Introduction. - Organ transplantation is associated with an increased risk
of neoplasia, which seems to be caused by the total effect of immunosuppres
sion, i.e., the combination of factors involved, rather than by the use of
a specific class of immunosuppressants. The presence and proliferation of v
iral oncogenes is frequently observed during this immunosuppressive state.
The neoplasia in immunosuppressed patients therefore has particular histolo
gical, clinical, evolutive, and therapeutical characteristics.
Current knowledge and key points. - The oncogenic mechanisms in immunosuppr
essed patients have been progressively clarified. A viral infection is asso
ciated with each type of neoplasia: thus, B lymphoma are generally associat
ed with Epstein-Barr viral infection. Skin and uterine cervical carcinomas
frequently appear after viral dysplasia due to papillomavirus. The signific
ant increase in the incidence of Kaposi sarcoma shows the role of the immun
e system in the control of the infection by the human herpes virus 8, which
has been recently discovered. Liver cancer is associated with a history of
hepatitis B or C chronic infection.
Future prospects and projects. - Post-transplantation neoplasia constitutes
a major problem in patient follow-up, as the number of transplant patients
has increased and their survival rare has improved. In addition, there is
an increasingly powerful new generation of immunosuppressive drugs. A preci
se knowledge of the immune system's control mechanisms regarding neoplasic
cells and viral infection is an important step in the prevention and effici
ent treatment of these forms of cancer Further research into the relationsh
ip between the immune system and viral oncogenesis should therefore be cons
idered a major aim. (C) 1999 Editions scientifiques et medicales Elsevier S
AS.