid of HHV-8 sequences; 20 had <1 vital copy/200,000 HHGE. The extremely low levels of infection rule out a role of HHV-8 in PCNSL pathogenesis and are consistent with HHV-8 infection of bystander cells contaminating the tumor clone.
UR - http://www.scopus.com/inward/record.url?scp=0030960870&partnerID=8YFLogxK
U2 - 10.1086/593456
DO - 10.1086/593456
M3 - Article
SN - 0022-1899
VL - 175
SP - 1193
EP - 1197
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 5
ER -