Tumour necrosis factor (TNF) alpha is involved in the pathogenesis of estab
lished lymphoproliferative disease. Serum levels of TNF alpha and its solub
le receptors are above normal Values in B-cell chronic lymphocytic leukaemi
a (B-CLL) and they are valuable prognostic markers in lymphoma patients. Th
e production of TNF alpha is genetically controlled. Altered synthesis of T
NF alpha has been associated with polymorphisms at the TNF gene cluster (i.
e. TNFA, TNFB and LTB). In the present study, we evaluated the prevalence o
f the known high TNF alpha- and TNF beta- producing alleles TNF1, TNF2 of t
he TNFA gene, TNFB1, TNFB2 alleles of the TNFB gene and of the polymorphic
alleles TNFd1. d2, d3, d4 and d5 of the microsatellite TNFd in patients wit
h B-CLL, non-Hodgkin's lymphoma (NHL) and Hodgkin's disease (HD). This stud
y demonstrates that there is no difference in the frequency of the tested T
NF alleles between normal controls and cohorts of patients with lymphoproli
ferative disease. These results indicate that TNF alleles are not genetic p
redisposing factors in the development of these diseases.