Background: African Kaposi's sarcoma (KS) lesions contain human herpesvirus
-8 (HHV-8) and Epstein-Barr virus (EBV, both of which are associated with v
arious types of non-Hodgkin's lymphomas and are known to produce several fa
ctors suspected of lymphomagenic potential. The aim of this study was to ev
aluate tumor-infiltrating lymphocytes for the evidence of clonal expansion
in African KS.
Methods: We used polymerase chain reaction (PCR)-based assays to determine
the clonality of tumor-infiltrating lymphocytes in African KS lesions and c
ompared the results to similar studies of patient-matched uninvolved skin a
nd peripheral blood.
Results: T cells were polyclonal in all samples tested. Peripheral blood B
cells were also polyclonal; however, a minority of lesional and uninvolved
skin samples exhibited evidence of restricted B-cell clonality. Correlation
with immunohistological analysis revealed that this clonal B-cell restrict
ion was secondary to the sparse nature of lesional B cells rather than thei
r clonal overgrowth.
Conclusions: We conclude that, despite the putative lymphomagenic potential
of HHV-8 and EBV and their co-existence in African KS lesions, tumor-infil
trating lymphocytes in these cases do not show evidence of clonal expansion
that might be an early manifestation of lymphoma. Nevertheless, these stud
ies are a case in point that sparse lymphoid subpopulations in lesional and
uninvolved extranodal tissues can give rise to restricted clonal patterns
that must be interpreted carefully to avoid the misdiagnosis of occult lymp
homa.